Preprint
Review

This version is not peer-reviewed.

Unlocking the Anti-Obesity Potential of the Genus Scutellaria: Pharmacological Insights and Therapeutic Perspectives

Submitted:

09 May 2026

Posted:

09 May 2026

You are already at the latest version

Abstract
Obesity represents a growing global health challenge, driving the need for safer and more effective therapeutic strategies. Natural products, particularly medicinal plants, have gained increasing attention as potential sources of anti-obesity agents due to their diverse bioactive compounds and multi-target mechanisms. The genus Scutellaria (Lamiaceae) is rich in phytochemicals, especially flavonoids such as baicalin, baicalein, and wogonin, which have been reported to modulate key metabolic pathways involved in obesity. This review aims to comprehensively summarize current evidence on selected Scutellaria species with potential anti-obesity activity, focusing on their phytochemical profiles and pharmacological mechanisms. A literature search was conducted using PubMed, Scopus, and Google Scholar databases, and relevant studies were selected based on predefined inclusion criteria. The findings indicate that Scutellaria-derived compounds may exert anti-obesity effects through multiple mechanisms, including inhibition of adipogenesis, regulation of lipid metabolism, improvement of energy homeostasis, and suppression of obesity-associated inflammation. Preclinical studies provide substantial evidence supporting these biological activities; however, clinical validation remains limited. In conclusion, Scutellaria species represent promising candidates for the development of novel anti-obesity therapies. Further studies, particularly well-designed clinical trials, are necessary to confirm their efficacy, safety, and therapeutic applicability in humans.
Keywords: 
;  ;  ;  ;  ;  ;  

1. Introduction

Obesity has become a major global public health concern, with its prevalence increasing markedly across diverse regions. Recent reports highlight a continuous rise in obesity rates, particularly in the Americas and Europe, where the burden remains among the highest worldwide [1]. Projections from the World Obesity Atlas further indicate a substantial increase in the number of individuals affected in the coming decades, underscoring the escalating scale of this health challenge [2]. In addition, obesity is strongly associated with a wide range of comorbidities, including type 2 diabetes, cardiovascular diseases, and metabolic syndrome, thereby emphasizing the urgent need for effective prevention and management strategies [3].
Pharmacological interventions are widely employed in the management of obesity; Nevertheless, currently available therapies present several limitations. Many synthetic anti-obesity agents exhibit variable efficacy and are often associated with adverse effects, particularly involving the gastrointestinal and pancreatic systems [4,5]. Furthermore, high treatment costs and limited accessibility remain significant barriers, especially in low- and middle-income populations [6,7]. These challenges have driven ongoing efforts to identify safer, more effective, and more accessible therapeutic alternatives targeting obesity-related metabolic disturbances.
In this context, phytochemical compounds derived from medicinal plants have attracted considerable attention due to their potential roles in metabolic regulation. Bioactive classes such as flavonoids, polyphenols, and alkaloids have been reported to influence key processes involved in obesity, including adipogenesis, lipid metabolism, and energy homeostasis [8,9,10,11]. Preclinical evidence suggests that these plant-derived compounds may improve metabolic parameters by modulating molecular pathways associated with fat accumulation and energy balance [12,13]. Such findings support the continued exploration of plant-based compounds as promising sources of novel anti-obesity agents.
Among these, the genus Scutellaria (family Lamiaceae) has gained increasing scientific interest due to its rich and diverse phytochemical composition. Notably, flavonoids such as baicalin, baicalein, and wogonin have been widely studied for their biological activities [12,13,14,15]. These compounds have been reported to regulate adipocyte differentiation, modulate lipid metabolism, and attenuate inflammatory processes involved in obesity pathogenesis. Moreover, accumulating evidence indicates that extracts and isolated constituents from Scutellaria species can influence key metabolic pathways related to lipid accumulation and energy regulation [14,16,17].
Therefore, this review aims to comprehensively summarize current studies on selected Scutellaria species and evaluate their potential as anti-obesity agents, with particular emphasis on their bioactive compounds and underlying mechanisms of action in obesity-related metabolic pathways.

2. Methods

A comprehensive literature search was conducted to identify studies investigating the phytochemistry and anti-obesity potential of Scutellaria species. Electronic databases, including PubMed, Scopus, Web of Science, and Google Scholar, were systematically searched for relevant articles published up to 2026. The search strategy employed combinations of keywords such as “Scutellaria”, “skullcap”, “anti-obesity”, “antiobesity”, “adipogenesis”, “lipid metabolism”, “flavonoids”, “baicalin”, “baicalein”, and “wogonin”. Additional records were identified through manual screening of reference lists from relevant articles.
The study selection process was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A total of 2,798 records were initially identified, including 2,687 records from electronic databases and 111 additional records from other sources. After removal of duplicates, 1,351 records remained for title and abstract screening.
During the screening phase, 871 records were excluded based on irrelevance to the topic. The remaining 498 full-text articles were assessed for eligibility. Of these, 334 articles were excluded for the following reasons: lack of relevance to obesity (n = 167), insufficient mechanistic or experimental detail (n = 113), non-English language (n = 17), and duplication or overlap with previously included reviews (n = 37).
Ultimately, 164 studies were included in the qualitative synthesis. Data from the selected studies were extracted and categorized according to Scutellaria species, phytochemical constituents, experimental models, and reported anti-obesity mechanisms. The findings were then synthesized narratively, with emphasis on mechanistic insights and critical evaluation of the available evidence.
Figure 1. PRISMA flow diagram showing the process of literature identification, screening, eligibility assessment, and inclusion. A total of 2,798 records were initially identified, with 1,351 remaining after duplicate removal. Following title and abstract screening, 498 articles were assessed for full-text eligibility, and 164 studies were ultimately included in the qualitative synthesis.
Figure 1. PRISMA flow diagram showing the process of literature identification, screening, eligibility assessment, and inclusion. A total of 2,798 records were initially identified, with 1,351 remaining after duplicate removal. Following title and abstract screening, 498 articles were assessed for full-text eligibility, and 164 studies were ultimately included in the qualitative synthesis.
Preprints 212759 g001

3. The Genus Scutellaria

The figure illustrates the remarkable morphological diversity within the genus Scutellaria, particularly in terms of floral architecture, pigmentation, and inflorescence arrangement. Despite sharing the characteristic bilabiate corolla and the distinctive dorsal appendage (scutellum), individual species exhibit substantial variation in flower size, color spectrum (ranging from white and yellow to deep purple and red), and structural complexity. This diversity reflects the broad ecological adaptability of the genus and its evolutionary radiation across different geographical regions [18,19,20,21,22].
From a taxonomic perspective, floral morphology remains a key diagnostic feature for species identification within Scutellaria. Variations in corolla shape, calyx structure, and reproductive organs contribute to species differentiation, although these traits may sometimes overlap, complicating classification. Recent phylogenomic studies suggest that morphological diversity within the genus is not always congruent with genetic relationships, indicating potential convergent evolution driven by environmental and pollination pressures [23,24].
Figure 2. Morphological and geographic diversity of genus Scutellaria. (A) Floral diversity of 24 representative species showing variation in color and inflorescence architecture. (B) Diagnostic floral and vegetative characters typical of Scutellaria. (C) Global distribution pattern of the genus, with the highest species richness in East Asia. Species list: (1) S. baicalensis, (2) S. barbata, (3) S. lateriflora, (4) S. galericulata, (5) S. miqueliana, (6) S. indica, (7) S. discolor, (8) S. orientalis, (9) S. tsinyuensis, (10) S. rubescens, (11) S. przewalskii, (12) S. amoena, (13) S. saxatilis, (14) S. setifera, (15) S. rivularis, (16) S. atropurpurea, (17) S.wrightii, (18) S. altissima, (19) S. brevicalyx, (20) S. umbrosa, (21) S. yunnanensis, (22) S. chinensis, (23) S. nelsonii, (24) S. Strigillosa.
Figure 2. Morphological and geographic diversity of genus Scutellaria. (A) Floral diversity of 24 representative species showing variation in color and inflorescence architecture. (B) Diagnostic floral and vegetative characters typical of Scutellaria. (C) Global distribution pattern of the genus, with the highest species richness in East Asia. Species list: (1) S. baicalensis, (2) S. barbata, (3) S. lateriflora, (4) S. galericulata, (5) S. miqueliana, (6) S. indica, (7) S. discolor, (8) S. orientalis, (9) S. tsinyuensis, (10) S. rubescens, (11) S. przewalskii, (12) S. amoena, (13) S. saxatilis, (14) S. setifera, (15) S. rivularis, (16) S. atropurpurea, (17) S.wrightii, (18) S. altissima, (19) S. brevicalyx, (20) S. umbrosa, (21) S. yunnanensis, (22) S. chinensis, (23) S. nelsonii, (24) S. Strigillosa.
Preprints 212759 g002
In the Indonesia endemic Scutellaria slametensis, differences in flower were observed between individuals from Cibodas Botanical Garden and Baturraden Botanical Garden. This variation may be related to environmental factors such as altitude, temperature, and light, as well as pollination pressure.
Notably, morphological variation may also have implications for phytochemical diversity. Differences in plant organs, particularly between aerial parts and roots, have been associated with distinct profiles of secondary metabolites, including flavonoids, terpenoids, and phenolic compounds. As these metabolites underpin the pharmacological activities of Scutellaria species, including their proposed anti-obesity effects, morphological diversity may indirectly reflect biochemical and functional heterogeneity within the genus [25].
However, current research rarely integrates morphological, phytochemical, and pharmacological data in a systematic manner. Most studies focus on a limited number of species, particularly S. baicalensis, without considering broader interspecies variation. This represents a critical gap, as comparative analyses across morphologically distinct species could provide valuable insights into structure–activity relationships and aid in the identification of novel bioactive compounds.
Overall, the diversity depicted in this figure underscores the complexity of the genus Scutellaria and highlights the need for integrative approaches that combine taxonomy, phytochemistry, and pharmacology to fully elucidate its therapeutic potential.
Figure 3. Variation in flower coloration of Scutellaria slametensis. (D1) Plant growing in its natural habitat on Mt. Slamet (in situ). (D2) Specimens collected from Cibodas Botanical Garden showing predominantly purplish flowers. (D3) Specimen from Baturraden Botanical Garden (ex situ collection) showing pinkish flowers.
Figure 3. Variation in flower coloration of Scutellaria slametensis. (D1) Plant growing in its natural habitat on Mt. Slamet (in situ). (D2) Specimens collected from Cibodas Botanical Garden showing predominantly purplish flowers. (D3) Specimen from Baturraden Botanical Garden (ex situ collection) showing pinkish flowers.
Preprints 212759 g003

4. Phytochemical Constituents of Selected Scutellaria Species

Species within the genus Scutellaria exhibit considerable chemical heterogeneity, reflecting variations in geographic distribution, plant part, and extraction methodologies [26,27,28]. Among the identified metabolites, flavonoids constitute the dominant class, accompanied by phenolic acids, terpenoids, iridoids, and other secondary metabolites. These compounds collectively contribute to the diverse biological activities attributed to the genus.
Despite this, despite extensive phytochemical characterization, the available data remain unevenly distributed across species, with a disproportionate focus on a limited number of well-studied taxa, particularly S. baicalensis. In addition, inconsistencies in analytical approaches and reporting standards complicate direct comparison between studies.
The phytochemical diversity of the genus Scutellaria is extensive and encompasses numerous species with distinct metabolite profiles. To improve clarity and emphasize the most pharmacologically relevant taxa, Table 1 summarizes representative Scutellaria species frequently investigated for their bioactive constituents and metabolic regulatory potential. A comprehensive phytochemical inventory of additional Scutellaria species is provided in Supplementary Table S1.
Although Scutellaria species contain a broad range of phytochemicals, current anti-obesity evidence is concentrated primarily on flavonoids from S. baicalensis, particularly baicalin, baicalein, and wogonin. These compounds appear to act through multi-target mechanisms, including suppression of adipogenesis, activation of AMPK-mediated lipid catabolism, inhibition of inflammatory signaling, and improvement of insulin sensitivity. Despite this most findings remain preclinical, and differences in experimental models, extract standardization, dose selection, and compound bioavailability limit direct translational interpretation.
As summarized in Table 2, AMPK activation appears to be one of the most consistently reported mechanism and the major proposed anti-obesity mechanisms of Scutellaria-derived compounds and highlights the current evidentiary limitations. Table 2 also highlights the predominance of cellular and animal models in anti-obesity research.

5. Results and Discussion

The included studies were analyzed and synthesized based on phytochemical composition and underlying anti-obesity mechanisms, as summarized below.

5.1. Phytochemical Drivers of Anti-Obesity Activity

The anti-obesity potential of Scutellaria species is largely attributed to their rich flavonoid content, particularly baicalin, baicalein, and wogonin, which have been consistently identified across multiple species. These compounds represent structurally related flavones that exhibit broad biological activities, including modulation of metabolic and inflammatory pathways relevant to obesity. In addition to flavonoids, other classes such as phenolic acids, terpenoids, and iridoids may contribute synergistically; Conversely, their roles remain comparatively underexplored.
A notable limitation across the literature is the predominant focus on a small subset of compounds, particularly those derived from S. baicalensis, while many other species remain chemically characterized but pharmacologically underinvestigated. This imbalance restricts the ability to generalize findings across the genus and suggests that the therapeutic potential of less-studied Scutellaria species may be underestimated.

5.2. Modulation of Adipogenesis and Lipid Metabolism

A central mechanism underlying the anti-obesity effects of Scutellaria-derived compounds is the regulation of adipogenesis. Several studies report that baicalin, baicalein, and related flavonoids inhibit adipocyte differentiation through downregulation of key transcription factors, including peroxisome proliferator-activated receptor gamma (PPARγ) and CCAAT/enhancer-binding proteins (C/EBPs). These transcription factors play critical roles in adipocyte maturation and lipid accumulation, and their suppression is associated with reduced adipogenesis in in vitro models.
In parallel, these compounds have been shown to influence lipid metabolism by activating AMP-activated protein kinase (AMPK), a central regulator of cellular energy homeostasis. Activation of AMPK promotes fatty acid oxidation while inhibiting lipogenesis, thereby contributing to reduced lipid accumulation in adipose and hepatic tissues. While these findings are mechanistically consistent, they are largely derived from controlled experimental systems, and their physiological relevance in humans remains to be fully established.

5.3. Anti-Inflammatory and Metabolic Regulatory Effects

Chronic low-grade inflammation is a hallmark of obesity and contributes significantly to metabolic dysfunction. Scutellaria-derived flavonoids, particularly wogonin and baicalein, have demonstrated anti-inflammatory properties through the suppression of pro-inflammatory cytokines and signaling pathways, including NF-κB. These effects may indirectly improve insulin sensitivity and metabolic homeostasis.
Despite this, the distinction between primary anti-obesity effects and secondary anti-inflammatory benefits is often unclear. Many studies do not differentiate whether observed metabolic improvements result from direct modulation of adipose tissue biology or from broader systemic anti-inflammatory effects. This ambiguity highlights the need for more targeted mechanistic studies to clarify causality.

5.4. Energy Homeostasis and Thermogenic Regulation

Emerging evidence suggests that certain Scutellaria extracts may influence energy expenditure by promoting thermogenesis and adipose tissue browning, potentially via AMPK-related pathways. Such effects represent a promising mechanism, as they address energy imbalance rather than solely inhibiting fat accumulation. Nonetheless, these findings are relatively limited and often involve combination extracts or multi-component formulations, making it difficult to attribute specific effects to individual Scutellaria-derived compounds.

5.5. Clinical Perspective

Despite substantial preclinical evidence, clinical evaluation of Scutellaria-derived compounds in obesity remains extremely limited. Current human studies primarily focus on the anti-inflammatory, hepatoprotective, or metabolic effects of Scutellaria baicalensis formulations rather than obesity-specific endpoints. Moreover, issues related to compound bioavailability, pharmacokinetic variability, and extract standardization continue to complicate clinical translation. Consequently, the therapeutic relevance of Scutellaria in obesity management remains largely unvalidated in human populations.

6. Translational Limitations and Research Gaps

Despite promising preclinical findings, several critical limitations hinder the translation of Scutellaria research into clinical application. First, the majority of studies are restricted to in vitro systems or animal models, with a notable lack of well-designed human trials. Second, variability in extraction methods, compound purity, and dosing regimens reduces reproducibility and comparability across studies. Third, issues related to bioavailability and pharmacokinetics of key flavonoids, such as baicalin and chrysin, remain insufficiently addressed, raising concerns about their in vivo efficacy.
Additionally, the frequent use of multi-component extracts complicates the identification of active constituents and their precise mechanisms of action. While synergistic effects are often proposed, they are rarely systematically evaluated. This gap underscores the importance of integrating phytochemical standardization with mechanistic and clinical research.

7. Implications for Future Research

To advance the therapeutic potential of Scutellaria species, future studies should prioritize standardized extraction protocols, comparative analyses across species, and detailed pharmacokinetic profiling of key compounds. Furthermore, well-designed clinical trials are essential to validate preclinical findings and assess safety, efficacy, and optimal dosing strategies. Expanding research beyond S. baicalensis to include underexplored species may also uncover novel bioactive compounds with distinct or complementary mechanisms of action.

8. Synthesis

Collectively, current evidence suggests that Scutellaria-derived compounds exert anti-obesity effects through multi-target mechanisms, including inhibition of adipogenesis, modulation of lipid metabolism, suppression of inflammation, and potential regulation of energy expenditure. Nevertheless, the predominance of preclinical data, coupled with methodological inconsistencies and limited clinical validation, underscores the need for a more rigorous and integrative research approach. Addressing these challenges will be essential to fully elucidate the role of Scutellaria as a viable source of anti-obesity therapeutics.
Figure 4. Graphical conclusion and Future perspectives.
Figure 4. Graphical conclusion and Future perspectives.
Preprints 212759 g004

9. Conclusion

The genus Scutellaria represents a promising yet underutilized source of bioactive compounds with potential applications in obesity management. Accumulating evidence indicates that Scutellaria-derived flavonoids, particularly baicalin, baicalein, and wogonin, exert multi-target effects on key pathways involved in obesity pathogenesis, including the regulation of adipogenesis, lipid metabolism, inflammation, and energy homeostasis. These findings support the concept that plant-derived compounds may offer a complementary or alternative approach to conventional anti-obesity therapies.
However, despite encouraging preclinical data, the current body of evidence remains limited by several critical challenges. Research efforts are disproportionately focused on a small number of species, primarily Scutellaria baicalensis, while the pharmacological potential of many other species within the genus remains largely unexplored. In addition, methodological inconsistencies, including variability in extraction procedures, compound standardization, and experimental models, hinder cross-study comparability and reproducibility. Critically, the lack of well-designed clinical studies represents a major barrier to translating preclinical findings into therapeutic applications.
Future research should prioritize systematic phytochemical profiling across a broader range of Scutellaria species, alongside standardized experimental frameworks to enable more robust comparisons. Elucidation of pharmacokinetic properties, bioavailability, and safety profiles of key compounds is essential to bridge the gap between experimental efficacy and clinical applicability. Moreover, integrative approaches combining phytochemistry, molecular pharmacology, and clinical investigation will be critical for identifying lead compounds and validating their therapeutic potential.
In conclusion, while Scutellaria species exhibit considerable promise as sources of anti-obesity agents, their translation into clinically relevant therapies requires a more rigorous, standardized, and multidisciplinary research strategy. Addressing these challenges will be essential to fully realize the therapeutic value of this chemically and biologically diverse genus.

Author Contributions

All the authors contributed equally to preparing and executing the idea for the article, design of the review, English language editing and formatting the article.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Boutari, C.; Mantzoros, C.S. A 2022 update on the epidemiology of obesity and a call to action: as its twin COVID-19 pandemic appears to be receding, the obesity and dysmetabolism pandemic continues to rage on. Metabolism;PubMed 2022, 133, 155217. [Google Scholar] [CrossRef] [PubMed]
  2. Powis, J.; Thompson, R.; Jackson-Leach, R. World Obesity Atlas 2025 [Internet]. 2025, 1. Available online: www.worldobesity.org.
  3. Chong, B.; Jayabaskaran, J.; Kong, G.; Chan, Y.H.; Chin, Y.H.; Goh, R.; et al. Trends and predictions of malnutrition and obesity in 204 countries and territories: an analysis of the Global Burden of Disease Study 2019. EClinicalMedicine;PubMed 2023, 57. [Google Scholar] [CrossRef] [PubMed]
  4. Wilding, J.P.H.; Batterham, R.L.; Calanna, S.; Davies, M.; Van Gaal, L.F.; Lingvay, I.; et al. Once-Weekly Semaglutide in Adults with Overweight or Obesity. N. Engl. J. Med.;PDF PubMed 2021, 384(11), 989–1002. [Google Scholar] [CrossRef] [PubMed]
  5. Jastreboff, A.M.; Aronne, L.J.; Ahmad, N.N.; Wharton, S.; Connery, L.; Alves, B.; et al. Tirzepatide Once Weekly for the Treatment of Obesity. N. Engl. J. Med.;PDF PubMed 2022, 387(3), 205–16. [Google Scholar] [CrossRef] [PubMed]
  6. Gómez Lumbreras, A.; Tan, M.S.; Villa-Zapata, L.; Ilham, S.; Earl, J.C.; Malone, D.C. Cost-effectiveness analysis of five anti-obesity medications from a US payer’s perspective. Nutr. Metab. Cardiovasc Dis. 2023, 33(6), 1268–76. [Google Scholar] [CrossRef] [PubMed]
  7. Alsuhibani, A.A.; Alrasheed, M.A.; Alhomoud, I.S.; Alsahali, S.; Almalki, Z.S.; Guo, J.J. Spending, utilization, and price trends for anti-obesity medications in U.S. Medicaid programs: an empirical analysis from 1999 to 2023. Front Med. 2025, 12, 1537181. [Google Scholar] [CrossRef]
  8. Varshney, S.; Kumar, D.; Choudhary, R.; Gupta, A.; Beg, M.; Shankar, K.; et al. Flavopiridol inhibits adipogenesis and improves metabolic homeostasis by ameliorating adipose tissue inflammation in a diet-induced obesity model. Biomed. Pharmacother.;PubMed 2024, 179, 117330. [Google Scholar] [CrossRef] [PubMed]
  9. Kim, J.H.; Lee, S.; Cho, E.J. Flavonoids from Acer okamotoanum Inhibit Adipocyte Differentiation and Promote Lipolysis in the 3T3-L1 Cells. Mol. 2020, Vol. 25, Page 1920 PubMed. 2020, 25(8), 1920. [Google Scholar] [CrossRef] [PubMed]
  10. Casado-díaz, A.; Rodríguez-ramos, Á.; Torrecillas-baena, B.; Dorado, G.; Quesada-gómez, J.M.; Gálvez-moreno, M.Á. Flavonoid Phloretin Inhibits Adipogenesis and Increases OPG Expression in Adipocytes Derived from Human Bone-Marrow Mesenchymal Stromal-Cells. Nutrients PubMed. 2021, 13(11). [Google Scholar] [CrossRef] [PubMed]
  11. Sung, Y.Y.; Son, E.; Im, G.; Kim, D.S. Herbal Combination of Phyllostachys pubescens and Scutellaria baicalensis Inhibits Adipogenesis and Promotes Browning via AMPK Activation in 3T3-L1 Adipocytes. Plants PubMed. 2020, 9(11), 1422. [Google Scholar] [CrossRef] [PubMed]
  12. Lin, Y.; Ren, N.; Li, S.; Chen, M.; Pu, P. Novel anti-obesity effect of scutellarein and potential underlying mechanism of actions. Biomed. Pharmacother.;PubMed 2019, 117, 109042. [Google Scholar] [CrossRef] [PubMed]
  13. Li, H.; Tang, S. Baicalin attenuates diet-induced obesity partially through promoting thermogenesis in adipose tissue. Obes. Res. Clin. Pract.;PubMed 2021, 15(5), 485–90. [Google Scholar] [CrossRef] [PubMed]
  14. Li, H.; Tang, S. Baicalin attenuates diet-induced obesity partially through promoting thermogenesis in adipose tissue. Obes. Res. Clin. Pract.;PubMed 2021, 15(5), 485–90. [Google Scholar] [CrossRef] [PubMed]
  15. Baygildieva, D.I.; Baygildiev, T.M.; Stavrianidi, A.N.; Shpigun, O.A.; Rodin, I.A. Simultaneous Determination of Wogonin, Scutellarin, Baicalin, and Baicalein in Extracts from Scutellariae Baicalensis by High-Performance Liquid Chromatography with Tandem Mass Spectrometry. J. Anal. Chem. 2018, 73(14), 1317–22. [Google Scholar] [CrossRef]
  16. Le, Yang L; Xiao, N.; Liu, J.; Liu, K.; Liu, B.; Li, P.; et al. Differential regulation of baicalin and scutellarin on AMPK and Akt in promoting adipose cell glucose disposal. Biochim Biophys. Acta Mol. Basis Dis. 2017, 1863(2), 598–606. [Google Scholar] [CrossRef] [PubMed]
  17. Zhang, Z.; Wang, R.; Cai, J.; Li, X.; Feng, X.; Xu, S.; et al. Baicalin alleviates lipid accumulation in adipocytes via inducing metabolic reprogramming and targeting Adenosine A1 receptor. Toxicon 2025, 258, 108339. [Google Scholar] [CrossRef] [PubMed]
  18. Wang, D.; Wang, J.; Wang, Y.; Yao, D.; Niu, Y. Metabolomic and Transcriptomic Profiling Uncover the Underlying Mechanism of Color Differentiation in Scutellaria baicalensis Georgi. Flowers. Front Plant Sci. 2022, 13, 884957. [Google Scholar] [CrossRef]
  19. Guo, F.; Guan, R.; Sun, X.; Zhang, C.; Shan, C.; Liu, M.; et al. Integrated metabolome and transcriptome analyses of anthocyanin biosynthesis reveal key candidate genes involved in colour variation of Scutellaria baicalensis flowers. BMC Plant Biol. 2023, 23(1), 643. [Google Scholar] [CrossRef] [PubMed]
  20. Costine, B.; Zhang, M.; Chhajed, S.; Pearson, B.; Chen, S.; Nadakuduti, S.S. Exploring native Scutellaria species provides insight into differential accumulation of flavones with medicinal properties. Sci. Rep.;PubMed 2022, 2022 12:1 12(1), 13201. [Google Scholar] [CrossRef] [PubMed]
  21. Wang, Y.; Xu, C.; Guo, X.; Wang, Y.; Chen, Y.; Shen, J.; et al. Phylogenomics analysis of Scutellaria (Lamiaceae) of the world. BMC Biol.;PubMed 2024, 22(1), 185. [Google Scholar] [CrossRef] [PubMed]
  22. Cheryomushkina, V.; Guseva, А.; Talovskaya, E.; Аstashenkov, А. Dwarf subshrub morphological structure variety in species of the genus Scutellaria (Lamiaceae) under different growing conditions. Taiwania 2022, 67(1), 146–54. [Google Scholar] [CrossRef]
  23. Guo, F.; Guan, R.; Sun, X.; Zhang, C.; Shan, C.; Liu, M.; et al. Integrated metabolome and transcriptome analyses of anthocyanin biosynthesis reveal key candidate genes involved in colour variation of Scutellaria baicalensis flowers. BMC Plant Biol.;PubMed 2023, 23(1). [Google Scholar] [CrossRef] [PubMed]
  24. Cha, Y.P.; Zhang, J.; Ma, Y.M.; Tong, Z.L.; Wu, Y.; Luo, L.; et al. Variations in pollinator-mediated selection of floral traits across flowering times. J. Plant Ecol. 2023, 16(6). [Google Scholar] [CrossRef]
  25. Huang, B.H.; Chen, Y.W.; Huang, C.L.; Gao, J.; Liao, P.C. Diversifying selection of the anthocyanin biosynthetic downstream gene UFGT accelerates floral diversity of island Scutellaria species. BMC Evol. Biol. 2016, 16(1), 191. [Google Scholar] [CrossRef] [PubMed]
  26. Costine, B.; Zhang, M.; Chhajed, S.; Pearson, B.; Chen, S.; Nadakuduti, S.S. Exploring native Scutellaria species provides insight into differential accumulation of flavones with medicinal properties. Sci. Rep. 2022, 12(1). [Google Scholar] [CrossRef] [PubMed]
  27. Lim, J.; Kim, K.; Kwon, D.Y.; Kim, J.K.; Sathasivam, R.; Park, S.U. Effects of Different Solvents on the Extraction of Phenolic and Flavonoid Compounds, and Antioxidant Activities, in Scutellaria baicalensis Hairy Roots. Horticulturae 2024, 10(2), 160. [Google Scholar] [CrossRef]
  28. Wala, M.; Wróblewska, K.; Janda-Milczarek, A.; Ecioł, M.; Wala, K.; Wróblewska, A.; et al. The Effect of the Extraction Conditions on the Antioxidant Activity and Bioactive Compounds Content in Ethanolic Extracts of Scutellaria baicalensis Root. Molecules 2024, Vol 29, Page 4153. PubMed 2024, 29(17), 4153. [Google Scholar] [CrossRef] [PubMed]
  29. Zhou, P.; Zuo, L.; Liu, C.; Xiong, B.; Li, Z.; Zhou, X.; et al. Unraveling spatial metabolome of the aerial and underground parts of Scutellaria baicalensis by matrix-assisted laser desorption/ionization mass spectrometry imaging. Phytomedicine;PubMed 2024, 123, 155259. [Google Scholar] [CrossRef] [PubMed]
  30. Lawson, S.K.; Satyal, P.; Setzer, W.N. Phytochemical Analysis of the Essential Oils From Aerial Parts of Four Scutellaria “Skullcap” Species Cultivated in South Alabama: Scutellaria baicalensis Georgi, S.; Barbata, D.; Don, S. Incana Biehler, and S. In Nat Prod Commun; Lateriflora, L., Ed.; 2021; 8, p. 16. [Google Scholar] [CrossRef]
  31. Sun, C.; Xiao, M.; Cui, B.; Mu, L.; Zhang, S.; Zhang, X.; et al. Identification of flavonoid isomers in Scutellaria baicalensis using QSRR modeling. J. Chromatogr. B Anal. Technol. BioMed Life Sci.;PubMed 2025, 1254. [Google Scholar] [CrossRef] [PubMed]
  32. Takeoka, G.R.; Rodriguez, D.M.; Dao, L.; Patterson, R. Headspace Volatiles of Scutellaria baicalensis Georgi Flowers. J. Essent. Oil Bear. Plants 2009, 12(4), 435–42. [Google Scholar] [CrossRef]
  33. Askey, B.C.; Liu, D.; Rubin, G.M.; Kunik, A.R.; Song, Y.H.; Ding, Y.; et al. Metabolite profiling reveals organ-specific flavone accumulation in Scutellaria and identifies a scutellarin isomer isoscutellarein 8-O-β-glucuronopyranoside. Plant Direct 2021, 5(12), e372. [Google Scholar] [CrossRef]
  34. Zheng, M.; Fang, Y.; Zhao, Q.; Zheng, M.; Fang, Y.; Zhao, Q. Comparative analysis of flavones from six commonly used Scutellaria species. Med. Plant Biol. 2023, 2023 1 2(1), 12. [Google Scholar] [CrossRef]
  35. Cheng, Y.; Cao, W.; Guo, R.; Chen, R.; Li, X.; Qian, D.; et al. A comparative study of the quality differences and seasonal dynamics of flavonoids between the aerial parts and roots of Scutellaria barbata. Front Plant Sci. 2024, 15, 1497664. [Google Scholar] [CrossRef] [PubMed]
  36. Li, H.Y.; Wei, W.J.; Ma, K.L.; Zhang, J.Y.; Li, Y.; Gao, K. Phytotoxic neo-clerodane diterpenoids from the aerial parts of Scutellaria barbata. Phytochemistry;PubMed 2020, 171, 112230. [Google Scholar] [CrossRef] [PubMed]
  37. Kawka, B.; Kwiecień, I.; Ekiert, H. Endogenous production of specific flavonoids and verbascoside in agar and agitated microshoot cultures of Scutellaria lateriflora L. and biotransformation potential. Plant Cell Tissue Organ Cult. 2020, 142(3), 471–82. [Google Scholar] [CrossRef]
  38. Wilczańska, A.; Sparzak-Stefanowska, B.; Kokotkiewicz, A.; Jesionek, A.; Królicka, A.; Łuczkiewicz, M.; et al. Biotechnological strategies for controlled accumulation of flavones in hairy root culture of Scutellaria lateriflora L. Scientific Reports 2023 13:1. PubMed 2023, 13(1), 20422. [Google Scholar] [CrossRef] [PubMed]
  39. Li, J.; Wang, Y.H.; Smillie, T.J.; Khan, I.A. Identification of phenolic compounds from Scutellaria lateriflora by liquid chromatography with ultraviolet photodiode array and electrospray ionization tandem mass spectrometry. J. Pharm. BioMed Anal. 2012, 63, 120–7. [Google Scholar] [CrossRef] [PubMed]
  40. Stepanova, A.Y.; Solov’eva, A.I.; Malunova, M.V.; Salamaikina, S.A.; Panov, Y.M.; Lelishentsev, A.A. Hairy Roots of Scutellaria spp. (Lamiaceae) as Promising Producers of Antiviral Flavones. Mol. 2021, Vol. 26, Page 3927;PubMed 2021, 26(13), 3927. [Google Scholar] [CrossRef] [PubMed]
  41. Karimov, A.; Botirov, E.K. Flavonoids from the Aerial Part and Roots of Scutellaria adenostegia. Chem. Nat. Compd. 2015, 51(4), 764–5. [Google Scholar] [CrossRef]
  42. Musakhonovich, K.A.; Mamadievich, B.K.; Vladimirovna, O.Y.; Khozhiakbarovich, B.E.; Akparalievich, M.A.; Jalilovich, A.N. ESSENTIAL OIL COMPOSITION OF TWO SPECIES OF SCUTELLARIA AERIAL PARTS. Химия Растительнoгo Сырья 2021, (4), 139–44. [Google Scholar] [CrossRef]
  43. Chemesova, I.I.; Budantsev, A.L. F L A V O N O I D F R O M ScuteUaria adsurgens. Chem. Nat. Compd. 1994, 30(2). [Google Scholar]
  44. Matsa, M.; Bardakci, H.; Gousiadou, C.; Kirmizibekmez, H.; Skaltsa, H. Secondary metabolites from Scutellaria albida L. ssp. velenovskyi (Rech. f.) Greuter & Burdet. Biochem Syst. Ecol. 2019, 83, 71–6. [Google Scholar] [CrossRef]
  45. Gousiadou, C.; Karioti, A.; Heilmann, J.; Skaltsa, H. Iridoids from Scutellaria albida ssp. albida. Phytochemistry 2007, 68(13), 1799–804. [Google Scholar] [CrossRef] [PubMed]
  46. Cicek, M.; Demirci, B.; Yilmaz, G.; Ketenoglu, O.; Baser, K.H.C. Composition of the essential oils of subspecies of scutellaria albida L. from Turkey. J. Essent. Oil Res. 2010, 22(1), 55–8. [Google Scholar] [CrossRef]
  47. Grzegorczyk-Karolak, I.; Kuźma, Ł.; Wysokińska, H. In vitro cultures of Scutellaria alpina as a source of pharmacologically active metabolites. Acta Physiol. Plant 2016, 38(1), 1–9. [Google Scholar] [CrossRef]
  48. Grzegorczyk-Karolak, I.; Kuźma, Ł.; Wysokińska, H. In vitro cultures of Scutellaria alpina as a source of pharmacologically active metabolites. Acta Physiol. Plant 2016, 38(1), 1–9. [Google Scholar] [CrossRef]
  49. Badalamenti, N.; Porrello, A.; Ilardi, V.; Bruno, M. The essential oil chemical composition of aerial parts of a new chemotype of Scutellaria altissima growing wild in North Macedonia. Nat. Prod. Res. 2025. [Google Scholar] [CrossRef] [PubMed]
  50. Grzegorczyk-Karolak, I.; Kuźma, Ł.; Wysokińska, H. Study on the chemical composition and antioxidant activity of extracts from shoot culture and regenerated plants of Scutellaria altissima L. Acta Physiol. Plant 2015, 37(1), 1736. [Google Scholar] [CrossRef]
  51. (PDF) HPLC analysis of flavonoids from Scutellaria altissima [Internet]. 2 May 2026. Available online: https://www.researchgate.net/publication/335034334_HPLC_analysis_of_flavonoids_from_Scutellaria_altissima.
  52. Miyaichi, Y.; Hanamitsu, E.; Kizu, H.; Tomimori, T. Studies on the Constituents of Scutellaria Species (XXII). Constituents of the Roots of Scutellaria amabilis HARA. Chem. Pharm. Bull. 2006, 54(4), 435–41. [Google Scholar] [CrossRef] [PubMed]
  53. Fang, Q.L.; Qiao, X.; qing, Yin X; cheng, Zeng Y; hong, Du C; mei, Xue Y; et al. Flavonoids from Scutellaria amoena C. H. Wright alleviate mitochondrial dysfunction and regulate oxidative stress via Keap1/Nrf2/HO-1 axis in rats with high-fat diet-induced nonalcoholic steatohepatitis. Biomed. Pharmacother. PubMed. 2023, 158, 114160. [Google Scholar] [CrossRef] [PubMed]
  54. Shock, C.C.; Poudel, A.; Satyal, P.; Setzer, W.N. Chemical Compositions of Scutellaria Essential Oils Cultivated in Eastern Oregon: S. angustifolia, S. baicalensis, S. barbata, and S. lateriflora. Plants 2026, 15(7), 1075. [Google Scholar] [CrossRef] [PubMed]
  55. Gharari, Z.; Bagheri, K.; Derakhshani, B.; Sharafi, A. HPLC-DAD-ESI/MSn analysis of phenolic components of Scutellaria araxensis, S. bornmuelleri and S. orientalis doi:10.1080/14786419.2020.1837810/ASSET/E6EFF6DF-0024-4661-BFF8-AB7963A1A901/ASSETS/IMAGES/GNPL_A_1837810_UF0001_C.JPG. Nat. Prod. Res.;PubMed 2022, 36(9), 2440–5. [Google Scholar] [CrossRef] [PubMed]
  56. Gharari, Z.; Bagheri, K.; Danafar, H.; Sharafi, A. Chemical Composition and Antimicrobial Activity of Scutellaria araxensis Essential Oil from Iran. Chem. Nat. Compd. 2020, 56(4), 745–7. [Google Scholar] [CrossRef]
  57. Gharari, Z.; Bagheri, K.; Sharafi, A. Fractional analysis of dichloromethane extract of Scutellaria araxensis Grossh root and shoot by HPLC-PDA-ESI-MSn. Nat. Prod. Res. PubMed. 2022, 36(15), 4031–5. [Google Scholar] [CrossRef] [PubMed]
  58. Costine, B.; Zhang, M.; Chhajed, S.; Pearson, B.; Chen, S.; Nadakuduti, S.S. Exploring native Scutellaria species provides insight into differential accumulation of flavones with medicinal properties. Sci. Rep. PubMed. 2022, 12(1). [Google Scholar] [CrossRef] [PubMed]
  59. Yılmaz, G.; Çiçek, M.; Demirci, B.; Başer, K.H.C. Essential oil compositions of subspecies of Scutellaria brevibracteata Stapf from Turkey. J. Essent. Oil Res. 2019, 31(4), 255–62. [Google Scholar] [CrossRef]
  60. Dogan, Z.; Telli, G.; Cahide Tel, B.; Saracoglu, I. Scutellaria brevibracteata Stapf and active principles with anti-inflammatory effects through regulation of NF-κB/COX-2/iNOS pathways [Internet]. 2022. [Google Scholar] [CrossRef]
  61. Gharari, Z.; Bagheri, K.; Danafar, H.; Sharafi, A. Enhanced flavonoid production in hairy root cultures of Scutellaria bornmuelleri by elicitor induced over-expression of MYB7 and FNSП2 genes. Plant Physiol. Biochem.;PubMed 2020, 148, 35–44. [Google Scholar] [CrossRef] [PubMed]
  62. Gharari, Z.; Shabani, H.; Bagheri, K.; Sharafi, A. Phytochemical composition profile of Scutellaria bornmuelleri methanolic extract using GC-MS analysiss. Future Nat. Prod. 2022, 8(1), 7–14. [Google Scholar] [CrossRef]
  63. Takeoka, G.R.; Dao, L.; Rodriguez, D.M.; Patterson, R. Headspace volatiles of scutellaria californica a. Gray flowers. J. Essent. Oil Res. 2008, 20(2), 169–71. [Google Scholar] [CrossRef]
  64. Giuliani, C.; Bottoni, M.; Ascrizzi, R.; Milani, F.; Flamini, G.; Fico, G. Scutellaria caucasica A. Ham.: Morphological features and headspace characterization. Flora Morphol. Distrib. Funct. Ecol. Plants 2020, 269. [Google Scholar] [CrossRef]
  65. Stojakowska, A.; Kisiel, W. Secondary metabolites from a callus culture of Scutellaria columnae. Fitoterapia 1999, 70(3), 324–5. [Google Scholar] [CrossRef]
  66. Siddikov, G.U.; Yuldashev, M.P.; Batirov, E.K.; Abdullaev, S. V. Flavonoids from Scutellaria cordifrons and S. phyllostachya roots. Chem. Nat. Compd. 2006, 42(3), 356–7. [Google Scholar] [CrossRef]
  67. Turginov, O.T.; Akbarova, M.H.; Turginov, O.T.; Akbarova, M.H. Distribution of the Species Genus Scutellaria, L. (Lamiaceae) Flora of the Ferghana Valley. Am. J. Plant Sci. 2020, 11(10), 1533–44. [Google Scholar] [CrossRef]
  68. Bruno, M.; Fazio, C.; Arnold, N.A. Neo-clerodane diterpenoids from Scutellaria cypria. Phytochemistry 1996, 42(2), 555–7. [Google Scholar] [CrossRef]
  69. Dehkordi, F.J.; Kharazian, N.; Lorigooini, Z. Characterization of flavonoid components in scutellaria L. Species (Lamiaceae) using fingerprinting analysis. Acta Biol. Crac. Ser. Bot. 2020, 62(1), 79–96. [Google Scholar] [CrossRef]
  70. Ismail Ahmadi, F.; Fathollahi, R.; Dastan, D. Phytochemical Constituents and Biological Properties of Scutellaria Condensata Subsp. Pycnotricha. J. Appl. Organomet. Chem. 2022, 2(3), 119–28. [Google Scholar] [CrossRef]
  71. Sarikurkcu, C.; Sihoglu, A.; Kirkan, B. LC-ESI-MS/MS-based phytochemical characterization and antioxidant – enzyme inhibitory correlation in Scutellaria diffusa. Spectrosc. Lett. 2026. [Google Scholar] [CrossRef]
  72. Cicek, M.; Demirci, B.; Yilmaz, G.; Baser, K.H.C. Essential oil composition of three species of Scutellaria from Turkey. Nat. Prod. Res. 2011, 25(18), 1720–6. [Google Scholar] [CrossRef] [PubMed]
  73. Tomimori, T.; Miyaichi, Y.; Yashitaicaimoto, Y.I.; Kizu, H.; Namba, T. Studies on the Nepalese Crude Drugs. XI.: On the Flavonoid Constituents of the Aerial Parts of Scutellaria discolor COLEBR. Chem. Pharm. Bull. 1988, 36(9), 3654–8. [Google Scholar] [CrossRef]
  74. Shah, M.; Murad, W.; Rehman, N.U.; Halim, S.A.; Ahmed, M.; Rehman, H.; et al. Biomedical Applications of Scutellaria edelbergii Rech. f.: In Vitro and In Vivo Approach. Molecules;PubMed 2021, 26(12), 3740. [Google Scholar] [CrossRef] [PubMed]
  75. Xiao, K.; Han, Q.T.; Zhang, L.; Dai, S.J. Two new flavanone glycosides from Scutellaria galericulata with anti-inflammatory activities. Phytochem Lett. 2017, 20, 151–4. [Google Scholar] [CrossRef]
  76. Zhang, D.W.; Wang, Y.; Liu, J.H.; Yue, X.D.; Dai, S.J. neo-Clerodane diterpenoids from Scutellaria galericulata and their anti-inflammatory activities. Phytochem Lett. 2026, 73, 104170. [Google Scholar] [CrossRef]
  77. Marrero Delange, D.; Morales Rico, C.L.; Canavaciolo, V.G.; Rodríguez Leyes, E.A.; Pérez, R.S. Volatile Constituents from Leaves of Endemic Scutellaria havanensis Jacq. in Cuba. J. Essent. Oil-Bear. Plants 2013, 16(3), 368–71. [Google Scholar] [CrossRef]
  78. Yuldashev, M.P.; Batirov, E.K.; Malikov, V.M. Flavonoids of the epigeal part of Scutellaria glabrata. Chem. Nat. Compd. 1994, 29(3), 410–1. [Google Scholar] [CrossRef]
  79. Dogan, Z.; Ishiuchi, K.; Makino, T.; Saracoglu, I. New acylated iridoid glucosides from Scutellaria glaphyrostachys Rech.f. and chemotaxonomic importance for the genus Scutellaria. Phytochem Lett. 2019, 32, 157–61. [Google Scholar] [CrossRef]
  80. Karimov, A.M.; BE, K. СТРУКТУРНОЕ РАЗНООБРАЗИЕ И СТЕПЕНЬ ИЗУЧЕННОСТИ ФЛАВОНОИДОВ РОДА SCUTELLARIA L. Chem. Plant Raw Mater. 2015. [Google Scholar] [CrossRef]
  81. Studies on the Nepalese Crude Drugs. XIII. On the Flavonoid and Iridoid Constituents of the Root of Scutellaria grossa WALL | CiNii Research [Internet]. 3 May 2026. Available online: https://cir.nii.ac.jp/crid/1570291227531014912.
  82. (PDF) ФЛАВОНОИДЫ SCUTELLARIA HAEMATOCHLORA JUZ. И S. OCELLATA JUZ. 3 May 2026. Available online: https://www.researchgate.net/publication/344728555_FLAVONOIDY_SCUTELLARIA_HAEMATOCHLORA_JUZ_I_S_OCELLATA_JUZ.
  83. Bai, M.; Zheng, C.J.; Wu, S.Y.; Chen, G.Y.; Song, X.P.; Han, C.R. Chemical constituents from Scutellaria hainanensis C. Y. Wu. Biochem Syst. Ecol. 2019, 82, 1–12. [Google Scholar] [CrossRef]
  84. Bardakci, H.; Skaltsa, H.; Milosevic-Ifantis, T.; Lazari, D.; Hadjipavlou-Litina, D.; Yeşilada, E.; et al. Antioxidant activities of several Scutellaria taxa and bioactive phytoconstituents from Scutellaria hastifolia L. Ind. Crops Prod. 2015, 77, 196–203. [Google Scholar] [CrossRef]
  85. Kamoldinov, K.S.; Eshbakova, K.A.; Bobakulov, K.M. Constituents of Scutellaria holosericea. Chem. Nat. Compd. 2012, 48(5), 889–90. [Google Scholar] [CrossRef]
  86. Miyazawa, M.; Nomura, M.; Marumoto, S.; Mori, K. Characteristic odor components of essential oil from Scutellaria laeteviolacea. J. Oleo Sci. 2013, 62(1), 51–6. [Google Scholar] [CrossRef] [PubMed]
  87. Diao, H.M.; Hao, Y.; Li, J.; Ling, H.W.; Shi, K.X.; Zhang, W.; et al. Flavonoids from Scutellaria likiangensis Diels and their antimalarial activities. Fitoterapia 2023, 164, 105357. [Google Scholar] [CrossRef] [PubMed]
  88. Firouznia, A.; Rustaiyana, A.; Masoudi, S.; Rahimizade, M.; Bigdeli, M.; Tabatabaei-Anaraki, M. Volatile Constituents of Salvia limbata, Stachys turcomanica, Scutellaria litwinowii and Hymenocrater elegans Four Lamiaceae Herbs from Iran. J. Essent. Oil Bear. Plants 2009, 12(4), 482–9. [Google Scholar] [CrossRef]
  89. Nikbin, M.; Kazemipour, N.; Maghsoodlou, M.T.; Valizadeh, J.; Sepehrimanesh, M.; Davarimanesh, A. Mineral elements and essential oil contents of Scutellaria luteo-caerulea Bornm. & Snit. Avicenna J. Phytomed;PubMed 2014, 4(3), 182. [Google Scholar] [PubMed]
  90. Mamadalieva, N.Z.; Sharopov, F.; Satyal, P.; Azimova, S.S.; Wink, M. Composition of the essential oils of three Uzbek Scutellaria species (Lamiaceae) and their antioxidant activities. Nat. Prod. Res. PubMed. 2017, 31(10), 1172–6. [Google Scholar] [CrossRef] [PubMed]
  91. Mamadalieva, N.Z.; Herrmann, F.; El-Readi, M.Z.; Tahrani, A.; Hamoud, R.; Egamberdieva, D.R.; et al. Flavonoids in Scutellaria immaculata and S. ramosissima (Lamiaceae) and their biological activity. J. Pharm. Pharmacol.;PubMed 2011, 63(10), 1346–57. [Google Scholar] [CrossRef] [PubMed]
  92. He, L.; Zhang, Z.; Lu, L.; Liu, Y.; Li, S.; Wang, J.; et al. Rapid identification and quantitative analysis of the chemical constituents in Scutellaria indica L. by UHPLC–QTOF–MS and UHPLC–MS/MS. J. Pharm. BioMed Anal.;PubMed 2016, 117, 125–39. [Google Scholar] [CrossRef] [PubMed]
  93. Ngu, T.N.; To, D.C.; Ngoc, T.V.T.; Thi, B.H.D. Chemical Constituents from the Whole Plant of Scutellaria indica. HPU2 J. Sci. Nat. Sci. Technol. 2022, 1(2), 44–51. [Google Scholar] [CrossRef]
  94. Karimov, A.M.; Slobodyanyuk, T.N.; Botirov, E.K. Flavonoids from the Aerial Part of Scutellaria intermedia. Chem. Nat. Compd. 2017, 53(4), 745–6. [Google Scholar] [CrossRef]
  95. Ismailov, A.I.; Karinmdzhanov, A.K.; Khudaibergenov, T.; Latvineuko, V.I.; Popova, T.P. Phenolic compounds of Scutellaria iscanderi. Chem. Nat. Compd. 1995, 31(3), 414–414. [Google Scholar] [CrossRef]
  96. Yunusov; Tashkent. View of Phytochemical Influence of Scutellaria iscanderi L. on Zinc Oxide Nanoparticle Biosynthesis. Journal of Science and Mathematic [Internet]. 2025. Available online: https://ejournal.upsi.edu.my/index.php/JSML/article/view/11853/6060.
  97. Gharari, Z.; Bagheri, K.; Danafar, H.; Sharafi, A. Simultaneous determination of baicalein, chrysin and wogonin in four Iranian Scutellaria species by high performance liquid chromatography. J. Appl. Res. Med. Aromat. Plants 2020, 16, 100232. [Google Scholar] [CrossRef]
  98. Yuldashev, M.P.; Karimov, A. Flavonoids of Scutellaria ocellata and S. nepetoides. Chem. Nat. Compd. 2001, 37(5), 431–3. [Google Scholar] [CrossRef]
  99. Shah, M.; Shahab, M.; Ullah, S.; Bibi, S.; Rahman, N.U.; Jamil, J.; et al. Exploring the aroma profile and biomedical applications of Scutellaria nuristanica Rech. F.: A new insight as a natural remedy. Phytomedicine;PubMed 2024, 133, 155928. [Google Scholar] [CrossRef] [PubMed]
  100. Rajendran, N.; Subramaniam, S.; Christena, L.R.; Muthuraman, M.S.; Subramanian, N.S.; Pemiah, B.; et al. Antimicrobial flavonoids isolated from Indian medicinal plant Scutellaria oblonga inhibit biofilms formed by common food pathogens. Nat. Prod. Res.;PubMed 2016, 30(17), 2002–6. [Google Scholar] [CrossRef] [PubMed]
  101. Yılmaz, G.; Çiçek, M.; Demirci, B.; Başer, K.H.C. Composition of the essential oils of five subspecies of Scutellaria orientalis from Turkey. J. Essent. Oil Res. 2020, 32(5), 429–35. [Google Scholar] [CrossRef]
  102. Sina İçen, M.; Arabacı, T.; Köstekci, S.; Gürhan, İ. Chemical Composition of the Essential Oil of Scutellaria orientalis L. subsp. virens (Boiss. &Kotschy) J. R. Edm. from Turkey Türkiye’de yetişen. J. Biol. Chem. 2016, 44(1), 25–8. [Google Scholar] [CrossRef]
  103. Muradov, M.T.; Khurramov, A.R.; Bobakulov, K.M.; Karimov, A.M.; Botirov, E.K. Constituents from the Aerial Part of Scutellaria oxystegia. Chem. Nat. Compd. 2023, 59(5), 939–40. [Google Scholar] [CrossRef]
  104. Lawrence, B.M.; Hogg, J.W.; Terhune, S.J.; Morton, J.K.; Gill, L.S. Terpenoid composition of some Canadian Labiatae. Phytochemistry 1972, 11(8), 2636–8. [Google Scholar] [CrossRef]
  105. Delazar, A.; Nazemiyeh, H.; Afshar, F.; Barghi, N.; Esnaashari, S.; Asgharian, P. Chemical compositions and biological activities of Scutellaria pinnatifida A. Hamilt aerial parts. Res. Pharm. Sci. 2017, 12(3), 187. [Google Scholar] [CrossRef]
  106. Heydari, F.; Tavakoli, S.; Shokravi, A.; Ahmadi, S.; Delnavazi, M.R.; Heydari, F.; et al. A Study of Karabaghian Skullcap (Scutellaria platystegia Juz.): Antioxidant and Antibacterial Activity Assays, Essential Oil Analysis, and Isolation of Its Phenolic Compounds. Jundishapur J. Nat. Pharm. Prod. 2022, 2022 17:2 17(2), e118896. [Google Scholar] [CrossRef]
  107. ERSÖZ, T.; ÜŞ, H.A.R.P.U.T.; SARACOĞLU, İ.; ÇALIŞ, İ.; OGIHARA, Y. Phenolic Compounds from Scutellaria pontica. Turk. J. Chem. 2002, 26(4), 581–8. [Google Scholar]
  108. Bhat, G.; Ganai, B.A.; Shawl, A.S. New phenolics from the root of Scutellaria prostrata JACQ. ex BENTH. Nat. Prod. Res. 2014, 28(20), 1685–90. [Google Scholar] [CrossRef] [PubMed]
  109. Bhat, G.; Lone, S.H.; Rather, M.A.; Shawl, A.S. Isolation, bioevaluation and RP-HPLC method development for the chemical constituents of aerial parts of Scutellaria prostrata Jacq. ex Benth. South Afr. J. Bot. 2022, 148, 720–6. [Google Scholar] [CrossRef]
  110. Denikeeva, M.F.; Litvinenko, V.I.; Borodin, L.I. Flavonoid compounds of Scutellaria przewalskii. Chem. Nat. Compd. 1970, 6(5), 552–5. [Google Scholar] [CrossRef]
  111. Solov’eva, A.I.; Stepanova, A.Y.; Panov, Y.M.; Gladkov, E.A. Metabolic Characteristics of Hairy Root Clones of Scutellaria pycnoclada and Scutellaria baicalensis. Processes 2023, 11(7), 2102. [Google Scholar] [CrossRef]
  112. Shah, M.; Shahab, M.; Ullah, S.; Bibi, S.; Rahman, N.U.; Jamil, J.; et al. Exploring the aroma profile and biomedical applications of Scutellaria nuristanica Rech. F.: A new insight as a natural remedy. Phytomedicine;PubMed 2024, 133, 155928. [Google Scholar] [CrossRef] [PubMed]
  113. Islam, M.N.; Downey, F.; Ng, C.K.Y. Comparative analysis of bioactive phytochemicals from Scutellaria baicalensis, Scutellaria lateriflora, Scutellaria racemosa, Scutellaria tomentosa and Scutellaria wrightii by LC-DAD-MS. Metabolomics 2011, 7(3), 446–53. [Google Scholar] [CrossRef]
  114. Su, Ya-In. Isolation and elucidation of antioxidant constituents from acetone extract in root of Scutellaria rehderiana | Request PDF [Internet]. 2004. Available online: https://www.researchgate.net/publication/8152832_Isolation_and_elucidation_of_antioxidant_constituents_from_acetone_extract_in_root_of_Scutellaria_rehderiana.
  115. Lin, Y.L.; Kuo, Y.H.; Cheng, M.C.; Wang, Y. Structures of Scutellones D and E Determined from X-Ray Diffraction, Spectral and Chemical Evidence. Neoclerodane-Type Diterpenoids from Scutellaria rivularis WALL. Chem. Pharm. Bull. 1988, 36(7), 2642–6. [Google Scholar] [CrossRef]
  116. Lin, C.C.; Shieh, D.E. The Anti-inflammatory Activity of Scutellaria rivularis Extracts and Its Active Components, Baicalin, Baicalein and Wogonin. PubMed. 2012, 24(1), 31–6. [Google Scholar] [CrossRef] [PubMed]
  117. Rosselli, S.; Bruno, M.; Simmonds, M.S.J.; Senatore, F.; Rigano, D.; Formisano, C. Volatile constituents of Scutellaria rubicunda Hornem subsp. linnaeana (Caruel) Rech. (Lamiaceae) endemic in Sicily. Biochem Syst. Ecol. 2007, 35(11), 797–800. [Google Scholar] [CrossRef]
  118. Watanabe, M.; Yahagi, T.; Kamikura, R.; Kotani, H.; Miyake, K.; Matsuzaki, K. Methoxyflavones isolated from the whole plant of Scutellaria rubropunctata Hayata var. rubropunctata promote osteoblast differentiation in MC3T3-E1 cells. J. Nat. Med.;PubMed 2023, 77(4), 748–60. [Google Scholar] [CrossRef] [PubMed]
  119. Dogan, Z.; Kutluay, V.M.; Genc, Y.; Saracoglu, I. Interactions between phenolic constituents of Scutellaria salviifolia and key targets associated with inflammation: network pharmacology, molecular docking analysis and in vitro assays. J. Biomol. Struct. Dyn. PubMed. 2023, 41(4), 1281–94. [Google Scholar] [CrossRef] [PubMed]
  120. Miyaichi, Y.; Imoto, Y.; Tomimori, T.; Namba, T. Studies on the Nepalese Crude Drugs. IX.: On the Flavonoid Constituents of the Root of Scutellaria scandens BUCH.-HAM. ex D. DON. Chem. Pharm. Bull. 1988, 36(7), 2371–6. [Google Scholar] [CrossRef]
  121. Melkani, A.B.; Nailwal, M.; Mohan, L.; Pant, C.C.; Dev, V. Steam volatile oil from Scutellaria repens Buch-Ham. ex D. Don; its composition and antibacterial activity. J. Essent. Oil Res. 2013, 25(5), 368–71. [Google Scholar] [CrossRef]
  122. Nurbyek, S.; Buyankhishig, B.; Suganuma, K.; Ishikawa, Y.; Kutsuma, M.; Abe, M.; et al. Phytochemical investigation of Scutellaria scordiifolia and its trypanocidal activity. Phytochemistry PubMed. 2023, 209, 113615. [Google Scholar] [CrossRef] [PubMed]
  123. Esquivel, B.; Calderón, J.S.; Flores, E. A neo-clerodane diterpenoid from Scutellaria seleriana. Phytochemistry 1998, 47(1), 135–7. [Google Scholar] [CrossRef]
  124. Glandular Trichomes Morphology, Chemical Composition and Antimicrobial Activity of the Essential Oil of Three Endemic Scutellaria Taxa (Lamiaceae) | Asian Journal of Chemistry [Internet]. 3 May 2026. Available online: https://asianpubs.org/index.php/ajchem/article/view/9794.
  125. Zhu, X.; Han, C.; Gao, T.; Shao, H. Chemical Composition, Phytotoxic and Antimicrobial Activities of the Essential Oil of Scutellaria strigillosa Hemsley. J. Essent. Oil Bear. Plants 2016, 19(3), 664–70. [Google Scholar] [CrossRef]
  126. Bai, C.; Xu, J.; Cao, B.; Li, X.; Li, G. Transcriptomic analysis and dynamic expression of genes reveal flavonoid synthesis in Scutellaria viscidula. Acta Physiol. Plant 2018, 40(9), 161. [Google Scholar] [CrossRef]
  127. Valarezo, E.; Castillo, A.; Guaya, D.; Morocho, V.; Malagón, O. Chemical composition of essential oils of two species of the Lamiaceae family: Scutellaria volubilis and Lepechinia paniculata from Loja, Ecuador. J. Essent. Oil Res. 2012, 24(1), 31–7. [Google Scholar] [CrossRef]
  128. Li, H.; Tang, S. Baicalin attenuates diet-induced obesity partially through promoting thermogenesis in adipose tissue. Obes. Res. Clin. Pract.;PubMed 2021, 15(5), 485–90. [Google Scholar] [CrossRef] [PubMed]
  129. Dai, J.; Liang, K.; Zhao, S.; Jia, W.; Liu, Y.; Wu, H.; et al. Chemoproteomics reveals baicalin activates hepatic CPT1 to ameliorate diet-induced obesity and hepatic steatosis. Proc. Natl. Acad. Sci. U S A PubMed. 2018, 115(26), E5896–905. [Google Scholar] [CrossRef] [PubMed]
  130. Zhang, Y.; Zhang, Z.; Zhang, Y.; Wu, L.; Gao, L.; Yao, R.; et al. Baicalin promotes the activation of brown and white adipose tissue through AMPK/PGC1α pathway. Eur. J. Pharmacol. PubMed. 2022, 922, 174913. [Google Scholar] [CrossRef] [PubMed]
  131. Zhang, Z.; Wang, R.; Cai, J.; Li, X.; Feng, X.; Xu, S.; et al. Baicalin alleviates lipid accumulation in adipocytes via inducing metabolic reprogramming and targeting Adenosine A1 receptor. Toxicon 2025, 258, 108339. [Google Scholar] [CrossRef] [PubMed]
  132. Seo, M.J.; Choi, H.S.; Jeon, H.J.; Woo, M.S.; Lee, B.Y. Baicalein inhibits lipid accumulation by regulating early adipogenesis and m-TOR signaling [Internet]. 2014. [Google Scholar] [CrossRef]
  133. Dunkhunthod, B.; Thumanu, K.; Eumkeb, G. Application of FTIR microspectroscopy for monitoring and discrimination of the anti-adipogenesis activity of baicalein in 3T3-L1 adipocytes [Internet]. 2017. [Google Scholar] [CrossRef]
  134. Zhang, S.; Yang, S.; Kong, B.; Zhang, Q.; Zhou, Z.; Zhao, W.; et al. Baicalein alleviates Western diet-induced obesity via metabolically activated adipose tissue macrophages by inducing Nrf2. J. Nutr. Biochem. 2026, 110381. [Google Scholar] [CrossRef] [PubMed]
  135. Li, S.; Shao, S.; Zhang, Z.; Wang, Z.; Han, X.; Jia, X.; et al. V8, a lysosomotropic wogonin derivative, alleviates hepatic steatosis by modulating GDF15-dependent mitochondrial homeostasis. Free Radic. Biol. Med. 2026, 242, 92–107. [Google Scholar] [CrossRef] [PubMed]
  136. Bak, E.J.; Kim, J.; Choi, Y.H.; Kim, J.H.; Lee, D.E.; Woo, G.H.; et al. Wogonin ameliorates hyperglycemia and dyslipidemia via PPARα activation in db/db mice. Clin. Nutr. 2014, 33(1), 156–63. [Google Scholar] [CrossRef] [PubMed]
  137. Chen, J.; Liu, J.; Wang, Y.; Hu, X.; Zhou, F.; Hu, Y.; et al. Wogonin mitigates nonalcoholic fatty liver disease via enhancing PPARα/AdipoR2, in vivo and in vitro. Biomed. Pharmacother. PubMed. 2017, 91, 621–31. [Google Scholar] [CrossRef] [PubMed]
  138. Jiang, G.; Chen, D.; Li, W.; Liu, C.; Liu, J.; Guo, Y. Effects of wogonoside on the inflammatory response and oxidative stress in mice with nonalcoholic fatty liver disease. Pharm. Biol. PubMed. 2020, 58(1), 1177–83. [Google Scholar] [CrossRef] [PubMed]
  139. Gao, Y.Z.; Zhao, L.F.; Ma, J.; Xue, W.H.; Zhao, H. Protective mechanisms of wogonoside against Lipopolysaccharide/D-galactosamine-induced acute liver injury in mice. Eur. J. Pharmacol.;PubMed 2016, 780, 8–15. [Google Scholar] [CrossRef] [PubMed]
  140. Lin, Y.; Ren, N.; Li, S.; Chen, M.; Pu, P. Novel anti-obesity effect of scutellarein and potential underlying mechanism of actions. Biomed. Pharmacother.;PubMed 2019, 117, 109042. [Google Scholar] [CrossRef] [PubMed]
  141. Zhang, X.; Huo, Z.; Luan, H.; Huang, Y.; Shen, Y.; Sheng, L.; et al. Scutellarin ameliorates hepatic lipid accumulation by enhancing autophagy and suppressing IRE1α/XBP1 pathway. Phyther. Res. 2022, 36(1), 433–47. [Google Scholar] [CrossRef] [PubMed]
  142. Park, M.Y.; Ha, S.E.; Kim, H.H.; Bhosale, P.B.; Abusaliya, A.; Jeong, S.H.; et al. Scutellarein Inhibits LPS-Induced Inflammation through NF-κB/MAPKs Signaling Pathway in RAW264.7 Cells. Molecules PubMed. 2022, 27(12). [Google Scholar] [CrossRef] [PubMed]
  143. Cho, W.; Choi, S.W.; Oh, H.; Abd El-Aty, A.M.; Hacimuftuoglu, A.; Jeong, J.H.; et al. Oroxylin-A alleviates hepatic lipid accumulation and apoptosis under hyperlipidemic conditions via AMPK/FGF21 signaling. Biochem Biophys. Res. Commun.;PubMed 2023, 648, 59–65. [Google Scholar] [CrossRef] [PubMed]
  144. Singh, J.; Kakkar, P. Oroxylin A, a constituent of Oroxylum indicum inhibits adipogenesis and induces apoptosis in 3T3-L1 cells. Phytomedicine PubMed. 2014, 21(12), 1733–41. [Google Scholar] [CrossRef] [PubMed]
  145. Jiang, Y.; Jiang, K.; Sun, P.; Liu, Y.; Nie, H. Oroxylin A ameliorates non-alcoholic fatty liver disease by modulating oxidative stress and ferroptosis through the Nrf2 pathway. Biochim. Et. Biophys. Acta (BBA) -Mol. Cell Biol. Lipids PubMed. 2025, 1870(5), 159628. [Google Scholar] [CrossRef] [PubMed]
  146. Choi, J.H.; Yun, J.W. Chrysin induces brown fat–like phenotype and enhances lipid metabolism in 3T3-L1 adipocytes. Nutrition 2016, 32(9), 1002–10. [Google Scholar] [CrossRef] [PubMed]
  147. Feng, X.; Qin, H.; Shi, Q.; Zhang, Y.; Zhou, F.; Wu, H.; et al. Chrysin attenuates inflammation by regulating M1/M2 status via activating PPARγ. Biochem Pharmacol.;PubMed 2014, 89(4), 503–14. [Google Scholar] [CrossRef] [PubMed]
  148. Pai, S.A.; Martis, E.A.; Munshi, R.P.; Gursahani, M.S.; Mestry, S.N.; Juvekar, A.R. Chrysin mitigated obesity by regulating energy intake and expenditure in rats. J. Tradit. Complement Med. 2020, 10(6), 577–85. [Google Scholar] [CrossRef]
  149. Feng, X.; Weng, D.; Zhou, F.; Owen, Y.D.; Qin, H.; Zhao, J.; et al. Activation of PPARγ by a Natural Flavonoid Modulator, Apigenin Ameliorates Obesity-Related Inflammation Via Regulation of Macrophage Polarization. EBioMedicine;PubMed 2016, 9, 61–76. [Google Scholar] [CrossRef] [PubMed]
  150. Yu, H.; Huang, X.; Zhu, H.H.; Wang, N.; Xie, C.; Zhou, Y.L.; et al. Apigenin ameliorates non-eosinophilic inflammation, dysregulated immune homeostasis and mitochondria-mediated airway epithelial cell apoptosis in chronic obese asthma via the ROS-ASK1-MAPK pathway. Phytomedicine;PubMed 2023, 111, 154646. [Google Scholar] [CrossRef] [PubMed]
  151. Mou, A.; Sun, F.; Tong, D.; Wang, L.; Lu, Z.; Cao, T.; et al. Dietary apigenin ameliorates obesity-related hypertension through TRPV4-dependent vasorelaxation and TRPV4-independent adiponectin secretion. Biochim. Et. Biophys. Acta (BBA) -Mol. Basis Dis.;PubMed 2024, 1870(8), 167488. [Google Scholar] [CrossRef] [PubMed]
  152. Xie, Y.; Berntsen, H.F.; Zimmer, K.E.; Ropstad, E.; Verhaegen, S.; Connolly, L. Luteolin protects against adipogenic and lipogenic potency induced by human relevant mixtures of persistent organic pollutants (POPs) in the 3T3-L1 model. Food Chem. Toxicol.;PubMed 2023, 173, 113608. [Google Scholar] [CrossRef] [PubMed]
  153. Baek, Y.; Lee, M.N.; Wu, D.; Pae, M. Luteolin reduces adipose tissue macrophage inflammation and insulin resistance in postmenopausal obese mice. J. Nutr. Biochem.;PubMed 2019, 71, 72–81. [Google Scholar] [CrossRef] [PubMed]
  154. Na, H.Y.; Lee, B.C. Scutellaria baicalensis Alleviates Insulin Resistance in Diet-Induced Obese Mice by Modulating Inflammation. Int. J. Mol. Sci. 2019, 20(3), 727. [Google Scholar] [CrossRef] [PubMed]
  155. Ma, L.; Wang, Y.; Ren, T.; Pan, L.; Li, X.; Wang, S.; et al. Scutellaria baicalensis extract prevents metabolic dysfunction-associated steatotic liver disease by modulating the gut-liver axis in high-fat diet mice. Phytochemistry.;PubMed 2026, 243, 114720. [Google Scholar] [CrossRef] [PubMed]
  156. Sung, Y.Y.; Kim, S.H.; Kim, D.S. Combined Phyllostachys pubescens and Scutellaria baicalensis Prevent High-Fat Diet-Induced Obesity via Upregulating Thermogenesis and Energy Expenditure by UCP1 in Male C57BL/6J Mice. Nutrients;PubMed 2022, 14(3), 446. [Google Scholar] [CrossRef] [PubMed]
  157. Li, S.T.; Xu, D.; Jia, J.; Zou, W.; Liu, J.Y.; Wang, Y.; et al. Structure and anti-inflammatory activity of neo-clerodane diterpenoids from Scutellaria barbata. Phytochemistry 2023, 213, 113771. [Google Scholar] [CrossRef] [PubMed]
  158. Liu, H.L.; Kao, T.H.; Shiau, C.Y.; Chen, B.H. Functional components in Scutellaria barbata D. Don with anti-inflammatory activity on RAW 264.7 cells. J. Food Drug Anal. 2018, 26(1), 31–40. [Google Scholar] [CrossRef] [PubMed]
  159. Kwiecień, I.; Miceli, N.; D’arrigo, M.; Marino, A.; Ekiert, H. Antioxidant Potential and Enhancement of Bioactive Metabolite Production in In Vitro Cultures of Scutellaria lateriflora L. by Biotechnological Methods. Molecules;PubMed 2022, 27(3). [Google Scholar] [CrossRef] [PubMed]
  160. Long, D.M.; Martinez, J.; Soumyanath, A.; Kretzschmar, D. Scutellaria lateriflora Extract Supplementation Provides Resilience to Age-Related Phenotypes in Drosophila melanogaster. Int. J. Mol. Sci.;PubMed 2026, 27(1), 461. [Google Scholar] [CrossRef] [PubMed]
  161. Cuong, T.D.; Hung, T.M.; Lee, J.S.; Weon, K.Y.; Woo, M.H.; Min, B.S. Anti-inflammatory activity of phenolic compounds from the whole plant of Scutellaria indica. Bioorg Med. Chem. Lett.;PubMed 2015, 25(5), 1129–34. [Google Scholar] [CrossRef] [PubMed]
  162. Kim, S.W.; Cuong, T.D.; Hung, T.M.; Ryoo, S.; Lee, J.H.; Min, B.S. Arginase II inhibitory activity of flavonoid compounds from Scutellaria indica. Arch. Pharm. Res. 2013, 36(8), 922–6. [Google Scholar] [CrossRef] [PubMed]
  163. Zhang, D.W.; Wang, Y.; Liu, J.H.; Yue, X.D.; Dai, S.J. neo-Clerodane diterpenoids from Scutellaria galericulata and their anti-inflammatory activities. Phytochem Lett. 2026, 73, 104170. [Google Scholar] [CrossRef]
  164. Xiao, K.; Han, Q.T.; Zhang, L.; Dai, S.J. Two new flavanone glycosides from Scutellaria galericulata with anti-inflammatory activities. Phytochem Lett. 2017, 20, 151–4. [Google Scholar] [CrossRef]
Table 1. Representative phytochemical profiles of selected Scutellaria species (condensed and standardized).
Table 1. Representative phytochemical profiles of selected Scutellaria species (condensed and standardized).
Species Plant Part Dominant Phytochemical Classes Representative Compounds References
S. baicalensis Root, aerial Flavonoids, phenolics, terpenoids Baicalin, baicalein, wogonin, wogonoside [29,30,31,32,33,34]
S. barbata Root, aerial Diterpenoids, flavonoids, volatiles Scutellarin, luteolin, neo-clerodanes [30,33,35,36]
S. lateriflora Aerial tissue Flavonoids, indole derivatives Baicalin, scutellarin, verbascoside [30,37,38,39,40]
S. adenostegia Aerial, root Flavonoids, volatiles Apigenin, luteolin, baicalein [41,42]
S. albida Aerial Iridoids, phenylethanoids, flavonoids Catalpol, verbascoside, scutellarin [44,45,46]
S. alpina Callus, aerial Flavonoids, terpenoids Baicalin, luteolin, wogonoside [47,48]
S. altissima Root, aerial Flavonoids, phenylpropanoids Baicalin, luteolin, myristicin [33,49,50,51]
S. amoena Aerial Flavonoids Baicalin, wogonin, oroxylin A [53]
S. araxensis Root, aerial Flavonoids, iridoids, phenolics Chrysin, wogonin, tricin [55,56,57]
S. bornmuelleri Root, aerial Flavonoids, phenylethanoids Wogonin, baicalin, verbascoside [55,61,62]
S. galericulata Aerial Flavonoids, diterpenoids Wogonin, scutellarein, baicalein [75,76,77]
S. indica Aerial, root Flavonoids Baicalin, wogonin, naringenin [34,92,93]
S. multicaulis Root, aerial Flavonoids, terpenoids Pectolinarin, chrysin, wogonin [69,97]
S. orientalis Root, aerial Flavonoids, volatiles Baicalein, chrysin, scutellarin [55,97,101,102]
S. rivularis Aerial Flavonoids, diterpenoids Baicalin, baicalein, scutellone D [115,116]
S. scordiifolia Aerial Flavonoid glycosides Scutellarein derivatives [122]
S. viscidula Aerial, root Flavonoids Baicalin, wogonin, viscidulin [126]
S. wrightii Aerial, root Flavonoids Chrysin, baicalin, scutellarin [33]
Table 2. Anti-obesity mechanisms of major Scutellaria-derived compounds and extracts.
Table 2. Anti-obesity mechanisms of major Scutellaria-derived compounds and extracts.
Compound / Extract Source species Experimental model Main anti-obesity mechanism Reported metabolic effects Critical note
Baicalin S. baicalensis, several Scutellaria spp 3T3-L1 adipocytes; HFD-induced obese models Activation of AMPK/ACC pathway; suppression of lipogenesis; promotion of adipose thermogenesis via UCP1 upregulation and browning pathways; activation of hepatic CPT1-mediated fatty acid β-oxidation [128,129,130,131] Reduced lipid accumulation, adipocyte hypertrophy, hepatic lipid deposition, and body-weight gain Strong preclinical evidence, but limited human validation
Baicalein S. baicalensis
several Scutellaria spp
Adipocytes; metabolic disease models; Western diet-induced obese mice Inhibition of adipogenesis via downregulation of PPAR γ/C/EBPα and suppression of mTOR signaling; reduction of lipogenesis (SREBP-1, Lipin1); Nrf-2 mediated immunometabolic activation of adipose tissue macrophages [132,133,134] Decreased adipocyte differentiation and intracellular triglyceride accumulation Mechanistic evidence predominantly cellular, with limited in vivo validation
Wogonin S. baicalensis
several Scutellaria spp
Adipocytes; obesity-associated inflammation models Suppression of inflammatory signaling; modulation of adipose tissue inflammation and insulin resistance [135,136,137] Improved inflammatory profile, glucose metabolism, and lipid regulation Promising, but often studied in combination or non-obesity models
Wogonoside/Norwogonoside S. baicalensis
several Scutellaria spp
Preclinical metabolic models Regulation of lipid metabolism and inflammatory mediators [138,139] Potential improvement in metabolic dysfunction and adipose inflammation Anti-obesity-specific data remain less extensive than baicalin
Scutellarin / Scutellarein S. baicalensis
several Scutellaria spp
Adipocyte and metabolic models Inhibition of adipogenesis and oxidative-inflammatory signaling; enhancement of autophagy and suppression of IRE1α/XBP1-mediated lipogenesis [140,141,142] Reduced lipid accumulation and obesity-related inflammatory responses Requires more direct obesity-focused validation
Oroxylin A S. baicalensis
several Scutellaria spp
In vitro and preclinical models Modulation of lipid metabolism, oxidative stress, and inflammatory pathways [143,144,145] Potential improvement in lipid homeostasis and metabolic stress Evidence is pharmacologically relevant but not yet obesity-specific enough
Chrysin Several Scutellaria spp. Adipocyte and metabolic models Downregulation of adipogenic transcription factors; antioxidant activity [146,147,148] Reduced adipogenesis and oxidative stress associated with metabolic dysfunction Poor bioavailability may limit translational relevance
Apigenin S. adenostegia, S. araxensis Adipocytes; metabolic models Inhibition of adipocyte differentiation; AMPK-related lipid regulation [149,150,151] Reduced lipid accumulation and improved metabolic signaling Not unique to Scutellaria; attribution should be cautious
Luteolin S. adenostegia, S. altissima Adipocyte and inflammation models Anti-inflammatory activity; regulation of adipogenesis and lipid metabolism [152,153] Suppressed adipocyte differentiation and inflammatory mediator production Needs species-specific anti-obesity confirmation
S. baicalensis extract S. baicalensis HFD-induced obesity; insulin resistance models Regulation of adipose inflammation, lipid metabolism, and insulin signaling [154,155] Improved insulin resistance, reduced inflammatory markers, and improved metabolic parameters Extract composition varies across studies
S. baicalensis + Phyllostachys pubescens combination S. baicalensis 3T3-L1 adipocytes; HFD-induced obese mice AMPK activation; browning/thermogenesis enhancement [156] Reduced adipogenesis; increased thermogenic markers and energy expenditure Combination design limits attribution to Scutellaria alone
S. barbata constituents S. barbata Mostly non-obesity pharmacological models Anti-inflammatory, antioxidant, and metabolic regulatory potential [157,158] Possible relevance to obesity-associated inflammation Direct anti-obesity evidence remains limited
S. lateriflora S. lateriflora Anti-inflammatory models, primarily neuropharmacology Putative AMPK, anti-inflammatory metabolic modulation, antioxidant [159,160] Possible relevance to obesity-associated inflammation No direct anti-obesity evidence
S. indica constituents S. indica Mostly non-obesity pharmacological models, no validated obesity-specific model reported Putative metabolic regulation via antioxidant, anti-inflammatory activity [161,162] Possible relevance to obesity-associated inflammation No direct anti-obesity evidence
S. galericulata
constituents
S. galericulata Non-obesity inflammatory models Antiinflammatory activity via suppression of TNF-α, IL-6, IL-8 [163,164] Possible relevance to obesity-associated inflammation No direct anti-obesity evidence
Scutellaria spp constituents Several scutellaria spp Non-obesity inflammatory models Antioxidant effect Possible relevance to obesity-associated oxidative stress No direct anti-obesity evidence
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.
Copyright: This open access article is published under a Creative Commons CC BY 4.0 license, which permit the free download, distribution, and reuse, provided that the author and preprint are cited in any reuse.
Prerpints.org logo

Preprints.org is a free preprint server supported by MDPI in Basel, Switzerland.

Subscribe

Disclaimer

Terms of Use

Privacy Policy

Privacy Settings

© 2026 MDPI (Basel, Switzerland) unless otherwise stated