Submitted:
09 May 2026
Posted:
09 May 2026
You are already at the latest version
Abstract
Keywords:
1. Introduction
2. Methods

3. The Genus Scutellaria


4. Phytochemical Constituents of Selected Scutellaria Species
5. Results and Discussion
5.1. Phytochemical Drivers of Anti-Obesity Activity
5.2. Modulation of Adipogenesis and Lipid Metabolism
5.3. Anti-Inflammatory and Metabolic Regulatory Effects
5.4. Energy Homeostasis and Thermogenic Regulation
5.5. Clinical Perspective
6. Translational Limitations and Research Gaps
7. Implications for Future Research
8. Synthesis

9. Conclusion
Author Contributions
Data Availability Statement
Conflicts of Interest
References
- 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]
- Powis, J.; Thompson, R.; Jackson-Leach, R. World Obesity Atlas 2025 [Internet]. 2025, 1. Available online: www.worldobesity.org.
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- Gousiadou, C.; Karioti, A.; Heilmann, J.; Skaltsa, H. Iridoids from Scutellaria albida ssp. albida. Phytochemistry 2007, 68(13), 1799–804. [Google Scholar] [CrossRef] [PubMed]
- 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]
- 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]
- 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]
- 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]
- 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]
- (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.
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- Stojakowska, A.; Kisiel, W. Secondary metabolites from a callus culture of Scutellaria columnae. Fitoterapia 1999, 70(3), 324–5. [Google Scholar] [CrossRef]
- 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]
- 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]
- Bruno, M.; Fazio, C.; Arnold, N.A. Neo-clerodane diterpenoids from Scutellaria cypria. Phytochemistry 1996, 42(2), 555–7. [Google Scholar] [CrossRef]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- Karimov, A.M.; BE, K. СТРУКТУРНОЕ РАЗНООБРАЗИЕ И СТЕПЕНЬ ИЗУЧЕННОСТИ ФЛАВОНОИДОВ РОДА SCUTELLARIA L. Chem. Plant Raw Mater. 2015. [Google Scholar] [CrossRef]
- 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.
- (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.
- 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]
- 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]
- Kamoldinov, K.S.; Eshbakova, K.A.; Bobakulov, K.M. Constituents of Scutellaria holosericea. Chem. Nat. Compd. 2012, 48(5), 889–90. [Google Scholar] [CrossRef]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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.
- 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]
- Yuldashev, M.P.; Karimov, A. Flavonoids of Scutellaria ocellata and S. nepetoides. Chem. Nat. Compd. 2001, 37(5), 431–3. [Google Scholar] [CrossRef]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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.
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- Esquivel, B.; Calderón, J.S.; Flores, E. A neo-clerodane diterpenoid from Scutellaria seleriana. Phytochemistry 1998, 47(1), 135–7. [Google Scholar] [CrossRef]
- 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.
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
| 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] |
| 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. |
© 2026 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.