163527-00-2
Chemical Structure
Resveratrol 12-C-β-glucopyranoside
- CAS No.: 163527-00-2
- Formula:C20H22O8
- Molecular Weight:390.38
InChIKey: URWNDISGXOTRRK-JIVMRSFOSA-N
SMILES: OC1=C([C@@H]2O[C@@H]([C@H]([C@@H]([C@H]2O)O)O)CO)C(O)=CC(/C=C/C3=CC=C(C=C3)O)=C1
Biological Activity: Resveratrol 12-C-β-glucopyranoside is a stilbene-type natural secondary metabolite. Resveratrol 12-C-β-glucopyranoside has the potential to target TNF-α, TGF-β1, and PPAR-α. As one of the core active components of MESR, Resveratrol 12-C-β-glucopyranoside exerts hepatoprotective, anti-inflammatory, and antioxidant effects in a rat liver injury model induced by Isoniazid (HY-B0329). Resveratrol 12-C-β-glucopyranoside can be used for studies related to drug-induced liver injury[1][2].
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Resveratrol 12-C-β-glucopyranoside | Resveratrol 12-C-β-glucopyranoside is a stilbene-type natural secondary metabolite. Resveratrol 12-C-β-glucopyranoside has the potential to target TNF-α, TGF-β1, and PPAR-α. As one of the core active components of MESR, Resveratrol 12-C-β-glucopyranoside exerts hepatoprotective, anti-inflammatory, and antioxidant effects in a rat liver injury model induced by Isoniazid (HY-B0329). Resveratrol 12-C-β-glucopyranoside can be used for studies related to drug-induced liver injury. | |||||||||||||||||||||
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References
- [1]. Samantaray B, et al. Hepatoprotective Mechanism of Shorea Robusta Gaertn. f. Against Isoniazid-induced Hepatotoxicity by Targeting TNF-α, TGF-β1, and PPAR-α: Insights from Computational Profiling To Immunohistochemical Confirmation. Cell biochemistry and biophysics. 2026 Jun;84(2):2209-2239. [Content Brief]
- [2]. Ito T, et al. Stilbenoids isolated from stem bark of Shorea hemsleyana. Chemical & pharmaceutical bulletin. 2000 Jul;48(7):1001-5. [Content Brief]
