Gomisin G

• CAT Number: I004370
• CAS Number: 62956-48-3
• Molecular Formula: C30H32O9
• Molecular Weight: 536.57
• Purity: ≥95%
• Target: HIV
• Solubility: 10 mM in DMSO
• Storage: Store at -20°C
• IUPAC Name: [(9S,10S,11S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-yl] benzoate
• InChI: InChI=1S/C30H32O9/c1-16-12-18-13-20(33-3)24(34-4)26(35-5)22(18)23-19(14-21-25(27(23)36-6)38-15-37-21)28(30(16,2)32)39-29(31)17-10-8-7-9-11-17/h7-11,13-14,16,28,32H,12,15H2,1-6H3/t16-,28-,30-/m0/s1
• InChIKey: OFDWKHIQKPKRKY-DSASHONVSA-N
• SMILES: C[C@H]1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3[C@@H]([C@@]1(C)O)OC(=O)C5=CC=CC=C5)OCO4)OC)OC)OC)OC

Gomisin G（Cat No.:I004370）is a bioactive lignan derived from Schisandra chinensis, widely recognized for its pharmacological properties. It exhibits potent antioxidant, anti-inflammatory, and hepatoprotective activities, making it a valuable tool in liver disease and oxidative stress research. Gomisin G is also studied for its potential to modulate metabolic pathways and enhance cellular protection against damage. With applications in natural product research and drug discovery, this compound is essential for exploring therapeutic strategies targeting inflammation, liver health, and metabolic disorders. Its high purity ensures reliable results in experimental setups.

Reference

[1]. Chen DF, et al. Anti-AIDS agents–XXVI. Structure-activity correlations of gomisin-G-related anti-HIV lignans from Kadsura interior and of related synthetic analogues. Bioorg Med Chem. 1997 Aug;5(8):1715-23.

[2]. Ikeya Y, et al. The constituents of Schizandra chinensis Baill. I. Isolation and structure determination of five new lignans, gomisin A, B, C, F and G, and the absolute structure of schizandrin. Chem Pharm Bull (Tokyo). 1979 Jun;27(6):1383-94.