Ganoderic acid D

• CAT Number: I018564
• CAS Number: 108340-60-9
• Molecular Formula: C₃₀H₄₂O₇
• Molecular Weight: 514.65
• Purity: ≥95%
• IUPAC Name: (6R)-6-[(5R,7S,10S,13R,14R,17R)-7-hydroxy-4,4,10,13,14-pentamethyl-3,11,15-trioxo-1,2,5,6,7,12,16,17-octahydrocyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoic acid
• InChI: InChI=1S/C30H42O7/c1-15(10-17(31)11-16(2)26(36)37)18-12-23(35)30(7)25-19(32)13-21-27(3,4)22(34)8-9-28(21,5)24(25)20(33)14-29(18,30)6/h15-16,18-19,21,32H,8-14H2,1-7H3,(H,36,37)/t15-,16?,18-,19+,21+,28+,29-,30+/m1/s1
• InChIKey: YTVGSCZIHGRVAV-IYAQLQCNSA-N
• SMILES: C[C@H](CC(=O)CC(C)C(=O)O)[C@H]1CC(=O)[C@@]2([C@@]1(CC(=O)C3=C2[C@H](C[C@@H]4[C@@]3(CCC(=O)C4(C)C)C)O)C)C

Ganoderic acid D (Cat.No:I018564) is a triterpenoid compound derived from the medicinal mushroom Ganoderma lucidum. It exhibits various biological activities, including anti-inflammatory, antioxidant, and anticancer effects. Ganoderic acid D has been studied for its potential in preventing tumor growth, suppressing angiogenesis, and modulating the immune system.

Reference

[1]. Liu Z, et al. Effect of ganoderic acid D on colon cancer Warburg effect: Role of SIRT3/cyclophilin D. Eur J Pharmacol. 2018 Apr 5;824:72-77.[2]. Yue QX, et al. Proteomics characterization of the cytotoxicity mechanism of ganoderic acid D and computer-automated estimation of the possible drug target network. Mol Cell Proteomics. 2008 May;7(5):949-61.