Asperosaponin VI

For research use only. Not for therapeutic Use.

  • CAT Number: R014530
  • CAS Number: 39524-08-8
  • Molecular Formula: C47H76O18
  • Molecular Weight: 929.10
  • Purity: ≥95%
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Asperosaponin VI(Cat No.:R014530)is a saponin compound isolated from the fungus Aspergillus species, specifically Aspergillus terreus. It is known for its bioactive properties, including anti-inflammatory, antioxidant, and anticancer activities. Asperosaponin VI has been shown to inhibit the growth of cancer cells by inducing apoptosis and modulating various signaling pathways. Additionally, it exhibits potential in protecting against oxidative stress and inflammatory diseases. Due to its diverse pharmacological effects, Asperosaponin VI is being investigated for potential therapeutic applications in cancer treatment, anti-inflammatory therapies, and as a natural product in drug discovery.


Catalog Number R014530
CAS Number 39524-08-8
Synonyms

Hederagenin 3-O-α-L-arabinopyranosyl-28-β-D-glucopyranosyl(1→6)-β-D-glucopyranoside?Leiyemudanoside A; Tauroside St-G0-1; -O-α-L-Arabinopyranosylhederagenin 28-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranoside?Akebia Saponin D;

Molecular Formula C47H76O18
Purity ≥95%
Target Caspase
Storage Store at 4℃
IUPAC Name [(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
InChI InChI=1S/C47H76O18/c1-42(2)13-15-47(41(59)65-40-37(58)34(55)32(53)26(63-40)20-61-38-36(57)33(54)31(52)25(18-48)62-38)16-14-45(5)22(23(47)17-42)7-8-28-43(3)11-10-29(64-39-35(56)30(51)24(50)19-60-39)44(4,21-49)27(43)9-12-46(28,45)6/h7,23-40,48-58H,8-21H2,1-6H3/t23-,24-,25+,26+,27+,28+,29-,30-,31+,32+,33-,34-,35+,36+,37+,38+,39-,40-,43-,44-,45+,46+,47-/m0/s1
InChIKey CCRXMHCQWYVXTE-HMRSNRLKSA-N
SMILES C[C@]12CC[C@@H]([C@@]([C@@H]1CC[C@@]3([C@@H]2CC=C4[C@]3(CC[C@@]5([C@H]4CC(CC5)(C)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O)O)O)O)O)O)C)C)(C)CO)O[C@H]8[C@@H]([C@H]([C@H](CO8)O)O)O

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