77394-03-7
Chemical Structure
Bivittoside A
- CAS No.: 77394-03-7
- Formula:C41H66O12
- Molecular Weight:750.96
IUPAC Name: (3S,3aS,5aS,5bS,7aR,9S,11aS,13S,13aS)-9-(((2S,3R,4S,5R)-4,5-dihydroxy-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)tetrahydro-2H-pyran-2-yl)oxy)-13-hydroxy-3,5a,8,8,11a-pentamethyl-3-(4-methylpentyl)-3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,13-tetradecahydro-1H,3H-naphtho[2',1':4,5]indeno[1,7a-c]furan-1-one
InChIKey: GOYXWSSENLVERY-YZRCTGSKSA-N
SMILES: C[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O[C@@H]2[C@@H](O)[C@H](O)CO[C@H]2O[C@H]3CC[C@@]4(C)[C@@H](CC[C@@H]5C4=C[C@H](O)[C@@]67[C@@]5(C)CC[C@@H]6[C@](C)(CCCC(C)C)OC7=O)C3(C)C)O1
Biological Activity: Bivittoside A is a non-sulfated hexoside analog derived from Bovine sea cucumber, exhibiting antifungal properties and potential for antitumor applications.
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Bivittoside A | Bivittoside A is a non-sulfated hexoside analog derived from Bovine sea cucumber, exhibiting antifungal properties and potential for antitumor applications. | |||||||||||||||||||||
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