77394-04-8

Bivittoside B Chemical Structure
77394-04-8

Chemical Structure

Bivittoside B

  • CAS No.: 77394-04-8
  • Formula:C54H88O22
  • Molecular Weight:1089.26

IUPAC Name: (3S,3aS,5aS,5bS,7aR,9S,11aS,13S,13aS)-9-(((2S,3R,4S,5R)-5-(((2S,3R,4S,5R,6R)-4-(((2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-methoxytetrahydro-2H-pyran-2-yl)oxy)-3,5-dihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)oxy)-4-hydroxy-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: OWKJBTKHYSAGRF-OMFWNHKNSA-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[C@H]3[C@H](O)[C@@H](O[C@H]4[C@H](O)[C@@H](OC)[C@H](O)[C@@H](CO)O4)[C@H](O)[C@@H](CO)O3)CO[C@H]2O[C@H]5CC[C@@]6(C)[C@@H](CC[C@@H]7C6=C[C@H](O)[C@@]89[C@@]7(C)CC[C@@H]8[C@](C)(CCCC(C)C)OC9=O)C5(C)C)O1

Biological Activity: Bivittoside B is a non-sulfated hexoside analog derived from Bovine sea cucumber, exhibiting antifungal and potential antitumor activities.

Cat. No. Product Name Purity Description Pricing
HY-130072
Bivittoside B Bivittoside B is a non-sulfated hexoside analog derived from Bovine sea cucumber, exhibiting antifungal and potential antitumor activities.
Pricing 
Expand Hide
loading...
/
  • /
loading...
Size Price
Stock Quantity Availability Operate
/
In-stock
(Estimated to ship on )
(Estimated to ship TODAY)
Estimated to ship on
(Estimated to ship TODAY)

Amount:

USD 0.00

This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

Pricing 
Expand Hide