2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)-

2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)- Suppliers list
Company Name: Zhejiang Huida Biotech Co., LTD  
Tel: 0571-89903022 18679456698
Email: zilong@hizyme.com
Company Name: TargetMol  
Tel: 400-821-0310 15002144251
Email: xuexiang.shao@tsbiochem.com
2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)- Basic information
Product Name:2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)-
Synonyms:2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)-
CAS:134769-19-0
MF:C21H26O6
MW:374.43
EINECS:
Product Categories:
Mol File:134769-19-0.mol
2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)- Structure
2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)- Chemical Properties
Boiling point 597.3±50.0 °C(Predicted)
density 1.29±0.1 g/cm3(Predicted)
pka14.38±0.60(Predicted)
Safety Information
MSDS Information
2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)- Usage And Synthesis
UsesCochleamycin A showed strong inhibitory activity against tumor cells, with IC50s (μg/mL) of P388, HL60, K562, COL0205 and HT29 cells of 1.6, 14.0, 6.2, 16.5 and 19.1, respectively. Cochleamycin A also has anti-Gram-positive bacteria activity[1].
References[1] Thomas A Dineen, et al. Total synthesis of cochleamycin A. Org Lett. 2004 Jun 10;6(12):2043-6.
2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)- Preparation Products And Raw materials
Tag:2,5-Ethanoindeno[4,5-e]oxecin-3,15(5H)-dione, 11-(acetyloxy)-6,7,8,8a,10a,11,12,13,13a,13b-decahydro-7-hydroxy-12-methyl-, (1Z,5R,7R,8aS,10aS,11S,12S,13aR,13bS)-(134769-19-0) Related Product Information
Rapamycin Carbonyl cyanide 3-chlorophenylhydrazone Brefeldin A Adenosine triphosphate Neomycin sulfate Streptozotocin