Name | (2Z,6Z)-6-[(3aS,6S,7S,9bS)-6-(2-Carboxyethyl)-7-isopropenyl-3a,6, 9b-trimethyl-1,2,3a,4,6,7,8,9,9a,9b-decahydro-3H-cyclopenta[a]nap hthalen-3-ylidene]-2-methyl-2-heptenoic acid |
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Synonyms |
(2Z,6Z)-6-[(3aS,6S,7S,9aS,9bS)-6-(2-Carboxyethyl)-7-isopropenyl-3a,6,9b-trimethyl-1,2,3a,4,6,7,8,9,9a,9b-decahydro-3H-cyclopenta[a]naphthalen-3-ylidene]-2-methyl-2-heptenoic acid
5'-CMP 5'-CYTIDYLIC ACID CMP MONOHYDRATE 1H-Benz[e]indene-6-propanoic acid, 3-[(4Z)-5-carboxy-1-methyl-4-hexen-1-ylidene]-2,3,3a,4,6,7,8,9,9a,9b-decahydro-3a,6,9b-trimethyl-7-(1-methylethenyl)-, (3Z,3aS,6S,7S,9aS,9bS)- 2',3'-dideoxy-[5']cytidylic acid 3,4-seco-lanosta-4(28),9(11),17(20),17(Z),24(Z)-tetraene-3,26-dioic acid Kadsuracoccinic acid A K-2',3'-dideoxy-cytidine monophosphate C-5-P 5'-CYTIDYLIC ACID MONOHYDRATE 5'-CYTIDINE MONOPHOSPHATE |
Description | Kadsuracoccinic acid A is a tetracyclic natural compound that can be isolated from the stems of Kadsura coccinea. Kadsuracoccinic acid A has vitro anti-HIV-1 activitiy with an EC50 value of 68.7 μM[1]. |
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Related Catalog | |
Target |
HIV-1:68.7 μM (EC50) |
References |
Density | 1.1±0.1 g/cm3 |
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Boiling Point | 622.6±55.0 °C at 760 mmHg |
Molecular Formula | C30H44O4 |
Molecular Weight | 468.668 |
Flash Point | 344.3±28.0 °C |
Exact Mass | 468.323975 |
PSA | 74.60000 |
LogP | 9.36 |
Vapour Pressure | 0.0±3.9 mmHg at 25°C |
Index of Refraction | 1.550 |
Hazard Codes | Xi |
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