Name | ((1S,4aR,6S,7R,7aS)-6-acetoxy-4a-hydroxy-1-((3-methylbutanoyl)oxy)-4a,5,6,7a-tetrahydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxiran]-4-yl)methyl 3-methyl-2-((3-methylbutanoyl)oxy)butanoate |
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Synonyms |
Butanoic acid, 3-methyl-2-(3-methyl-1-oxobutoxy)-, [6-(acetyloxy)-4a,5,6,7a-tetrahydro-4a-hydroxy-1-(3-methyl-1-oxobutoxy)spiro[cyclopenta[c]pyran-7(1H),2'-oxiran]-4-yl]methyl ester
{6-Acetoxy-4a-hydroxy-1-[(3-methylbutanoyl)oxy]-4a,5,6,7a-tetrahydro-1H-spiro[cyclopenta[c]pyran-7,2'-oxiran]-4-yl}methyl 3-methyl-2-[(3-methylbutanoyl)oxy]butanoate |
Description | IVHD-valtrate, an active Valeriana jatamansi derivative, is against human ovarian cancer cells in vitro and in vivo. IVHD-valtrate induces cancer cells apoptosis and arrests the ovarian cancer cells in the G2/M phase. IVHD-valtrate has the potential to be a novel chemotherapeutic agent for the human ovarian cancer research[1]. |
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Related Catalog | |
Target |
IC50: apoptosis[1] |
In Vitro | IVHD-valtrate inhibits the growth and proliferation of the A2780 and OVCAR-3 ovarian cancer cell lines in a concentration-dependent manner[1]. IVHD-valtrate results in a relatively low cytotoxicity to immortalized non-tumorigenic human ovarian surface epithelial cells (IOSE-144)[1]. |
References |
Density | 1.2±0.1 g/cm3 |
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Boiling Point | 616.5±55.0 °C at 760 mmHg |
Molecular Formula | C27H40O11 |
Molecular Weight | 540.600 |
Flash Point | 193.9±25.0 °C |
Exact Mass | 540.257080 |
PSA | 147.19000 |
LogP | 2.95 |
Vapour Pressure | 0.0±4.0 mmHg at 25°C |
Index of Refraction | 1.526 |
Hazard Codes | Xi |
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