| Name | (1R,4S,5S,8R,9R,12S,13S,16S)-16-Hydroxy-8-[(2R,4E)-6-hydroxy-6-methyl-4-hepten-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-19-one |
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| Synonyms |
(1R,4S,5S,8R,9R,12S,13S,16S)-16-Hydroxy-8-[(2R,4E)-6-hydroxy-6-methyl-4-hepten-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.0.0.0]nonadec-2-en-19-one
5,9-(Epoxymethano)-2H-cyclopenta[a]phenanthren-18-one, 1,3,4,8,10,11,12,13,14,15,16,17-dodecahydro-3-hydroxy-17-[(1R,3E)-5-hydroxy-1,5-dimethyl-3-hexen-1-yl]-4,4,13,14-tetramethyl-, (3S,5R,8S,9S,10S,13R,14S,17R)- |
| Description | Karavilagenin D, a cucurbitane-type triterpene isolated from Japanese bitter melon leaves, is a potential tumor-promoting inhibitor[1]. |
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| Related Catalog | |
| References |
| Density | 1.1±0.1 g/cm3 |
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| Boiling Point | 595.8±50.0 °C at 760 mmHg |
| Molecular Formula | C30H46O4 |
| Molecular Weight | 470.684 |
| Flash Point | 188.0±23.6 °C |
| Exact Mass | 470.339600 |
| PSA | 66.76000 |
| LogP | 5.83 |
| Vapour Pressure | 0.0±3.8 mmHg at 25°C |
| Index of Refraction | 1.566 |
| Hazard Codes | Xi |
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