Balsaminol B
![]() | |
| Names | |
|---|---|
| IUPAC name
(3S,4S,7S,8R,9S,10S,13R,14S,17R)-17-((2R,4R)-4-hydroxy-6-methylhept-5-en-2-yl)-4-(hydroxymethyl)-7-methoxy-4,9,13,14-tetramethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol | |
| Other names
7β-Methoxycucurbita-5,24-diene-3β,23(R),29-triol; (3β,4β,7β,9β,10α,23R)-4-(Hydroxymethyl)-7-methoxy-4,9,14-trimethyl-19-norcholesta-5,24-diene-3,23-diol | |
| Identifiers | |
| 1189131-53-0 | |
| ChEMBL | ChEMBL1078437 |
| ChemSpider | 24676126 |
| Jmol interactive 3D | Image |
| |
| |
| Properties | |
| C31H52O4 | |
| Molar mass | 488.75 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| | |
| Infobox references | |
Balsaminol B or 7β-methoxycucurbita-5,24-diene-3β,23(R),29-triol, is a chemical compound with formula C
31H
52O
4, found in the balsam apple vine (Momordica balsamina). It is a cucurbitane-type triterpenoid, related to cucurbitacin, isolated by C. Ramalhete and others in 2009.[1]
Balsaminol B is an amorphous powder soluble in methanol and ethyl acetate, but insoluble in n-hexane. It is cytotoxic at about 50 μM.[1]
See also
References
This article is issued from Wikipedia - version of the Sunday, February 22, 2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.
