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Karavilagenin E

From Wikipedia, the free encyclopedia
Karavilagenin E
Names
IUPAC name
(3S,5R,8S,9S,10S,13R,14S,17R)-17-((2R)-4-hydroxy-6-methylhept-5-en-2-yl)-4,4,13,14-tetramethyl-2,3,4,8,10,11,12,13,14,15,16,17-dodecahydro-1H-5,9-(epoxymethano)cyclopenta[a]phenanthren-3-ol
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
UNII
  • InChI=1S/C30H48O3/c1-19(2)16-21(31)17-20(3)22-10-12-28(7)23-11-13-30-24(8-9-25(32)26(30,4)5)29(23,18-33-30)15-14-27(22,28)6/h11,13,16,20-25,31-32H,8-10,12,14-15,17-18H2,1-7H3/t20-,21+,22-,23+,24+,25+,27-,28+,29+,30-/m1/s1 checkY
    Key: BZKMSMPQWDQSDS-ZRBXTNFGSA-N checkY
  • C[C@H](CC(O)/C=C(C)/C)[C@@]1([H])CC[C@@]2(C)[C@]3([H])C=C[C@]45C(C)(C)[C@@H](O)CC[C@@]4([H])[C@]3(CO5)CC[C@@]21C
Properties
C30H48O3
Molar mass 456.711 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Karavilagenin E is a chemical compound found in the Balsam apple vine (Momordica balsamina). It is a cucurbitane-type triterpenoid, related to cucurbitacin.[1]

Karavilagenin E is soluble in methanol and ethyl acetate but insoluble in n-hexane.[1]

See also

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References

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  1. ^ a b Cátia Ramalhete; Tayyab A. Mansoor; Silva Mulhovo; Joseph Molnár; Maria-José U. Ferreira (2009). "Cucurbitane-Type Triterpenoids from the African Plant Momordica balsamina". Journal of Natural Products. 72 (11): 2009–2013. doi:10.1021/np900457u. hdl:10884/1322. PMID 19795842.