EUCOSTEROL
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 14634458
Name
EUCOSTEROL
IUPAC name
(3S,3'R,4S,5R,5'S,10S,13S,14S,17S)-3-hydroxy-4-(hydroxymethyl)-3',4,10,13,14-pentamethyl-5'-propionyl-1,2,3,4,4',5,5',6,7,10,11,12,13,14-tetradecahydro-3'H-spiro[cyclopenta[a]phenanthrene-17,2'-furan]-15(16H)-one
SMILES
[H][C@@]45CCC1=C(CC[C@@]2(C)[C@@]1(C)C(=O)C[C@@]23O[C@H](C(=O)CC)C[C@H]3C)[C@@]4(C)CC[C@H](O)[C@]5(C)CO
Molecular formula
C29H44O5
Molecular weight
472.67 g/mol
Monoisotopic mass
472.3189 Da
Pathway:
Superclass:
Class:
Glycoside:
No
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Muscari comosum (L.) Mill. | bulb | - |
Adinolfi, M., Barone, G., Lanzetta, R., Laonigro, G., Mangoni, L., Parrilli, M. (1983). Triterpenes from bulbs of Muscari comosum, 1. isolation of nortriterpenes and structure of (23s,24s)-17,23-epoxy-24,31-dihydroxy-27-nor-5-alpha-lanost-8-ene,3,15-dione. J Nat Prod, 46(4), 559-562 doi:10.1021/np50028a022
|
| Muscari comosum (L.) Mill. | bulb | - |
Parrilli, M., Adinolfi, M., Mangoni, L. (1979). 13c-nmr study of two spirocyclic furanoid notriterpenes from Muscari comosum. Gazz Chim Ital, 109, 611-613
|