OBTUSIFOLIOL
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 65252
Name
OBTUSIFOLIOL
IUPAC name
(3S,4S,5S,10S,13R,14R,17R)-4,10,13,14-tetramethyl-17-((R)-6-methyl-5-methyleneheptan-2-yl)-2,3,4,5,6,7,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES
C[C@H]1[C@@H]2CCC3=C([C@]2(CC[C@@H]1O)C)CC[C@]4([C@]3(CC[C@@H]4[C@H](C)CCC(=C)C(C)C)C)C
Molecular formula
C30H50O
Molecular weight
426.73 g/mol
Monoisotopic mass
426.3862 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Bryonia dioica Jacq. | root | - |
Akihisa, T., Kimura, Y., Kokke, W.C.M.C., Itoh, T., Tamura, T. (1996). Eight novel sterols from the roots of Bryonia dioica jacq. Chem Pharm Bull, 44(6), 1202-1207 doi:10.1248/cpb.44.1202
|
| Corylus avellana L. | - | - |
J.S. Glasby Dict.Pls Containing 2ndary Metabolite. 1991.
|
| Cyperus esculentus L. | tuber | - |
Yan, M.H., Guan, Z.X. (1983). Studies on fatty acids and unsaponifiable constituents of oil from tubers of Cyperus esculentus L. Chih Wu Hsueh Pao, 25(3), 254-263
|
| Euphorbia peplus L. | - | - |
Ferreira, M.J.U., Lobo, A.M., Wyler, H. (1993). Triterpenoids and steroids from Euphorbia peplus. Fitoterapia, 64(1), 85-87
|
| Euphorbia peplus L. | exudate | - |
Giner, J.L., Berkowitz, J.D., Andersson, T. (2000). Nonpolar components of the latex of Euphorbia peplus. J Nat Prod, 63(2), 267-269 doi:10.1021/np990081g
|