ALPHA-FERNENOL

Structure

2D structure of ALPHA-FERNENOL
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 621134

Names and identifiers

Name

ALPHA-FERNENOL

Also reported as

FERN-9(11)-EN-3-BETA-OL; FERNENOL

IUPAC name

(3R,3aR,5aR,5bR,7aR,9S,11aS,13aS,13bR)-3-isopropyl-3a,5a,8,8,11a,13a-hexamethyl-2,3,3a,4,5,5a,5b,6,7,7a,8,9,10,11,11a,13,13a,13b-octadecahydro-1H-cyclopenta[a]chrysen-9-ol

SMILES

CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C

General information

Molecular formula

C30H50O

Molecular weight

426.73 g/mol

Monoisotopic mass

426.3862 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
No

Chemical classification: NPClassifier (Kim et al., 2021)

Plants with the compound

Plant Plant part Amount Reference
Artemisia vulgaris L. - -
List, P.H. and Horhammer, L., Hager's Handbuch der Pharmazeutischen Praxis, Vols. 2-6, Springer-Verlag, Berlin, 1969-1979.
Dactylis glomerata L. subsp. glomerata seed -
Ohmoto, T., Ikuse, M., Natori, S. (1970). Triterpenoids of the Gramineae. Phytochemistry, 9, 2137 doi:10.1016/s0031-9422(00)85379-0
Euphorbia peplus L. - -
Hemmers, H., Gulz, P.G., Marner, F.J. (1988). Triterpenoids in epicuticular waxes of three european Euphorbia species. Z Naturforsch Ser C, 43(11/12), 799-805 doi:10.1515/znc-1988-11-1202
Euphorbia peplus L. stem -
Hemmers, H., Gulz, P.G., Marner, F.J. (1988). Triterpenoids in epicuticular waxes of three european Euphorbia species. Z Naturforsch Ser C, 43(11/12), 799-805 doi:10.1515/znc-1988-11-1202