ERGOSTEROL
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 444679
Name
ERGOSTEROL
IUPAC name
(3S,9S,10R,13R,14R,17R)-17-((2R,5R,E)-5,6-dimethylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,10,11,12,13,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
SMILES
C[C@H](/C=C/[C@H](C)C(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3C2=CC=C4[C@@]3(CC[C@@H](C4)O)C)C
Molecular formula
C28H44O
Molecular weight
396.66 g/mol
Monoisotopic mass
396.3392 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| Plant | Plant part | Amount | Reference |
|---|---|---|---|
| Alcea rosea L. | - | - |
Chouhan, U.K., Skukla, R.N. (1984). Sterols of some Malvaceae with particular emphasis on cholesterol occurrence. J Sci Res(Bhopal), 6(1), 49-50
|
| Chelidonium majus L. | root | - |
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
|
| Dactylis glomerata L. subsp. glomerata | - | - |
Pollard, A. (1936). The isolation of carotene and sterols from the unsaponifiable matter of cocksfoot. Biochem J, 30, 382-386 doi:10.1042/bj0300382
|
| Lolium arundinaceum (Schreb.) Darbysh. subsp. arundinaceum | aerial parts | - |
Davis, N.D., Cole, R.J., Dorner, J.W., Weete, J.D., Backman, P.A., Clark, E.M., King, C.C., Schmidt, S.P., Diener, U.L. (1986). Steroid metabolites of Acremonium coenophialum, an endophyte of tall fescue. J Agr Food Chem, 34(1), 108-112 doi:10.1021/jf00067a029
|
| Triticum aestivum L. subsp. aestivum | seed | 12 ppm |
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
|