STIGMASTEROL-GLUCOSIDE

Structure

2D structure of STIGMASTEROL-GLUCOSIDE
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 6602508

Names and identifiers

Name

STIGMASTEROL-GLUCOSIDE

IUPAC name

(2R,3R,4S,5S,6R)-2-(((3S,8S,9S,10R,13R,14S,17R)-17-((2R,5S,E)-5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl)oxy)-6-(hydroxymethyl)tetrahydro-2H-pyran-3,4,5-triol

SMILES

CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC=C4[C@@]3(CC[C@@H](C4)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)C)C)C(C)C

General information

Molecular formula

C35H58O6

Molecular weight

574.84 g/mol

Monoisotopic mass

574.4233 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
Yes

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

Plants with the compound

Plant Plant part Amount Reference
Clematis vitalba L. - -
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
Matricaria chamomilla L. aerial parts -
Mericli, A.H. (1990). The lipophilic compounds of a turkish Matricaria chamomilla variety with no chamazulene in the volatile oil. Int J Crude Drug Res, 28(2), 145-147 doi:10.3109/13880209009082799