CIS-VIOLAXANTHIN

Structure

2D structure of CIS-VIOLAXANTHIN
2D structure
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3D model

Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 5282218

Names and identifiers

Name

CIS-VIOLAXANTHIN

IUPAC name

(1R,1'R,3S,3'S,6S,6'S)-6,6'-((1E,3Z,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaene-1,18-diyl)bis(1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol)

SMILES

C/C(=C\C=C\C=C(/C)\C=C\C=C(\C)/C=C/[C@]12[C@](O1)(C[C@H](CC2(C)C)O)C)/C=C/C=C(\C)/C=C/[C@]34[C@](O3)(C[C@H](CC4(C)C)O)C

General information

Molecular formula

C40H56O4

Molecular weight

600.88 g/mol

Monoisotopic mass

600.4179 Da

Classification

Pathway:
Superclass:
Class:
Glycoside:
No

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

Plants with the compound

Plant Plant part Amount Reference
Arabidopsis thaliana (L.) Heynh. root -
Parry, A., Horgan, R. (1992). Abscisic acid biosynthesis in roots. I. the identification of potential abscisic acid precursors, and other carotenoids. Planta, 187(2), 185-191
Rosa canina L. fruit 2 ppm
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.