ANTHERAXANTHIN
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Drawn and modelled with RDKit, 3D viewer 3Dmol.js. PubChem CID 5281223
Name
ANTHERAXANTHIN
Also reported as
ANTHEROXANTHIN
IUPAC name
(1R,3S,6S)-6-((1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-((R)-4-hydroxy-2,6,6-trimethylcyclohex-1-en-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaen-1-yl)-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol
SMILES
CC1=C(C(C[C@@H](C1)O)(C)C)/C=C/C(=C/C=C/C(=C/C=C/C=C(\C)/C=C/C=C(\C)/C=C/[C@]23[C@](O2)(C[C@H](CC3(C)C)O)C)/C)/C
Molecular formula
C40H56O3
Molecular weight
584.89 g/mol
Monoisotopic mass
584.4229 Da
Chemical classification: NPClassifier (Kim et al., 2021)
| 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
|
| Asplenium trichomanes L. | leaf | - |
Czeczuga, B. (1985). Carotenoids in sixty-six representatives of the Pteridophyta. Biochem Syst Ecol, 13(3), 221-230 doi:10.1016/0305-1978(85)90030-4
|
| Daucus carota L. | leaf | - |
Duke, James A. 1992. Handbook of phytochemical constituents of GRAS herbs and other economic plants. Boca Raton, FL. CRC Press.
|