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(1R)-4-[18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol

PubChem CID: 5362770

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Compound Synonyms Anchovixanthin, b,b-Carotene-3,3'-diol, SCHEMBL822867, (1R)-4-[18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol, 29472-68-2
Topological Polar Surface Area 40.5
Hydrogen Bond Donor Count 2.0
Inchi Key JKQXZKUSFCKOGQ-DKLMTRRASA-N
Rotatable Bond Count 10.0
State Solid
Synonyms Zeaxanthin, (3R,3'R,9Z)-form, Anchovixanthin, b,b-Carotene-3,3'-diol, beta,beta-Carotene-3,3'-diol, Zeaxanthol, Β,β-carotene-3,3'-diol, (3R,3's)-Zeaxanthin
Heavy Atom Count 42.0
Compound Name (1R)-4-[18-[(4R)-4-hydroxy-2,6,6-trimethylcyclohexen-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol
Kingdom Organic compounds
Description Beta,beta-carotene-3,3'-diol, also known as (3r,3's)-zeaxanthin or anchovixanthin, is a member of the class of compounds known as xanthophylls. Xanthophylls are carotenoids containing an oxygenated carotene backbone. Carotenes are characterized by the presence of two end-groups (mostly cyclohexene rings, but also cyclopentene rings or acyclic groups) linked by a long branched alkyl chain. Carotenes belonging form a subgroup of the carotenoids family. Xanthophylls arise by oxygenation of the carotene backbone. Beta,beta-carotene-3,3'-diol is practically insoluble (in water) and an extremely weak acidic compound (based on its pKa). Beta,beta-carotene-3,3'-diol can be found in channel catfish, crustaceans, and fishes, which makes beta,beta-carotene-3,3'-diol a potential biomarker for the consumption of these food products.
Exact Mass 568.428
Formal Charge 0.0
Monoisotopic Mass 568.428
Isotope Atom Count 0.0
Molecular Complexity 1190.0
Hydrogen Bond Acceptor Count 2.0
Molecular Weight 568.9
Database Name fooddb_chem_all;hmdb_chem_all;pubchem
Covalent Unit Count 1.0
Defined Atom Stereocenter Count 0.0
Iupac Name 4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-(4-hydroxy-2,6,6-trimethylcyclohexen-1-yl)-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-3,5,5-trimethylcyclohex-3-en-1-ol
Total Atom Stereocenter Count 2.0
Molecular Framework Aliphatic homomonocyclic compounds
Total Bond Stereocenter Count 9.0
Class Prenol lipids
Inchi InChI=1S/C40H56O2/c1-29(17-13-19-31(3)21-23-37-33(5)25-35(41)27-39(37,7)8)15-11-12-16-30(2)18-14-20-32(4)22-24-38-34(6)26-36(42)28-40(38,9)10/h11-24,35-36,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+
Smiles CC1=C(C(CC(C1)O)(C)C)/C=C/C(=C/C=C/C(=C/C=C/C=C(/C=C/C=C(/C=C/C2=C(CC(CC2(C)C)O)C)\C)\C)/C)/C
Xlogp 10.9
Superclass Lipids and lipid-like molecules
Defined Bond Stereocenter Count 9.0
Subclass Tetraterpenoids
Taxonomy Direct Parent Xanthophylls
Molecular Formula C40H56O2

  • 1. Outgoing r'ship FOUND_IN to/from Capsicum Annuum (Plant) Rel Props:Source_db:fooddb_chem_all