CHEBI:35328 - spirilloxanthin

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ChEBI Name spirilloxanthin ChEBI ID CHEBI:35328 Definition A carotenoid ether that is (3E,3'E)-1,1'-dihydroxy-3,3',4,4'-tetradehydro-1,1',2,2'-tetrahydro-ψ,ψ-carotene in which both hydroxyl hydrogens are replaced by methyl groups. Stars This entity has been manually annotated by the ChEBI Team. Supplier Information Download Molfile XML SDF Find compounds which contain this structure Find compounds which resemble this structure Take structure to the Advanced Search Formula C42H60O2 Net Charge 0 Average Mass 596.92460 Monoisotopic Mass 596.45933 InChI InChI=1S/C42H60O2/c1-35(23-15-25-37(3)27-17-29-39(5)31-19-33-41(7,8)43-11)21-13-14-22-36(2)24-16-26-38(4)28-18-30-40(6)32-20-34-42(9,10)44-12/h13-32H,33-34H2,1-12H3/b14-13+,23-15+,24-16+,27-17+,28-18+,31-19+,32-20+,35-21+,36-22+,37-25+,38-26+,39-29+,40-30+ InChIKey VAZQBTJCYODOSV-HZUCFJANSA-N SMILES COC(C)(C)C\C=C\C(C)=C\C=C\C(C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C=C\C=C(C)\C=C\CC(C)(C)OC Roles Classification Biological Role(s): bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. View more via ChEBI Ontology ChEBI Ontology Outgoing spirilloxanthin (CHEBI:35328) has role bacterial metabolite (CHEBI:76969) spirilloxanthin (CHEBI:35328) is a carotenoid ether (CHEBI:35329) Incoming 2',2'-dihydroxy-2-oxospirilloxanthin (CHEBI:91230) has functional parent spirilloxanthin (CHEBI:35328) 2'-hydroxy-2-oxospirilloxanthin (CHEBI:91229) has functional parent spirilloxanthin (CHEBI:35328) 2,2-dihydroxyspirilloxanthin (CHEBI:91228) has functional parent spirilloxanthin (CHEBI:35328) 2-hydroxyspirilloxanthin (CHEBI:91227) has functional parent spirilloxanthin (CHEBI:35328) IUPAC Name (3E,3'E)-1,1'-dimethoxy-3,3',4,4'-tetradehydro-1,1',2,2'-tetrahydro-ψ,ψ-carotene Synonyms Sources 3,3',4,4'-tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-ψ,ψ-carotene ChemIDplus rhodoviolascin ChemIDplus spirilloxanthin UniProt spirilloxanthin ChemIDplus Manual Xrefs Databases C00022893 KNApSAcK C15881 KEGG COMPOUND CPD-12615 MetaCyc LMPR01070122 LIPID MAPS MOL000088 COMe View more database links Registry Numbers Types Sources 1717970 Beilstein Registry Number Beilstein 1717970 Reaxys Registry Number Reaxys 34255-08-8 CAS Registry Number ChemIDplus Citations Types Sources 19287491 PubMed citation Europe PMC 20887710 PubMed citation Europe PMC 21229315 PubMed citation Europe PMC 22228659 PubMed citation Europe PMC 22428121 PubMed citation Europe PMC 22428122 PubMed citation Europe PMC 22623302 PubMed citation Europe PMC Last Modified 11 April 2016