CHEBI:63067 - zeaxanthin bis(β-D-glucoside)

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ChEBI Name zeaxanthin bis(β-D-glucoside) ChEBI ID CHEBI:63067 ChEBI ASCII Name zeaxanthin bis(beta-D-glucoside) Definition A β-D-glucoside that is zeaxanthin in which both hydroxy groups have been converted to the corresponding glucosides. It is one of the most polar carotenoids found in nature (solubility in water is 800 ppm, compared with only 12.6 ppm for zeaxanthin itself). 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 C52H76O12 Net Charge 0 Average Mass 893.15260 Monoisotopic Mass 892.53368 InChI InChI=1S/C52H76O12/c1-31(17-13-19-33(3)21-23-39-35(5)25-37(27-51(39,7)8)61-49-47(59)45(57)43(55)41(29-53)63-49)15-11-12-16-32(2)18-14-20-34(4)22-24-40-36(6)26-38(28-52(40,9)10)62-50-48(60)46(58)44(56)42(30-54)64-50/h11-24,37-38,41-50,53-60H,25-30H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,31-15+,32-16+,33-19+,34-20+/t37-,38-,41-,42-,43-,44-,45+,46+,47-,48-,49-,50-/m1/s1 InChIKey DHNSFMNURMJEQV-OIBMWOCGSA-N SMILES CC(\C=C\C=C(C)\C=C\C1=C(C)C[C@H](CC1(C)C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O)=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)C[C@H](CC1(C)C)O[C@@H]1O[C@H](CO)[C@@H](O)[C@H](O)[C@H]1O ChEBI Ontology Outgoing zeaxanthin bis(β-D-glucoside) (CHEBI:63067) has functional parent zeaxanthin (CHEBI:27547) zeaxanthin bis(β-D-glucoside) (CHEBI:63067) is a β-D-glucoside (CHEBI:22798) zeaxanthin bis(β-D-glucoside) (CHEBI:63067) is a carotenoid (CHEBI:23044) IUPAC Name (3R,3'R)-3-(β-D-glucopyranosyloxy)-β,β-caroten-3'-yl β-D-glucopyranoside Synonyms Sources (all-E,3R,3'R)-zeaxanthin di-β-D-glucopyranoside ChEBI zeaxanthin bis(β-D-glucoside) UniProt zeaxanthin diglucoside MetaCyc zeaxanthin-β-D-diglucoside MetaCyc Zeaxanthin-beta-D-diglucoside KEGG COMPOUND Manual Xrefs Databases C00000932 KNApSAcK C15969 KEGG COMPOUND CPD-11471 MetaCyc View more database links Registry Number Type Source 7901386 Reaxys Registry Number Reaxys Citations Types Sources 1409639 PubMed citation Europe PMC 2254247 PubMed citation Europe PMC Last Modified 28 July 2014