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+ |
VAZQBTJCYODOSV-HZUCFJANSA-N |
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 |
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bacterial metabolite
Any prokaryotic metabolite produced during a metabolic reaction in bacteria.
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View more via ChEBI Ontology
(3E,3'E)-1,1'-dimethoxy-3,3',4,4'-tetradehydro-1,1',2,2'-tetrahydro-ψ,ψ-carotene
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3,3',4,4'-tetradehydro-1,1',2,2'-tetrahydro-1,1'-dimethoxy-ψ,ψ-carotene
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ChemIDplus
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rhodoviolascin
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ChemIDplus
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spirilloxanthin
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UniProt
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spirilloxanthin
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ChemIDplus
|
1717970
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Reaxys Registry Number
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Reaxys
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34255-08-8
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CAS Registry Number
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ChemIDplus
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19287491
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PubMed citation
|
Europe PMC
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20887710
|
PubMed citation
|
Europe PMC
|
21229315
|
PubMed citation
|
Europe PMC
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22228659
|
PubMed citation
|
Europe PMC
|
22428121
|
PubMed citation
|
Europe PMC
|
22428122
|
PubMed citation
|
Europe PMC
|
22623302
|
PubMed citation
|
Europe PMC
|
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