CHEBI:80167 - chlorobactene

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ChEBI Name chlorobactene ChEBI ID CHEBI:80167 Definition A carotenoid that is 1,2,4-trimethylmenzene in which the hydrogen at position 3 has been replaced by an all-trans-3,7,12,16,20,24-hexamethylpentacosa-1,3,5,7,9,11,13,15,17,19,23-undecaen-1-yl group. Found in photosynthetic green bacteria. 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 C40H52 Net Charge 0 Average Mass 532.842 Monoisotopic Mass 532.40690 InChI InChI=1S/C40H52/c1-31(2)17-13-20-34(5)23-15-25-35(6)24-14-21-32(3)18-11-12-19-33(4)22-16-26-36(7)27-30-40-38(9)29-28-37(8)39(40)10/h11-12,14-19,21-30H,13,20H2,1-10H3/b12-11+,21-14+,22-16+,25-15+,30-27+,32-18+,33-19+,34-23+,35-24+,36-26+ InChIKey VJASLAGEYVTOGS-IQAIWTHGSA-N SMILES C=1(/C=C/C(=C/C=C/C(=C/C=C/C=C(/C=C/C=C(/C=C/C=C(/CCC=C(C)C)\C)\C)\C)/C)/C)C(=CC=C(C1C)C)C Metabolite of Species Details Chlorobium limicola (NCBI:txid1092) See: Acta Chem. Scand., 1964, 18, 1703 Chlorobaculum tepidum (NCBI:txid1097) See: PubMed Chlorobium vibrioforme f. thiosulfatophilum (NCBI:txid115853) See: Acta Chem. Scand., 1964, 18, 1703 Chlorobaculum macestae (NCBI:txid44314) of strain Strain M See: PubMed Desulfuromonas acetoxidans (NCBI:txid891) See: Acta Chem. Scand., 1964, 18, 1703 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 chlorobactene (CHEBI:80167) has role bacterial metabolite (CHEBI:76969) chlorobactene (CHEBI:80167) is a benzenes (CHEBI:22712) chlorobactene (CHEBI:80167) is a carotenoid (CHEBI:23044) chlorobactene (CHEBI:80167) is a carotenoid φ-end group (CHEBI:139129) IUPAC Name φ,ψ-carotene Synonym Source trans-chlorobactene ChEBI Manual Xrefs Databases C00022819 KNApSAcK C15908 KEGG COMPOUND LMPR01070163 LIPID MAPS View more database links Registry Numbers Types Sources 2489575 Reaxys Registry Number Reaxys 2932-09-4 CAS Registry Number KEGG COMPOUND 2932-09-4 CAS Registry Number ChemIDplus Citations Types Sources 16923888 PubMed citation Europe PMC 18365725 PubMed citation Europe PMC 25920497 PubMed citation Europe PMC 4774401 PubMed citation Europe PMC 526104 PubMed citation Europe PMC 9297463 PubMed citation Europe PMC Last Modified 21 September 2017