EMBL-EBI | Chemical Biology | ChEBI
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| Formula | C40H58O |
| Net Charge | 0 |
| Average Mass | 554.903 |
| Monoisotopic Mass | 554.44877 |
| SMILES | CC(C)=CCC/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)CCCC(C)(C)O |
| InChI | InChI=1S/C40H58O/c1-33(2)19-13-22-36(5)25-16-28-37(6)26-14-23-34(3)20-11-12-21-35(4)24-15-27-38(7)29-17-30-39(8)31-18-32-40(9,10)41/h11-12,14-17,19-21,23-30,41H,13,18,22,31-32H2,1-10H3/b12-11+,23-14+,24-15+,28-16+,29-17+,34-20+,35-21+,36-25+,37-26+,38-27+,39-30+ |
| InChIKey | CNYVJTJLUKKCGM-RGGGOQHISA-N |
| Wikipedia |
|---|
| Roles Classification |
|---|
| Biological Role: | bacterial metabolite Any prokaryotic metabolite produced during a metabolic reaction in bacteria. |
| ChEBI Ontology |
|---|
| Outgoing Relation(s) |
| rhodopin (CHEBI:35331) has role bacterial metabolite (CHEBI:76969) |
| rhodopin (CHEBI:35331) is a carotenol (CHEBI:23045) |
| rhodopin (CHEBI:35331) is a tertiary alcohol (CHEBI:26878) |
| Incoming Relation(s) |
| (3E)-3,4-didehydrorhodopin (CHEBI:62481) has functional parent rhodopin (CHEBI:35331) |
| IUPAC Name |
|---|
| 1,2-dihydro-ψ,ψ-caroten-1-ol |
| Synonyms | Source |
|---|---|
| rhodopin | ChemIDplus |
| 1,2-dihydro-1-hydroxy-ψ,ψ-carotene | ChemIDplus |
| 1-hydroxylycopene | ChEBI |
| 1-hydroxy-1,2-dihydrolycopene | ChEBI |
| (6E,8E,10E,12E,14E,16E,18E,20E,22E,24E,26E)-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,14,16,18,20,22,24,26,30-dodecaen-2-ol | IUPAC |
| all-trans-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,8,10,12,14,16,18,20,22,24,26,30-dodecaen-2-ol | ChEBI |
| UniProt Name | Source |
|---|---|
| rhodopin | UniProt |
| Manual Xrefs | Databases |
|---|---|
| LMPR01070114 | LIPID MAPS |
| CPD-11447 | MetaCyc |
| CN101368191 | Patent |
| C19795 | KEGG COMPOUND |
| Rhodopin | Wikipedia |
| C00022854 | KNApSAcK |
| Registry Numbers | Sources |
|---|---|
| Beilstein:1730253 | Beilstein |
| Reaxys:1730252 | Reaxys |
| CAS:105-92-0 | ChemIDplus |
| CAS:105-92-0 | KEGG COMPOUND |
| Citations |
|---|