all-trans-retinol (CHEBI:17336)

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ChEBI Name	all-trans-retinol

ChEBI ID	CHEBI:17336

ChEBI ASCII Name	all-trans-retinol

Definition	A retinol in which all four exocyclic double bonds have E- (trans-) geometry.

Stars	This entity has been manually annotated by the ChEBI Team.

Secondary ChEBI IDs	CHEBI:8816, CHEBI:12783, CHEBI:22349

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Formula

C20H30O

Net Charge

Average Mass

286.459

Monoisotopic Mass

286.22967

InChI

InChI=1S/C20H30O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,21H,7,10,14-15H2,1-5H3/b9-6+,12-11+,16-8+,17-13+

InChIKey

FPIPGXGPPPQFEQ-OVSJKPMPSA-N

SMILES

C\C(=C/CO)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C

Metabolite of Species	Details
Mus musculus (NCBI:txid10090)	Source: BioModels - MODEL1507180067 See: PubMed
Taxus chinensis (NCBI:txid29808)	See: PubMed
Pandanus tectorius (NCBI:txid4726)	See: PubMed
Homo sapiens (NCBI:txid9606)	See: DOI
Homo sapiens (NCBI:txid9606)	Found in blood (UBERON:0000178). See: Geigy Scientific Tables, 8th Rev edition, pp. 165-177. Edited by C. Lentner, West Cadwell, N.J.: Medical education Div., Ciba-Geigy Corp., Basel, Switzerland c1981-1992.
Homo sapiens (NCBI:txid9606)	Found in saliva (UBERON:0001836). See: Dame, ZT. et al. (2014) The Human Saliva Metabolome (manuscript in preparation)

Roles Classification
Biological Role(s):	human metabolite Any mammalian metabolite produced during a metabolic reaction in humans (Homo sapiens). (via retinol ) plant metabolite Any eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms. mouse metabolite Any mammalian metabolite produced during a metabolic reaction in a mouse (Mus musculus). metabolite Any intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites. (via vitamin A ) fat-soluble vitamin (role) Any vitamin that dissolves in fats and are stored in body tissues. Unlike the water-soluble vitamins, they are stored in the body for long periods of time and generally pose a greater risk for toxicity when consumed in excess. (via vitamin A )

ChEBI Ontology
Outgoing	all-trans-retinol (CHEBI:17336) has role human metabolite (CHEBI:77746) all-trans-retinol (CHEBI:17336) has role mouse metabolite (CHEBI:75771) all-trans-retinol (CHEBI:17336) has role plant metabolite (CHEBI:76924) all-trans-retinol (CHEBI:17336) is a retinol (CHEBI:50211) all-trans-retinol (CHEBI:17336) is a vitamin A (CHEBI:12777)

Incoming	all-trans-3,4-didehydroretinol (CHEBI:132246) has functional parent all-trans-retinol (CHEBI:17336) all-trans-3-hydroxyretinol (CHEBI:156530) has functional parent all-trans-retinol (CHEBI:17336) all-trans-4-hydroxyretinol (CHEBI:132259) has functional parent all-trans-retinol (CHEBI:17336) all-trans-4-oxoretinol (CHEBI:44597) has functional parent all-trans-retinol (CHEBI:17336) all-trans-retinyl ester (CHEBI:63410) has functional parent all-trans-retinol (CHEBI:17336) all-trans-retinyl linoleate (CHEBI:70762) has functional parent all-trans-retinol (CHEBI:17336) all-trans-retinyl oleate (CHEBI:70760) has functional parent all-trans-retinol (CHEBI:17336) all-trans-retinyl palmitate (CHEBI:17616) has functional parent all-trans-retinol (CHEBI:17336) all-trans-retinyl stearate (CHEBI:70761) has functional parent all-trans-retinol (CHEBI:17336) retinyl acetate (CHEBI:32095) has functional parent all-trans-retinol (CHEBI:17336)

IUPAC Name

all-trans-retinol

Synonyms	Sources
(2E,4E,6E,8E)-3,7-dimethyl-9-(2,6,6-trimethylcyclohex-1-en-1-yl)nona-2,4,6,8-tetraen-1-ol	IUPAC
(all-E)-3,7-dimethyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2,4,6,8-nonatetraen-1-ol	HMDB
all-trans retinol	ChemIDplus
all-trans-Retinol	KEGG COMPOUND
all-trans-retinol	UniProt
all-trans-retinyl alcohol	ChemIDplus
all-trans-vitamin A	ChemIDplus
all-trans-vitamin A alcohol	NIST Chemistry WebBook
retinol (vit A)	DrugCentral
trans-retinol	HMDB
vitamin A	KEGG COMPOUND
vitamin A alcohol	ChemIDplus
Vitamin A1	KEGG COMPOUND
vitamin A₁	ChEBI
vitamin A1 alcohol	ChemIDplus

Last Modified

28 July 2021