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(Q28529715)
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all-trans-retinal
chemical compound
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Statements
instance of
type of chemical entity
0 references
subclass of
10,15-cyclophytane diterpenoid
0 references
retinal
0 references
part of
all-trans retinal binding
subject has role
reactant
1 reference
stated in
Gene Ontology release 2019-11-16
beta-carotene 15,15'-dioxygenase activity
1 reference
stated in
Gene Ontology release 2020-05-02
Rhea release 113
NAD-retinol dehydrogenase activity
1 reference
stated in
Gene Ontology release 2020-05-02
Rhea release 113
NADP-retinol dehydrogenase activity
1 reference
stated in
Gene Ontology release 2020-05-02
Rhea release 113
all-trans-8'-apo-beta-carotenal 15,15'-oxygenase
1 reference
stated in
Gene Ontology release 2020-05-02
Rhea release 113
chemical structure
All-trans-Retinal.svg
423 × 120; 7 KB
0 references
mass
284.214015516
dalton
1 reference
based on heuristic
inferred from isomeric SMILES
chemical formula
C₂₀H₂₈O
0 references
canonical SMILES
CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=O)C)C
0 references
isomeric SMILES
CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=O)C(C)(C)CCC1
0 references
found in taxon
Homo sapiens
2 references
stated in
Recon 2.2: from reconstruction to model of human metabolism
stated in
A community-driven global reconstruction of human metabolism.
Galleria mellonella
1 reference
stated in
NinaB combines carotenoid oxygenase and retinoid isomerase activity in a single polypeptide
Mycobacterium tuberculosis
1 reference
stated in
The Mycobacterium tuberculosis ORF Rv0654 encodes a carotenoid oxygenase mediating central and excentric cleavage of conventional and aromatic carotenoids
Suberites domuncula
1 reference
stated in
Differential expression of the demosponge (Suberites domuncula) carotenoid oxygenases in response to light: protection mechanism against the self-produced toxic protein (Suberitine)
Haloarcula japonica
1 reference
stated in
Complete biosynthetic pathway of the C50 carotenoid bacterioruberin from lycopene in the extremely halophilic archaeon Haloarcula japonica
Nostoc
1 reference
stated in
Identification of carotenoid cleavage dioxygenases from Nostoc sp. PCC 7120 with different cleavage activities
Rana temporaria
1 reference
stated in
Carotenoids, vitamin A and 7-dehydrosteroid in the frog, Rana temporaria
Panax ginseng
1 reference
stated in
Comparative research of chemical constituents, antifungal and antitumor properties of ether extracts of Panax ginseng and its endophytic fungus
tomato
1 reference
stated in
Identification of retinal in higher plants: Is a rhodopsinlike protein the blue light receptor?
subject has role
primary metabolite
1 reference
stated in
Reactome
reference URL
https://reactome.org/PathwayBrowser/#/R-HSA-1430728&DTAB=MT
Identifiers
InChI
InChI=1S/C20H28O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,15H,7,10,14H2,1-5H3/b9-6+,12-11+,16-8+,17-13+
0 references
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
1 reference
stated in
ChEBI release 2020-09-01
CAS Registry Number
116-31-4
1 reference
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
stated in
CAS Common Chemistry
retrieved
10 April 2021
reference URL
https://commonchemistry.cas.org/detail?cas_rn=116-31-4
PubChem CID
638015
0 references
ChEBI ID
17898
mapping relation type
exact match
1 reference
matched by identifier from
International Chemical Identifier
InChI
InChI=1S/C20H28O/c1-16(8-6-9-17(2)13-15-21)11-12-19-18(3)10-7-14-20(19,4)5/h6,8-9,11-13,15H,7,10,14H2,1-5H3/b9-6+,12-11+,16-8+,17-13+
ChEMBL ID
CHEMBL81379
1 reference
stated in
IUPHAR/BPS Guide to PHARMACOLOGY
retrieved
8 February 2021
SureChEMBL ID
SCHEMBL106994
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
SCHEMBL106993
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
UniChem compound ID
209499
1 reference
stated in
UniChem
CCDC Number
1275673
1 reference
stated in
Cambridge Structural Database
retrieved
10 January 2023
based on heuristic
InChIKey match
CSD Refcode
TRETAL03
1 reference
stated in
Cambridge Structural Database
retrieved
10 January 2023
based on heuristic
InChIKey match
MassBank accession ID
MSBNK-BGC_Munich-RP014201
0 references
MSBNK-BGC_Munich-RP014202
0 references
MSBNK-BGC_Munich-RP014203
0 references
NMRShiftDB structure ID
10016299
1 reference
matched by identifier from
InChIKey
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
DSSTox substance ID
DTXSID5025998
1 reference
stated in
Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
DSSTOX compound identifier
DTXCID205998
0 references
NSC number
20811
0 references
122757
0 references
626581
0 references
Guide to Pharmacology Ligand ID
2350
1 reference
stated in
IUPHAR/BPS Guide to PHARMACOLOGY
retrieved
5 February 2021
Human Metabolome Database ID
HMDB0001358
2 references
based on heuristic
inferred from InChIKey
matched by identifier from
InChIKey
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
UNII
RR725D715M
1 reference
matched by identifier from
InChIKey
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
Probes And Drugs ID
PD017224
0 references
LIPID MAPS ID
LMPR01090002
1 reference
stated in
LIPID MAPS
reference URL
http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download
retrieved
30 June 2018
SwissLipids ID
SLM:000000435
2 references
stated in
SwissLipids
reference URL
https://www.swisslipids.org/#/downloads
retrieved
6 November 2021
matched by identifier from
InChIKey
InChIKey
NCYCYZXNIZJOKI-OVSJKPMPSA-N
PDB ligand ID
RET
0 references
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