(Q28529715)

English

all-trans-retinal

chemical compound

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Statements

type of chemical entity

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10,15-cyclophytane diterpenoid

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chemical structure

All-trans-Retinal.svg
423 × 120; 7 KB

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284.214015516 dalton

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based on heuristic

inferred from isomeric SMILES

chemical formula

C₂₀H₂₈O

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canonical SMILES

CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=O)C)C

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isomeric SMILES

CC1=C(/C=C/C(C)=C/C=C/C(C)=C/C=O)C(C)(C)CCC1

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2 references

Recon 2.2: from reconstruction to model of human metabolism

A community-driven global reconstruction of human metabolism.

Galleria mellonella

1 reference

NinaB combines carotenoid oxygenase and retinoid isomerase activity in a single polypeptide

Mycobacterium tuberculosis

1 reference

The Mycobacterium tuberculosis ORF Rv0654 encodes a carotenoid oxygenase mediating central and excentric cleavage of conventional and aromatic carotenoids

Suberites domuncula

1 reference

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

Complete biosynthetic pathway of the C50 carotenoid bacterioruberin from lycopene in the extremely halophilic archaeon Haloarcula japonica

1 reference

Identification of carotenoid cleavage dioxygenases from Nostoc sp. PCC 7120 with different cleavage activities

Rana temporaria

1 reference

Carotenoids, vitamin A and 7-dehydrosteroid in the frog, Rana temporaria

1 reference

Comparative research of chemical constituents, antifungal and antitumor properties of ether extracts of Panax ginseng and its endophytic fungus

1 reference

Identification of retinal in higher plants: Is a rhodopsinlike protein the blue light receptor?

subject has role

primary metabolite

1 reference

https://reactome.org/PathwayBrowser/#/R-HSA-1430728&DTAB=MT

Identifiers

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+

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NCYCYZXNIZJOKI-OVSJKPMPSA-N

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ChEBI release 2020-09-01

CAS Registry Number

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NCYCYZXNIZJOKI-OVSJKPMPSA-N

CAS Common Chemistry

10 April 2021

https://commonchemistry.cas.org/detail?cas_rn=116-31-4

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mapping relation type

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1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

8 February 2021

UniChem compound ID

1 reference

1 reference

Cambridge Structural Database

10 January 2023

based on heuristic

1 reference

Cambridge Structural Database

10 January 2023

based on heuristic

MassBank accession ID

MSBNK-BGC_Munich-RP014201

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MSBNK-BGC_Munich-RP014202

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MSBNK-BGC_Munich-RP014203

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DSSTox substance ID

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Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

DSSTOX compound identifier

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Guide to Pharmacology Ligand ID

1 reference

IUPHAR/BPS Guide to PHARMACOLOGY

5 February 2021

Human Metabolome Database ID

1 reference

based on heuristic

inferred from InChIKey

Probes And Drugs ID

0 references

1 reference

http://www.lipidmaps.org/rest/compound/lm_id/LM/all/download

30 June 2018

1 reference

https://www.swisslipids.org/#/downloads

6 November 2021

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Sitelinks

Wikipedia(0 entries)

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Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

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Wikivoyage(0 entries)

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Multilingual sites(0 entries)

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