Structure Database (LMSD)

Common Name
all-trans-5,6-Epoxyretinoic acid
Systematic Name
(2E,4E,6E,8E)-3,7-dimethyl-9-{2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl}nona-2,4,6,8-tetraenoic acid
Synonyms
LM ID
LMPR01090055
Formula
Exact Mass
Calculate m/z
316.203845
Status
Curated


Classification

Biological Context

all-trans-5,6-epoxy Retinoic acid (5,6-epoxy RA) is an agonist of all isoforms of the retinoic acid receptor (RAR; EC50s = 77, 35, and 4 nM for RARα, RARβ, and RARγ, respectively).1 5,6-epoxy RA (1 µM) also induces growth arrest of MCF-7 and NB4 cells in vitro.2,3 It is a natural metabolite of all-trans retinoic acid , which is a metabolite of vitamin A.4

This information has been provided by Cayman Chemical

References

1. McCormick, A.M., and Napoli, J.L. Identification of 5,6-epoxyretinoic acid as an endogenous retinol metabolite. The Journal of Biological Chemisty 257(4), 1730-1735 (1982).
2. Idrest, N., Marill, J., Flexor, M.A., et al. Activation of retinoic acid receptor-dependent transcription by all-trans-retinoic acid metabolites and isomers. The Journal of Biological Chemisty 277(25), 31491-31498 (2002).
4. Idres, N., Benoît, G., Flexor, M.A., et al. Granulocytic differentiation of human NB4 promyelocytic leukemia cells induced by all-trans retinoic acid metabolites. Cancer Res. 61(2), 700-705 (2001).

References

Taxonomy Information

Curated from
NCBI taxonomy class
Reference
Rattus norvegicus (#10116)
Mammalia (#40674)
Identification of 5,6-epoxyretinoic acid as an endogenous retinol metabolite.,
J Biol Chem, 1982
Pubmed ID: 7056740

String Representations

InChiKey (Click to copy)
KEEHJLBAOLGBJZ-WEDZBJJJSA-N
InChi (Click to copy)
InChI=1S/C20H28O3/c1-15(8-6-9-16(2)14-17(21)22)10-13-20-18(3,4)11-7-12-19(20,5)23-20/h6,8-10,13-14H,7,11-12H2,1-5H3,(H,21,22)/b9-6+,13-10+,15-8+,16-14+
SMILES (Click to copy)
C12(OC1(C)CCCC2(C)C)/C=C/C(/C)=C/C=C/C(/C)=C/C(=O)O

Other Databases

KEGG ID
HMDB ID
CHEBI ID
PubChem CID
Cayman ID

Calculated Physicochemical Properties

Heavy Atoms 23
Rings 2
Aromatic Rings 0
Rotatable Bonds 5
Van der Waals Molecular Volume 343.01
Topological Polar Surface Area 49.83
Hydrogen Bond Donors 1
Hydrogen Bond Acceptors 3
logP 5.39
Molar Refractivity 94.31

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Created at
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Updated at
20th Dec 2022