U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C14H12O
Molecular Weight 196.2445
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of STILBENE OXIDE, CIS-

SMILES

O1[C@@H]([C@@H]1C2=CC=CC=C2)C3=CC=CC=C3

InChI

InChIKey=ARCJQKUWGAZPFX-OKILXGFUSA-N
InChI=1S/C14H12O/c1-3-7-11(8-4-1)13-14(15-13)12-9-5-2-6-10-12/h1-10,13-14H/t13-,14+

HIDE SMILES / InChI

Molecular Formula C14H12O
Molecular Weight 196.2445
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Expression and activity of microsomal epoxide hydrolase in follicles isolated from mouse ovaries.
2002 Jul
Activation of nitrous oxide and selective epoxidation of alkenes catalyzed by the manganese-substituted polyoxometalate, [Mn(III)2ZnW(Zn2W9O34)2]10-.
2002 Jul 31
Brassica napus soluble epoxide hydrolase (BNSEH1).
2002 Nov
Overexpression of Arabidopsis thaliana soluble epoxide hydrolase 1 in Pichia pastoris and characterisation of the recombinant enzyme.
2002 Oct
Characterization and cDNA cloning of a clofibrate-inducible microsomal epoxide hydrolase in Drosophila melanogaster.
2003 Dec
Non-synonymous single nucleotide alterations in the microsomal epoxide hydrolase gene and their functional effects.
2003 Mar
Kinetics and mechanism of rhenium-catalyzed O atom transfer from epoxides.
2003 Sep 10
Functional analysis of human microsomal epoxide hydrolase genetic variants.
2004 Nov 20
Parallel mechanistic studies on the counterion effect of manganese salen and porphyrin complexes on olefin epoxidation by iodosylarenes.
2005 Feb
Regulation of JH epoxide hydrolase versus JH esterase activity in the cabbage looper, Trichoplusia ni, by juvenile hormone and xenobiotics.
2005 May
The Saccharomyces cerevisiae ORF YNR064c protein has characteristics of an 'orphaned' epoxide hydrolase.
2005 May 15
Modular, active, and robust Lewis acid catalysts supported on a metal-organic framework.
2010 Jul 19
Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:50:49 GMT 2023
Edited
by admin
on Fri Dec 15 19:50:49 GMT 2023
Record UNII
GIX80CN6Z7
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
STILBENE OXIDE, CIS-
Common Name English
CIS-2,3-DIPHENYLOXIRANE
Systematic Name English
CIS-1,2-DIPHENYLETHYLENE OXIDE
Common Name English
OXIRANE, 2,3-DIPHENYL-, (2R,3S)-REL-
Common Name English
STILBENE OXIDE, MESO-
Common Name English
MESO-STILBENE OXIDE
Common Name English
STILBENE CIS-EPOXIDE
Common Name English
CIS-STILBENE OXIDE
Common Name English
NSC-133513
Code English
Code System Code Type Description
EPA CompTox
DTXSID20937561
Created by admin on Fri Dec 15 19:50:49 GMT 2023 , Edited by admin on Fri Dec 15 19:50:49 GMT 2023
PRIMARY
FDA UNII
GIX80CN6Z7
Created by admin on Fri Dec 15 19:50:49 GMT 2023 , Edited by admin on Fri Dec 15 19:50:49 GMT 2023
PRIMARY
PUBCHEM
98511
Created by admin on Fri Dec 15 19:50:49 GMT 2023 , Edited by admin on Fri Dec 15 19:50:49 GMT 2023
PRIMARY
CHEBI
50004
Created by admin on Fri Dec 15 19:50:49 GMT 2023 , Edited by admin on Fri Dec 15 19:50:49 GMT 2023
PRIMARY
NSC
133513
Created by admin on Fri Dec 15 19:50:49 GMT 2023 , Edited by admin on Fri Dec 15 19:50:49 GMT 2023
PRIMARY
CAS
1689-71-0
Created by admin on Fri Dec 15 19:50:49 GMT 2023 , Edited by admin on Fri Dec 15 19:50:49 GMT 2023
PRIMARY