Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H12O |
Molecular Weight | 184.2338 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
C(OC1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=BOTNYLSAWDQNEX-UHFFFAOYSA-N
InChI=1S/C13H12O/c1-3-7-12(8-4-1)11-14-13-9-5-2-6-10-13/h1-10H,11H2
Molecular Formula | C13H12O |
Molecular Weight | 184.2338 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
Crystal structures of leukotriene A4 hydrolase in complex with captopril and two competitive tight-binding inhibitors. | 2002 Oct |
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1,5-Disubstituted imidazoles inhibit juvenile hormone biosynthesis by the corpora allata of the mosquito Aedes aegypti. | 2003 Nov |
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A sensitive class specific immunoassay for the detection of pyrethroid metabolites in human urine. | 2004 Feb |
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The exchanger inhibitory peptide region-dependent inhibition of Na+/Ca2+ exchange by SN-6 [2-[4-(4-nitrobenzyloxy)benzyl]thiazolidine-4-carboxylic acid ethyl ester], a novel benzyloxyphenyl derivative. | 2004 Jul |
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Structural variations of 1-(4-(phenoxymethyl)benzyl)piperidines as nonimidazole histamine H3 receptor antagonists. | 2004 May 15 |
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Forefront of Na+/Ca2+ exchanger studies: molecular pharmacology of Na+/Ca2+ exchange inhibitors. | 2004 Sep |
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Discovery of N-(3-{4-[(3-fluorobenzyl)oxy]phenoxy}propyl)-2-pyridin-4-ylacetamide as a potent and selective reverse NCX inhibitor. | 2005 Aug |
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Synthesis and structure-activity relationships of benzyloxyphenyl derivatives as a novel class of NCX inhibitors: effects on heart failure. | 2005 Feb 1 |
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Sodium-calcium exchange inhibitors: therapeutic potential in cardiovascular diseases. | 2005 Jul |
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Photochemical reactions of triplet p-phenylbenzyl derivatives studied by using laser flash triplet-sensitization techniques. | 2005 Mar |
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SAR, species specificity, and cellular activity of cyclopentene dicarboxylic acid amides as DHODH inhibitors. | 2005 Nov 1 |
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Mimetics of the tri- and tetrasaccharide epitope of GQ1balpha as myelin-associated glycoprotein (MAG) ligands. | 2007 Dec 1 |
|
Na+/Ca2+ exchange as a drug target--insights from molecular pharmacology and genetic engineering. | 2007 Mar |
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Three Na+/Ca2+ exchanger (NCX) variants are expressed in mouse osteoclasts and mediate calcium transport during bone resorption. | 2007 May |
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Efficacy of various pyrethroid structures against a highly metabolically resistant isogenic strain of Helicoverpa armigera (Lepidoptera: Noctuidae) from China. | 2007 Oct |
|
Na+/Ca2+ exchange inhibitors: a new class of calcium regulators. | 2007 Sep |
|
Novel high-affinity and selective biaromatic 4-substituted gamma-hydroxybutyric acid (GHB) analogues as GHB ligands: design, synthesis, and binding studies. | 2008 Dec 25 |
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2-(2-Benzyl-oxyphen-yl)-1H-benzimid-azole. | 2008 Feb 20 |
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Discovery of leukotriene A4 hydrolase inhibitors using metabolomics biased fragment crystallography. | 2009 Aug 13 |
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Anti human immunodeficiency virus-1 (HIV-1) agents 1. Discovery of benzyl phenyl ethers as new HIV-1 inhibitors in vitro. | 2009 Jan |
|
Molecular determinants on the insect sodium channel for the specific action of type II pyrethroid insecticides. | 2009 Jan 15 |
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Evidence for dose-additive effects of pyrethroids on motor activity in rats. | 2009 Oct |
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Inhibition of beta-cell sodium-calcium exchange enhances glucose-dependent elevations in cytoplasmic calcium and insulin secretion. | 2010 Jul |
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Biomimetic synthesis and anti-HIV activity of dimeric phloroglucinols. | 2010 Mar 1 |
|
Design, synthesis, and preliminary biological evaluation of pyrrolo[3,4-c]quinolin-1-one and oxoisoindoline derivatives as aggrecanase inhibitors. | 2010 May 3 |
|
1-Benz-yloxy-4-(2-nitro-ethen-yl)benzene. | 2010 Oct 30 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:18:17 GMT 2023
by
admin
on
Fri Dec 15 18:18:17 GMT 2023
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Record UNII |
BUE863N0L8
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Record Status |
Validated (UNII)
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Record Version |
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BUE863N0L8
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70352
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DTXSID70870813
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