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1H-Imidazole-4-carboxylic acid, 1,2-diphenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

475595-57-4

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475595-57-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 475595-57-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,5,5,9 and 5 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 475595-57:
(8*4)+(7*7)+(6*5)+(5*5)+(4*9)+(3*5)+(2*5)+(1*7)=204
204 % 10 = 4
So 475595-57-4 is a valid CAS Registry Number.

475595-57-4Relevant academic research and scientific papers

Asymmetric synthesis and biological evaluation of imidazole- and oxazole-containing synthetic lipoxin A4 mimetics (sLXms)

de Gaetano, Monica,Butler, Eibhlín,Gahan, Kevin,Zanetti, Andrea,Marai, Mariam,Chen, Jianmin,Cacace, Antonino,Hams, Emily,Maingot, Catherine,McLoughlin, Alisha,Brennan, Eoin,Leroy, Xavier,Loscher, Christine E.,Fallon, Padraic,Perretti, Mauro,Godson, Catherine,Guiry, Patrick J.

, p. 80 - 108 (2018/11/21)

Lipoxins (LXs) are endogenously generated eicosanoids with potent bio-actions consistent with attenuation of inflammation. The costly synthesis and metabolic instability of LXs may limit their therapeutic potential. Here we report the synthesis and charac

HETEROCYCLIC LIPXON ANALOGS AND USES THEROF

-

, (2018/03/09)

The present invention relates to a compound of formula (I): wherein L is an optionally substituted heterocyclic group excluding unsubstituted monocyclic pyridine groups; wherein a is 0, 1 or 2; wherein R1 is H or with R2 is a bond; wherein R2 is an optionally substituted alkoxy or aryloxy group, or with R1 forms a bond; wherein R3 is an optionally substituted alkyl group; and wherein R4 is CH2, CMe2 or O. Such compounds may be used in the treatment or prophylaxis of a disease or condition in which inhibition of acute inflammation and/or promotion of its resolution and/or suppression of fibrosis.

Synthesis and pharmacological evaluation of 1-[(1,2-diphenyl-1H-4-imidazolyl)methyl]-4-phenylpiperazines with clozapine-like mixed activities at dopamine D2, serotonin, and GABAA receptors

Asproni, Battistina,Pau, Amedeo,Bitti, Mauro,Melosu, Marilena,Cerri, Riccardo,Dazzi, Laura,Seu, Emanuele,Maciocco, Elisabetta,Sanna, Enrico,Busonero, Fabiol,Talani, Giuseppe,Pusceddu, Luca,Altomare, Cosimo,Trapani, Giuseppe,Biggio, Giovanni

, p. 4655 - 4668 (2007/10/03)

A series of 18 1-[(1,2-diphenyl-1H-4-imidazolyl)methyl]-4-piperazines (1a-r) were designed and synthesized as possible ligands with mixed dopamine (DA) D2/serotonin 5-HT1A affinity, with the aim of identifying novel compounds with ne

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