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275812-32-3

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  • Urea,N-(5-acetyl-4-methyl-2-thiazolyl)-N'-[(1R,2S)-2-[[(3S)-3-[(4-fluorophenyl)methyl]-1-piperidinyl]methyl]cyclohexyl]-

    Cas No: 275812-32-3

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275812-32-3 Usage

General Description

CCR3 antagonist refers to a class of chemicals that inhibit the function of the C-C chemokine receptor type 3 (CCR3), a protein involved in immune and inflammatory responses. These antagonists work by blocking the binding of specific chemokines to the CCR3 receptor, thereby preventing the activation and migration of certain immune cells, such as eosinophils and basophils, that are involved in allergic and inflammatory diseases. By inhibiting CCR3, these chemicals have the potential to reduce inflammation and tissue damage associated with conditions such as asthma, allergic rhinitis, and atopic dermatitis. Therefore, CCR3 antagonists are being researched and developed as potential treatments for these and other diseases characterized by excessive immune responses.

Check Digit Verification of cas no

The CAS Registry Mumber 275812-32-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,5,8,1 and 2 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 275812-32:
(8*2)+(7*7)+(6*5)+(5*8)+(4*1)+(3*2)+(2*3)+(1*2)=153
153 % 10 = 3
So 275812-32-3 is a valid CAS Registry Number.

275812-32-3Downstream Products

275812-32-3Related news

The small molecular CCR3 Antagonist (cas 275812-32-3) YM344031 attenuates neurodegenerative pathologies and improves learning and memory performance in a mouse model of Alzheimer’s disease07/15/2019

The chemokine C-C receptor 3 (CCR3) plays a role in the pathogenesis of Alzheimer’s disease (AD). Based on our previous observations that deletion of CCR3 prevented neurodegenerative pathologies in amyloid precursor protein/presenilin 1 (APP/PS1) double-transgenic mice, we hypothesize that CCR3...detailed

275812-32-3Relevant articles and documents

Stereoselective process for a CCR3 antagonist

Yue, Tai-Yuen,McLeod, Douglas D.,Albertson, Kevin B.,Beck, Steven R.,Deerberg, Joerg,Fortunak, Joseph M.,Nugent, William A.,Radesca, Lilian A.,Tang, Liya,Xiang, Cathie Dong

, p. 262 - 271 (2012/12/22)

A convergent, multikilogram, stereoselective synthesis of 1 is described. A key fragment, (S)-3-(4-fluorobenzyl)piperidine (2) was synthesized from valerolactam in three steps using our recently discovered Ir-BDPP-catalyzed asymmetric hydrogenation. Anoth

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