4,4-Difluoro-N-((S)-3-((1R,3R,5S)-3-(3-Isopropyl-5-Methyl-4H-1,2,4-Triazol-4-Yl)-8-Azabicyclo[3.2.1]Octan-8-Yl)-1-Phenylpropyl)Cyclohexane-1-Carboxamide 4,4-二氟-N-((S)-3-((1R,3R,5S)-3-(3-异丙基-5-甲基-4H-1,2,4-三唑-4-基)-8-氮杂双环[3.2.1]辛烷-8-基)-1-苯基丙基)环己烷-1-酰胺
CAS 376348-65-1 MFCD09953791
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专业采购外包团队在线服务
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分类
- Chiral Reagents
- Inhibitors
- Pharmaceuticals
- Intermediates & Fine Chemicals
- Pfizer compounds
产品应用
- Potent, non-competitive CCR5 receptor antagonist; inhibits binding of HIV viral coat protein gp120. Antiviral.
相关文献及参考
- [2]. Mencarelli A, et al. Highly specific blockade of CCR5 inhibits leukocyte trafficking and reduces mucosal inflammation in murine colitis. Sci Rep. 2016 Aug 5;6:30802.
- [3]. Romero-Sánchez MC, et al. Effect of maraviroc on HIV-disease progression-related biomarkers. Antimicrob Agents Chemother. 2012 Nov;56(11):5858-64.
- [4]. Huilin Mou, et al. NRSF and CCR5 Established Neuron-glia Communication during Acute and Chronic Stresses. Journal of Drug Metabolism & Toxicology. January 10, 2016.
- Fumero, E., et al.: Clin. Microbiol. Infect., 9, 1077 (2003),
- Walker, D.K., et al.: Drug Metab. Dispos., 33, 587 (2005),
- Wood, A., et al.: Prog. Med. Chem., 43, 239 (2005),
- [1]. Dor
- [1]. Dorr P, et al. Maraviroc (UK-427,857), a potent, orally bioavailable, and selective small-molecule inhibitor of chemokine receptor CCR5 with broad-spectrum anti-human immunodeficiency virus type 1 activity. Antimicrob Agents Chemother. 2005 Nov;49(11):472