Cenicriviroc

    
97%

Cenicriviroc

源叶(MedMol)
S85553 一键复制产品信息
497223-25-3
C41H52N4O4S
696.94
货号 产品规格 价格(RMB) 库存(上海) 北京 武汉 南京 购买数量
S85553-1mg 97% ¥250.00 2 - - -
S85553-5mg 97% ¥1040.00 6 - - -
S85553-10mg 97% ¥1530.00 5 - - -
S85553-50mg 97% ¥4080.00 5 - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品

产品介绍

Cenicriviroc (CVC, TAK-652, TBR-652) 是一种有效的、口服活性的 CC chemokine receptor 2 (CCR2) 和 CCR5 的双效抑制剂。Cenicriviroc 还可抑制 HIV-1 和 HIV-2 并具有有效的抗炎和抗感染活性

产品描述:

Cenicriviroc (CVC, TAK-652, TBR-652) 是一种有效的、口服活性的 CC chemokine receptor 2 (CCR2) 和 CCR5 的双效抑制剂。Cenicriviroc 还可抑制 HIV-1 和 HIV-2 并具有有效的抗炎和抗感染活性

靶点: CCR2;CCR5;HIV-1;HIV-2;HIVProtease;CCR
体内研究: Cenicriviroc significantly reduces monocyte/macrophage recruitment in vivo at doses >= 20 mg/kg/day (p < 0.05). At these doses, Cenicriviroc shows antifibrotic effects, with significant reductions in collagen deposition (p < 0.05), and collagen type 1 protein and mRNA expression across the three animal models of fibrosis. In the NASH model, Cenicriviroc significantly reduces the nonalcoholic fatty liver disease activity score (p < 0.05 vs. controls). Cenicriviroc treatment has no notable effect on body or liver/kidney weight.
细胞实验: Cell lines: activated macrophages Concentrations: 1 μM Incubation Time: 2 h Method: TG is injected intraperitoneally into male C57BL/6 mice and activated macrophages are collected 48 hours later by peritoneal lavage. Chemotaxis is assayed using a Transwell1 Chamber with a 5 μm-pore size polycarbonate filter. Briefly, cells are incubated for 2 hours in the presence of 1 nM CCL2 and/or 1 μM Cenicriviroc (dissolved in dimethyl sulfoxide with 0.5% acetic acid and diluted 1:1000 with serum-free Roswell Park Memorial Institute-1640 medium and 0.5% bovine serum albumin). Cells are harvested from the lower compartment and analyzed by flow cytometry to enumerate F4/80+CD11b+ macrophages using a 3-laser BD FACSCanto. Results are analyzed using FlowJo software.
动物实验: Animal Models: 8–10 weeks old male C57BL/6 mice, 10–12 weeks old male Sprague-Dawley rats Dosages: 5 mg/kg, 20 mg/kg, 100 mg/kg, 30 mg/kg Administration: Oral gavage, IP
参考文献: 1. Jacob Lalezari, et al. J Acquir Immune Defic Syndr. 2011 Jun 1;57(2):118-25. 2. Eric Lefebvre, et al. PLoS One. 2016 Jun 27;11(6):e0158
溶解性: Soluble  in  DMSO、Ethanol
保存条件: 2-8℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 1.435 ml 7.174 ml 14.348 ml
5 mM 0.287 ml 1.435 ml 2.87 ml
10 mM 0.143 ml 0.717 ml 1.435 ml
50 mM 0.029 ml 0.143 ml 0.287 ml
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参考文献

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摩尔浓度计算器

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