
Cenicriviroc
CAS No. 497223-25-3
Cenicriviroc ( TAK-652 | TBR-652 )
产品货号. M24457 CAS No. 497223-25-3
Cenicriviroc 是一种口服活性的 CCR2/CCR5 双重拮抗剂。它还可以抑制 HIV-1 和 HIV-2,并具有有效的抗感染和抗炎活性。
纯度: >98% (HPLC)






规格 | 价格/人民币 | 库存 | 数量 |
2MG | ¥729 | 有现货 |
![]() ![]() |
5MG | ¥1045 | 有现货 |
![]() ![]() |
10MG | ¥1661 | 有现货 |
![]() ![]() |
25MG | ¥3337 | 有现货 |
![]() ![]() |
50MG | ¥4309 | 有现货 |
![]() ![]() |
100MG | ¥6221 | 有现货 |
![]() ![]() |
200MG | 获取报价 | 有现货 |
![]() ![]() |
500MG | 获取报价 | 有现货 |
![]() ![]() |
1G | 获取报价 | 有现货 |
![]() ![]() |
生物学信息
-
产品名称Cenicriviroc
-
注意事项本公司产品仅用于科研实验,不得用于人体或动物的临床与诊断
-
产品简述Cenicriviroc 是一种口服活性的 CCR2/CCR5 双重拮抗剂。它还可以抑制 HIV-1 和 HIV-2,并具有有效的抗感染和抗炎活性。
-
产品描述Cenicriviroc is an orally active, dual antagonist of CCR2/CCR5. It also inhibits both HIV-1 and HIV-2, and displays potent anti-infective and anti-inflammatory activity.(In Vitro):Cenicriviroc prevents human immunodeficiency virus type 1 (HIV-1) from cellular entry. Regarding the 4 R5 HIV-2 clinical isolates tested, effective concentration 50% EC50 for cenicriviroc are 0.03, 0.33, 0.45 and 0.98 nM. The dual-tropic and the X4-tropic HIV-2 strains are resistant to cenicriviroc with EC50 at >1000 nM, and MPI at 33% and 4%, respectively.(In Vivo):Cenicriviroc (≥20 mg/kg/day) significantly reduces monocyte/macrophage recruitment in vivo. At these doses, cenicriviroc shows antifibrotic effects, with significant reductions in collagen deposition, and collagen type 1 protein and mRNA expression across the three animal models of fibrosis. In the NASH model, cenicriviroc significantly reduces the non-alcoholic fatty liver disease activity score. Cenicriviroc treatment has no notable effect on body or liver/kidney weight.
-
体外实验Cenicriviroc prevents human immunodeficiency virus type 1 (HIV-1) from cellular entry. Regarding the 4 R5 HIV-2 clinical isolates tested, effective concentration 50% EC50?for cenicriviroc are 0.03, 0.33, 0.45 and 0.98 nM. The dual-tropic and the X4-tropic HIV-2 strains are resistant to cenicriviroc with EC50 at >1000 nM, and MPI at 33% and 4%, respectively.
-
体内实验Cenicriviroc (≥20 mg/kg/day) significantly reduces monocyte/macrophage recruitment in vivo. At these doses, cenicriviroc shows antifibrotic effects, with significant reductions in collagen deposition, and collagen type 1 protein and mRNA expression across the three animal models of fibrosis. In the NASH model, cenicriviroc significantly reduces the non-alcoholic fatty liver disease activity score. Cenicriviroc treatment has no notable effect on body or liver/kidney weight.
-
同义词TAK-652 | TBR-652
-
通路Autophagy
-
靶点CCR
-
受体CCR2| CCR5| HIV-1| HIV-2
-
研究领域——
-
适应症——
化学信息
-
CAS Number497223-25-3
-
分子量696.94
-
分子式C42H52N4O4
-
纯度>98% (HPLC)
-
溶解度DMSO:120 mg/mL (172.19 mM)
-
SMILESCCCCOCCOC1=CC=C(C=C1)C2=CC/3=C(C=C2)N(CCC/C(=C3)/C(=O)NC4=CC=C(C=C4)[S@@](=O)CC5=CN=CN5CCC)CC(C)C
-
化学全称——
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1.Lefebvre E, et al. Antifibrotic Effects of the Dual CCR2/CCR5 Antagonist Cenicriviroc in Animal Models of Liver and Kidney Fibrosis. PLoS One. 2016 Jun 27;11(6):e0158156
产品手册




关联产品
-
CCR1 antagonist 6
CCR1 antagonist 6 (compound 16q) 是 CCR1 的一个拮抗剂,IC50 值为 3 nM。
-
Cenicriviroc
Cenicriviroc 是一种口服活性的 CCR2/CCR5 双重拮抗剂。它还可以抑制 HIV-1 和 HIV-2,并具有有效的抗感染和抗炎活性。
-
Leronlimab
Leronlimab (PRO 140) 是一种人源化 IgG4 抗 CCR5 单克隆抗体。leronlimumab 抑制 CCR 介导的 HIV-1 病毒和小鼠肿瘤模型肺转移。Leronlimab 可用于 HIV 非酒精性脂肪性肝炎 (NASH) 和癌症的研究。