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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)

COA Datasheet HNMR HPLC MSDS Handing Instructions
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 Number
    497223-25-3
  • 分子量
    696.94
  • 分子式
    C42H52N4O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO:120 mg/mL (172.19 mM)
  • SMILES
    CCCCOCCOC1=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
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