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Maribavir

CAS No. 176161-24-3

Maribavir ( Maribavir | 1263W-94 | BW-1263W-94 | GW-1263 )

产品货号. M17375 CAS No. 176161-24-3

Maribavir 是一种口服苯并咪唑核苷化合物,具有抗巨细胞病毒 (CMV) 活性。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
5MG ¥1169 有现货
10MG ¥1891 有现货
25MG ¥3329 有现货
50MG ¥4622 有现货
100MG ¥6201 有现货
200MG ¥8532 有现货
500MG 获取报价 有现货
1G 获取报价 有现货
1 mL x 10 mM in DMSO ¥1292 有现货

生物学信息

  • 产品名称
    Maribavir
  • 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
    Maribavir 是一种口服苯并咪唑核苷化合物,具有抗巨细胞病毒 (CMV) 活性。
  • 产品描述
    Maribavir, also known as 1263W-94; BW-1263W-94; GW-1263; GW-257406X; SHP-620; VP-41263; BW-1263W94, is an UL97 kinase inhibitor potentially for the treatment of cytomegalovirus (CMV) infection. The mechanism by which maribavir inhibits HCMV replication is by inhibition of an HCMV encoded protein kinase enzyme called UL97 or pUL97.(In Vitro):Maribavir is a potent inhibitor of the autophosporylation of the wild type and all the major Ganciclovir (GCV) resistant UL97 mutants analysed with a mean IC50 of 35 nM. The M460I mutation results in hypersensitivity to Maribavir with an IC50 of 4.8 nM. A Maribavir resistant mutant of UL97 (L397R) is functionally compromised as both a Ganciclovir kinase and a protein kinase (~ 10% of wild type levels). Enzyme kinetic experiments demonstrate that Maribavir is a competitive inhibitor of ATP with a Ki of 10 nM. Maribavir (1263W94) inhibits viral replication in a dose-dependent manner, with IC50 of 0.12±0.01 μM as measured by a multicycle DNA hybridization assay. The pUL97 protein kinase is strongly inhibited by Maribavir, with 50% inhibition occurring at 3 nM.
  • 体外实验
    Maribavir is a potent inhibitor of the autophosporylation of the wild type and all the major Ganciclovir (GCV) resistant UL97 mutants analysed with a mean IC50 of 35 nM. The M460I mutation results in hypersensitivity to Maribavir with an IC50 of 4.8 nM. A Maribavir resistant mutant of UL97 (L397R) is functionally compromised as both a Ganciclovir kinase and a protein kinase (~ 10% of wild type levels). Enzyme kinetic experiments demonstrate that Maribavir is a competitive inhibitor of ATP with a Ki of 10 nM. Maribavir (1263W94) inhibits viral replication in a dose-dependent manner, with IC50 of 0.12±0.01 μM as measured by a multicycle DNA hybridization assay. The pUL97 protein kinase is strongly inhibited by Maribavir, with 50% inhibition occurring at 3 nM.
  • 体内实验
    ——
  • 同义词
    Maribavir | 1263W-94 | BW-1263W-94 | GW-1263
  • 通路
    GPCR/G Protein
  • 靶点
    S1P Receptor
  • 受体
    HCMV
  • 研究领域
    Infection
  • 适应症
    ——

化学信息

  • CAS Number
    176161-24-3
  • 分子量
    376.24
  • 分子式
    C15H19Cl2N3O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : ≥ 51 mg/mL 135.55 mM
  • SMILES
    Clc1cc2n([C@@H]3O[C@@H]([C@@H](O)[C@H]3O)CO)c(NC(C)C)nc2cc1Cl
  • 化学全称
    5,6-Dichloro-2-(isopropylamino)-1-beta-L-ribofuranosyl-1H-benzimidazole

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. Karen KB, et al. Antimicrob Agents ChemOthers. August 2002 vol. 46 no. 8 2365-2372 2. Whitehurst CB, et al. MJ Virol. 2013 May;87(9):5311-5.
产品手册
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