• 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号

Ledipasvir

CAS No. 1256388-51-8

Ledipasvir ( GS5885 | GS-5885 | GS 5885 | Ledipasvir )

产品货号. M17226 CAS No. 1256388-51-8

Ledipasvir 是一种丙型肝炎病毒 NS5A 抑制剂。雷迪帕韦的作用机制是作为 P-糖蛋白抑制剂和乳腺癌抗性蛋白抑制剂。

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
2MG ¥365 有现货
5MG ¥583 有现货
10MG ¥729 有现货
25MG ¥1312 有现货
50MG ¥2187 有现货
100MG ¥3791 有现货
500MG ¥8667 有现货
1G 获取报价 有现货

生物学信息

  • 产品名称
    Ledipasvir
  • 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
    Ledipasvir 是一种丙型肝炎病毒 NS5A 抑制剂。雷迪帕韦的作用机制是作为 P-糖蛋白抑制剂和乳腺癌抗性蛋白抑制剂。
  • 产品描述
    Ledipasvir, also known as GS-5885; is an inhibitor of the hepatitis C virus NS5A protein and is a drug for the treatment of hepatitis C that was developed by Gilead Sciences. On October 10, 2014 the FDA approved the combination product ledipasvir 90 mg/sofosbuvir 400 mg (trade name Harvoni). The ledipasvir/sofosbuvir combination is a direct-acting antiviral agent that interferes with HCV replication and can be used to treat patients with genotypes 1a or 1b without PEG-interferon or ribavirin.
  • 体外实验
    Ledipasvir has GT1a and 1b EC50 values of 31 and 4 pM, respectively, and protein-adjusted EC50 values of 210 pM (GT1a) and 27 pM (GT1b) and the intrinsic EC50 of 39 is 310 fM for GT1a and 40 fM for GT1b. Ledipasvir is highly protein-bound both in human serum and in the cell-culture medium (containing 10% BSA) of the replicon assay. Ledipasvir exhibits an EC50 value of 141 nM against the JFH/3a-NS5A replicon.
  • 体内实验
    Ledipasvir is remarkable not only on the basis of its high replicon potency but also on the basis of its low clearance, good bioavailability, and long half-lives in rat, dog, and monkey and low predicted clearance in human. The pharmacokinetics of Ledipasvir is measured in rats and dogs. Ledipasvir shows good half-lives (rat 1.83 ± 0.22 hr, dog 2.63 ± 0.18 hr) in plasma, low systemic clearance (CL), and moderate volumes of distribution (Vss) that are greater than total body water volume.
  • 同义词
    GS5885 | GS-5885 | GS 5885 | Ledipasvir
  • 通路
    Cell Cycle/DNA Damage
  • 靶点
    HDAC
  • 受体
    GT1a| GT1b
  • 研究领域
    Infection
  • 适应症
    ——

化学信息

  • CAS Number
    1256388-51-8
  • 分子量
    889
  • 分子式
    C49H54F2N8O6
  • 纯度
    >98% (HPLC)
  • 溶解度
    DMSO : 50 mg/mL. 56.24 mM;H2O : < 0.1 mg/mL
  • SMILES
    O=C(OC)N[C@H](C(=O)N1[C@H](c2ncc(c3cc4C(F)(F)c5c(ccc(c6ccc7nc([C@H]8N(C(=O)[C@@H](NC(=O)OC)C(C)C)[C@@H]9CC[C@H]8C9)[nH]c7c6)c5)c4cc3)[nH]2)CC2(C1)CC2)C(C)C
  • 化学全称
    Methyl N-[(2S)-1-[(6S)-6-[5-[9,9-Difluoro-7-[2-[(1S,2S,4R)-3-[(2S)-2-(methoxycarbonylamino)-3-methylbutanoyl]-3-azabicyclo[2.2.1]heptan-2-yl]-3H-benzimidazol-5-yl]fluoren-2-yl]-1H-imidazol-2-yl]-5-azaspiro[2.4]heptan-5-yl]-3-methyl-1-oxobutan-2-yl]carbamate

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. Smith MA, et al. Ann Pharmacother. 2015 Mar;49(3):343-50.
产品手册
关联产品
  • SS-208

    SS-208 是一种选择性 HDAC6 抑制剂 (IC50 = 12 nM),具有抗肿瘤活性。 SS-208 显示出优于其他 HDAC 亚型的选择性。

  • BRD2492

    BRD2492 是一种高效、选择性 HDAC1/2 抑制剂(IC50 分别为 2/19 nM)。

  • HDAC-IN-52

    HDAC-IN-52 是一种含吡啶的 HDAC 抑制剂,抑制 HDAC1,HDAC2,HDAC3 和 HDAC10 的 IC50 分别为 0.189,0.227,0.440 和 0.446 μM。HDAC-IN-52 可用于癌症研究。