021-51111890/在线客服
购物车（）
sales@molnova.cn
  • 咨询热线
    客服服务热线 13671568941/15317326293
  • 在线咨询
    963389683
  • 微信客服
    微信客服
  • 公众号
    扫码关注公众号
首页- Products - Others - Other Targets - HCV-IN-30

HCV-IN-30

CAS No. 1007882-23-6

HCV-IN-30 ( —— )

产品货号. M26246 CAS No. 1007882-23-6

HCV-IN-30 is an HCV NS5A replication complex inhibitor (IC50s: 901 and 102 nM for genotypes 1a and 1b replicons).

纯度: >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
规格 价格/人民币 库存 数量
10MG ￥316 有现货
25MG ￥518 有现货
50MG ￥786 有现货
100MG ￥1272 有现货
500MG ￥3329 有现货
1G 获取报价 有现货
拼团 产品询价 大包装询价 加入购物车

生物学信息

  • 产品名称
    HCV-IN-30
  • 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
    HCV-IN-30 is an HCV NS5A replication complex inhibitor (IC50s: 901 and 102 nM for genotypes 1a and 1b replicons).
  • 产品描述
    HCV-IN-30 is an HCV NS5A replication complex inhibitor (IC50s: 901 and 102 nM for genotypes 1a and 1b replicons).
  • 同义词
    ——
  • 通路
    Others
  • 靶点
    Other Targets
  • 受体
    CDK1/CyclinB; Cdk5/p25; GSK-3β
  • 研究领域
    ——
  • 适应症
    ——

化学信息

  • CAS Number
    1007882-23-6
  • 分子量
    624.8
  • 分子式
    C36H44N6O4
  • 纯度
    >98% (HPLC)
  • 溶解度
    ——
  • SMILES
    O=C(N1[C@H](C2=NC=C(C3=CC=C(C4=CC=C(C5=CN=C([C@H](CCC6)N6C(OC(C)(C)C)=O)N5)C=C4)C=C3)N2)CCC1)OC(C)(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.Leclerc S, et al. Indirubins inhibit glycogen synthase kinase-3 beta and CDK5/p25, two protein kinases involved in abnormal tau phosphorylation in Alzheimer's disease. A property common to most cyclin-dependent kinase inhibitors? J Biol Chem. 2001 Jan 5;276(1):251-60.
计算器

浓度计算器

摩尔计算器

分子量计算器

产品手册
关联产品

  • Ganoderic acid GS-1

    Ganoderic acid GS-1, a highly oxygenated lanostane-type triterpenoid, has anti-HIV-1 protease activities with an IC 50 of 58 μM.

  • Rhodamine 800

    Rhodamine 800 is a near-infrared fluorescent dye. The absorption maximum at 683 nm in acetone shifts to 696 nm in DMSO without a significant change of the overall spectral profile.

  • EMPA

    EMPA is a selective, high-affinity and reversible antagonist of orexin OX2 receptor(human and rat OX2-HEK293 membranes with KD values of 1.1 and 1.4 nM respectively)EMPA displaces the EMPA binding from cell membranes containing human and rat OX2 receptors, with Ki values of 1.10±0.24 nM and 1.45±0.13 nM, respectively.?

登录 注册