1. Anti-infection Metabolic Enzyme/Protease Cell Cycle/DNA Damage
  2. HCV HCV Protease Nucleoside Antimetabolite/Analog
  3. Valopicitabine

Valopicitabine (NM283) 是一种核苷类似物,是强效抗 HCV 剂的 2'-C-甲基胞苷 (NM107) 的口服生物利用前体。NM107 竞争性抑制 NS5B 聚合酶,导致链终止。

在相同的摩尔浓度下,化合物盐形式与游离形式有相同的生物活性,但盐形式 Valopicitabine dihydrochloride 通常具有更好的水溶性和稳定性。

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Valopicitabine Chemical Structure

Valopicitabine Chemical Structure

CAS No. : 640281-90-9

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Valopicitabine 的其他形式现货产品:

Customer Review

Other Forms of Valopicitabine:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Valopicitabine (NM283) is a nucleoside analog and the orally bioavailable proagent of the potent anti-HCV agent 2'-C-methylcytidine (NM107). NM107competitively inhibits NS5B polymerase, causing chain termination[1][2].

IC50 & Target

HCV[1]

细胞效力
(Cellular Effect)
Cell Line Type Value Description References
Huh-7 CC50
> 100 μM
Compound: valopicitabaine
Cytotoxicity against Huh7 cells after 24 hrs by MTS assay
Cytotoxicity against Huh7 cells after 24 hrs by MTS assay
[PMID: 17521911]
Huh-7 EC50
1.5 μM
Compound: valopicitabaine
Antiviral activity against HCV genotype 1b in Huh7 cells assessed as inhibition of viral RNA replication after 72 hrs by ribonuclease protection assay
Antiviral activity against HCV genotype 1b in Huh7 cells assessed as inhibition of viral RNA replication after 72 hrs by ribonuclease protection assay
[PMID: 17521911]
Huh-7 EC50
7.45 μM
Compound: valopicitabaine
Antiviral activity against HCV genotype 1b in Huh7 cells assessed as inhibition of viral RNA replication after 24 hrs by ribonuclease protection assay
Antiviral activity against HCV genotype 1b in Huh7 cells assessed as inhibition of viral RNA replication after 24 hrs by ribonuclease protection assay
[PMID: 17521911]
Huh-7 EC50
7.6 μM
Compound: 1
Antiviral activity against HCV infected in human HuH7 cells by cell-based subgenomic replicon assay
Antiviral activity against HCV infected in human HuH7 cells by cell-based subgenomic replicon assay
[PMID: 19493593]
体内研究
(In Vivo)

Valopicitabine (NM283) (100 mg/kg;口服给药;Sprague-Dawley 大鼠) 显示 Cmax、AUC、t1/2 和 tmax 分别为3.624 μg/mL、8.95 μg·h/mL、0.64小时和1小时[2]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Clinical Trial
分子量

356.37

同用名

NM283

Formula

C15H24N4O6

CAS 号
运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
Valopicitabine
目录号:
HY-108060
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