Tegobuvir
CAS No. 1000787-75-6
Tegobuvir ( GS 333126 | GS 9190 | GS333126 | GS9190 )
产品货号. M10009 CAS No. 1000787-75-6
HCV NS5B 聚合酶的非核苷抑制剂,可作为 HCV 基因型 1 的有效抑制剂。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
规格 | 价格/人民币 | 库存 | 数量 |
5MG | ¥1968 | 有现货 |
|
10MG | ¥3345 | 有现货 |
|
25MG | ¥5573 | 有现货 |
|
50MG | ¥7930 | 有现货 |
|
100MG | ¥10692 | 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Tegobuvir
-
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 NS5B 聚合酶的非核苷抑制剂,可作为 HCV 基因型 1 的有效抑制剂。
-
产品描述A nonnucleoside inhibitor of HCV NS5B polymerase that acts as a potent inhibitor of HCV genotype 1; inhibits 1a (H77) and 1b (Con-1) replicons with EC50 of 13.8 nM and 0.8 nM respectively, and displays a loss in potency against 2a (JFH-1) virus with EC50 of 2.9 uM.(In Vitro):Tegobuvir rapidly increases the proportion of replicons with the Y448H mutation in a dose-dependent manner. After 3 days of treatment, 1.2%, 6.8%, and > 50% of the replicon population expresses Y448H with the use of Tegobuvir at 1, 10, and 20 times its 50% effective concentration, respectively. Tegobuvir exerts anti-HCV activity utilizing a unique chemical activation and subsequent direct interaction with the NS5B protein. Treatment of HCV subgenomic replicon cells with Tegobuvir results in a modified form of NS5B with a distinctly altered mobility on a SDS-PAGE gel. Tegobuvir is potent in GT1a and 1b with mean EC50s of 19.8 and 1.5 nM respectively. For genotype 3a, 4a, and 6a Con chimeras, tegobuvir EC50s are all greater than 100 nM. The F445C NS5B mutations in GT3a, 4a, and 6a chimeric replicons restore tegobuvir potency to EC50 levels comparable to GT1a.
-
体外实验Tegobuvir rapidly increases the proportion of replicons with the Y448H mutation in a dose-dependent manner. After 3 days of treatment, 1.2%, 6.8%, and > 50% of the replicon population expresses Y448H with the use of Tegobuvir at 1, 10, and 20 times its 50% effective concentration, respectively. Tegobuvir exerts anti-HCV activity utilizing a unique chemical activation and subsequent direct interaction with the NS5B protein. Treatment of HCV subgenomic replicon cells with Tegobuvir results in a modified form of NS5B with a distinctly altered mobility on a SDS-PAGE gel. Tegobuvir is potent in GT1a and 1b with mean EC50s of 19.8 and 1.5 nM respectively. For genotype 3a, 4a, and 6a Con chimeras, tegobuvir EC50s are all greater than 100 nM. The F445C NS5B mutations in GT3a, 4a, and 6a chimeric replicons restore tegobuvir potency to EC50 levels comparable to GT1a.
-
体内实验——
-
同义词GS 333126 | GS 9190 | GS333126 | GS9190
-
通路Microbiology/Virology
-
靶点HCV
-
受体HCV
-
研究领域Infection
-
适应症——
化学信息
-
CAS Number1000787-75-6
-
分子量517.401
-
分子式C25H14F7N5
-
纯度>98% (HPLC)
-
溶解度10 mM in DMSO
-
SMILESFC1=CC=CC=C1C2=NC3=CN(CC4=NN=C(C5=CC=C(C(F)(F)F)C=C5C(F)(F)F)C=C4)C=CC3=N2
-
化学全称5H-Imidazo[4,5-c]pyridine, 5-[[6-[2,4-bis(trifluoromethyl)phenyl]-3-pyridazinyl]methyl]-2-(2-fluorophenyl)-
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. Shih IH, et al. Antimicrob Agents Chemother. 2011 Sep;55(9):4196-203.
2. Zeuzem S, et al. Hepatology. 2012 Mar;55(3):749-58.
3. Wong KA, et al. Virology. 2012 Jul 20;429(1):57-62.
产品手册
关联产品
-
Sofosbuvir impurity ...
索磷布韦杂质 F 既是索磷布韦的非对映异构体,也是丙型肝炎病毒 RNA 复制抑制剂索磷布韦的杂质。
-
HCV-IN-31
HCV-IN-31 是一种 HCV 抑制剂,EC50/EC95 为 15.7 μM。
-
Platycodin D3
Platycodin D3 是一种 NF-κB 抑制剂,可作为多种炎症性肺部疾病的祛痰剂,可调节气道粘蛋白的产生和分泌。