Cat. No. | Product Name | CAS No. | Purity | Chemical Structure |
---|---|---|---|---|
TN1033 | Sennidin A
番泻苷元A
|
641-12-3 | 100% |
|
Sennidin A 是从狭叶番泻分离得到的一种天然产物,能够抑制 HCV NS3 解旋酶,其 IC50值为0.8 μM。它诱导 Akt 和葡萄糖转运蛋白4的磷酸化,刺激葡萄糖掺入。 | ||||
TN1138 | γ-Fagarine
γ-崖椒碱
|
524-15-2 |
|
|
gamma-Fagarine possesses moderate levels of anti-HCV activities with IC50 values being 20.4 ± 0.4 ug/ml, respectively. It has sister chromatid exchanges (SCEs)-i... | ||||
TN1034 | Sennidin B
番泻苷元B
|
517-44-2 |
|
|
Sennidin B 是从Cassia angustifolia 分离得到的Sennidin A 异构体,它刺激葡萄糖掺入,诱导Akt 和葡萄糖转运蛋白4 的磷酸化。 | ||||
T5539 | GS-443902
瑞德西韦代谢物
|
1355149-45-9 |
|
|
Remdesivir triphosphate 是一种有效的病毒 RNA 依赖的 RNA 聚合酶抑制剂,对RSVRdRp 和 HCVRdRp 的IC50分别为 1.1 µM 和 5 µM。它是 Remdesivir 的活性三磷酸代谢物。 | ||||
TN3809 | Dehydrojuncusol
化合物 TN3809
|
117824-04-1 | 98% |
|
Dehydrojuncusol, a new inhibitor of hepatitis C virus RNA replication, it inhibits infection of different HCV genotypes by targeting the NS5A protein and is acti... | ||||
T12966 | Sofosbuvir impurity K
索非布韦杂质 K
|
1496552-51-2 | 98% |
|
Sofosbuvir impurity K is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | ||||
T12969 | Sofosbuvir impurity N
索非布韦杂质 N
|
1394157-34-6 | 98% |
|
Sofosbuvir impurity N is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | ||||
T12033 | Micrococcin P1
微球菌素 P1
|
67401-56-3 | 98% |
|
Micrococcin P1 is a macrocyclic peptide antibiotic and is a potent hepatitis C virus (HCV) inhibitor(EC50 range of 0.1-0.5 μM) | ||||
T12965 | Sofosbuvir impurity J
索非布韦杂质 J
|
1334513-10-8 | 98% |
|
Sofosbuvir impurity J is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | ||||
T12963 | Sofosbuvir impurity H
化合物 T12963
|
T12963 | 98% |
|
Sofosbuvir impurity H, an diastereoisomer of Sofosbuvir, is the impurity of Sofosbuvir. Sofosbuvir (PSI-7977) is a diastereoisomer of Sofosbuvir.Sofosbuvir is an... | ||||
T10067 | 2',5-Difluoro-2'-deoxycytidine
化合物 T10067
|
581772-30-7 | 98% |
|
2',5-Difluoro-2'-deoxycytidine has potent anti-HCV activity and toxicity to rRNA. | ||||
T12967 | Sofosbuvir impurity L
化合物 T12967
|
T12967 | 98% |
|
Sofosbuvir impurity L is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | ||||
T12968 | Sofosbuvir impurity M
索非布韦杂质 M
|
2095551-10-1 | 98% |
|
Sofosbuvir impurity M is an diastereoisomer of Sofosbuvir.Sofosbuvir is an HCV RNA replication inhibitor, with potent anti-hepatitis C virus activity. | ||||
T73223 | NS5A-IN-3
化合物 NS5A-IN-3
|
2764786-56-1 | 98% |
|
NS5A-IN-3 (Compound 15) 为高效NS5A抑制剂,对HCV基因型1b显示出高效力,并对基因型3a (GT 3a) 活性提升以及展现出良好的代谢稳定性。NS5A-IN-3相较于daclatasvir,对基因型1b具有更高的耐药门槛。 | ||||
T73834 | NS5A-IN-2
化合物 NS5A-IN-2
|
2764786-74-3 | 98% |
|
NS5A-IN-2 (Compound 33)为一种高效的NS5A抑制剂,对HCV基因型1b展现出极高效力,并对基因型3a (GT 3a) 亦具备增强活性与良好的代谢稳定性。 | ||||
T16675 | PSI-352938
化合物 T16675
|
1231747-17-3 | 98% |
|
PSI-352938 is an inhibitor of hepatitis C virus nucleotide. | ||||
TN3438 | Arborinine
化合物 TN3438
|
5489-57-6 | 98% |
|
Arborinine shows mild in vitro antibacterial activity, it possesses moderate levels of anti-hepatitis C virus(HCV) activities with the IC50 values being 6.4 ± 0.... | ||||
TN5079 | Sulochrin
化合物 TN5079
|
519-57-3 | 98% |
|
Sulochrin shows antifungal and antibacterial activities, it can inhibit hepatitis C virus (HCV) infection in a dose-dependent manner without any apparent cytotox... | ||||
T13281 | Valopicitabine
化合物 T13281
|
640281-90-9 | 98% |
|
Valopicitabine is an effective prodrug of the effective anti-HCV drug 2'-C-methylcytidine and can be used as a promising antiviral drug for the study of chronic ... | ||||
TQ0122 | VCH-916
化合物VCH-916
|
1200133-34-1 | 98% |
|
VCH-916 是一种新型非核苷类 HCV NS5B 聚合酶抑制剂。 |