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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T1525 | Ritonavir | RTV,Abbott 84538,A 84538,ABT 538 | Apoptosis , SARS-CoV , HIV Protease |
Ritonavir (ABT 538) is a peptidomimetic agent that inhibits both HIV-1 and HIV-2 proteases. Ritonavir is highly inhibited by serum proteins but boosts the effect of other HIV proteases by blocking their degradation by cy... | |||
T12735 | Ritonavir metabolite | Desthiazolylmethyloxycarbonyl Ritonavir | Others |
Ritonavir metabolite is a Ritonavir metabolite, which is a inhibitor of HIV protease. | |||
T74106 | Hydroxy ritonavir | ||
Hydroxy ritonavir, a metabolite of ritonavir, functions as an inhibitor of the HIV protease, thereby serving as a treatment for HIV infection and AIDS [1]. | |||
T22394 | Paritaprevir | ABT450,ABT-450,Veruprevir | HCV Protease |
Paritaprevir (ABT450) is an inhibitor of non-structural protein 3/4A protease with EC50 values of 1 and 0.21 nM for HCV 1a and HCV 1b, respectively. | |||
T1623 | Lopinavir | ABT-378 | SARS-CoV , HIV Protease |
Lopinavir (ABT-378) is a peptidomimetic HIV protease inhibitor that retains activity against HIV protease with the Val 82 mutation. Lopinavir is less affected by binding to serum proteins than the structurally-related dr... | |||
T64037 | CYP3A4-IN-2 | ||
CYP3A4-IN-2 is a specific inhibitor of cytochrome P450 3A4 (CYP3A4) (IC50: 0.055 μM). CYP3A4-IN-2 is a ritonavir analogue with a more hydrophobic R2 side group and stronger inhibition than ritonavir. CYP3A4-IN-2 is capab... | |||
T20562 | Ureidovaline | ||
Ureidovaline is an intermediate in the Ritonavir synthesis. | |||
T64032 | CYP3A4-IN-3 | ||
CYP3A4-IN-3 is a specific, highly affinity cytochrome P450 3A4 (CYP3A4) (cytochrome P450 3A4 (CYP3A4)) inhibitor (IC50: 0.075 μM). CYP3A4-IN-3 is an analogue of ritonavir with a simpler structure and twice as much inhibi... | |||
T73898 | Paritaprevir dihydrate | ||
Paritaprevir dihydrate (ABT-450), a highly effective and orally administered antiviral, acts as a non-structural protein 3/4A (NS3/4A) protease inhibitor, displaying EC50 values of 1 and 0.21 nM against HCV genotypes 1a ... |