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HIV Protease

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HIV Protease

Chemical Structure Cat. No. Product Name CAS No.
Tipranavir Chemical Structure
BCP22007 Tipranavir 174484-41-4
Tipranavir is an HIV-1 protease inhibitor. It has a role as a HIV protease inhibitor and an antiviral drug.
Deuterated Atazanivir-D3-1 Chemical Structure
BCP03513 Deuterated Atazanivir-D3-1 1092540-56-1
Atazanivir-D3-2 is a azapeptide derivative and inhibits HIV protease.
GSK2838232A Chemical Structure
BCP23646 GSK2838232A N/A
GSK2838232 is a novel human immune virus (HIV) maturation inhibitor being developed for the treatment of chronic HIV infection.
Amprenavir Chemical Structure
BCP04651 Amprenavir 161814-49-9
Amprenavir is an HIV protease inhibitor with IC50 of 14.6 ng/mL in wild-type HIV isolates.
Darunavir Chemical Structure
BCP04563 Darunavir 206361-99-1
Darunavir HIV-1 antiviral structurally is similar to amprenavir and it is second generation HIV-1-protease inhibitor.
Darunavir Ethanolate Chemical Structure
BCP02153 Darunavir Ethanolate 635728-49-3
Darunavir Ethanolate is an HIV protease inhibitor.
Indinavir Chemical Structure
BCP05711 Indinavir 150378-17-9
Indinavir(MK-639; L735524) is a potent and specific HIV protease inhibitor that appears to have good oral bioavailability.
Indinavir sulfate Chemical Structure
BCP13525 Indinavir sulfate 157810-81-6
Indinavir sulfate(MK-639 sulfate; L735524 sulfate ) is a potent and specific HIV protease inhibitor that appears to have good oral bioavailability.
Fosamprenavir calcium Chemical Structure
BCP06334 Fosamprenavir calcium 226700-81-8
GW433908 is a phosphate ester prodrug of the antiretroviral protease inhibitor amprenavir, with improved solubility over the parent molecule and a potential for reduced pill burden on current dosing regimens. GW433908G is the calcium salt of the prodrug.
Fosamprenavir Chemical Structure
BCP09504 Fosamprenavir 226700-79-4
GW433908 is a phosphate ester prodrug of the antiretroviral protease inhibitor amprenavir, with improved solubility over the parent molecule and a potential for reduced pill burden on current dosing regimens.
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