| Cat. No. |
Product Name |
Information |
| PC-43335 |
HIV-1 integrase inhibitor
|
HIV-1 integrase inhibitor is an HIV-1 integrase inhibitor.. |
| PC-62778 |
YIR-819 TFA salt
|
YIR-819 is a small-molecule CD4 mimic that acts as a highly potent HIV entry inhibitor with IC50 of 2.6 uM against YTA48P virus with no significant cytotoxicity (CC50=33 uM). |
| PC-62258 |
HIV-1 inhibitor 18A
|
HIV-1 inhibitor 18A is a novel broad HIV-1 inhibitor that blocks envelope glycoprotein transitions critical for entry, specifically inhibits the entry of a wide range of HIV-1 isolates with mean IC50 of 6.4 uM. |
| PC-62243 |
HIV-1 Integrase Inhibitor 7
|
HIV-1 Integrase Inhibitor 7 is an allosteric HIV-1 integrase inhibitor that inhibits the LEDGF/p75-integrase interaction with IC50 of 0.58 uM, antiviral activity EC50 of 0.76 uM.. |
| PC-70237 |
SCH 350581 dihydrochloride
|
A specific small molecule inhibitor of CCR5, inhibits HIV-1 entry.. |
| PC-60172 |
HIV-1 Integrase Inhibitor 1
|
A novel compound that disrupts the HIV-1 integrase LEDGF interaction. |
| PC-45129 |
Saquinavir mesylate
|
Apotent and selective inhibitor of HIV-1 protease with IC50 of 0.5-6 nM in cell assays. |
| PC-42549 |
Raltegravir potassium salt
|
A potent, selective, orally bioavailable HIV-integrase inhibitor with IC50 of 15 nM. |
| PC-45165 |
Darunavir ethanolate
|
A potent, selective HIV-1 protease inhibitor that is extremely potent against laboratory HIV-1 strains and primary clinical isolates with IC50 of 3 nM, IC90 of 9 nM. |
| PC-42659 |
Delavirdine mesylate
|
A potent HIV-1 reverse transcriptase inhibitor with IC50 of 0.26 uM for recombinant HIV-1 RT. |
| PC-45974 |
NBD-557
|
A potent HIV-1 entry inhibitor that blocks the gp120-CD4 interaction. |
| PC-45254 |
Fosamprenavir calcium
|
A phosphate ester prodrug of the HIV-1 protease inhibitor amprenavir with improved solubility.. |
