Cat. No. |
Product Name |
Information |
PC-22959 |
HT-7
BST2 modulator
|
HT-7 is a specific, heterocyclic HIV-1 inhibitor inhibits viral release by inducing cell surface bone marrow stromal antigen 2 (BST2)/Tetherin/CD317/HM1.24, increases cell surface BST2 coupled with HIV-1 release reduction in Jurkat cells but not Jurkat/KO-BST2 cells. |
PC-22715 |
Ainuovirine
NNRTI
|
Ainuovirine is a third-generation non-nucleoside reverse-transcriptase inhibitor (NNRTI) as anti-HIV-1 agent. |
PC-22328 |
Bevirimat
HIV-1 maturation inhibitor
|
Bevirimat (PA-457) is a potent HIV inhibitor that inhibits HIV Gag protein processing and viral maturation. |
PC-22327 |
JRC-II-191
CD4 mimic
|
JRC-II-191 is a small-molecule CD4 mimic with Kd of 760 nM for gp120 envelope glycoprotein, inhibits HIV-1 entry by blocking the binding of the HIV-1 envelope glycoprotein gp120 to the CD4 receptor. |
PC-22321 |
Lamivudine
NRTI
|
Lamivudine (BCH-189) is an orally active nucleoside reverse transcriptase inhibitor (NRTI), inhibits HIV reverse transcriptase and also the reverse transcriptase of HBV, also inhibits long interspersed nuclear element-1 (LINE-1 or L1) reverse transcriptase. |
PC-21968 |
Bavtavirine
NNRTI
|
Bavtavirine is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) against HIV-1. |
PC-20513 |
BDM2
IN-LEDGF/p75 inhibitor
|
BDM2 is a potent, HIV-1 Integrase IN-LEDGF allosteric inhibitor (INLAI), shows potent anti-HIV activity. |
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-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-42659 |
Delavirdine mesylate
|
A potent HIV-1 reverse transcriptase inhibitor with IC50 of 0.26 uM for recombinant HIV-1 RT. |
PC-45254 |
Fosamprenavir calcium
|
A phosphate ester prodrug of the HIV-1 protease inhibitor amprenavir with improved solubility.. |