| Cat.No. | Name | Information |
|---|---|---|
| M6094 | Darunavir | Darunavir is a nonpeptidic HIV protease inhibitor, used to treat HIV infection. |
| M5949 | Saquinavir Mesylate | Saquinavir mesylate is an HIV Protease Inhibitor used in antiretroviral therapy. |
| M5948 | Saquinavir | Saquinavir(Ro 31-8959) is an HIV Protease inhibitor used in antiretroviral therapy. |
| M5706 | Indinavir sulfate | Indinavir sulfate(MK-639 sulfate; L735524 sulfate ) is a potent and specific HIV protease inhibitor that appears to have good oral bioavailability. |
| M5427 | Atazanavir | Atazanavir (BMS-232632) is an azapeptide and HIV-protease inhibitor. Atazanavir (BMS-232632) is a substrate and inhibitor of CYP3A4, and an inhibitor and inducer of P-glycoprotein (P-gp). Atazanavir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM. |
| M5182 | Glabranin | Glabranin |
| M5052 | Tenofovir Disoproxil Fumarate | Tenofovir Disoproxil Fumarate belongs to a class of antiretroviral compounds, it inhibits the activity of HIV reverse transcriptase by competing with the natural substrate deoxyadenosine 5’-triphosphate and, after incorporation into DNA, by DNA chain termination. |
| M5049 | Abacavir | Abacavir is an orally active and competitive nucleoside reverse transcriptase inhibitor. Abacavir can inhibits the replication of HIV. |
| M4958 | Tenofovir alafenamide | Tenofovir alafenamide (GS-7340) is an investigational oral proagent of tenofovir (TFV) that more efficiently delivers TFV into lymphoid cells and tissues than TFV disoproxil fumarate. |
| M4752 | l-Chicoric-acid | L-chicoric Acid ((-)-Chicoric Acid), a dicafoyl tartaric Acid, is a potent, selective and reversible INHIBITOR of HIV-1 integrase with an IC50 of approximately 100 nM. L-chicoric Acid also inhibits HIV-1 replication in tissue cultures. |
| M4727 | Pseudohypericin | Pseudohypericin and its homolog Hypericin are the main hydroxyphenanthroflinones in hypericum. Pseudohypericin has anti-HIV activity. |
| M4635 | 1,3,5-tricaffeoylquinic-acid | 1,3,5-Tricaffeoylquinic acid is a Tricaffeoylquinic acid derivative isolated from H. populifolium and has anti-HIV effects. |
| M4566 | Escin-IA | Escin IA, a triterpenoid saponin isolated from horse chestnut, inhibits HIV-1 protease with IC50 value of 35 μM. Escin IA has anti-metastasis activity of triple negative breast cancer, and its mechanism includes down-regulation of LOXL expression and inhibition of epithelial mesenchymal transformation. |
| M4515 | Fangchinoline | Fangchinoline, a bisbenzylisoquinoline alkaloid, is a novel HIV-1 inhibitor with pain-relieving, blood pressure-depressing, and antibiotic activities. |
| M4418 | Sennoside-A | Sennoside A is an anthraquinone glycoside found in abundance in the leaves and pods of senna (Cassia Angustifolia). Sennoside A is an HIV-1 inhibitor that inhibits HIV-1 replication. |
| M4257 | Gomisin-G | Gomisin G is a natural compound for anti-HIV activity. |
| M3743 | Lersivirine | Lersivirine (UK-453061) is an investigational second-generation NNRTI that (in in vitro studies) is active against many HIV strains with NNRTI resistance mutations. |
| M3715 | GSK2838232A | GSK2838232 is a novel human immune virus (HIV) maturation inhibitor being developed for the treatment of chronic HIV infection. |
| M3654 | Nelfinavir Mesylate | Nelfinavir is a potent HIV-1 protease inhibitor (Ki=2 nM) and is widely prescribed in combination with HIV reverse transcriptase inhibitors for the treatment of HIV infection. |
| M3578 | Amprenavir | Amprenavir is an HIV protease inhibitor with IC50 of 14.6 ng/mL in wild-type HIV isolates. |
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