| Cat.No. | Name | Information |
|---|---|---|
| M3568 | Darunavir Ethanolate | Darunavir Ethanolate is an HIV protease inhibitor. |
| M3485 | BMS-378806 | BMS-378806 selectively inhibits the binding of HIV-1 gp120 to the CD4 receptor with EC50 of 0.85-26.5 nM in virus. |
| M3179 | 9-Aminoacridine | 9-Aminoacridine is a highly fluorescent dye used clinically as a topical antiseptic and experimentally as a mutagen, an intracellular pH indicator and a negative mode small molecule MALDI matrix. |
| M3133 | YYA-021 | YYA-021 is a CD4-mimic HIV entry inhibitor, competitively inhibiting the interaction between gp120 and CD4. |
| M2994 | Salicylanilide | Salicylanilides are a group of compounds with a wide range of biological activities including antiviral potency, antibacterial (including antimycobacterial) and antifungal activities. |
| M2605 | Des(benzylpyridyl) Atazanavir | Des(benzylpyridyl) Atazanavir is a HIV protease inhibitor, the N-dealkylated metabolite (M1) of Atazanavir (A790051). |
| M2463 | BMS-663068 | BMS-663068 is a novel small-molecule attachment inhibitor that targets HIV-1 gp120 and prevents its binding to CD4+ T cells with EC50 of < 10 nM. |
| M2173 | Delavirdine mesylate | Delavirdine mesylate is a nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1 (HIV-1). |
| M2159 | Ritonavir | Ritonavir is an HIV protease inhibitor used in the study of HIV infection and AIDS. Ritonavir (ABT 538) |
| M2158 | Lopinavir | Lopinavir (ABT-378) is a potent protease inhibitor. |
| M1865 | Bevirimat | Bevirimat (BVM), also known as PA-457 or MPC-4326, is a novel Human Immunodeficiency Virus type 1 (HIV-1) maturation inhibitor. |
| M1657 | Atazanavir Sulfate | Atazanavir sulfate (BMS-232632, Reyataz) is an azapeptide inhibitor of HIV-1 protease. Atazanavir sulfate is a substrate and inhibitor of CYP3A4, and an inhibitor and inducer of P-glycoprotein (P-gp). Atazanavir sulfate is also a SARS-CoV 3CLpro inhibitor with an IC50 of 3.49 μM. |
| M53468 | Arg-Val-(Nle-p-nitro)-Phe-Glu-Ala-Nle-NH2 | Arg-Val-(Nle-p-nitro)-Phe-Glu-Ala-Nle-NH2 is a fluorogenic substrate of HIV-1 protease. |
| M53467 | Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2 | Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2 is a substrato peptídico of HIV-1 protease. |
| M53466 | HIV-1, HIV-2 Protease Substrate | HIV-1, HIV-2 Protease Substrate is the substrate of HIV-1, HIV-2 protease. |
| M53465 | HIV Protease Substrate IV | HIV Protease Substrate IV is a substrate of HIV protease. |
| M53464 | Herpes virus inhibitor 2 | Herpes virus inhibitor 2 is a herpes virus inhibitor and disrupts herpes virus ribonucleotide reductase quaternary structure. |
| M53463 | HIV Protease Substrate 1 | HIV Protease Substrate 1, a fiuorogenic HIV protease substrate, can be used to study enzymatic activity of HIV protease. |
| M53462 | HIV Protease Substrate I | HIV Protease Substrate I is a chromogenic substrate of HIV-1 protease. |
| M53461 | HIV-1 protease-IN-7 | HIV-1 protease-IN-7 is an orally active HIV-1 protease inhibitor (IC50=3.52 nM, EC50=37 nM). |
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