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HIV Protease

HIV Protease

HIV Protease inhibitors are a class of antiretroviral drugs that specifically target the protease enzyme of the Human Immunodeficiency Virus (HIV). By inhibiting this enzyme, these compounds prevent the virus from processing its polyproteins into mature, functional proteins, thereby blocking the production of new infectious virions. HIV Protease inhibitors are a cornerstone of highly active antiretroviral therapy (HAART) used to manage HIV/AIDS. At CymitQuimica, we provide a variety of HIV Protease inhibitors to support your research in HIV treatment, drug resistance, and virology.

Found 447 products of "HIV Protease"

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  • Gardiquimod hydrochloride

    CAS:
    <p>Gardiquimod (hydrochloride) is an imidazoquinoline class TLR7/8 agonist. It can inhibit HIV-1 infection in macrophages and activated peripheral blood mononuclear cells (PBMCs). At concentrations below 10 μM, Gardiquimod (hydrochloride) specifically activates TLR7.</p>
    Formula:C17H24ClN5O
    Color and Shape:Solid
    Molecular weight:349.858
  • Fipravirimat

    CAS:
    <p>Fipravirimat is a potent inhibitor of HIV-1 with potential applications in HIV and AIDS research.</p>
    Formula:C43H67FN2O4S
    Color and Shape:Solid
    Molecular weight:727.07
  • Integrase-LEDGF/p75 allosteric inhibitor 1

    CAS:
    <p>Oral HIV-1 allosteric integrase inhibitor, blocks DNA integration, antiviral, potent against NL432 (EC50: 3.9 nM).</p>
    Formula:C33H41NO6S
    Color and Shape:Solid
    Molecular weight:579.75
  • HIV-1 inhibitor-52

    CAS:
    <p>HIV-1 inhibitor-52: potent, broad-spectrum with EC50s 1.6-6.4 nM against various HIV-1 strains.</p>
    Formula:C46H72FNO5S
    Color and Shape:Solid
    Molecular weight:770.13
  • (S)-Batylalcohol

    CAS:
    <p>(S)-Batylalcohol (1-O-Octadecyl-sn-glycerol) is an analogue of phosphonoformic acid (PFA) and demonstrates higher in vitro antiviral activity against human immunodeficiency virus type 1 (HIV-1) compared to PFA. This compound is applicable in antiretroviral research.</p>
    Formula:C21H44O3
    Color and Shape:Solid
    Molecular weight:344.572
  • 4'-Ethynyl-2'-deoxyadenosine

    CAS:
    <p>4'-E-dA is a potent nucleoside RT inhibitor for drug-resistant HIV (EC50: 98 nM in MT-4 cells).</p>
    Formula:C12H13N5O3
    Purity:98%
    Color and Shape:Solid
    Molecular weight:275.26
  • BMS-818251

    CAS:
    <p>BMS-818251 is a potent small-molecule inhibitor that targets HIV-1 entry, with an EC50 value of 0.019 nM. It exhibits over 10 times greater efficacy on the cross-subtype panels of the 208-HIV-1 strain compared to BMS-626529. BMS-818251 enhances potency through interactions with gp120 residues in the conserved β20-β21 hairpin.</p>
    Formula:C29H26N6O5S
    Color and Shape:Solid
    Molecular weight:570.619
  • ZLM-66


    <p>ZLM-66: Doravirine analog, HIV-1 NNRTI inhibitor, IC50: 41nM, EC50: HIV-1 13nM, cIAP1 0.32nM; useful in AIDS research.</p>
    Color and Shape:Solid
  • HIV-IN-3


    <p>HIV-IN-3 (Compound 22a) is a potent inhibitor of HIV (IC50: 1.5 μM). HIV-IN-3 has potential for the study of HIV-related diseases.</p>
    Formula:C21H32ClN7O3
    Color and Shape:Solid
    Molecular weight:465.98
  • Lamivudine, (+/-)-trans-

    CAS:
    <p>Lamivudine, a drug for HIV-1 and HBV, inhibits reverse transcriptase and resembles zalcitabine.</p>
    Formula:C8H11N3O3S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:229.26
  • NBD-10007

    CAS:
    <p>NBD-10007 is an inhibitor of HIV-1 entry.</p>
    Formula:C20H25ClN4O3S
    Purity:98%
    Color and Shape:Solid
    Molecular weight:436.96
  • Saphenamycin

    CAS:
    <p>Saphenamycin is an antibiotic from a strain of Streptomyces.</p>
    Formula:C23H18N2O5
    Purity:98%
    Color and Shape:Solid
    Molecular weight:402.40
  • Emtricitabine triphosphate

    CAS:
    <p>Emtricitabine triphosphate is an active metabolite of Emtricitabine, a drug for HIV/HBV that inhibits reverse transcriptase.</p>
    Formula:C8H13FN3O12P3S
    Color and Shape:Solid
    Molecular weight:487.19
  • L 702007

    CAS:
    <p>L 702007 is an inhibitor of HIV-1 reverse transcriptase.</p>
    Formula:C18H25N3O2
    Purity:98%
    Color and Shape:Solid
    Molecular weight:315.41
  • HIV-1 inhibitor-41


    <p>HIV-1 inhibitor-41 (B23): Oral non-nucleoside reverse transcriptase blocker, EC50 of 50 nM (E138K), 20.8 nM (WT), low hERG/CYP impact, non-toxic.</p>
    Formula:C16H15F2N3OS
    Color and Shape:Solid
    Molecular weight:335.37
  • HIV-1 inhibitor-14


    <p>HIV-1 inhibitor-14: potent, broad HIV-1 RT inhibitor. IC50=0.14μM. Effective against wild-type and resistant strains, EC50=5.79-28.3nM.</p>
    Formula:C29H32N6O4S
    Color and Shape:Solid
    Molecular weight:560.67
  • HIV-1 inhibitor-18


    <p>HIV-1 inhibitor-18 blocks HIV-1 capsid, effective on NL4-3 strain (EC50: 5.14 μM), slightly toxic (MT-4CC50&gt;9.51).</p>
    Formula:C27H31N3O6S
    Color and Shape:Solid
    Molecular weight:525.62
  • HIV-1 inhibitor-13


    <p>HIV-1 inhibitor-13: oral NNRTI, IC50=0.14μM for HIV-1 RT, effective on resistant strains (EC50=2.85-18nM).</p>
    Formula:C30H32N6O3
    Color and Shape:Solid
    Molecular weight:524.61
  • HIV-1 inhibitor-8


    <p>HIV-1 inhibitor-8: potent oral NNRTI, low toxicity, IC50: 0.081 μM, effective on multiple strains, EC50: 4.44-54.5 nM.</p>
    Formula:C25H21N5OS
    Color and Shape:Solid
    Molecular weight:439.53
  • HIV-1 inhibitor-61

    CAS:
    <p>HIV-1 Inhibitor-61 (2c) serves as a potent inhibitor of HIV-1 reverse transcriptase, exhibiting an EC50 value of 0.07 nM in NL4-3 wt MT-4 cells [1].</p>
    Formula:C24H24F2N2O2S
    Color and Shape:Solid
    Molecular weight:442.52