
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 474 products of "HIV Protease"
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HIV-1 inhibitor-39
CAS:HIV-1 inhibitor-39: blocks HIV-1, anti-RT (IC50=15.75 μM), toxic to MT-4 cells (CC50=112.9 μM).Formula:C20H17ClN4O4S4Color and Shape:SolidMolecular weight:541.09Antiviral agent 9
Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.Formula:C38H50N7O8PColor and Shape:SolidMolecular weight:763.82HIV-1 inhibitor-48
CAS:HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .Formula:C19H16BrN5Color and Shape:SolidMolecular weight:394.27HIV-1 inhibitor-35
CAS:HIV-1 inhibitor-35, potent against HIV (EC50: 80 nM LTR, 70 nM CMV), also suppresses HepG2 cells (CC50: 40 nM), may reverse HIV-1 latency.Formula:C13H12Cl3N5OSColor and Shape:SolidMolecular weight:392.69HIV-1 inhibitor-9
CAS:HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.Formula:C24H21N5OColor and Shape:SolidMolecular weight:395.46HIV-1 inhibitor-56
CAS:HIV-1 inhibitor-56 (compound 12126065) is a potent non-nucleoside reverse transcriptase inhibitor with significant antiviral activity against wild-type HIV-1,Formula:C22H14ClN7O2SColor and Shape:SolidMolecular weight:475.91Cgp 53820
CAS:CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.Formula:C31H51N5O5Color and Shape:SolidMolecular weight:573.77HIV-1 inhibitor-33
CAS:HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.Formula:C25H28N6OColor and Shape:SolidMolecular weight:428.53ML67-33
CAS:<p>ML67-33 selectively activates K2P channels; EC50: 36.3 μM (cell-free), 9.7 μM (HEK293). Reversible TREK-1 modulation.</p>Formula:C18H17Cl2N5Purity:98%Color and Shape:SolidMolecular weight:374.27HEPT
CAS:HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription.Formula:C14H16N2O4SPurity:98%Color and Shape:SolidMolecular weight:308.35L-Ristosamine nucleoside
CAS:<p>L-Ristosamine nucleoside shows antiviral activity.</p>Formula:C21H21N3O7Color and Shape:SolidMolecular weight:427.41Suberosol
CAS:Suberosol possesses anti-HIV replication activity.Formula:C31H50O2Purity:98%Color and Shape:SolidMolecular weight:454.73ZP7
CAS:ZP7 is a HIV-1 replication inhibitor.Formula:C15H9Br2ClN4OS2Purity:98%Color and Shape:SolidMolecular weight:520.65APA-APA-MPO
CAS:APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor.Formula:C12H25Cl2N5OPurity:98%Color and Shape:SolidMolecular weight:326.27Ingenol 3-Hexanoate
CAS:Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1.Formula:C26H38O6Purity:98%Color and Shape:SolidMolecular weight:446.58BM 21.1298
CAS:<p>BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.</p>Formula:C16H13NOSPurity:98%Color and Shape:SolidMolecular weight:267.35D4DAP
CAS:D4DAP is an inhibitor of HIV virus replication.Formula:C10H12N6O2Purity:98%Color and Shape:SolidMolecular weight:248.24Nitrobenzofuroxan
CAS:Nitrobenzofuroxan, is a HIV-1 and IDO1 inhibitor.Formula:C6H3N3O4Purity:98%Color and Shape:SolidMolecular weight:181.11BMS-663749 lysine
CAS:BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.Formula:C29H39N6O11PPurity:98%Color and Shape:SolidMolecular weight:678.63GSK5750
CAS:GSK5750 is the ribonuclease H activity inhibitor.Formula:C16H12N4O2SColor and Shape:SolidMolecular weight:324.36
