
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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DMP 323
CAS:<p>DMP 323 is a potent inhibitor of HIV-1 protease.</p>Formula:C35H38N2O5Purity:98%Color and Shape:SolidMolecular weight:566.69Berlopentin
CAS:<p>Berlopentin is splenopentin analog used to treat HIV-positive patients. It also has immunostimulatory properties.</p>Formula:C35H55N9O11Color and Shape:SolidMolecular weight:777.86Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C20H20Cl2N4O2SPurity:98%Color and Shape:SolidMolecular weight:451.37L-697661
CAS:<p>L-697661, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C16H15Cl2N3O2Color and Shape:SolidMolecular weight:352.22A 77003
CAS:<p>A 77003 is a HIV-1 protease inhibitor. A77003 impairs HIV-1 protease-mediated Gag processing.</p>Formula:C44H58N8O6Color and Shape:SolidMolecular weight:794.98PYR01
CAS:<p>PYR01 is a potent nonnucleoside reverse transcriptase inhibitor of HIV-1 and concurrently acts as a targeted activator to eliminate cells expressing HIV-1 [1].</p>Formula:C21H13F7N4O3Color and Shape:SolidMolecular weight:502.34Indinavir, threo-
CAS:<p>Indinavir, threo- is a protease inhibitor utilized as a component of highly active antiretroviral treatment to HIV/AIDS.</p>Formula:C36H47N5O4Purity:98%Color and Shape:SolidMolecular weight:613.79A 74704
CAS:<p>A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.</p>Formula:C43H52N4O7Purity:98%Color and Shape:SolidMolecular weight:736.9BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C14H12ClF3N2OColor and Shape:SolidMolecular weight:316.71Droxinavir HCl
CAS:<p>Droxinavir HCl is an antiviral agent and HIV protease inhibitor.</p>Formula:C29H52ClN5O4Purity:98%Color and Shape:SolidMolecular weight:570.22Bavtavirine
CAS:<p>Bavtavirine is a non-nucleoside reverse HIV-1 transcriptase inhibitor (NNRTIs),inhibits HIV replication by preventing the transcription of viral RNA into DNA.</p>Formula:C26H20N6Purity:97.2%Color and Shape:SolidMolecular weight:416.48HIV-1 inhibitor-10
CAS:<p>HIV-1 inhibitor-10 is a nanomolar HIV-1 maturation inhibitor.</p>Formula:C39H54O6Color and Shape:SolidMolecular weight:618.84U 104489
CAS:<p>U 104489 (PNU-104489) is a novel specific inhibitor of human immunodeficiency virus 1 (HIV-1), showing effective activity against BHA-P-resistant HIV-1MF.</p>Formula:C26H36N6O3SColor and Shape:SolidMolecular weight:512.67U 89360E
CAS:<p>U 89360E is a peptidic inhibitor.</p>Formula:C28H52N8O6Purity:98%Color and Shape:SolidMolecular weight:596.76Palinavir
CAS:<p>Palinavir is an antiviral, it inhibits HIV-1 protease.</p>Formula:C41H52N6O5Purity:98%Color and Shape:SolidMolecular weight:708.89BILR-355
CAS:<p>BILR-355 is a reverse transcriptase inhibitor.</p>Formula:C25H23N5O3Purity:98%Color and Shape:SolidMolecular weight:441.48XZ426
CAS:<p>XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .</p>Formula:C22H24F2N4O4Color and Shape:SolidMolecular weight:446.45HIV-1 integrase inhibitor 3
CAS:<p>HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).</p>Formula:C21H22F2N4O4Purity:98%Color and Shape:SolidMolecular weight:432.427-Deaza-2',3'-dideoxyguanosine
CAS:<p>7-Deaza-2',3'-dideoxyguanosine (7-Deaza-ddG) is a 2′,3′-dideoxynucleoside 5′-triphosphate that inhibits HIV-1 reverse transcriptase with a Ki of 25 nM [1].</p>Formula:C11H14N4O3Color and Shape:SolidMolecular weight:250.25GSK3532795
CAS:<p>GSK3532795: potent oral HIV-1 maturation inhibitor; EC50: 1.9-13 nM for various strains.</p>Formula:C42H62N2O4SPurity:98%Color and Shape:SolidMolecular weight:691.02L-696229
CAS:<p>L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.</p>Formula:C17H18N2O2Purity:98%Color and Shape:SolidMolecular weight:282.34Murabutide
CAS:<p>Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,</p>Formula:C23H40N4O11Color and Shape:SolidMolecular weight:548.58L-689502
CAS:<p>L-689502 is a potent HIV-l protease inhibitor (IC50: 1 nM).</p>Formula:C39H51N3O7Purity:98%Color and Shape:SolidMolecular weight:673.84Fosalvudine tidoxil
CAS:<p>Fosalvudine tidoxil, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C35H64FN2O8PSPurity:98%Color and Shape:SolidMolecular weight:722.93GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Formula:C36H46ClN3O3Color and Shape:SolidMolecular weight:604.22Reverse transcriptase-IN-1
CAS:<p>Reverse transcriptase-IN-1 is a diarylbenzopyrimidine (DABP) analogue and a potent inhibitor of HIV-1 nonnucleoside reverse transcriptase with an IC50of 13.7</p>Formula:C25H17N7O2Purity:99.61%Color and Shape:SolidMolecular weight:447.45Hinokinin
CAS:<p>Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.</p>Formula:C20H18O6Color and Shape:SolidMolecular weight:354.35HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Formula:C9H10F2N2O5Purity:98%Color and Shape:SolidMolecular weight:264.18HIV-1 protease-IN-11
CAS:<p>HIV-1 protease-IN-11 (compound 34a), an HIV-1 protease inhibitor, demonstrates potent inhibition with an IC50 of 0.41 nM and maintains substantial efficacy</p>Formula:C26H37N3O5SPurity:98%Color and Shape:SolidMolecular weight:503.65HIV-1 protease-IN-8
CAS:<p>HIV-1 protease-IN-8 (compound 34b) is a potent inhibitor of the HIV-1 protease enzyme, exhibiting an IC50 of 0.32 nM.</p>Formula:C25H35N3O5SPurity:98%Color and Shape:SolidMolecular weight:489.63HIV-1 protease-IN-7
CAS:<p>HIV-1 protease-IN-7 (compound 16) is an orally active inhibitor of HIV-1 protease, exhibiting an IC50 of 3.52 nM and an EC50 of 37 nM [1].</p>Formula:C68H104N10O12SPurity:98%Color and Shape:SolidMolecular weight:1285.68HIV-1 protease-IN-12
CAS:<p>HIV-1 protease-IN-12 (compound 35b) serves as a potent inhibitor of HIV-1 protease, exhibiting an IC50 value of 0.51 nM, and demonstrates efficacy against drug-</p>Formula:C25H35N3O5SPurity:98%Color and Shape:SolidMolecular weight:489.63HIV-1 protease-IN-9
CAS:<p>HIV-1 protease-IN-9 (compound 5b), a potent HIV-1 protease inhibitor, exhibits strong antiviral efficacy with a dissociation constant (K_i) of 0.028 nM and a</p>Formula:C37H41N7O4SPurity:98%Color and Shape:SolidMolecular weight:679.83NNRTIs-IN-1
CAS:<p>NNRTIs-IN-1 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) with notable anti-resistance efficacy, effectively inhibiting both the wild-type</p>Formula:C28H22N6O3Color and Shape:SolidMolecular weight:490.51L 687908
CAS:<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Formula:C40H51N5O5Purity:98%Color and Shape:SolidMolecular weight:681.86HIV-IN-8
CAS:<p>HIV-IN-8 (Compound 9) acts as an HIV inhibitor, suppressing HIV replication with an effective concentration (EC50) of 13 μg/mL [1].</p>Formula:C36H30O16Color and Shape:SolidMolecular weight:718.61PNU-103017
CAS:<p>PNU-103017 is an inhibitor of HIV protease.</p>Formula:C28H28N2O5SPurity:98%Color and Shape:SolidMolecular weight:504.6R 87366
CAS:<p>R 87366 is used as a water-soluble HIV protease inhibitor.</p>Formula:C32H39N7O6Purity:98%Color and Shape:SolidMolecular weight:617.7L 694746
CAS:<p>L 694746 is an inhibitor of HIV-1 protease.</p>Formula:C35H42N2O8Purity:98%Color and Shape:SolidMolecular weight:618.72DGKα-IN-8
CAS:<p>DGKα-IN-8 (Example 51) is a potent diacylglycerol kinase alpha (DGKα) inhibitor, exhibiting an IC50 of 22.491 nM and an EC50 of 0.256 nM.</p>Formula:C23H19ClF3N5OColor and Shape:SolidMolecular weight:473.88I-XW-053
CAS:<p>I-XW-053 is an inhibitor of capsid targeted HIV-1 replication using the hybrid structure based method to block the interface between CA N-terminal domains (NTD-</p>Formula:C22H16N2O2Purity:99.05%Color and Shape:SolidMolecular weight:340.37Ulonivirine
CAS:<p>Ulonivirine is an orally active non-nucleoside reverse transcriptase inhibitor that exhibits high antiviral activity and can be used to study HIV-1 infection.</p>Formula:C18H8ClF6N5O3Color and Shape:SolidMolecular weight:491.73Teropavimab
CAS:<p>Teropavimab (3BNC117-LS), an antibody, is utilized in the research of HIV infection [1].</p>Color and Shape:LiquidRo 31-8588
CAS:<p>Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.</p>Formula:C33H56N4O5Color and Shape:SolidMolecular weight:588.82Azt-pmap
CAS:<p>AZT-PMPA, an aryl phosphate derivative of AZT and a nucleoside analogue, demonstrates anti-HIV activity[1].</p>Formula:C20H25N6O8PPurity:98%Color and Shape:SolidMolecular weight:508.42WRNA10
CAS:<p>WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).</p>Formula:C25H32N4O4Color and Shape:SolidMolecular weight:452.55Glycolithocholic acid 3-sulfate disodium
CAS:<p>Glycolithocholic acid 3-sulfate (disodium) demonstrates inhibitory effects on in vitro HIV-1 replication and has potential applications in HIV infection and</p>Formula:C26H41NNa2O7SColor and Shape:SolidMolecular weight:557.65HIV-1 inhibitor-54
CAS:<p>HIV-1 inhibitor-54: potent anti-HIV (EC50: 32 nM), targets WT HIV-1 IIIB in MT-4 cells for infection research.</p>Formula:C27H30N6O4SPurity:98.05% - 99.44%Color and Shape:SoildMolecular weight:534.63PDDC inhibitor
CAS:<p>PDDC inhibitor (Phenyl (R)-(1-(3-(3,4-dimethoxyphenyl)-2,6-dimethylimidazo[1,2-b]pyridazin-8-yl)pyrrolidin-3-yl)carbamate) is an nSMase2 inhibitor.</p>Formula:C27H29N5O4Purity:96.09% - 99.39%Color and Shape:SolidMolecular weight:487.55HIV-1 inhibitor-17
<p>HIV-1 inhibitor-18 blocks HIV-1 capsid, acts on NL4-3 strain (EC50: 2.57 μM), has low cytotoxicity (MT-4 CC50: >8.55).</p>Formula:C32H32N4O5SColor and Shape:SolidMolecular weight:584.69

