
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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Probenecid
CAS:<p>Probenecid (Benemid) is a benzoic acid derivative with antihyperuricemic property.</p>Formula:C13H19NO4SPurity:98.95% - 99.84%Color and Shape:Crystals From Dil Alcohol Pleasant Aftertaste (Ntp 1992)Molecular weight:285.36(S)-(+)-N-3-Benzylnirvanol
CAS:<p>(S)-(+)-N-3-Benzylnirvanol is a cytochrome P450 CYP2C19 inhibitor with a ki value of 82.5μM for CYP2C9 and 0.25μM for CYP2C19.Cost-effective and quality-assured.</p>Formula:C18H18N2O2Purity:98.90%Color and Shape:SoildMolecular weight:294.35(Rac)-Telinavir
CAS:<p>N1 compound with anti-HIV activity; contains dimethyl, phenyl, quinoline groups.</p>Formula:C33H44N6O5Purity:99.30%Color and Shape:SolidMolecular weight:604.74Islatravir
CAS:<p>Islatravir (MK-8591) is an effective anti-HIV-1 agent.</p>Formula:C12H12FN5O3Purity:98.77%Color and Shape:SolidMolecular weight:293.25Salicylanilide
CAS:<p>Salicylanilide (2-Hydroxybenzanilide)s are a group of compounds with antiviral potency, antibacterial and antifungal activities.</p>Formula:C13H11NO2Purity:99.55%Color and Shape:White To Off-White Crystalline PowderMolecular weight:213.23Dolutegravir intermediate-1
CAS:<p>Dolutegravir intermediate-1 is a synthetic precursor for HIV-1 treatment from patent WO 2016125192 A2.</p>Formula:C13H17NO8Purity:99.52%Color and Shape:SolidMolecular weight:315.28Ibalizumab
CAS:<p>Ibalizumab(TMB-355) is a humanized IgG4 monoclonal antibody that acts as a CD4 receptor inhibitor, blocking the entry of HIV-1 into cells by binding to the CD4</p>Purity:SDS-PAGE:96.4%;SEC-HPLC:97.7%Color and Shape:LiquidMolecular weight:147.3 kDaGSK2838232
CAS:<p>GSK2838232 inhibit HIV reverse transcriptase activity across a broad panel of HIV-1 isolates,GSK2838232 is novel human immune virus (HIV) maturation inhibitor.</p>Formula:C48H73ClN2O6Purity:97.97%Color and Shape:SolidMolecular weight:809.56Elsulfavirine
CAS:<p>Elsulfavirine (VM-1500) is an HIV-1 infection reverse transcriptase inhibitor. It is a new anti-HIV drug.</p>Formula:C24H17BrCl2FN3O5SPurity:99.66%Color and Shape:SolidMolecular weight:629.28Zalcitabine
CAS:<p>Zalcitabine (ddC) is a nucleoside analog inhibiting HIV by blocking reverse transcriptase and halting viral DNA synthesis.</p>Formula:C9H13N3O3Purity:99.08% - ≥95%Color and Shape:White To Off-White Crystalline PowderMolecular weight:211.223-Deazaadenosine hydrochloride
CAS:<p>3-Deazaadenosine HCl blocks SAH hydrolase (Ki: 3.9 μM), with anti-inflammatory, anti-proliferative, and anti-HIV effects.</p>Formula:C11H15ClN4O4Purity:98.48%Color and Shape:SolidMolecular weight:302.71Nevirapine
CAS:<p>Nevirapine (NVP) is a benzodiazepine non-nucleoside reverse transcriptase inhibitor.</p>Formula:C15H14N4OPurity:99.58% - 99.59%Color and Shape:White Or Off-White Crystalline PowderMolecular weight:266.3Fostemsavir Tris
CAS:<p>Fostemsavir Tris (BMS-663068 Tris) is the prodrug of BMS-626529,is a oral, safe and effective inhibitor of HIV-1 attachment.</p>Formula:C29H37N8O11PPurity:99.45%Color and Shape:SolidMolecular weight:704.62BRD-6929
CAS:<p>BRD-6929, a brain-targeted HDAC1/2 inhibitor (IC50 1/8 nM), enhances gnidimacrin's anti-HIV effect, useful in mood behavior studies.</p>Formula:C19H17N3O2SPurity:98.01% - 99.05%Color and Shape:SolidMolecular weight:351.42Pepstatin
CAS:<p>Pepstatin (Pepsin Inhibitor S 735A) is a specific and orally aspartate protease inhibitor that also inhibits HIV protease activity. Cost effective and quality assured.</p>Formula:C34H63N5O9Purity:96.74% - 99.94%Color and Shape:SolidMolecular weight:685.89Benfotiamine
CAS:<p>Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.</p>Formula:C19H23N4O6PSPurity:99.2% - 99.91%Color and Shape:Shinning Black PowderMolecular weight:466.45Atazanavir
CAS:<p>Atazanavir (BMS-232632)(BMS-232632) is an highly effective HIV-1 protease inhibitor.</p>Formula:C38H52N6O7Purity:98% - 99.95%Color and Shape:Crystalline SolidMolecular weight:704.86Ritonavir
CAS:<p>Ritonavir (ABT 538) inhibits HIV-1/2 proteases; serum proteins limit it but it enhances other HIV drugs by hindering P450 degradation.</p>Formula:C37H48N6O5S2Purity:99.38% - 99.96%Color and Shape:White PowderMolecular weight:720.94Tenofovir diphosphate TEA
CAS:<p>Tenofovir diphosphate TEA (TFV-DP TEA) is an ATP-competitive DNA polymerase inhibitor that inhibits HIV-1 reverse transcriptase that\has anti-HIV/HBV potential.</p>Formula:C9H16N5O10P3·C6H15NPurity:93.45% - 98.51%Color and Shape:SolidMolecular weight:548.36Hck-IN-1
CAS:<p>Hck-IN-1 selectively inhibits Nef:Hck, IC50: 2.8 μM; >20 μM for Hck alone. Potent HIV-1 Nef antagonist, IC50: 100-300 nM for HIV-1 replication.</p>Formula:C16H11ClN6O3SPurity:99.07%Color and Shape:SolidMolecular weight:402.81Atazanavir sulfate
CAS:<p>Atazanavir sulfate, an azapeptide HIV-protease inhibitor, treats HIV/AIDS alongside other anti-HIV drugs.</p>Formula:C38H52N6O7·H2SO4Purity:99.31% - 99.40%Color and Shape:SolidMolecular weight:802.93TERT-IN-1
CAS:<p>TERT-IN-1 has anti-HIV activity and can be used to study HIV infection.</p>Formula:C16H20ClN3SPurity:99.31%Color and Shape:SoildMolecular weight:321.87NBD-556
CAS:<p>NBD-556 is a small molecule mimetic of CD4. NBD-556 recognizes the HIV-1 envelope protein gp120 and induces restructuring of gp120 analogous to CD4 binding.</p>Formula:C17H24ClN3O2Purity:99.79%Color and Shape:SolidMolecular weight:337.84PF-3450074
CAS:<p>PF-3450074 (PF-74) is a specific HIV-1 inhibitor, blocking viral replication and uncoating at submicromolar EC50=8-640 nM.</p>Formula:C27H27N3O2Purity:99.92%Color and Shape:SolidMolecular weight:425.52L 754394
CAS:<p>L 754394 is an effective and specific inhibitor of the HIV-1 protease.</p>Formula:C38H47N5O5Color and Shape:SolidMolecular weight:653.81HIV p17 Gag (77-85)
CAS:<p>Targeting HIV Gag p17 (77-85) with intracellular Ab cDNA disrupts viral replication pre/post-integration.</p>Formula:C44H72N10O15Purity:98%Color and Shape:SolidMolecular weight:981.1Bictegravir Sodium
CAS:<p>Bictegravir Sodium is an HIV-1 integrase inhibitor with 7.5 nM IC50, offering strong, selective anti-HIV effects and minimal toxicity.</p>Formula:C21H17F3N3NaO5Purity:99.97%Color and Shape:SolidMolecular weight:471.36Globotriaosylceramides (porcine)
CAS:<p>Globotriaosylceramides, cell membrane glycosphingolipids, act as Shiga toxin receptors and accumulate in Fabry disease, resisting HIV by blocking gp120.</p>Formula:C60H113NO18Color and Shape:SolidMolecular weight:1136.553HIV-1 protease-IN-14
<p>HIV-1protease-IN-14 (compound 5ae) is an effective inhibitor of HIV-1protease, exhibiting Ki values of 0.28 nM and 56.9 nM against WTHIV-1PR and R41THIV-1PR, respectively. This compound also demonstrates low cytotoxicity.</p>Color and Shape:Odour SolidHIV-1 inhibitor-81
<p>HIV-1inhibitor-81 (Compound 14g) is an HIV-1 protease inhibitor with a Ki of 1.6 nM. This compound exhibits antiviral activity against HIV-1, with an EC50 value of 250 nM.</p>Formula:C32H44N2O8SColor and Shape:SolidMolecular weight:616.77HIV-1 protease-IN-10
<p>HIV-1 protease-IN-10 (Compound 2), exhibiting HIV-1 latency reversing activity (IC50: 0.22 μM), selectively binds to the PKCδ C1b domain (IC50: 0.69 μM) and</p>Formula:C23H40O5Purity:98%Color and Shape:SolidMolecular weight:396.56Protease Inhibitor Library
<p>A unique collection of 343 protease and proteasome inhibitors for research in chemical genomics, and drug screening;</p>Color and Shape:Odour SolidScirpusin A
CAS:<p>Scirpusin A is a hydroxystilbene dimer from the rhizome of Scirpus fluviatilis and Xinjiang wine grape.</p>Formula:C28H22O7Color and Shape:SolidMolecular weight:470.47HIV gag peptide (197-205)
CAS:<p>HIV gag peptide (197-205) is a H-2Kd-restricted epitope derived from the p24 portion of the HIV-1 gag protein and composed of the amino acid 197-205 (AMQMLKETI</p>Formula:C45H81N11O14S2Purity:98%Color and Shape:SolidMolecular weight:1064.32Peptide T TFA
CAS:<p>Peptide T (TFA), an octapeptide from HIV-1 gp120, inhibits HIV binding to CD4.</p>Formula:C37H56F3N9O18Purity:98%Color and Shape:SolidMolecular weight:971.89HIV-1 inhibitor-11
<p>HIV-1 inhibitor-11, a fused pyridine ring derivative, is a HIV-1 inhibitor.</p>Formula:C42H36ClF10N7O5S2Color and Shape:SolidMolecular weight:1008.35Kuguacin N
<p>Kuguacin N is a useful organic compound for research related to life sciences and the catalog number is T126345.</p>Formula:C30H46O4Color and Shape:SolidMolecular weight:470.694MPG, HIV related
CAS:<p>MPG: 27-amino acid peptide from HIV-1 gp41 & SV40 T antigen, delivers nucleic acids into cells efficiently.</p>Formula:C126H201N35O33SPurity:98%Color and Shape:SolidMolecular weight:2766.22NF279
CAS:<p>P2X1 antagonist</p>Formula:C49H36N6Na6O23S6Purity:98%Color and Shape:SolidMolecular weight:1407.17VIR-165
<p>VIR-165, a derivative of VIRIP (353-372 of alpha1-antitrypsin), blocks several HIV-1 strains.</p>Formula:C109H158N22O25S2Purity:98%Color and Shape:SolidMolecular weight:2240.7Delavirdine
CAS:<p>Delavirdine, an NNRTI for HIV-1, is used in HAART.</p>Formula:C22H28N6O3SColor and Shape:SolidMolecular weight:456.56NNRT-IN-6
<p>NNRT-IN-6 (Compound 13a) is a non-nucleoside reverse transcriptase inhibitor (NNRT) used to inhibit HIV-1 reverse transcriptase (HIV-1RT), with an IC50 of 0.41 μM. It effectively suppresses both wild-type HIV-1 and mutants L100I, K103N, Y181C, Y188L, E138K, F227L/V106A, and RES056, with an EC50 range of 6.2-250 nM.</p>Formula:C32H31N9O3SColor and Shape:SolidMolecular weight:621.71Peptide T
CAS:<p>Peptide T, an HIV-1 derived octapeptide, may inhibit gp120 binding to CD4 and cytokines, and affect VIP receptors.</p>Formula:C35H55N9O16Purity:98%Color and Shape:SolidMolecular weight:857.86Cys-TAT(47-57)
CAS:<p>Cys-TAT(47-57): arginine-rich peptide from HIV-1 TAT protein's transduction domain.</p>Formula:C67H124N34O14SPurity:98%Color and Shape:SolidMolecular weight:1661.99MB-66
<p>MB-66 (MAPP-66) is a fully human IgG1 antibody targeting HSV and HIV. It is a monoclonal antibody membrane intended for vaginal application. The isotype control for MB-66 can be referred to as HumanIgG1kappa, Isotype Control.</p>Color and Shape:Odour LiquidSPD-756
CAS:<p>SPD-756, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Formula:C12H16N6O3Purity:98%Color and Shape:SolidMolecular weight:292.29HIV-1 inhibitor-59
<p>HIV-1 Inhibitor-59 (Compound I-5b) effectively inhibits both wild-type and mutant strains of HIV-1, with EC50 values ranging from 5.62 to 171 nM.</p>Formula:C28H28FN5O3SColor and Shape:SolidMolecular weight:533.62Clavirolide L
<p>Clavirolide L (Compound 3), a dolabellane-type diterpenoid isolated from Clavularia viridis, demonstrates significant inhibition against HIV-1 without</p>Formula:C20H28O3Color and Shape:SolidMolecular weight:316.43HIV-1 inhibitor-6
CAS:<p>HIV-1 inhibitor-6 (3-Pyridinecarboxamide, 1,4-dihydro-1-methyl-N-(5-nitro-1,2-benzisothiazol-3-yl)-4-oxo-) is a potent HIV-1 pre-mRNA selective splicing</p>Formula:C14H10N4O4SPurity:99.33%Color and Shape:SolidMolecular weight:330.32Hinnuliquinone
CAS:<p>Hinnuliquinone is an anti-HIV agent.</p>Formula:C32H30N2O4Purity:98%Color and Shape:SolidMolecular weight:506.59

