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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HIV 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:981.1Clavirolide 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:316.43SPD-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:292.29Scirpusin 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-1 inhibitor-58
<p>HIV-1 Inhibitor-58 (Compound 10c) is a non-nucleoside reverse transcriptase inhibitor with broad-spectrum antiviral properties, effective against both wild-type</p>Formula:C26H24N6O2Color and Shape:SolidMolecular weight:452.51Salvianan A
CAS:<p>1,6,11-Trimethyl-1,2-dihydrofuro[2',3':1,2]phenanthro[4,3-d]oxazole (compound 1) serves as an effective anti-HIV-1 agent [1].</p>Formula:C20H17NO2Color and Shape:SolidMolecular weight:303.35Tenofovir-C3-O-C15-CF3 ammonium
CAS:<p>Tenofovir-C3-O-C15-CF3 (ammonium) has a longer half-life and stronger anti-HIV action, improving pharmacokinetics in vivo.</p>Formula:C28H52F3N6O5PColor and Shape:SolidMolecular weight:640.73Kadsuralignan A
CAS:<p>Kadsuralignan A (compound 1), a dibenzocyclooctadiene lignan extracted from the leaves and stems of Schisandra lancifolia, exhibits anti-HIV activity, with an</p>Formula:C22H26O7Color and Shape:SolidMolecular weight:402.44Globotriaosylceramides (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:1136.553(Iso)-Fosdevirine
CAS:<p>(Iso)-Fosdevirine ( (Iso)-GSK2248761), a reverse transcriptase (NNRTI) inhibitor with anti-HIV activity, is used in the study of neurological diseases.</p>Formula:C20H17ClN3O3PPurity:99.93%Color and Shape:SoildMolecular weight:413.79Bictegravir 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:471.36(2S,5S)-Censavudine
<p>(2S,5S)-Censavudine, a potent HIV inhibitor and nucleoside reverse transcriptase blocker.</p>Formula:C12H12N2O4Color and Shape:SolidMolecular weight:248.23Decanoyl-RVKR-CMK
CAS:<p>Inhibits all seven proprotein convertases; stops proET-1 processing; hinders VGF secretion in PC12 cells.</p>Formula:C34H66ClN11O5Purity:98%Color and Shape:SolidMolecular weight:744.42Schineolignin B
<p>Schineolignin B is a useful organic compound for research related to life sciences and the catalog number is T126011.</p>Formula:C22H30O5Color and Shape:SolidMolecular weight:374.477BNM-III-170
CAS:<p>BNM-III-170 is able to inhibit HIV-1 viral entry into target cells.</p>Formula:C25H26ClF7N6O6Color and Shape:SolidMolecular weight:674.96Peptide 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:857.86N36Mut(e,g)
<p>N36Mut(e,g) is an HIV fusion peptide inhibitor targeting gp41. It functions by disrupting the formation of the homotrimeric coiled coil of the N-terminal helix in the pre-hairpin intermediate, leading to the creation of a heterotrimer.</p>Formula:C189H317N55O56Color and Shape:SolidMolecular weight:4255.87PROTAC Vif degrader-1
<p>PROTACVif degrader-1 (Compound L15) is a Vif-targeted PROTAC degrader exhibiting anti-HIV-1 virucidal activity, with an EC50 of 33.35 μM against HIV-1IIIB.</p>Color and Shape:Odour SolidInteriorin
CAS:<p>Interiorin, extracted from Kadsura heteroclita, exhibits moderate anti-HIV activity, exhibiting an EC_50 of 1.6 μg/mL [1].</p>Formula:C27H30O8Color and Shape:SolidMolecular weight:482.52Indoline
CAS:<p>Compound PDK0239, with CAS No. 496-15-1, is a fragment molecule that serves as an important scaffold for molecular linking, expansion, and modification. Compound PDK0239 provides a structural basis and research tool for the design and screening of novel drug candidates, and is commonly used in drug discovery, drug synthesis, and related research.</p>Formula:C8H9NColor and Shape:Clear To Yellow LiquidMolecular weight:119.16Pol (476-484), HIV-1 RT Epitope
CAS:<p>Pol (476-484), HIV-1 RT Epitope is a biologically active peptide and represents the dominant HLA A*0201-restricted epitope within HIV-1 reverse transcriptase (</p>Formula:C46H78N12O12Color and Shape:SolidMolecular weight:991.18[(Cys(Bzl)84,Glu(OBzl)85)]CD4 (81-92)
CAS:<p>[(Cys(Bzl)84, Glu(OBzl)85)]CD4 (81-92) is a selective HIV-1 inhibitor that blocks the interaction between HIV-1 and CD4 molecules, thereby inhibiting viral infection and cell fusion. At a concentration of 25 μM, it can completely prevent fusion formation [1].</p>Formula:C76H108N14O26SColor and Shape:SolidMolecular weight:1665.81NF279
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:2240.7GP120, HIV-1 MN
<p>GP120, HIV-1 MN, a peptide, is utilized in researching HIV infection [1] [2].</p>Formula:C135H221N45O33Color and Shape:SolidMolecular weight:3002.5Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2
CAS:<p>Ac-Ser-Gln-Asn-Tyr-Pro-Val-Val-NH2, a peptide substrate for HIV-1 protease, is used in inhibition assays.</p>Formula:C38H58N10O12Color and Shape:SolidMolecular weight:846.93HIV-1 inhibitor-12
<p>HIV-1 inhibitor-12: potent at inhibiting HIV-1 capsid protein polymerization with 9 nM IC50.</p>Formula:C42H36ClF10N7O5S2Color and Shape:SolidMolecular weight:1008.35UK-88947 HCl
CAS:<p>UK 88947 is a protease inhibitor.</p>Formula:C41H63ClN6O6Purity:98%Color and Shape:SolidMolecular weight:771.44MPG, 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:2766.22HIV-1 inhibitor-75
<p>HIV-1inhibitor-75 is a human immunodeficiency virus 1 (HIV-1) inhibitor with an EC50 range of 0.0039-0.338 μM. Its target is the reverse transcriptase, exhibiting an IC50 value of 0.055 μM. Additionally, HIV-1inhibitor-75 demonstrates good metabolic stability in vitro, presenting moderate clearance rates and an extended half-life in human plasma and liver microsomes.</p>Formula:C25H20ClN3O3SColor and Shape:SolidMolecular weight:477.96Pirmitegravir
CAS:<p>Pirmitegravir (STP0404) is a potent ALLINI, blocks LEDGF/p75 site, shows antiviral action against HIV.</p>Formula:C27H31ClN4O3Purity:99.79% - 99.79%Color and Shape:SolidMolecular weight:495.01Enfuvirtide
CAS:<p>Enfuvirtide (INN) is an HIV fusion inhibitor, the first of a class of antiretroviral drugs used in combination therapy for the treatment of HIV-1 infection.</p>Formula:C204H301N51O64Purity:98%Color and Shape:White To Off-White Amorphous SolidMolecular weight:4491.945HIV-IN-2
CAS:<p>HIV-IN-2 (Compound 100) is a potent inhibitor of HIV, showing potential for research into HIV infection [1].</p>Formula:C34H27ClF7N9O3SColor and Shape:SolidMolecular weight:810.14CI-39
CAS:<p>CI-39, an NNRTI with EC50 of 3.40 µM, inhibits HIV-1 reverse transcriptase and RNase H, with CC50 >30 µM.</p>Formula:C19H18N2O4Color and Shape:SolidMolecular weight:338.36HIV protease-IN-1
CAS:<p>HIV protease-IN-1 (compound 1·succinate), a potent non-peptidic inhibitor of HIV protease, is utilized for AIDS research [1].</p>Formula:C39H40ClF7N10O7Color and Shape:SolidMolecular weight:929.24(±)-BI-D
CAS:<p>(±)-BI-D is an effective ALLINI(An allosteric IN inhibitor) that binds integrase at the LEDGF/p75 binding site (IC50: 2.4–2.9 μM).</p>Formula:C25H27NO4Color and Shape:SolidMolecular weight:405.49Saquinavir mesylate
CAS:<p>Saquinavir mesylate (Ro 31-8959/003) is an Inhibitor of HIV Proteaseused in antiretroviral therapy</p>Formula:C39H54N6O8SPurity:99.19%Color and Shape:White Or Pale Yellow PowderMolecular weight:766.9Dideoxyadenosine
CAS:<p>2',3'-Dideoxyadenosine is an inhibitor of HIV replication with antiretroviral activity and antiviral efficacy [1].</p>Formula:C10H13N5O2Purity:99.28%Color and Shape:Physical Description Off-White Powder (Ntp 1992)Molecular weight:235.242'-Deoxy-2'-fluoroarabinoadenosine
CAS:<p>2'-Deoxy-2'-fluoroarabinoadenosine is a nucleoside analogue with extensive anti-tumor activity and can be used for the study of tumor diseases.</p>Formula:C10H12FN5O3Purity:99.95%Color and Shape:SolidMolecular weight:269.23Pseudothymidine
CAS:<p>Pseudothymidine is a C-nucleoside analog of thymidine.</p>Formula:C10H14N2O5Purity:98%Color and Shape:SolidMolecular weight:242.23(Z)-9-Propenyladenine
CAS:<p>(Z)-9-Propenyladenine is a mutagenic impurity in tenofovir disoproxil fumarate.</p>Formula:C8H9N5Color and Shape:SolidMolecular weight:175.19TAT (48-57)
CAS:<p>TAT (48-57) is a cell-permeable HIV-1 Tat protein fragment, amino acids 48-57.</p>Formula:C55H109N31O12Purity:98%Color and Shape:SolidMolecular weight:1396.65Abacavir hydroxyacetate
CAS:<p>Abacavir hydroxyacetate is a nucleoside analog reverse transcriptase inhibitor used in the study of HIV infection.</p>Formula:C16H20N6O3Purity:98.29%Color and Shape:SolidMolecular weight:344.37Pentosan Polysulfate Sodium (W/W 43%)
CAS:<p>Pentosan Polysulfate Sodium: anti-HIV, anti-inflammatory, aids cartilage, treats interstitial cystitis.</p>Purity:98%Color and Shape:SolidMolecular weight:N/ATenofovir hydrate
CAS:<p>Tenofovir hydrate (GS 1278 hydrate) is a nucleotide reverse transcriptase inhibitor with antiviral activity.</p>Formula:C9H16N5O5PPurity:99.63%Color and Shape:SolidMolecular weight:305.23Letrazuril
CAS:<p>Letrazuril is a compound of the anti-HIV.</p>Formula:C17H9Cl2FN4O2Color and Shape:SolidMolecular weight:391.18PL 100
CAS:<p>PL 100 could inhibit HIV-1 protease.</p>Formula:C33H44N4O6SPurity:98%Color and Shape:SolidMolecular weight:624.79Betulin diacetate
CAS:<p>Betulin diacetate is a bioactive chemical.</p>Formula:C34H54O4Color and Shape:SolidMolecular weight:526.8Etravirine D4
CAS:<p>Etravirine is a non-nucleoside reverse transcriptase inhibitor (NNRTI) used for the treatment of HIV. Etravirine D4 is the deuterium labeled Etravirine.</p>Formula:C20H15BrN6OPurity:98%Color and Shape:SolidMolecular weight:439.3Cabotegravir sodium
CAS:<p>Cabotegravir sodium inhibits HIV integrase (IC50: 2.5 nM), metabolized by UGT1A1, with minimal ARV interaction.</p>Formula:C19H16F2N3NaO5Color and Shape:SolidMolecular weight:427.34
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