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 497 products of "HIV Protease"
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GSK-364735
CAS:GSK-364735 is an HIV-1 IN inhibitor.Formula:C19H18FN3O4Purity:97.73%Color and Shape:SolidMolecular weight:371.36KM-023
CAS:KM-023 is a new second-generation non-nucleoside reverse transcriptase inhibitor for the study of human immunodeficiency virus (HIV) type 1 infection.Formula:C18H19N3O3Purity:99.03% - 99.47%Color and Shape:SolidMolecular weight:325.36L 756423
CAS:L756423 is a potent, selective HIV protease inhibitor (Ki=0.049 nM), effective against HIV spread in MT25 lymphocytes at 0.1-0.5 nM, useful for AIDS research.Formula:C39H48N4O5Purity:99.34% - 99.88%Color and Shape:SolidMolecular weight:652.82Atevirdine
CAS:<p>Atevirdine is an HIV-1 reverse transcriptase inhibitor with antiviral activity for the study of the AIDS dementia complex (ADC).</p>Formula:C21H25N5O2Purity:98.20%Color and Shape:SolidMolecular weight:379.46HIV-1 integrase inhibitor 8
CAS:<p>HIV-1 integrase inhibitor 8 is an inhibitor of HIV-1 integrase. Integration is a required step in HIV replication [1].</p>Formula:C21H24O2Purity:98.91%Color and Shape:SolidMolecular weight:308.41Emivirine
CAS:Emivirine (MKC-442) is a potent and selective nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1.Formula:C17H22N2O3Purity:99.8%Color and Shape:SolidMolecular weight:302.37Opaviraline
CAS:<p>Opaviraline (GW-420867X) is a potent reverse transcriptase inhibitor that inhibits Human immunodeficiency virus 1 and has the potential to treat HIV infection.</p>Formula:C14H17FN2O3Purity:99.94%Color and Shape:SolidMolecular weight:280.29Suksdorfin
CAS:Suksdorfin has hypoglycemic effects and activates PPARγ, which promotes insulin-dependent glucose uptake by adipocytes and can be used to study obesity .Formula:C21H24O7Purity:98.54%Color and Shape:SolidMolecular weight:388.41AzddMeC
CAS:<p>AzddMeC (Az-Dcme) is an HIV-1 reverse transcriptase and HIV-1 replication inhibitor with antiretroviral activity.AzddMeC is used in the study of HIV-1 infection</p>Formula:C10H14N6O3Purity:97.14% - 99.62%Color and Shape:SolidMolecular weight:266.26Lenacapavir
CAS:Lenacapavir (GS-6207) is the first HIV-1 capsid inhibitor approved by the U.S. Food and Drug Administration, the European Medicines Agency, and Health Canada for the treatment of MDR HIV-1 infection.Cost-effective and quality-assured.Formula:C39H32ClF10N7O5S2Purity:99.61% - 99.87%Color and Shape:SolidMolecular weight:968.28BMS-488043
CAS:BMS-488043 is a novel and unique oral small molecule HIV fusion inhibitor that inhibits the attachment of Human Immunodeficiency Virus type 1 (HIV-1) to CD4(+)Formula:C22H22N4O5Purity:99.95%Color and Shape:SolidMolecular weight:422.43(2RS)-FPMPA
CAS:(2RS)-FPMPA（FPMPA） has antiviral activity with an IC50 value of 1.85 μM measured in human MT12 cells infected with SHIV (DH4R).Formula:C9H13FN5O4PPurity:99.9% - >99.99%Color and Shape:SolidMolecular weight:305.2Ulonivirine
CAS:Ulonivirine is an orally active non-nucleoside reverse transcriptase inhibitor that exhibits high antiviral activity and can be used to study HIV-1 infection.Formula:C18H8ClF6N5O3Color and Shape:SolidMolecular weight:491.73Teropavimab
CAS:Teropavimab (3BNC117-LS), an antibody, is utilized in the research of HIV infection [1].Color and Shape:Liquid3′-Deoxy Thymidine
CAS:3′-Deoxy Thymidine is a nucleoside analog of thymidine with antiviral activity. 3′-Deoxy Thymidine inhibit HIV replication in peripheral blood mononuclear cells (EC50 = 0.17 µM). 3′-Deoxy Thymidine also decreases plaque formation in CV-1 cells infected with HSV-1 at micromolar concentrations. These properties support the use of 3′-Deoxy Thymidine in antiviral mechanism studies and nucleoside analog evaluation.Formula:C10H14N2O4Purity:99.89%Color and Shape:SolidMolecular weight:226.23Rp-dGTPαS
CAS:Rp-dGTPαS, an enantiomer of the dNTPαS nucleotide, serves as the substrate for SAMHD1, a critical regulator of cellular dNTP levels that curtails the replication of viruses (HIV-1, etc.) in CD4+ myeloid lineage and resting T cells. The SAMHD1 tetrameric complex facilitates the hydrolysis of Rp-dGQTPαS into 2'-deoxynucleosides and triphosphates [1].Formula:C10H16N5O12P3SColor and Shape:SolidMolecular weight:523.25Ro 31-8588
CAS:Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.Formula:C33H56N4O5Color and Shape:SolidMolecular weight:588.82Cgp 57813
CAS:CGP 57813 is a lipophilic compound, which can be used as an inhibitor of HIV-1 protease.Formula:C43H58N4O8Color and Shape:SolidMolecular weight:758.94WRNA10
CAS:WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).Formula:C25H32N4O4Color and Shape:SolidMolecular weight:452.55SW106
CAS:SW106 blocks PTHR1 cAMP signaling, not affecting mutant PTHR1-T410P/H223R.Formula:C16H14F5NO2Color and Shape:SolidMolecular weight:347.28
