HIV Protease
Os inibidores da protease do HIV são uma classe de medicamentos antirretrovirais que têm como alvo específico a enzima protease do vírus da imunodeficiência humana (HIV). Ao inibir esta enzima, esses compostos impedem o vírus de processar suas poliproteínas em proteínas maduras e funcionais, bloqueando assim a produção de novos virions infecciosos. Os inibidores da protease do HIV são um pilar da terapia antirretroviral altamente ativa (HAART) utilizada para o tratamento do HIV/AIDS. Na CymitQuimica, oferecemos uma variedade de inibidores da protease do HIV para apoiar sua pesquisa em tratamento do HIV, resistência a medicamentos e virologia.
Foram encontrados 506 produtos de "HIV Protease"
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AQ 148
CAS:AQ 148 is a potent competitive inhibitor of HIV-1 PR.Fórmula:C30H37N3O4Cor e Forma:SolidPeso molecular:503.63HIV-1 integrase inhibitor 9
CAS:HIV-1 integrase inhibitor 9 (compound 8a) is a potent inhibitor of HIV-1 RNase H (IC50: 12.3 μM) and has antiviral effects.Fórmula:C18H12N2O10Cor e Forma:SolidPeso molecular:416.3Reverse transcriptase-IN-4
Reverse transcriptase-IN-4: potent, selective NNRT inhibitor; EC50 = 0.053 μM for HIV-1, 0.26 μM for E138K mutant.Fórmula:C17H21N5OSCor e Forma:SolidPeso molecular:343.45Rovafovir Etalafenamide
CAS:Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.Fórmula:C21H24FN6O6PPureza:98%Cor e Forma:SolidPeso molecular:506.42SARS-CoV-IN-2
CAS:SARS-CoV-IN-2 is an effective SARS-CoV replication inhibitorFórmula:C24H26ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:463.78Navuridine
CAS:Navuridine (AZdU) is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.Fórmula:C9H11N5O4Pureza:99.83%Cor e Forma:SolidPeso molecular:253.22Ref: TM-T21474
5mg48,00€10mg71,00€25mg131,00€50mg188,00€100mg298,00€500mg1.216,00€1mL*10mM (DMSO)52,00€Emivirine
CAS:Emivirine (MKC-442) is a potent and selective nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1.Fórmula:C17H22N2O3Pureza:99.8%Cor e Forma:SolidPeso molecular: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>Fórmula:C14H17FN2O3Pureza:99.94%Cor e Forma:SolidPeso molecular:280.29Tenofovir alafenamide fumarate
CAS:Tenofovir alafenamide fumarate (GS-7340) is an oral anti-HIV drug that prevents infection.Fórmula:C25H33N6O9PPureza:99.99%Cor e Forma:SolidPeso molecular:592.54(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).Fórmula:C9H13FN5O4PPureza:99.9% - >99.99%Cor e Forma:SolidPeso molecular:305.2GSK-364735
CAS:GSK-364735 is an HIV-1 IN inhibitor.Fórmula:C19H18FN3O4Pureza:97.73%Cor e Forma:SolidPeso molecular:371.36L 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.Fórmula:C39H48N4O5Pureza:99.34% - 99.88%Cor e Forma:SolidPeso molecular:652.82Lenacapavir
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.Fórmula:C39H32ClF10N7O5S2Pureza:99.61% - 99.87%Cor e Forma:SolidPeso molecular:968.28Ref: TM-T11465
1mg187,00€5mg376,00€10mg565,00€25mg998,00€50mg1.388,00€100mg1.882,00€200mg2.622,00€1mL*10mM (DMSO)615,00€Atevirdine
CAS:<p>Atevirdine is an HIV-1 reverse transcriptase inhibitor with antiviral activity for the study of the AIDS dementia complex (ADC).</p>Fórmula:C21H25N5O2Pureza:98.20%Cor e Forma:SolidPeso molecular:379.46AzddMeC
CAS: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 infectionFórmula:C10H14N6O3Pureza:97.14% - 99.62%Cor e Forma:SolidPeso molecular:266.26BMS-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(+)Fórmula:C22H22N4O5Pureza:99.95%Cor e Forma:SolidPeso molecular:422.43KM-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.Fórmula:C18H19N3O3Pureza:99.03% - 99.47%Cor e Forma:SolidPeso molecular:325.36Ref: TM-T67804
1mg150,00€5mg361,00€10mg542,00€25mg870,00€50mg1.188,00€100mg1.596,00€500mg3.202,00€1mL*10mM (DMSO)359,00€Suksdorfin
CAS:Suksdorfin has hypoglycemic effects and activates PPARγ, which promotes insulin-dependent glucose uptake by adipocytes and can be used to study obesity .Fórmula:C21H24O7Pureza:98.54%Cor e Forma:SolidPeso molecular:388.41HIV-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>Fórmula:C21H24O2Pureza:98.91%Cor e Forma:SolidPeso molecular:308.41I-XW-053
CAS: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-Fórmula:C22H16N2O2Pureza:99.05%Cor e Forma:SolidPeso molecular:340.37
