
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"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
(S)-BI-1001
CAS:(S)-BI-1001 is an active S-enantiomer of BI-1001. (S)-BI-1001 has antiviral potency against HIV-1 integrase (IC50: 28 nM, and EC50: 450 nM and a Kd: 4.7 μM).Fórmula:C19H15BrClNO3Pureza:98%Cor e Forma:SolidPeso molecular:420.68HIV-IN-4
CAS:HIV-IN-4 (Compound 12) is a potent HIV inhibitor that exhibits promising anti-HIV activities [1].Fórmula:C14H18N2O3Cor e Forma:SolidPeso molecular:262.3HIV-1 inhibitor-16
CAS:HIV-1 inhibitor-16: potent with EC50 1.3 nM for wild-type; inhibits K103N, E138K, Y181C, L100I strains; good solubility; stable; low CYP impact; non-toxic.Fórmula:C23H16F2N6Cor e Forma:SolidPeso molecular:414.41HIV-1 inhibitor-57
CAS:<p>HIV-1 Inhibitor-57 (Compound 12g) is an antiviral agent that potently inhibits both wild-type and five common NNRTI-resistant strains of HIV-1, exhibiting EC50</p>Fórmula:C25H24FN5O3SCor e Forma:SolidPeso molecular:493.55SARS-CoV-IN-3
CAS:SARS-CoV-IN-3 is an effective SARS-CoV replication inhibitor.Fórmula:C25H28ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:477.81Mesoxalic acid
CAS:Mesoxalic acid is a dicarboxylic acid and a ketonic acid which blocks RT translocation.Fórmula:C3H2O5Pureza:98%Cor e Forma:SolidPeso molecular:118.04SAMT-247
CAS:SAMT-247 is an HIV inhibitor that acts by modifying the nucleocapsid NCp7 region of Gag in infected cells and blocking Gag processing and reducing infectivity.Fórmula:C12H14N2O3SCor e Forma:SolidPeso molecular:266.32TMC310911
CAS:TMC310911 is an oral HIV-1 protease inhibitor with an EC50 of 2.2-14.2 nM, effective against various HIV-1 strains.Fórmula:C38H53N5O7S2Pureza:98%Cor e Forma:SolidPeso molecular:755.99Reverse transcriptase-IN-3
Reverse transcriptase-IN-3, a pyrimidine carboxamide, inhibits HIV-1 including mutant strains.Fórmula:C28H31N7O4SCor e Forma:SolidPeso molecular:561.66DQBS
CAS:DQBS is an HIV-1 Nef function antagonist.Fórmula:C22H17ClN4O4SPureza:98%Cor e Forma:SolidPeso molecular:468.91HIV-1 integrase inhibitor 7
CAS:HIV-1 integrase inhibitor 7 is a potent HIV-1 integrase inhibitor (IC50: 33.3 nM).Fórmula:C30H26O16Pureza:98%Cor e Forma:SolidPeso molecular:642.52β-L-D4A
CAS:beta-L-D4A inhibits HIV-1 reverse transcriptase, stopping DNA synthesis.Fórmula:C10H11N5O2Pureza:99.45%Cor e Forma:SolidPeso molecular:233.23MK-4965
CAS:MK-4965 is a new type of non-nucleoside reverse transcriptase inhibitor with antiviral activity.Fórmula:C20H13Cl2N5O2Cor e Forma:SolidPeso molecular:426.26gp120-IN-1
CAS:gp120-IN-1 (4e) is a potent HIV-1 inhibitor, IC50 2.2 μM, CC50 100.90 μM, and blocks HIV entry.Fórmula:C15H18N2O4SCor e Forma:SolidPeso molecular:322.38HIV-1 inhibitor-25
CAS:Compound R-12a is a potent HIV-1 reverse transcriptase inhibitor (IC50: 0.1061 nM), with low cytotoxicity and effective against multiple mutants.Fórmula:C26H19N5O2Cor e Forma:SolidPeso molecular:433.46LEDGIN6
CAS:HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection.Fórmula:C21H20ClNO2Cor e Forma:SolidPeso molecular:353.84NIT
CAS:NIT is an HIV-1 protease inhibitor.Fórmula:C15H7N3O4S2Pureza:98%Cor e Forma:SolidPeso molecular:357.36HIV-1 inhibitor-36
CAS:HIV-1 inhibitor-36 (Compound 2) is a potent HIV-1 inhibitor with significant potential as a novel latency reversing agent [1].Fórmula:C14H14Cl2N2O2SCor e Forma:SolidPeso molecular:345.24HIV-1 inhibitor-24
CAS:HIV-1 inhibitor-24 (S-12a) blocks HIV reverse transcription effectively (IC50: 9.5 nM), low toxicity, well-tolerated in mice, good heart safety.Fórmula:C26H19N5O2Cor e Forma:SolidPeso molecular:433.46DPC-681
CAS:DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).Fórmula:C35H48FN5O5SCor e Forma:SolidPeso molecular:669.85
