
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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L-696229
CAS:L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.Fórmula:C17H18N2O2Pureza:98%Cor e Forma:SolidPeso molecular:282.34Hinokinin
CAS:Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35SW106
CAS:SW106 blocks PTHR1 cAMP signaling, not affecting mutant PTHR1-T410P/H223R.Fórmula:C16H14F5NO2Cor e Forma:SolidPeso molecular:347.28HIV-1 protease-IN-9
CAS:HIV-1 protease-IN-9 (compound 5b), a potent HIV-1 protease inhibitor, exhibits strong antiviral efficacy with a dissociation constant (K_i) of 0.028 nM and aFórmula:C37H41N7O4SPureza:98%Cor e Forma:SolidPeso molecular:679.83Ro 31-8588
CAS:Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.Fórmula:C33H56N4O5Cor e Forma:SolidPeso molecular:588.8212-Bromododecanoic Acid
CAS:12-Bromododecanoic acid, a halogenated derivative of lauric acid, serves in the synthesis of clickable myristic acid derivatives and functions as a model fatty acid ligand for elucidating the X-ray crystal structure of bovine β-lactoglobulin-ligand complexes. This compound, at a concentration of 10 µg/ml, has been shown to diminish virion DNA in the culture supernatant of primary hepatocytes from a duckling model of hepatitis B virus (HBV) infection and exhibits inhibitory activity against HIV replication in CEM-SS T cells with an EC50 value of 38 µM.Fórmula:C12H23BrO2Cor e Forma:SolidPeso molecular:279.218XZ426
CAS:XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .Fórmula:C22H24F2N4O4Cor e Forma:SolidPeso molecular:446.45DMP 323
CAS:DMP 323 is a potent inhibitor of HIV-1 protease.Fórmula:C35H38N2O5Pureza:98%Cor e Forma:SolidPeso molecular:566.69WRNA10
CAS:WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).Fórmula:C25H32N4O4Cor e Forma:SolidPeso molecular:452.55GSK3532795
CAS:<p>GSK3532795: potent oral HIV-1 maturation inhibitor; EC50: 1.9-13 nM for various strains.</p>Fórmula:C42H62N2O4SPureza:98%Cor e Forma:SolidPeso molecular:691.02Murabutide
CAS:Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,Fórmula:C23H40N4O11Cor e Forma:SolidPeso molecular:548.58HIV-1 inhibitor-3
CAS:HIV-1 inhibitor-3 is an HIV infection inhibitor.Fórmula:C9H10F2N2O5Pureza:98%Cor e Forma:SolidPeso molecular:264.18Hydroxy Darunavir
CAS:Hydroxy darunavir, a metabolite of the HIV-1 protease inhibitor darunavir, is generated through isobutyl aliphatic hydroxylation of darunavir.Fórmula:C27H37N3O8SCor e Forma:SolidPeso molecular:563.66KNI-272
CAS:Kynostatin-272 is a HIV protease inhibitor. KNI-272 blocked the maturation of viral particles.Fórmula:C33H41N5O6S2Cor e Forma:SolidPeso molecular:667.84L 694746
CAS:L 694746 is an inhibitor of HIV-1 protease.Fórmula:C35H42N2O8Pureza:98%Cor e Forma:SolidPeso molecular:618.72A 77003
CAS:A 77003 is a HIV-1 protease inhibitor. A77003 impairs HIV-1 protease-mediated Gag processing.Fórmula:C44H58N8O6Cor e Forma:SolidPeso molecular:794.98BMS-561390
CAS:BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.Fórmula:C14H12ClF3N2OCor e Forma:SolidPeso molecular:316.71R 87366
CAS:R 87366 is used as a water-soluble HIV protease inhibitor.Fórmula:C32H39N7O6Pureza:98%Cor e Forma:SolidPeso molecular:617.7GSK3839919A
CAS:GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].Fórmula:C36H46ClN3O3Cor e Forma:SolidPeso molecular:604.22HIV-1 integrase inhibitor 3
CAS:HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).Fórmula:C21H22F2N4O4Pureza:98%Cor e Forma:SolidPeso molecular:432.42
