Proteasa del VIH
Los inhibidores de la proteasa del VIH son una clase de fármacos antirretrovirales que atacan específicamente la enzima proteasa del virus de la inmunodeficiencia humana (VIH). Al inhibir esta enzima, estos compuestos evitan que el virus procese sus poliproteínas en proteínas maduras y funcionales, bloqueando así la producción de nuevos viriones infecciosos. Los inhibidores de la proteasa del VIH son una piedra angular de la terapia antirretroviral altamente activa (TARGA) utilizada para manejar el VIH/SIDA. En CymitQuimica, ofrecemos una variedad de inhibidores de la proteasa del VIH para apoyar su investigación en el tratamiento del VIH, la resistencia a los medicamentos y la virología.
Se han encontrado 449 productos de "Proteasa del VIH"
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HIV-1 inhibitor-31
CAS:<p>HIV-1 inhibitor-31 (compound 4) is a potent inhibitor of HIV-1. HIV-1 inhibitor-31 can be used in the study of AIDS.</p>Fórmula:C21H13Cl2N3O2Forma y color:SolidPeso molecular:410.25Deaminase inhibitor-1
CAS:<p>Deaminase inhibitor-1 is an APOBEC3G DNA Deaminase inhibitor with an IC 50 value of 18.9 μM [1].</p>Fórmula:C11H12BrN3OSForma y color:SolidPeso molecular:314.2HIV-1 inhibitor-50
CAS:<p>HIV-1 inhibitor-50 is a non-nucleoside reverse transcriptase inhibitor (NNRTI) that targets HIV-1 reverse transcriptase (IC50 = 50 nM).</p>Fórmula:C24H18FN5O2Forma y color:SolidPeso molecular:427.43S-1360
CAS:<p>S-1360 is an inhibitor of HIV-1 integrase.</p>Fórmula:C16H12FN3O3Pureza:98%Forma y color:SolidPeso molecular:313.28PF-46396
CAS:<p>PF-46396 is a HIV maturation inhibitor and can be used against HIV-1 clade B and C.</p>Fórmula:C27H29F3N2OForma y color:SolidPeso molecular:454.53HIV-1 inhibitor-39
CAS:<p>HIV-1 inhibitor-39: blocks HIV-1, anti-RT (IC50=15.75 μM), toxic to MT-4 cells (CC50=112.9 μM).</p>Fórmula:C20H17ClN4O4S4Forma y color:SolidPeso molecular:541.09Antiviral agent 9
<p>Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.</p>Fórmula:C38H50N7O8PForma y color:SolidPeso molecular:763.82HIV-1 inhibitor-48
CAS:<p>HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .</p>Fórmula:C19H16BrN5Forma y color:SolidPeso molecular:394.27HIV-1 inhibitor-35
CAS:<p>HIV-1 inhibitor-35, potent against HIV (EC50: 80 nM LTR, 70 nM CMV), also suppresses HepG2 cells (CC50: 40 nM), may reverse HIV-1 latency.</p>Fórmula:C13H12Cl3N5OSForma y color:SolidPeso molecular:392.69HIV-1 inhibitor-9
CAS:<p>HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.</p>Fórmula:C24H21N5OForma y color:SolidPeso molecular:395.46HIV-1 inhibitor-56
CAS:<p>HIV-1 inhibitor-56 (compound 12126065) is a potent non-nucleoside reverse transcriptase inhibitor with significant antiviral activity against wild-type HIV-1,</p>Fórmula:C22H14ClN7O2SForma y color:SolidPeso molecular:475.91Cgp 53820
CAS:<p>CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.</p>Fórmula:C31H51N5O5Forma y color:SolidPeso molecular:573.77HIV-1 inhibitor-33
CAS:<p>HIV-1 inhibitor-33, potent against HIV-1 (EC50: 8.6 nM), low toxicity to MT-4 cells (CC50: 18 μM), useful for AIDS research.</p>Fórmula:C25H28N6OForma y color:SolidPeso molecular:428.53ML67-33
CAS:<p>ML67-33 selectively activates K2P channels; EC50: 36.3 μM (cell-free), 9.7 μM (HEK293). Reversible TREK-1 modulation.</p>Fórmula:C18H17Cl2N5Pureza:98%Forma y color:SolidPeso molecular:374.27HEPT
CAS:<p>HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription.</p>Fórmula:C14H16N2O4SPureza:98%Forma y color:SolidPeso molecular:308.35L-Ristosamine nucleoside
CAS:<p>L-Ristosamine nucleoside shows antiviral activity.</p>Fórmula:C21H21N3O7Forma y color:SolidPeso molecular:427.41Suberosol
CAS:<p>Suberosol possesses anti-HIV replication activity.</p>Fórmula:C31H50O2Pureza:98%Forma y color:SolidPeso molecular:454.73ZP7
CAS:<p>ZP7 is a HIV-1 replication inhibitor.</p>Fórmula:C15H9Br2ClN4OS2Pureza:98%Forma y color:SolidPeso molecular:520.65APA-APA-MPO
CAS:<p>APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor.</p>Fórmula:C12H25Cl2N5OPureza:98%Forma y color:SolidPeso molecular:326.27Ingenol 3-Hexanoate
CAS:<p>Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1.</p>Fórmula:C26H38O6Pureza:98%Forma y color:SolidPeso molecular:446.58BM 21.1298
CAS:<p>BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.</p>Fórmula:C16H13NOSPureza:98%Forma y color:SolidPeso molecular:267.35D4DAP
CAS:<p>D4DAP is an inhibitor of HIV virus replication.</p>Fórmula:C10H12N6O2Pureza:98%Forma y color:SolidPeso molecular:248.24Nitrobenzofuroxan
CAS:<p>Nitrobenzofuroxan, is a HIV-1 and IDO1 inhibitor.</p>Fórmula:C6H3N3O4Pureza:98%Forma y color:SolidPeso molecular:181.11BMS-663749 lysine
CAS:<p>BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.</p>Fórmula:C29H39N6O11PPureza:98%Forma y color:SolidPeso molecular:678.63GSK5750
CAS:<p>GSK5750 is the ribonuclease H activity inhibitor.</p>Fórmula:C16H12N4O2SForma y color:SolidPeso molecular:324.365-Et-ddU
CAS:<p>5-Et-ddU: A pyrimidine nucleoside with anti-HIV-1 activity in human blood cells.</p>Fórmula:C11H16N2O4Pureza:98%Forma y color:SolidPeso molecular:240.26L-708906
CAS:<p>L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.</p>Fórmula:C24H20O6Pureza:98%Forma y color:SolidPeso molecular:404.41Dacopafant
CAS:<p>Dacopafant is an antagonist of platlet activationg factor receptor.</p>Fórmula:C12H11N3OSForma y color:SolidPeso molecular:245.35M038
CAS:5M038, a novel inhibitor of HIV envelope-mediated fusion, strongly inhibits gp41-mediated membrane fusion.Fórmula:C17H8F6N4Pureza:98%Forma y color:SolidPeso molecular:382.26L 738372
CAS:<p>L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase.</p>Fórmula:C18H15N3OForma y color:SolidPeso molecular:289.33Vif-A3G Inhibitor N.41
CAS:<p>Vif-A3G Inhibitor N.41 is a HIV-1 inhibitor-targeting drug. It causes Vif-dependent degradation of human APOBEC3G, thereby inhibiting the Vif-A3G interaction.</p>Fórmula:C15H14N2O2Pureza:98%Forma y color:SolidPeso molecular:254.28A 75925
CAS:<p>A 75925, a nonnucleoside reverse transcriptase inhibitors (NNRTI), works to inhibit HIV-1 replication.</p>Fórmula:C44H54N4O8Pureza:98%Forma y color:SolidPeso molecular:766.92Sp-TTPαS
CAS:Sp-TTPαS is a competitive inhibitor of the catalytic activity of sterile alpha motif and HD domain containing protein 1 (SAMHD1). It competitively inhibits TTP hydrolysis, with a Ki value of 46 µM.Fórmula:C10H17N2O13P3SPeso molecular:498.23HIV-1 inhibitor-53
CAS:<p>HIV-1 Inhibitor-53 targets HIV-1 protease (IC50: 1.93 nM) and reverse transcriptase (IC50: 2.35 μM), aiding AIDS research.</p>Fórmula:C30H34N2O8SPureza:98%Forma y color:SolidPeso molecular:582.66Fosdevirine
CAS:<p>Fosdevirine (GSK2248761), a non-nucleoside reverse transcriptase (NNRTI) inhibitor with anti-HIV activity, is used in the study of neurological related diseases</p>Fórmula:C20H17ClN3O3PPureza:99.92%Forma y color:SolidPeso molecular:413.79(S)-BI-1001
CAS:<p>(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).</p>Fórmula:C19H15BrClNO3Pureza:98%Forma y color:SolidPeso molecular:420.68Navuridine
CAS:<p>Navuridine (AZdU) is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.</p>Fórmula:C9H11N5O4Pureza:99.83%Forma y color:SolidPeso molecular:253.22Isoescin IA
CAS:<p>Isoescin IA is a triterpenoid saponin isolated from the seeds of Aesculus chinensis. It has anti-HIV-1 protease activity.</p>Fórmula:C55H86O24Pureza:96.00%Forma y color:SolidPeso molecular:1131.26L 756423
CAS:<p>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.</p>Fórmula:C39H48N4O5Pureza:99.34% - 99.88%Forma y color:SolidPeso molecular: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>Fórmula:C21H25N5O2Pureza:98.20%Forma y color:SolidPeso molecular:379.46GSK-364735
CAS:<p>GSK-364735 is an HIV-1 IN inhibitor.</p>Fórmula:C19H18FN3O4Pureza:97.73%Forma y color:SolidPeso molecular:371.36Opaviraline
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%Forma y color:SolidPeso molecular:280.29Emivirine
CAS:<p>Emivirine (MKC-442) is a potent and selective nonnucleoside reverse transcriptase inhibitor of human immunodeficiency virus type 1.</p>Fórmula:C17H22N2O3Pureza:99.8%Forma y color:SolidPeso molecular:302.37AzddMeC
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>Fórmula:C10H14N6O3Pureza:97.14% - 99.62%Forma y color:SolidPeso molecular:266.26Lenacapavir
CAS:<p>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.</p>Fórmula:C39H32ClF10N7O5S2Pureza:99.61% - 99.87%Forma y color:SolidPeso molecular:968.28BMS-488043
CAS:<p>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(+)</p>Fórmula:C22H22N4O5Pureza:99.95%Forma y color:SolidPeso molecular:422.43KM-023
CAS:<p>KM-023 is a new second-generation non-nucleoside reverse transcriptase inhibitor for the study of human immunodeficiency virus (HIV) type 1 infection.</p>Fórmula:C18H19N3O3Pureza:99.47% - >99.99%Forma y color:SolidPeso molecular:325.36(2RS)-FPMPA
CAS:<p>(2RS)-FPMPA（FPMPA） has antiviral activity with an IC50 value of 1.85 μM measured in human MT12 cells infected with SHIV (DH4R).</p>Fórmula:C9H13FN5O4PPureza:99.9% - >99.99%Forma y color:SolidPeso molecular:305.2Tenofovir alafenamide fumarate
CAS:<p>Tenofovir alafenamide fumarate (GS-7340) is an oral anti-HIV drug that prevents infection.</p>Fórmula:C25H33N6O9PPureza:99.95%Forma y color:SolidPeso molecular:592.54Suksdorfin
CAS:<p>Suksdorfin has hypoglycemic effects and activates PPARγ, which promotes insulin-dependent glucose uptake by adipocytes and can be used to study obesity .</p>Fórmula:C21H24O7Pureza:98.54%Forma y color:SolidPeso molecular:388.41
