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 447 produtos de "HIV Protease"
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Lopinavir
CAS:<p>Lopinavir (ABT-378) is a peptidomimetic HIV protease inhibitor that retains activity against HIV protease with the Val 82 mutation.</p>Fórmula:C37H48N4O5Pureza:98% - 99.62%Cor e Forma:White Crystalline SolidPeso molecular:628.8Didanosine
CAS:<p>Didanosine (ddI) is a nucleoside reverse transcriptase inhibitor analog of adenosine (IC50: 0.49 μM).</p>Fórmula:C10H12N4O3Pureza:99.64%Cor e Forma:White Crystalline PowderPeso molecular:236.23Rilpivirine
CAS:<p>Rilpivirine (R278474) is a diarylpyrimidine derivative and reverse transcriptase inhibitor with antiviral activity against HIV-1 that is used in the treatment</p>Fórmula:C22H18N6Pureza:97.22% - 98.83%Cor e Forma:SolidPeso molecular:366.42Obefazimod
CAS:<p>Obefazimod (ABX-464) is a potent anti-HIV agent. ABX464 inhibits HIV-1 replication in stimulated peripheral blood mononuclear cells (PBMCs).</p>Fórmula:C16H10ClF3N2OPureza:99.86%Cor e Forma:SolidPeso molecular:338.712,4-Dihydroxypyridine
CAS:<p>2,4-Dihydroxypyridine: a pyridine derivative, chelates metals, assesses ion levels, measures enzymatic reactions, and quantifies biomolecules.</p>Fórmula:C5H5NO2Pureza:97.79%Cor e Forma:White To Yellow-Beige Crystals OrPeso molecular:111.1Dimercaprol
CAS:<p>Dimercaprol (Dicaptol) is an anti-gas warfare agent that is effective against Lewisite (dichloro(2-chlorovinyl)arsine) and formerly known as British Anti-</p>Fórmula:C3H8OS2Pureza:98.91% - 99.64%Cor e Forma:Viscous Oily LiquidPeso molecular:124.22Raltegravir potassium
CAS:<p>Raltegravir potassium (MK 0518 potassium salt) salt(MK0518 potassium salt) is a potent integrase (IN) inhibitor, used to treat HIV infection.</p>Fórmula:C20H20FN6O5·KPureza:98% - 99.55%Cor e Forma:Off-White SolidPeso molecular:482.51NBD-557
CAS:<p>NBD-557 is a potentially HIV-1 inhibitor.</p>Fórmula:C17H24BrN3O2Pureza:99.52%Cor e Forma:SolidPeso molecular:382.3Raltegravir
CAS:<p>Raltegravir (MK-0518) is a pyrrolidinone derivative and HIV INTEGRASE INHIBITOR that is used in combination with other ANTI-HIV AGENTS for the treatment of HIV</p>Fórmula:C20H21FN6O5Pureza:99.86% - >99.99%Cor e Forma:SolidPeso molecular:444.42IMB-301
CAS:<p>IMB-301 is a small molecular inhibitor via virtual screening according to the hA3G model.</p>Fórmula:C19H17Cl2FN2OPureza:99.72%Cor e Forma:SolidPeso molecular:379.26Lamivudine 13C,15N2
CAS:<p>Lamivudine 13C,15N2, a BCH-189 impurity, blocks HIV/HBV reverse transcriptase as an NRTI.</p>Fórmula:C8H9N3O4SPureza:98%Cor e Forma:SolidPeso molecular:246.22Nelfinavir
CAS:<p>Nelfinavir (AG1341), with Ki=2 nM, is an HIV treatment and broad-spectrum anticancer drug.</p>Fórmula:C32H45N3O4SPureza:98.16% - 99.5%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:567.78Elipovimab
CAS:<p>Elipovimab, a potent and broadly neutralizing antibody against HIV-1, targets and eliminates HIV-infected cells [1].</p>Cor e Forma:LiquidSemzuvolimab
CAS:<p>Semzuvolimab, a murine IgG1κ antibody, targets the p55 T-cell surface antigen T4/Leu-3 (CD4).</p>Cor e Forma:LiquidSuvizumab
CAS:<p>Suvizumab (KD-247) is a neutralizing anti-HIV-1 antibody with IC50 values of 0.1-1.0 µg/mL; it lowers viral load and prevents infection.</p>Cor e Forma:LiquidAntiviral agent 55
CAS:<p>Antiviralagent 55 (Compound 95) is an inhibitor of human immunodeficiency viruses 1 and 2 (HIV1 and HIV2), demonstrating antiviral activity.</p>Fórmula:C21H20N2O4Cor e Forma:SolidPeso molecular:364.39Benzalphthalide
CAS:<p>Benzalphthalide (NSC-2824) is a chemical compound with anti-HIV activity.</p>Fórmula:C15H10O2Pureza:99.94%Cor e Forma:Pale Yellow To Yellow Crystalline PowderPeso molecular:222.24Zinlirvimab
CAS:<p>Zinlirvimab is a humanized IgG1-λ2 monoclonal antibody that neutralizes HIV by targeting the HIV-1 gp120 envelope glycoprotein, specifically the IIIB gp120 V3</p>Cor e Forma:LiquidNipamovir
CAS:<p>Nipamovir is a nitroimidazole prodrug that exhibits antiviral activity comparable to SAMT-247 and NS-1040 in cellular assays and a human ex vivo model of HIV infection, with low toxicity. Nipamovir has EC50 values of 3.64±3.28 and 3.23±2.81 μM for CEM-SS/HIV-1RF and hPBMC/HIV-192HT599, respectively [1].</p>Fórmula:C14H15N5O4SCor e Forma:SolidPeso molecular:349.37Antiviral agent 9
<p>Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.</p>Fórmula:C38H50N7O8PCor e Forma:SolidPeso molecular:763.82APOBEC3G-IN-1
CAS:<p>APOBEC3G-IN-1 (MN136.0185) is a targeted APOBEC3G inhibitor with anti-HIV activity for the study of infectious diseases and cancer.</p>Fórmula:C15H11NO3Pureza:96.54%Cor e Forma:SolidPeso molecular:253.25HIV-IN-6
CAS:<p>HIV-IN-6, an anti-HIV agent, blocks replication by targeting SFKs like Hck involved with Nef protein.</p>Fórmula:C20H16N4O3SPureza:97.12%Cor e Forma:SolidPeso molecular:392.43HIV-1 inhibitor-49
<p>HIV-1 inhibitor-49, an oral HEPT analog, has strong pharmacokinetics, potent reverse transcriptase inhibition (IC50=30nM), and is safe in mice.</p>Fórmula:C21H18F2N2O3SCor e Forma:SolidPeso molecular:416.44MK-2048
CAS:<p>MK-2048 is a potent inhibitor of integrase (IN) and INR263K with IC50 of 2.6 nM and 1.5 nM, respectively.</p>Fórmula:C21H21ClFN5O4Pureza:98%Cor e Forma:SolidPeso molecular:461.87HIV-1 inhibitor-22
CAS:<p>HIV-1 inhibitor-22 effectively blocks HIV-1 RT (IC50=3.63 μM) with low cytotoxicity (CC50 > 227 μM).</p>Fórmula:C30H26N6O3SCor e Forma:SolidPeso molecular:550.63HIV-1 integrase inhibitor 4
CAS:<p>HIV-1 integrase inhibitor 4 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 3.7 nM).</p>Fórmula:C24H20F2N4O5SPureza:98%Cor e Forma:SolidPeso molecular:514.5HIV-1 inhibitor-29
CAS:<p>HIV-1 inhibitor-29: Blocks HIV-1 IIIB (EC50: 2.18μM), resists F227L/V106A (EC50: 0.974μM), low toxicity (CC50: 211μM), for AIDS research.</p>Fórmula:C30H36N6O5Cor e Forma:SolidPeso molecular:560.64D77
CAS:<p>D77 is anti-HIV-1 inhibitor. D77 inhibits HIV-1(IIIB) replication by EC50 value of 23.8 μg/ml in MT-4 cell (5.03 μg/ml for C8166 cells).</p>Fórmula:C28H22BrNO7SPureza:98%Cor e Forma:SolidPeso molecular:596.45HIV-1 inhibitor-34
CAS:<p>HIV-1 inhibitor-34 (5q): potent, selective; EC50: 6.4 nM; MT-4 CC50: 16 μM; useful in AIDS research.</p>Fórmula:C26H27N7OCor e Forma:SolidPeso molecular:453.54HIV-IN-4
CAS:<p>HIV-IN-4 (Compound 12) is a potent HIV inhibitor that exhibits promising anti-HIV activities [1].</p>Fórmula:C14H18N2O3Cor e Forma:SolidPeso molecular:262.3HIV-1 inhibitor-16
CAS:<p>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.</p>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:<p>SARS-CoV-IN-3 is an effective SARS-CoV replication inhibitor.</p>Fórmula:C25H28ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:477.81Mesoxalic acid
CAS:<p>Mesoxalic acid is a dicarboxylic acid and a ketonic acid which blocks RT translocation.</p>Fórmula:C3H2O5Pureza:98%Cor e Forma:SolidPeso molecular:118.04SAMT-247
CAS:<p>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.</p>Fórmula:C12H14N2O3SCor e Forma:SolidPeso molecular:266.32TMC310911
CAS:<p>TMC310911 is an oral HIV-1 protease inhibitor with an EC50 of 2.2-14.2 nM, effective against various HIV-1 strains.</p>Fórmula:C38H53N5O7S2Pureza:98%Cor e Forma:SolidPeso molecular:755.99Reverse transcriptase-IN-3
<p>Reverse transcriptase-IN-3, a pyrimidine carboxamide, inhibits HIV-1 including mutant strains.</p>Fórmula:C28H31N7O4SCor e Forma:SolidPeso molecular:561.66DQBS
CAS:<p>DQBS is an HIV-1 Nef function antagonist.</p>Fórmula:C22H17ClN4O4SPureza:98%Cor e Forma:SolidPeso molecular:468.91HIV-1 integrase inhibitor 7
CAS:<p>HIV-1 integrase inhibitor 7 is a potent HIV-1 integrase inhibitor (IC50: 33.3 nM).</p>Fórmula:C30H26O16Pureza:98%Cor e Forma:SolidPeso molecular:642.52β-L-D4A
CAS:<p>beta-L-D4A inhibits HIV-1 reverse transcriptase, stopping DNA synthesis.</p>Fórmula:C10H11N5O2Pureza:99.45%Cor e Forma:SolidPeso molecular:233.23MK-4965
CAS:<p>MK-4965 is a new type of non-nucleoside reverse transcriptase inhibitor with antiviral activity.</p>Fórmula:C20H13Cl2N5O2Cor e Forma:SolidPeso molecular:426.26gp120-IN-1
CAS:<p>gp120-IN-1 (4e) is a potent HIV-1 inhibitor, IC50 2.2 μM, CC50 100.90 μM, and blocks HIV entry.</p>Fórmula:C15H18N2O4SCor e Forma:SolidPeso molecular:322.38HIV-1 inhibitor-25
CAS:<p>Compound R-12a is a potent HIV-1 reverse transcriptase inhibitor (IC50: 0.1061 nM), with low cytotoxicity and effective against multiple mutants.</p>Fórmula:C26H19N5O2Cor e Forma:SolidPeso molecular:433.46LEDGIN6
CAS:<p>HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection.</p>Fórmula:C21H20ClNO2Cor e Forma:SolidPeso molecular:353.84NIT
CAS:<p>NIT is an HIV-1 protease inhibitor.</p>Fórmula:C15H7N3O4S2Pureza:98%Cor e Forma:SolidPeso molecular:357.36HIV-1 inhibitor-36
CAS:<p>HIV-1 inhibitor-36 (Compound 2) is a potent HIV-1 inhibitor with significant potential as a novel latency reversing agent [1].</p>Fórmula:C14H14Cl2N2O2SCor e Forma:SolidPeso molecular:345.24HIV-1 inhibitor-24
CAS:<p>HIV-1 inhibitor-24 (S-12a) blocks HIV reverse transcription effectively (IC50: 9.5 nM), low toxicity, well-tolerated in mice, good heart safety.</p>Fórmula:C26H19N5O2Cor e Forma:SolidPeso molecular:433.46DPC-681
CAS:<p>DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).</p>Fórmula:C35H48FN5O5SCor e Forma:SolidPeso molecular:669.85HIV-1 inhibitor-19
CAS:<p>HIV-1 inhibitor-19 is a potent NNRTI targeting L100I, K103N, V106A/F227L mutants; EC50s: 7.3, 9.2, 21.0 nM respectively.</p>Fórmula:C24H22BClN2O5SCor e Forma:SolidPeso molecular:496.77HIV-1 inhibitor-15
CAS:<p>HIV-1 inhibitor-15 (compound 9d): Potent, broad-spectrum, EC50=1.7-9 nM for various strains, good solubility/safety, oral use.</p>Fórmula:C24H20N6Cor e Forma:SolidPeso molecular:392.46TX-1918
CAS:<p>TX-1918, a tyrphostin, blocks eEF-2K to hinder HepG2, HCT116 cell growth.</p>Fórmula:C14H12O3Cor e Forma:SolidPeso molecular:228.24S 2720
CAS:<p>S 2720 is a human immunodeficiency virus type 1 (HIV-1)-specific reverse transcriptase (RT) inhibitor quinoxaline.</p>Fórmula:C14H15ClN2O2SCor e Forma:SolidPeso molecular:310.81E7-03
CAS:<p>1E7-03 is an inhibitor of HIV-1 transcription, by targeting host Protein Phosphatase-1 (PP1).</p>Fórmula:C28H29N3O6Cor e Forma:SolidPeso molecular:503.55DPC-961
CAS:<p>DPC-961, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C14H10ClF3N2OCor e Forma:SolidPeso molecular:314.69B07 hydrochloride
CAS:<p>B07 hydrochloride is a CCR5 antagonist-based inhibitor of HIV-1 entry.</p>Fórmula:C29H38ClFN4O2Pureza:98%Cor e Forma:SolidPeso molecular:529.09GCA-186
CAS:<p>GCA-186 is an effective non-nucleoside HIV-1 reverse transcriptase inhibitor.</p>Fórmula:C19H26N2O3Pureza:98%Cor e Forma:SolidPeso molecular:330.42HIV-1 inhibitor-20
CAS:<p>HIV-1 inhibitor-20 is a potent HIV-1 inhibitor.</p>Fórmula:C19H11ClF3N3O2Cor e Forma:SolidPeso molecular:405.76BMS-585248
CAS:<p>BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120.</p>Fórmula:C22H18FN7O3Cor e Forma:SolidPeso molecular:447.42AIC-292
CAS:<p>AIC-292 is a potent, tolerable reverse transcriptase inhibitor active against various HIV-1 strains, including NNRTI-resistant K103N, G190A, Y181C.</p>Fórmula:C19H12Cl2F2N4O2Cor e Forma:SolidPeso molecular:437.23L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Fórmula:C31H47N3O6Pureza:98%Cor e Forma:SolidPeso molecular:557.72HIV-1 inhibitor-28
CAS:<p>HIV-1 inhibitor-28: potent, selective, EC50=58 nM, low MT-4 cell toxicity (CC50=38.6 μM), valuable in AIDS research.</p>Fórmula:C26H32N6O3SCor e Forma:SolidPeso molecular:508.64HIV-1 inhibitor-45
CAS:<p>HIV-1 inhibitor-45 is a potent inhibitor of HIV-1 RNase H (IC50: 0.067 μM) and has antiviral effects.</p>Fórmula:C23H24N4O8SCor e Forma:SolidPeso molecular:516.52HIV-1 inhibitor-21
CAS:<p>HIV-1 inhibitor-21 (compound 9b) blocks HIV-1 RT effectively (IC50: 0.55 μM), targeting wild-type and K103N strains, with low toxicity (CC50: 10.2 μM).</p>Fórmula:C28H24N6O2Cor e Forma:SolidPeso molecular:476.53HI-236
CAS:<p>HI-236 is used as a non-nucleoside HIV-1 reverse-transcriptase inhibitor.</p>Fórmula:C16H18BrN3O2SPureza:98%Cor e Forma:SolidPeso molecular:396.3Adenallene
CAS:<p>Adenallene inhibits replication and cytopathic effects of HIV in vitro.</p>Fórmula:C9H9N5OPureza:98%Cor e Forma:SolidPeso molecular:203.2AQ 148
CAS:<p>AQ 148 is a potent competitive inhibitor of HIV-1 PR.</p>Fórmula:C30H37N3O4Cor e Forma:SolidPeso molecular:503.63HIV-1 integrase inhibitor 9
CAS:<p>HIV-1 integrase inhibitor 9 (compound 8a) is a potent inhibitor of HIV-1 RNase H (IC50: 12.3 μM) and has antiviral effects.</p>Fórmula:C18H12N2O10Cor e Forma:SolidPeso molecular:416.3Reverse transcriptase-IN-4
<p>Reverse transcriptase-IN-4: potent, selective NNRT inhibitor; EC50 = 0.053 μM for HIV-1, 0.26 μM for E138K mutant.</p>Fórmula:C17H21N5OSCor e Forma:SolidPeso molecular:343.45Rovafovir Etalafenamide
CAS:<p>Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.</p>Fórmula:C21H24FN6O6PPureza:98%Cor e Forma:SolidPeso molecular:506.42SARS-CoV-IN-2
CAS:<p>SARS-CoV-IN-2 is an effective SARS-CoV replication inhibitor</p>Fórmula:C24H26ClFeN3OPureza:98%Cor e Forma:SolidPeso molecular:463.78HIV-1 inhibitor-23
CAS:<p>HIV-1 inhibitor-23 suppresses HIV reverse transcriptase, effective on wild-type (EC50: 24.9 nM) and K103N mutant (EC50: 10.4 nM), with in vitro stability.</p>Fórmula:C30H26N6O4SCor e Forma:SolidPeso molecular:566.63R 82150
CAS:<p>R 82150 is an antiviral and a member of the tetrahydroimidazo[4,5,1-jk]-[1,4]-benzodiazepin-2(1H)-thione family.</p>Fórmula:C16H21N3SPureza:98%Cor e Forma:SolidPeso molecular:287.42DLC27-14
CAS:<p>DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.</p>Fórmula:C25H25NO4Cor e Forma:SolidPeso molecular:403.47HIV-1 inhibitor-32
CAS:<p>HIV-1 inhibitor-32 is a potent inhibitor of HIV-1 that acts on wild-type HIV (IC50: 34 nM) and can be used in AIDS research.</p>Fórmula:C26H29N5O3SCor e Forma:SolidPeso molecular:491.61HIV-1 protease-IN-2
CAS:<p>HIV-1 protease-IN-2: strong HIV-1 protease blocker, IC50 2.53 nM, fights DRV-sensitive/resistant HIV-1.</p>Fórmula:C27H34N4O7SCor e Forma:SolidPeso molecular:558.65HIV-1 inhibitor-46
CAS:<p>HIV-1 inhibitor-46, compound 13d, is a potent non-nucleoside reverse transcriptase inhibitor with an EC50 of 1.425 μM, useful in AIDS research.</p>Fórmula:C24H21ClN4OSCor e Forma:SolidPeso molecular:448.97HIV-1 inhibitor-37
CAS:<p>HIV-1 inhibitor-37, a potent HIV-1 suppressant, shows promise as a novel latent reactivator.</p>Fórmula:C14H11Cl3N4OCor e Forma:SolidPeso molecular:357.62Tenofovir maleate
CAS:<p>Tenofovir Disoproxil Fumarate is a nucleotide reverse transcriptase inhibitor used in the treatment of HIV and chronic Hepatitis B.</p>Fórmula:C13H18N5O8PCor e Forma:SolidPeso molecular:403.28Stampidine
CAS:<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Fórmula:C20H23BrN3O8PPureza:98%Cor e Forma:SolidPeso molecular:544.29HIV-1 inhibitor-30
CAS:<p>HIV-1 inhibitor-30 (10i) targets RT enzyme, EC50=40nM, IC50=80nM. Effective against seven NNRTI-resistant HIV-1 strains.</p>Fórmula:C19H20ClN3O2Cor e Forma:SolidPeso molecular:357.83Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Fórmula:C27H58NO6PPureza:98%Cor e Forma:SolidPeso molecular:523.73(+)-Dihydrocalanolide A
CAS:<p>DHCal A (NSC 678323) is an oral nonnucleoside Reverse Transcriptase inhibitor for HIV research.</p>Fórmula:C22H28O5Cor e Forma:SolidPeso molecular:372.45HIV-IN-5
CAS:<p>HIV-IN-5 (5r) inhibits HIV-1 with 0.16 μM IC50, targeting NNIBP as a NNRTI.</p>Fórmula:C30H24N2O8SCor e Forma:SolidPeso molecular:572.59HIV-1 inhibitor-47
CAS:<p>HIV-1 Inhibitor-47 blocks Vif-APOBEC3G interaction, has 14.33 μM IC50, and may yield antianxiety and antipsychotic derivatives.</p>Fórmula:C12H14N6Cor e Forma:SolidPeso molecular:242.28L 870810
CAS:<p>L 870810 is a small-molecule inhibitor of HIV-1 integrase with potent antiviral activity in cell culture and good pharmacokinetic properties.</p>Fórmula:C20H19FN4O4SCor e Forma:SolidPeso molecular:430.45HIV-1 protease-IN-5
CAS:<p>HIV-1 protease-IN-5 is an HIV-1 protease inhibitor (IC50: 1.64 nM). HIV-1 protease-IN-5 exhibits significant effects on wild-type and DRV-resistant HIV-1.</p>Fórmula:C27H29F3N2O7SCor e Forma:SolidPeso molecular:582.59DPC-963
CAS:<p>DPC-963 is a RNA-directed DNA polymerase inhibitor.</p>Fórmula:C14H9F5N2OCor e Forma:SolidPeso molecular:316.23Brecanavir
CAS:<p>Brecanavir is a tyrosyl-based arylsulfonamide, high affinity, protease inhibitor (PI) for the treatment of human immunodeficiency virus type 1.</p>Fórmula:C33H41N3O10S2Cor e Forma:SolidPeso molecular:703.82ZINC04177596
CAS:<p>ZINC04177596 is a novel Nef Protein Inhibitor with anti-HIV activity.</p>Fórmula:C22H16N6O4Cor e Forma:SolidPeso molecular:428.4HIV-1 inhibitor-42
CAS:<p>HIV-1 inhibitor-42 (5b) strongly blocks HIV-1 (IC50: 0.06μM) and its RT RNA/DNA polymerases (IC50: 0.518/0.072μM).</p>Fórmula:C22H20N2O5SCor e Forma:SolidPeso molecular:424.47EP39
<p>EP39 is a potent HIV-1 inhibitor, stabilizing the SP1 domain's helix and blocking virus maturation.</p>Fórmula:C38H62N2O5Cor e Forma:SolidPeso molecular:626.91SJ-3366
CAS:<p>SJ3366 is a unique and highly potent nonnucleoside reverse transcriptase human immunodeficiency virus type 1 and HIV-2 inhibitor.</p>Fórmula:C21H24N2O3Cor e Forma:SolidPeso molecular:352.43HIV-1 protease-IN-1
CAS:<p>HIV-1 protease-IN-1, potent HIV inhibitor; IC50=90pM, fights B/C-HIV strains with EC50=89-13.59/8.23nM.</p>Fórmula:C25H35N3O6SCor e Forma:SolidPeso molecular:505.63VEC-5
CAS:<p>VEC-5: an HIV-1 inhibitor, outperforms RN18 by better binding with Vif in studies.</p>Fórmula:C29H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:447.48HIV-1 inhibitor-38
CAS:<p>HIV-1 inhibitor-38, or Compound 91, shows promise as a strong latency reversing agent against HIV-1.</p>Fórmula:C15H13Cl3N6Cor e Forma:SolidPeso molecular:383.66A3N19
CAS:<p>A3N19 is a potent inhibitor of HIV-1 non-nucleoside reverse transcriptase and is able to act on HIV-1 IIIB (EC50: 3.28 nM).</p>Fórmula:C31H31N9O2SCor e Forma:SolidPeso molecular:593.7DMJ-I-228
CAS:<p>DMJ-I-228 is a specific inhibitor of HIV-1 entry through interaction with the Env spike by virtue of the incorporation of a guandinium group.</p>Fórmula:C19H19ClFN5O4Cor e Forma:SolidPeso molecular:435.84gp120-IN-2
CAS:<p>gp120-IN-2 is a potent HIV-1 inhibitor (IC50 = 7.5 μM) with low cytotoxicity (CC50 = 112.93 μM).</p>Fórmula:C15H18N2O5Cor e Forma:SolidPeso molecular:306.31A 80987
CAS:<p>A 80987 is an inhibitor of HIV-1 protease.</p>Fórmula:C37H43N5O6Cor e Forma:SolidPeso molecular:653.77GW-695634
CAS:<p>GW-695634, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C26H21Cl2N3O6SCor e Forma:SolidPeso molecular:574.43HIV-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:C21H13Cl2N3O2Cor e Forma: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:C11H12BrN3OSCor e Forma: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:C24H18FN5O2Cor e Forma:SolidPeso molecular:427.43S-1360
CAS:<p>S-1360 is an inhibitor of HIV-1 integrase.</p>Fórmula:C16H12FN3O3Pureza:98%Cor e Forma: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:C27H29F3N2OCor e Forma: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:C20H17ClN4O4S4Cor e Forma:SolidPeso molecular:541.09HIV-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:C19H16BrN5Cor e Forma: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:C13H12Cl3N5OSCor e Forma: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:C24H21N5OCor e Forma: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:C22H14ClN7O2SCor e Forma:SolidPeso molecular:475.91Cgp 53820
CAS:<p>CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.</p>Fórmula:C31H51N5O5Cor e Forma: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:C25H28N6OCor e Forma: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%Cor e Forma:SolidPeso molecular:374.27HEPT
CAS:<p>HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription.</p>Fórmula:C14H16N2O4SPureza:98%Cor e Forma:SolidPeso molecular:308.35L-Ristosamine nucleoside
CAS:<p>L-Ristosamine nucleoside shows antiviral activity.</p>Fórmula:C21H21N3O7Cor e Forma:SolidPeso molecular:427.41Suberosol
CAS:<p>Suberosol possesses anti-HIV replication activity.</p>Fórmula:C31H50O2Pureza:98%Cor e Forma:SolidPeso molecular:454.73ZP7
CAS:<p>ZP7 is a HIV-1 replication inhibitor.</p>Fórmula:C15H9Br2ClN4OS2Pureza:98%Cor e Forma:SolidPeso molecular:520.65APA-APA-MPO
CAS:<p>APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor.</p>Fórmula:C12H25Cl2N5OPureza:98%Cor e Forma:SolidPeso molecular:326.27Ingenol 3-Hexanoate
CAS:<p>Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1.</p>Fórmula:C26H38O6Pureza:98%Cor e Forma:SolidPeso molecular:446.58BM 21.1298
CAS:<p>BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.</p>Fórmula:C16H13NOSPureza:98%Cor e Forma:SolidPeso molecular:267.35D4DAP
CAS:<p>D4DAP is an inhibitor of HIV virus replication.</p>Fórmula:C10H12N6O2Pureza:98%Cor e Forma:SolidPeso molecular:248.24Nitrobenzofuroxan
CAS:<p>Nitrobenzofuroxan, is a HIV-1 and IDO1 inhibitor.</p>Fórmula:C6H3N3O4Pureza:98%Cor e Forma: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%Cor e Forma:SolidPeso molecular:678.63GSK5750
CAS:<p>GSK5750 is the ribonuclease H activity inhibitor.</p>Fórmula:C16H12N4O2SCor e Forma: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%Cor e Forma:SolidPeso molecular:240.26L-708906
CAS:<p>L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.</p>Fórmula:C24H20O6Pureza:98%Cor e Forma:SolidPeso molecular:404.41Dacopafant
CAS:<p>Dacopafant is an antagonist of platlet activationg factor receptor.</p>Fórmula:C12H11N3OSCor e Forma:SolidPeso molecular:245.35M038
CAS:<p>5M038, a novel inhibitor of HIV envelope-mediated fusion, strongly inhibits gp41-mediated membrane fusion.</p>Fórmula:C17H8F6N4Pureza:98%Cor e Forma:SolidPeso molecular:382.26L 738372
CAS:<p>L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase.</p>Fórmula:C18H15N3OCor e Forma: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%Cor e Forma: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%Cor e Forma:SolidPeso molecular:766.92HIV-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%Cor e Forma: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%Cor e Forma: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%Cor e Forma: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%Cor e Forma: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%Cor e Forma: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%Cor e Forma:SolidPeso molecular:652.82Opaviraline
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:280.29Emivirine
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%Cor e Forma:SolidPeso molecular:302.37GSK-364735
CAS:<p>GSK-364735 is an HIV-1 IN inhibitor.</p>Fórmula:C19H18FN3O4Pureza:97.73%Cor e Forma:SolidPeso molecular:371.36Lenacapavir
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%Cor e Forma:SolidPeso molecular:968.28AzddMeC
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%Cor e Forma:SolidPeso molecular:266.26HIV-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:308.41KM-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%Cor e Forma:SolidPeso molecular:325.36BMS-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%Cor e Forma:SolidPeso molecular:422.43(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%Cor e Forma: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%Cor e Forma:SolidPeso molecular:592.54Atevirdine
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:379.46Suksdorfin
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%Cor e Forma:SolidPeso molecular:388.41KNI-272
CAS:<p>Kynostatin-272 is a HIV protease inhibitor. KNI-272 blocked the maturation of viral particles.</p>Fórmula:C33H41N5O6S2Cor e Forma:SolidPeso molecular:667.84DMP 323
CAS:<p>DMP 323 is a potent inhibitor of HIV-1 protease.</p>Fórmula:C35H38N2O5Pureza:98%Cor e Forma:SolidPeso molecular:566.69Berlopentin
CAS:<p>Berlopentin is splenopentin analog used to treat HIV-positive patients. It also has immunostimulatory properties.</p>Fórmula:C35H55N9O11Cor e Forma:SolidPeso molecular:777.86Capravirine
CAS:<p>Capravirine, a non-nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C20H20Cl2N4O2SPureza:98%Cor e Forma:SolidPeso molecular:451.37L-697661
CAS:<p>L-697661, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C16H15Cl2N3O2Cor e Forma:SolidPeso molecular:352.22A 77003
CAS:<p>A 77003 is a HIV-1 protease inhibitor. A77003 impairs HIV-1 protease-mediated Gag processing.</p>Fórmula:C44H58N8O6Cor e Forma:SolidPeso molecular:794.98PYR01
CAS:<p>PYR01 is a potent nonnucleoside reverse transcriptase inhibitor of HIV-1 and concurrently acts as a targeted activator to eliminate cells expressing HIV-1 [1].</p>Fórmula:C21H13F7N4O3Cor e Forma:SolidPeso molecular:502.34Indinavir, threo-
CAS:<p>Indinavir, threo- is a protease inhibitor utilized as a component of highly active antiretroviral treatment to HIV/AIDS.</p>Fórmula:C36H47N5O4Pureza:98%Cor e Forma:SolidPeso molecular:613.79A 74704
CAS:<p>A 74704 is a pseudo C2-symmetric inhibitor of HIV-1 protease and its diester analog.</p>Fórmula:C43H52N4O7Pureza:98%Cor e Forma:SolidPeso molecular:736.9BMS-561390
CAS:<p>BMS-561390, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C14H12ClF3N2OCor e Forma:SolidPeso molecular:316.71Droxinavir HCl
CAS:<p>Droxinavir HCl is an antiviral agent and HIV protease inhibitor.</p>Fórmula:C29H52ClN5O4Pureza:98%Cor e Forma:SolidPeso molecular:570.22Bavtavirine
CAS:<p>Bavtavirine is a non-nucleoside reverse HIV-1 transcriptase inhibitor (NNRTIs),inhibits HIV replication by preventing the transcription of viral RNA into DNA.</p>Fórmula:C26H20N6Pureza:97.2%Cor e Forma:SolidPeso molecular:416.48HIV-1 inhibitor-10
CAS:<p>HIV-1 inhibitor-10 is a nanomolar HIV-1 maturation inhibitor.</p>Fórmula:C39H54O6Cor e Forma:SolidPeso molecular:618.84U 104489
CAS:<p>U 104489 (PNU-104489) is a novel specific inhibitor of human immunodeficiency virus 1 (HIV-1), showing effective activity against BHA-P-resistant HIV-1MF.</p>Fórmula:C26H36N6O3SCor e Forma:SolidPeso molecular:512.67U 89360E
CAS:<p>U 89360E is a peptidic inhibitor.</p>Fórmula:C28H52N8O6Pureza:98%Cor e Forma:SolidPeso molecular:596.76Palinavir
CAS:<p>Palinavir is an antiviral, it inhibits HIV-1 protease.</p>Fórmula:C41H52N6O5Pureza:98%Cor e Forma:SolidPeso molecular:708.89BILR-355
CAS:<p>BILR-355 is a reverse transcriptase inhibitor.</p>Fórmula:C25H23N5O3Pureza:98%Cor e Forma:SolidPeso molecular:441.48XZ426
CAS:<p>XZ426 is a potent integrase strand transfer inhibitor with anti- HIV activity .</p>Fórmula:C22H24F2N4O4Cor e Forma:SolidPeso molecular:446.45HIV-1 integrase inhibitor 3
CAS:<p>HIV-1 integrase inhibitor 3 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 2.7 nM).</p>Fórmula:C21H22F2N4O4Pureza:98%Cor e Forma:SolidPeso molecular:432.427-Deaza-2',3'-dideoxyguanosine
CAS:<p>7-Deaza-2',3'-dideoxyguanosine (7-Deaza-ddG) is a 2′,3′-dideoxynucleoside 5′-triphosphate that inhibits HIV-1 reverse transcriptase with a Ki of 25 nM [1].</p>Fórmula:C11H14N4O3Cor e Forma:SolidPeso molecular:250.25GSK3532795
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:691.02L-696229
CAS:<p>L-696229: specific HIV-1 RT inhibitor, blocks viral spread in various cells.</p>Fórmula:C17H18N2O2Pureza:98%Cor e Forma:SolidPeso molecular:282.34Murabutide
CAS:<p>Murabutide, a safe synthetic immunomodulator, diminishes the expression of CD4 and CCR5 receptors and promotes the secretion of high levels of beta-chemokines,</p>Fórmula:C23H40N4O11Cor e Forma:SolidPeso molecular:548.58L-689502
CAS:<p>L-689502 is a potent HIV-l protease inhibitor (IC50: 1 nM).</p>Fórmula:C39H51N3O7Pureza:98%Cor e Forma:SolidPeso molecular:673.84Fosalvudine tidoxil
CAS:<p>Fosalvudine tidoxil, a nucleoside reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C35H64FN2O8PSPureza:98%Cor e Forma:SolidPeso molecular:722.93GSK3839919A
CAS:<p>GSK3839919A is a potent allosteric inhibitor of HIV-1 integrase [1].</p>Fórmula:C36H46ClN3O3Cor e Forma:SolidPeso molecular:604.22Reverse transcriptase-IN-1
CAS:<p>Reverse transcriptase-IN-1 is a diarylbenzopyrimidine (DABP) analogue and a potent inhibitor of HIV-1 nonnucleoside reverse transcriptase with an IC50of 13.7</p>Fórmula:C25H17N7O2Pureza:99.61%Cor e Forma:SolidPeso molecular:447.45Hinokinin
CAS:<p>Hinokinin (Cubebinolide), a bioactive lignan, exhibits a broad spectrum of pharmacological activities.</p>Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35HIV-1 inhibitor-3
CAS:<p>HIV-1 inhibitor-3 is an HIV infection inhibitor.</p>Fórmula:C9H10F2N2O5Pureza:98%Cor e Forma:SolidPeso molecular:264.18HIV-1 protease-IN-11
CAS:<p>HIV-1 protease-IN-11 (compound 34a), an HIV-1 protease inhibitor, demonstrates potent inhibition with an IC50 of 0.41 nM and maintains substantial efficacy</p>Fórmula:C26H37N3O5SPureza:98%Cor e Forma:SolidPeso molecular:503.65HIV-1 protease-IN-8
CAS:<p>HIV-1 protease-IN-8 (compound 34b) is a potent inhibitor of the HIV-1 protease enzyme, exhibiting an IC50 of 0.32 nM.</p>Fórmula:C25H35N3O5SPureza:98%Cor e Forma:SolidPeso molecular:489.63HIV-1 protease-IN-7
CAS:<p>HIV-1 protease-IN-7 (compound 16) is an orally active inhibitor of HIV-1 protease, exhibiting an IC50 of 3.52 nM and an EC50 of 37 nM [1].</p>Fórmula:C68H104N10O12SPureza:98%Cor e Forma:SolidPeso molecular:1285.68HIV-1 protease-IN-12
CAS:<p>HIV-1 protease-IN-12 (compound 35b) serves as a potent inhibitor of HIV-1 protease, exhibiting an IC50 value of 0.51 nM, and demonstrates efficacy against drug-</p>Fórmula:C25H35N3O5SPureza:98%Cor e Forma:SolidPeso molecular:489.63HIV-1 protease-IN-9
CAS:<p>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 a</p>Fórmula:C37H41N7O4SPureza:98%Cor e Forma:SolidPeso molecular:679.83NNRTIs-IN-1
CAS:<p>NNRTIs-IN-1 is a potent non-nucleoside reverse transcriptase inhibitor (NNRTI) with notable anti-resistance efficacy, effectively inhibiting both the wild-type</p>Fórmula:C28H22N6O3Cor e Forma:SolidPeso molecular:490.51L 687908
CAS:<p>L 687908 is a potent inhibitor of hydroxyethylene-containing HIV protease.</p>Fórmula:C40H51N5O5Pureza:98%Cor e Forma:SolidPeso molecular:681.86HIV-IN-8
CAS:<p>HIV-IN-8 (Compound 9) acts as an HIV inhibitor, suppressing HIV replication with an effective concentration (EC50) of 13 μg/mL [1].</p>Fórmula:C36H30O16Cor e Forma:SolidPeso molecular:718.61PNU-103017
CAS:<p>PNU-103017 is an inhibitor of HIV protease.</p>Fórmula:C28H28N2O5SPureza:98%Cor e Forma:SolidPeso molecular:504.6R 87366
CAS:<p>R 87366 is used as a water-soluble HIV protease inhibitor.</p>Fórmula:C32H39N7O6Pureza:98%Cor e Forma:SolidPeso molecular:617.7L 694746
CAS:<p>L 694746 is an inhibitor of HIV-1 protease.</p>Fórmula:C35H42N2O8Pureza:98%Cor e Forma:SolidPeso molecular:618.72DGKα-IN-8
CAS:<p>DGKα-IN-8 (Example 51) is a potent diacylglycerol kinase alpha (DGKα) inhibitor, exhibiting an IC50 of 22.491 nM and an EC50 of 0.256 nM.</p>Fórmula:C23H19ClF3N5OCor e Forma:SolidPeso molecular:473.88I-XW-053
CAS:<p>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-</p>Fórmula:C22H16N2O2Pureza:99.05%Cor e Forma:SolidPeso molecular:340.37Ulonivirine
CAS:<p>Ulonivirine is an orally active non-nucleoside reverse transcriptase inhibitor that exhibits high antiviral activity and can be used to study HIV-1 infection.</p>Fórmula:C18H8ClF6N5O3Cor e Forma:SolidPeso molecular:491.73Teropavimab
CAS:<p>Teropavimab (3BNC117-LS), an antibody, is utilized in the research of HIV infection [1].</p>Cor e Forma:LiquidRo 31-8588
CAS:<p>Talviraline (HBY 097) inhibits HIV-1 replication and reduces cell death in various cells and immune cells.</p>Fórmula:C33H56N4O5Cor e Forma:SolidPeso molecular:588.82Azt-pmap
CAS:<p>AZT-PMPA, an aryl phosphate derivative of AZT and a nucleoside analogue, demonstrates anti-HIV activity[1].</p>Fórmula:C20H25N6O8PPureza:98%Cor e Forma:SolidPeso molecular:508.42WRNA10
CAS:<p>WRNA10 is a potent binding agent for HIV-1TAR RNA (IC50: 10 μM, CC50: 40 μM).</p>Fórmula:C25H32N4O4Cor e Forma:SolidPeso molecular:452.55Glycolithocholic acid 3-sulfate disodium
CAS:<p>Glycolithocholic acid 3-sulfate (disodium) demonstrates inhibitory effects on in vitro HIV-1 replication and has potential applications in HIV infection and</p>Fórmula:C26H41NNa2O7SCor e Forma:SolidPeso molecular:557.65HIV-1 inhibitor-54
CAS:<p>HIV-1 inhibitor-54: potent anti-HIV (EC50: 32 nM), targets WT HIV-1 IIIB in MT-4 cells for infection research.</p>Fórmula:C27H30N6O4SPureza:98.05% - 99.44%Cor e Forma:SoildPeso molecular:534.63PDDC inhibitor
CAS:<p>PDDC inhibitor (Phenyl (R)-(1-(3-(3,4-dimethoxyphenyl)-2,6-dimethylimidazo[1,2-b]pyridazin-8-yl)pyrrolidin-3-yl)carbamate) is an nSMase2 inhibitor.</p>Fórmula:C27H29N5O4Pureza:96.09% - 99.39%Cor e Forma:SolidPeso molecular:487.55HIV-1 inhibitor-17
<p>HIV-1 inhibitor-18 blocks HIV-1 capsid, acts on NL4-3 strain (EC50: 2.57 μM), has low cytotoxicity (MT-4 CC50: >8.55).</p>Fórmula:C32H32N4O5SCor e Forma:SolidPeso molecular:584.69
