Proteasi HIV
Gli inibitori della proteasi dell'HIV sono una classe di farmaci antiretrovirali che bersagliano specificamente l'enzima proteasi del virus dell'immunodeficienza umana (HIV). Inibendo questo enzima, questi composti impediscono al virus di elaborare le sue poliproteine in proteine mature e funzionali, bloccando così la produzione di nuovi virioni infettivi. Gli inibitori della proteasi dell'HIV sono una pietra miliare della terapia antiretrovirale altamente attiva (HAART) utilizzata per gestire l'HIV/AIDS. Presso CymitQuimica, offriamo una varietà di inibitori della proteasi dell'HIV per supportare la vostra ricerca nel trattamento dell'HIV, nella resistenza ai farmaci e nella virologia.
Trovati 506 prodotti di "Proteasi HIV"
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FGF22-IN-1
CAS:FGF22-IN-1 is a CD4 N-terminal immunoglobulin variable region-like structural domain (CD4 D1) inhibitor that suppresses the immune response.Formula:C14H11N3OSPurezza:99.18%Colore e forma:SolidPeso molecolare:269.32Antiviral agent 9
Antiviral agent 9: EC50 0.006 nM vs HIV-1, 300x more selective than TAF.Formula:C38H50N7O8PColore e forma:SolidPeso molecolare:763.82HIV-1 inhibitor-48
CAS:HIV-1 inhibitor-48 is a novel non-nucleoside reverse transcriptase inhibitor (NNRTI) and exhibits anti-HIV-1 activity .Formula:C19H16BrN5Colore e forma:SolidPeso molecolare:394.27HIV-1 inhibitor-35
CAS: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.Formula:C13H12Cl3N5OSColore e forma:SolidPeso molecolare:392.69HIV-1 inhibitor-9
CAS:HIV-1 inhibitor-9 potently blocks WT and NNRTI-resistant HIV strains at low nanomolar levels.Formula:C24H21N5OColore e forma:SolidPeso molecolare:395.46HIV-1 inhibitor-56
CAS:HIV-1 inhibitor-56 (compound 12126065) is a potent non-nucleoside reverse transcriptase inhibitor with significant antiviral activity against wild-type HIV-1,Formula:C22H14ClN7O2SColore e forma:SolidPeso molecolare:475.91Cgp 53820
CAS:CGP 53820 is a pseudosymmetric inhibitor of HIV-1 Protease.Formula:C31H51N5O5Colore e forma:SolidPeso molecolare:573.77HIV-1 inhibitor-33
CAS: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.Formula:C25H28N6OColore e forma:SolidPeso molecolare:428.53HI-253
CAS:HI-253 is a potent non-nucleoside inhibitor of drug-resistant human immunodeficiency virus (HIV).Formula:C14H13BrClN3SColore e forma:SolidPeso molecolare:370.7APOBEC3G-IN-1
CAS:APOBEC3G-IN-1 (MN136.0185) is a targeted APOBEC3G inhibitor with anti-HIV activity for the study of infectious diseases and cancer.Formula:C15H11NO3Purezza:96.54%Colore e forma:SolidPeso molecolare:253.25ML67-33
CAS:ML67-33 selectively activates K2P channels; EC50: 36.3 μM (cell-free), 9.7 μM (HEK293). Reversible TREK-1 modulation.Formula:C18H17Cl2N5Purezza:98%Colore e forma:SolidPeso molecolare:374.27HIV-1 inhibitor-53
CAS:HIV-1 Inhibitor-53 targets HIV-1 protease (IC50: 1.93 nM) and reverse transcriptase (IC50: 2.35 μM), aiding AIDS research.Formula:C30H34N2O8SPurezza:98%Colore e forma:SolidPeso molecolare:582.66MK-2048
CAS:MK-2048 is a potent inhibitor of integrase (IN) and INR263K with IC50 of 2.6 nM and 1.5 nM, respectively.Formula:C21H21ClFN5O4Purezza:98%Colore e forma:SolidPeso molecolare:461.87HIV-1 inhibitor-49
HIV-1 inhibitor-49, an oral HEPT analog, has strong pharmacokinetics, potent reverse transcriptase inhibition (IC50=30nM), and is safe in mice.Formula:C21H18F2N2O3SColore e forma:SolidPeso molecolare:416.44HEPT
CAS:HEPT is a non-nucleoside inhibitor of HIV-1 reverse transcription.Formula:C14H16N2O4SPurezza:98%Colore e forma:SolidPeso molecolare:308.35L-Ristosamine nucleoside
CAS:L-Ristosamine nucleoside shows antiviral activity.Formula:C21H21N3O7Colore e forma:SolidPeso molecolare:427.41Suberosol
CAS:Suberosol possesses anti-HIV replication activity.Formula:C31H50O2Purezza:98%Colore e forma:SolidPeso molecolare:454.73ZP7
CAS:ZP7 is a HIV-1 replication inhibitor.Formula:C15H9Br2ClN4OS2Purezza:98%Colore e forma:SolidPeso molecolare:520.65APA-APA-MPO
CAS:APA-APA-MPO is a PCAF bromodomain/Tat-AcK50 association inhibitor.Formula:C12H25Cl2N5OPurezza:98%Colore e forma:SolidPeso molecolare:326.27Ingenol 3-Hexanoate
CAS:Ingenol 3-Hexanoate is a novel potent reactivator of latent HIV-1.Formula:C26H38O6Purezza:98%Colore e forma:SolidPeso molecolare:446.58BM 21.1298
CAS:BM 21.1298 is a inhibition of HIV-1 reverse transcriptase.Formula:C16H13NOSPurezza:98%Colore e forma:SolidPeso molecolare:267.35D4DAP
CAS:D4DAP is an inhibitor of HIV virus replication.Formula:C10H12N6O2Purezza:98%Colore e forma:SolidPeso molecolare:248.24Nitrobenzofuroxan
CAS:Nitrobenzofuroxan, is a HIV-1 and IDO1 inhibitor.Formula:C6H3N3O4Purezza:98%Colore e forma:SolidPeso molecolare:181.11BMS-663749 lysine
CAS:BMS-663749 lysine is used as a phosphonooxymethyl prodrug 4 for HIV-1 attachment inhibitor.Formula:C29H39N6O11PPurezza:98%Colore e forma:SolidPeso molecolare:678.63GSK5750
CAS:GSK5750 is the ribonuclease H activity inhibitor.Formula:C16H12N4O2SColore e forma:SolidPeso molecolare:324.365-Et-ddU
CAS:5-Et-ddU: A pyrimidine nucleoside with anti-HIV-1 activity in human blood cells.Formula:C11H16N2O4Purezza:98%Colore e forma:SolidPeso molecolare:240.26L-708906
CAS:L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.Formula:C24H20O6Purezza:98%Colore e forma:SolidPeso molecolare:404.41Fosdevirine
CAS:Fosdevirine (GSK2248761), a non-nucleoside reverse transcriptase (NNRTI) inhibitor with anti-HIV activity, is used in the study of neurological related diseasesFormula:C20H17ClN3O3PPurezza:99.92%Colore e forma:SolidPeso molecolare:413.79Dacopafant
CAS:Dacopafant is an antagonist of platlet activationg factor receptor.Formula:C12H11N3OSColore e forma:SolidPeso molecolare:245.3HIV-IN-6
CAS:HIV-IN-6, an anti-HIV agent, blocks replication by targeting SFKs like Hck involved with Nef protein.Formula:C20H16N4O3SPurezza:97.78%Colore e forma:SolidPeso molecolare:392.435M038
CAS:5M038, a novel inhibitor of HIV envelope-mediated fusion, strongly inhibits gp41-mediated membrane fusion.Formula:C17H8F6N4Purezza:98%Colore e forma:SolidPeso molecolare:382.26L 738372
CAS:L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase.Formula:C18H15N3OColore e forma:SolidPeso molecolare:289.33Vif-A3G Inhibitor N.41
CAS: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.Formula:C15H14N2O2Purezza:98%Colore e forma:SolidPeso molecolare:254.28A 75925
CAS:A 75925, a nonnucleoside reverse transcriptase inhibitors (NNRTI), works to inhibit HIV-1 replication.Formula:C44H54N4O8Purezza:98%Colore e forma:SolidPeso molecolare:766.92HIV-1 inhibitor-22
CAS:HIV-1 inhibitor-22 effectively blocks HIV-1 RT (IC50=3.63 μM) with low cytotoxicity (CC50 > 227 μM).Formula:C30H26N6O3SColore e forma:SolidPeso molecolare:550.63HIV-1 integrase inhibitor 4
CAS:HIV-1 integrase inhibitor 4 is an HIV-1 integrase strand transfer (INST) inhibitor (IC50: 3.7 nM).Formula:C24H20F2N4O5SPurezza:98%Colore e forma:SolidPeso molecolare:514.5HIV-1 inhibitor-29
CAS:HIV-1 inhibitor-29: Blocks HIV-1 IIIB (EC50: 2.18μM), resists F227L/V106A (EC50: 0.974μM), low toxicity (CC50: 211μM), for AIDS research.Formula:C30H36N6O5Colore e forma:SolidPeso molecolare:560.64D77
CAS: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).Formula:C28H22BrNO7SPurezza:98%Colore e forma:SolidPeso molecolare:596.45Sp-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.Formula:C10H17N2O13P3SPeso molecolare:498.23HIV-1 inhibitor-34
CAS:HIV-1 inhibitor-34 (5q): potent, selective; EC50: 6.4 nM; MT-4 CC50: 16 μM; useful in AIDS research.Formula:C26H27N7OColore e forma:SolidPeso molecolare:453.54(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).Formula:C19H15BrClNO3Purezza:98%Colore e forma:SolidPeso molecolare:420.68HIV-IN-4
CAS:HIV-IN-4 (Compound 12) is a potent HIV inhibitor that exhibits promising anti-HIV activities [1].Formula:C14H18N2O3Colore e forma:SolidPeso molecolare: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.Formula:C23H16F2N6Colore e forma:SolidPeso molecolare: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>Formula:C25H24FN5O3SColore e forma:SolidPeso molecolare:493.55SARS-CoV-IN-3
CAS:SARS-CoV-IN-3 is an effective SARS-CoV replication inhibitor.Formula:C25H28ClFeN3OPurezza:98%Colore e forma:SolidPeso molecolare:477.81Mesoxalic acid
CAS:Mesoxalic acid is a dicarboxylic acid and a ketonic acid which blocks RT translocation.Formula:C3H2O5Purezza:98%Colore e forma:SolidPeso molecolare: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.Formula:C12H14N2O3SColore e forma:SolidPeso molecolare: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.Formula:C38H53N5O7S2Purezza:98%Colore e forma:SolidPeso molecolare:755.99Reverse transcriptase-IN-3
Reverse transcriptase-IN-3, a pyrimidine carboxamide, inhibits HIV-1 including mutant strains.Formula:C28H31N7O4SColore e forma:SolidPeso molecolare:561.66DQBS
CAS:DQBS is an HIV-1 Nef function antagonist.Formula:C22H17ClN4O4SPurezza:98%Colore e forma:SolidPeso molecolare:468.91HIV-1 integrase inhibitor 7
CAS:HIV-1 integrase inhibitor 7 is a potent HIV-1 integrase inhibitor (IC50: 33.3 nM).Formula:C30H26O16Purezza:98%Colore e forma:SolidPeso molecolare:642.52β-L-D4A
CAS:beta-L-D4A inhibits HIV-1 reverse transcriptase, stopping DNA synthesis.Formula:C10H11N5O2Purezza:99.45%Colore e forma:SolidPeso molecolare:233.23MK-4965
CAS:MK-4965 is a new type of non-nucleoside reverse transcriptase inhibitor with antiviral activity.Formula:C20H13Cl2N5O2Colore e forma:SolidPeso molecolare: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.Formula:C15H18N2O4SColore e forma:SolidPeso molecolare: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.Formula:C26H19N5O2Colore e forma:SolidPeso molecolare:433.46LEDGIN6
CAS:HIV-1 integrase inhibitor 2 is used for the treatment of human immunodeficiency virus (HIV) infection.Formula:C21H20ClNO2Colore e forma:SolidPeso molecolare:353.84NIT
CAS:NIT is an HIV-1 protease inhibitor.Formula:C15H7N3O4S2Purezza:98%Colore e forma:SolidPeso molecolare: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].Formula:C14H14Cl2N2O2SColore e forma:SolidPeso molecolare: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.Formula:C26H19N5O2Colore e forma:SolidPeso molecolare:433.46DPC-681
CAS:DPC-681 is a potent and selective HIV protease inhibitor (IC90s: 4 to 40 nM for wild-type HIV-1).Formula:C35H48FN5O5SColore e forma:SolidPeso molecolare:669.85HIV-1 inhibitor-19
CAS:HIV-1 inhibitor-19 is a potent NNRTI targeting L100I, K103N, V106A/F227L mutants; EC50s: 7.3, 9.2, 21.0 nM respectively.Formula:C24H22BClN2O5SColore e forma:SolidPeso molecolare:496.77HIV-1 inhibitor-15
CAS:HIV-1 inhibitor-15 (compound 9d): Potent, broad-spectrum, EC50=1.7-9 nM for various strains, good solubility/safety, oral use.Formula:C24H20N6Colore e forma:SolidPeso molecolare:392.46TX-1918
CAS:TX-1918, a tyrphostin, blocks eEF-2K to hinder HepG2, HCT116 cell growth.Formula:C14H12O3Colore e forma:SolidPeso molecolare:228.24S 2720
CAS:S 2720 is a human immunodeficiency virus type 1 (HIV-1)-specific reverse transcriptase (RT) inhibitor quinoxaline.Formula:C14H15ClN2O2SColore e forma:SolidPeso molecolare:310.81E7-03
CAS:1E7-03 is an inhibitor of HIV-1 transcription, by targeting host Protein Phosphatase-1 (PP1).Formula:C28H29N3O6Colore e forma:SolidPeso molecolare:503.55DPC-961
CAS:DPC-961, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.Formula:C14H10ClF3N2OColore e forma:SolidPeso molecolare:314.69B07 hydrochloride
CAS:B07 hydrochloride is a CCR5 antagonist-based inhibitor of HIV-1 entry.Formula:C29H38ClFN4O2Purezza:98%Colore e forma:SolidPeso molecolare:529.09GCA-186
CAS:GCA-186 is an effective non-nucleoside HIV-1 reverse transcriptase inhibitor.Formula:C19H26N2O3Purezza:98%Colore e forma:SolidPeso molecolare:330.42HIV-1 inhibitor-20
CAS:HIV-1 inhibitor-20 is a potent HIV-1 inhibitor.Formula:C19H11ClF3N3O2Colore e forma:SolidPeso molecolare:405.76BMS-585248
CAS:BMS-585248 is a highly effective HIV-1 adhesion inhibitor that targets the viral envelope protein gp120.Formula:C22H18FN7O3Colore e forma:SolidPeso molecolare:447.42AIC-292
CAS:AIC-292 is a potent, tolerable reverse transcriptase inhibitor active against various HIV-1 strains, including NNRTI-resistant K103N, G190A, Y181C.Formula:C19H12Cl2F2N4O2Colore e forma:SolidPeso molecolare:437.23Tivirapine
CAS:Tivirapine, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.Formula:C16H20ClN3SColore e forma:SolidPeso molecolare:321.87L 739594
CAS:L 739594 is an inhibitor of HIV-1 protease.Formula:C31H47N3O6Purezza:98%Colore e forma:SolidPeso molecolare:557.72HIV-1 inhibitor-28
CAS:HIV-1 inhibitor-28: potent, selective, EC50=58 nM, low MT-4 cell toxicity (CC50=38.6 μM), valuable in AIDS research.Formula:C26H32N6O3SColore e forma:SolidPeso molecolare:508.64BMS-663749
CAS:BMS-663749 is an attachment inhibitor of human immunodeficiency virus type 1 (HIV-1).Formula:C23H25N4O9PColore e forma:SolidPeso molecolare:532.44HIV-1 inhibitor-45
CAS:HIV-1 inhibitor-45 is a potent inhibitor of HIV-1 RNase H (IC50: 0.067 μM) and has antiviral effects.Formula:C23H24N4O8SColore e forma:SolidPeso molecolare:516.52HIV-1 inhibitor-21
CAS: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).Formula:C28H24N6O2Colore e forma:SolidPeso molecolare:476.53GSK-364735 potassium
CAS:GSK-364735 potassium is an HIV-1 IN inhibitor.Formula:C19H17FKN3O4Colore e forma:SolidPeso molecolare:409.46HI-236
CAS:HI-236 is used as a non-nucleoside HIV-1 reverse-transcriptase inhibitor.Formula:C16H18BrN3O2SPurezza:98%Colore e forma:SolidPeso molecolare:396.3Adenallene
CAS:Adenallene inhibits replication and cytopathic effects of HIV in vitro.Formula:C9H9N5OPurezza:98%Colore e forma:SolidPeso molecolare:203.2AQ 148
CAS:AQ 148 is a potent competitive inhibitor of HIV-1 PR.Formula:C30H37N3O4Colore e forma:SolidPeso molecolare: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.Formula:C18H12N2O10Colore e forma:SolidPeso molecolare: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.Formula:C17H21N5OSColore e forma:SolidPeso molecolare:343.45Rovafovir Etalafenamide
CAS:Rovafovir Etalafenamide is a prodrug of anti-HIV nucleoside phosphonate.Formula:C21H24FN6O6PPurezza:98%Colore e forma:SolidPeso molecolare:506.42SARS-CoV-IN-2
CAS:SARS-CoV-IN-2 is an effective SARS-CoV replication inhibitorFormula:C24H26ClFeN3OPurezza:98%Colore e forma:SolidPeso molecolare:463.78Navuridine
CAS:Navuridine (AZdU) is an oral active inhibitor of HIV reverse transcriptase with a relatively short half-life.Formula:C9H11N5O4Purezza:99.83%Colore e forma:SolidPeso molecolare: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.Formula:C17H22N2O3Purezza:99.8%Colore e forma:SolidPeso molecolare: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>Formula:C14H17FN2O3Purezza:99.94%Colore e forma:SolidPeso molecolare:280.29Tenofovir alafenamide fumarate
CAS:Tenofovir alafenamide fumarate (GS-7340) is an oral anti-HIV drug that prevents infection.Formula:C25H33N6O9PPurezza:99.99%Colore e forma:SolidPeso molecolare: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).Formula:C9H13FN5O4PPurezza:99.9% - >99.99%Colore e forma:SolidPeso molecolare:305.2GSK-364735
CAS:GSK-364735 is an HIV-1 IN inhibitor.Formula:C19H18FN3O4Purezza:97.73%Colore e forma:SolidPeso molecolare: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.Formula:C39H48N4O5Purezza:99.34% - 99.88%Colore e forma:SolidPeso molecolare: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.Formula:C39H32ClF10N7O5S2Purezza:99.61% - 99.87%Colore e forma:SolidPeso molecolare: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>Formula:C21H25N5O2Purezza:98.20%Colore e forma:SolidPeso molecolare: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 infectionFormula:C10H14N6O3Purezza:97.14% - 99.62%Colore e forma:SolidPeso molecolare: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(+)Formula:C22H22N4O5Purezza:99.95%Colore e forma:SolidPeso molecolare: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.Formula:C18H19N3O3Purezza:99.03% - 99.47%Colore e forma:SolidPeso molecolare: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 .Formula:C21H24O7Purezza:98.54%Colore e forma:SolidPeso molecolare: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>Formula:C21H24O2Purezza:98.91%Colore e forma:SolidPeso molecolare: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-Formula:C22H16N2O2Purezza:99.05%Colore e forma:SolidPeso molecolare:340.37
