Microbiologia/Virologia
Os inibidores de microbiologia e virologia são compostos que têm como alvo microrganismos, incluindo bactérias, vírus e fungos, interrompendo seu crescimento, replicação ou sobrevivência. Esses inibidores são essenciais para estudar a patogênese microbiana, entender os mecanismos de resistência e desenvolver novas terapias antimicrobianas e antivirais. Os inibidores nessa categoria são usados para combater doenças infecciosas, explorar a ecologia microbiana e investigar as interações hospedeiro-patógeno. Na CymitQuimica, oferecemos uma ampla seleção de inibidores de alta qualidade para microbiologia e virologia para apoiar sua pesquisa em doenças infecciosas, microbiologia e virologia.
Subcategorias de "Microbiologia/Virologia"
- Antibacteriano(2.966 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(710 produtos)
- HBV(177 produtos)
- HIV Protease(450 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5858 produtos de "Microbiologia/Virologia"
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Netzahualcoyonol
CAS:<p>Netzahualcoyonol has antibacterial/cytotoxic effects; isolated with tingenone as active compounds.</p>Fórmula:C30H38O5Pureza:98%Cor e Forma:SolidPeso molecular:478.62Levovirin valinate HCl
CAS:Levovirin valinate HCl is a valine ester prodrug of levovirin as a new investigational drug for the therapy of the hepatitis C virus.Fórmula:C13H22ClN5O6Pureza:98%Cor e Forma:SolidPeso molecular:379.8HIV-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:582.59TachypleginA
CAS:<p>TachypleginA is a parasite motility and invasion inhibitor.</p>Fórmula:C22H21F2NOPureza:98%Cor e Forma:SolidPeso molecular:353.4Antibacterial agent 65
CAS:<p>Antibacterial agent 65 is a potential antimicrobial agent and antioxidant agent.</p>Fórmula:C17H16O3Cor e Forma:SolidPeso molecular:268.31Flaviviruses-Inhibitor-I
CAS:Flaviviruses-Inhibitor-I is several viruses belonging to the family of Flaviviridae inhibitor.Fórmula:C17H17N3O3SPureza:98%Cor e Forma:SolidPeso molecular:343.4HIV-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:582.66Zimet 38-74
CAS:<p>Zimet 38-74 is an agent of antiviral.</p>Fórmula:C27H28N4O2SPureza:98%Cor e Forma:SolidPeso molecular:472.6HBV-IN-10
CAS:<p>HBV-IN-10, an isomer of compound 6, inhibits HBsAg with EC50 between 0.1-1 μM (Patent WO2021204258A1).</p>Fórmula:C23H24FN7OCor e Forma:SolidPeso molecular:433.48Caspofungin
CAS:<p>Caspofungin is a cyclic lipopeptide echinocandin and beta-(1,3)-D-glucan synthase inhibitor that is used to treat internal or systemic mycoses.</p>Fórmula:C52H88N10O15Cor e Forma:SolidPeso molecular:1093.31Thiamphenicol glycinate hydrochloride
CAS:<p>Thiamphenicol glycinate hydrochloride is a broad-spectrum antibacterial agent utilized in research on respiratory tract infections.</p>Fórmula:C14H19Cl3N2O6SCor e Forma:SolidPeso molecular:449.73Liriodenine methiodide
CAS:<p>Liriodenine methiodide shows antibacterial and antifungal activity against several microorganisms.</p>Fórmula:C18H12INO3Pureza:98%Cor e Forma:SolidPeso molecular:417.2CA-IN-5g
CAS:<p>CA-IN-5g is an effective carbonic anhydrase (CA) inhibitor. Carbonic anhydrase is isolated from Trypanosoma cruzi (TcCA).</p>Fórmula:C17H16N2O4Cor e Forma:SolidPeso molecular:312.32MTC420
CAS:<p>MTC420: Anti-TB drug, Mtb IC50=525nM, Wayne IC50=76nM, MDR IC50=140nM.</p>Fórmula:C20H16F4N2OPureza:98%Cor e Forma:SolidPeso molecular:376.35Antitrypanosomal agent 9
CAS:<p>Agent 9 inhibits T. b. brucei (IC50: 1.15 μM), used in HAT research.</p>Fórmula:C22H27NO3Cor e Forma:SolidPeso molecular:353.45Antitrypanosomal agent 7
CAS:<p>Compound 18c, an antitrypanosomal, is twice as potent as Nifurtimox against T. brucei (IC50: 0.71 μM), with favorable ADME and AT-DNA binding affinity.</p>Fórmula:C23H29N5O2Cor e Forma:SolidPeso molecular:407.51HBV-IN-29
CAS:<p>HBV-IN-29 (ex8), a flavone derivative, inhibits cccDNA in HBV research.</p>Fórmula:C22H19ClO6Cor e Forma:SolidPeso molecular:414.84Pomotrelvir
CAS:<p>Pomotrelvir (PBI-0451) is an oral SARS-CoV-2 3CL protease inhibitor with antiviral properties for COVID-19 research.</p>Fórmula:C23H26ClN5O3Cor e Forma:SolidPeso molecular:455.946BrW
CAS:<p>6BrW is an analog of tryptophan effector.</p>Fórmula:C11H11BrN2O2Pureza:98%Cor e Forma:SolidPeso molecular:283.12Antiparasitic agent-7
CAS:<p>Compound 5d, antiparasitic for L. infantum, IC50 of 2.85μM; cytotoxic to HepG2 cells, CC50 of 10.61μM.</p>Fórmula:C18H15N3O5Cor e Forma:SolidPeso molecular:353.33Juncin E
CAS:<p>Juncin E is an 18.9 kDa antifungal protein.</p>Fórmula:C30H37ClO14Pureza:98%Cor e Forma:SolidPeso molecular:657.06BoNT-IN-1
CAS:<p>BoNT-IN-1 (compound 8) is a potent inhibitor of Clostridium botulinum neurotoxin serotype A light chain (BoNT/A LC), with an IC50 of 0.9 μM.</p>Fórmula:C23H20N4O3Cor e Forma:SolidPeso molecular:400.43Deoxypheganomycin D
CAS:<p>Deoxypheganomycin D is a specific mycobacteria inhibitor.</p>Fórmula:C30H47N9O11Pureza:98%Cor e Forma:SolidPeso molecular:709.75BioA-IN-13
CAS:<p>BioA-IN-13 is a highly effective inhibitor of the Mycobacterium tuberculosis BioA enzyme, displaying potent cell permeability and whole-cell activity [1].</p>Fórmula:C19H16N2O4SCor e Forma:SolidPeso molecular:368.41AM-TS23
CAS:AM-TS23 is used as a DNA polymerase lambda and beta inhibitor.Fórmula:C17H12N2O3S3Pureza:98%Cor e Forma:SolidPeso molecular:388.48ML366
CAS:<p>ML366 is a Vibrio cholerae Quorum Sensing inhibitor Acting via the LuxO response regulator.</p>Fórmula:C17H19N3O4Pureza:98%Cor e Forma:SolidPeso molecular:329.35Antibacterial agent 126
<p>Antibacterial agent 126 combats biofilm, disrupts membranes, and boosts ROS/RNS to prevent drug resistance.</p>Fórmula:C21H24NO6PCor e Forma:SolidPeso molecular:417.39HBV-IN-14
CAS:<p>HBV-IN-14: a pyridinopyrimidinone, potent cccDNA inhibitor for HBV study (patent WO2021190502A1, comp 5).</p>Fórmula:C22H21ClN2O5Cor e Forma:SolidPeso molecular:428.87Meturedepa
CAS:<p>Meturedepa is an antineoplastic agent.</p>Fórmula:C11H22N3O3PPureza:98%Cor e Forma:SolidPeso molecular:275.28PknB-IN-1
CAS:<p>PknB-IN-1 inhibits PknB (IC50: 14.4 μM), has anti-mycobacterial effects (MIC: 6.2 μg/mL) against M. tuberculosis H37Rv.</p>Fórmula:C25H30N2O2Cor e Forma:SolidPeso molecular:390.52ICI-56780
CAS:<p>ICI-56780, a antimalarial agent, displays blood schizonticidal activity against P.berghei.</p>Fórmula:C23H25NO5Cor e Forma:SolidPeso molecular:395.45Aranotin
CAS:<p>Aranotin, from Arachniotus aureus, inhibits RNA viruses by blocking RNA polymerase.</p>Fórmula:C20H18N2O7S2Cor e Forma:SolidPeso molecular:462.5A 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:766.92Ornidazole diol
CAS:<p>Ornidazole diol is a diol produced through ornidazole rapidly hydrolyzing in basic solutions.</p>Fórmula:C7H11N3O4Pureza:98%Cor e Forma:SolidPeso molecular:201.18Antibacterial agent 74
CAS:<p>Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].</p>Fórmula:C16H20N2O3Cor e Forma:SolidPeso molecular:288.34Lincophenicol
CAS:<p>Lincophenicol is an Escherichia coli ribosomal peptidyltransferase-catalyzed puromycin reaction inhibitor.</p>Fórmula:C18H27N3O5Pureza:98%Cor e Forma:SolidPeso molecular:365.42Bioresmethrin
CAS:<p>Bioresmethrin is a pesticide of synthetic pyrethroid.</p>Fórmula:C22H26O3Pureza:98%Cor e Forma:SolidPeso molecular:338.45Vif-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:254.28Penamecillin
CAS:<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Fórmula:C19H22N2O6SCor e Forma:SolidPeso molecular:406.45SARS-CoV-2 Mpro-IN-6
CAS:<p>SARS-CoV-2 Mpro-IN-6: irreversible Mpro inhibitor, IC50 0.18 μM, selective; doesn't block cathepsins B/F/K/L or caspase 3.</p>Fórmula:C18H18Cl3N3O2SCor e Forma:SolidPeso molecular:446.78pUL89 Endonuclease-IN-1
CAS:<p>Compound 13d: potent pUL89 endonuclease inhibitor, IC50 0.88 μM, anti-HCMV activity.</p>Fórmula:C10H8N2O4SCor e Forma:SolidPeso molecular:252.25Diamthazole
CAS:<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Fórmula:C15H23N3OSCor e Forma:SolidPeso molecular:293.43Antiparasitic agent-2
CAS:<p>Compound 8a: potent against L. infantum (IC50=7.28μM) & T. cruzi (IC50=2.30μM); mildly toxic to HepG2 (CC50=26.79μM).</p>Fórmula:C20H17N3O3Cor e Forma:SolidPeso molecular:347.37CAY10760
CAS:<p>CAY10760 inhibits RAD51-BRCA2 interaction (EC50=19 μM), reduces homologous recombination by 54%, and hinders BxPC-3/Capan-1 cancer cell proliferation.</p>Fórmula:C28H24ClN3O3Cor e Forma:SolidPeso molecular:485.96ANT431
CAS:<p>ANT431 is a novel metallo-β-lactamase inhibitor for the treatment of carbapenem-resistant enterobacteriaceae infections</p>Fórmula:C9H7N3O4S2Cor e Forma:SolidPeso molecular:285.3MMV676584
CAS:<p>MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .</p>Fórmula:C12H8ClFN2OS2Cor e Forma:SolidPeso molecular:314.79HBV-IN-21
CAS:<p>HBV-IN-21 inhibits HBV DNA replication (IC50: 2.2 μM) and binds HBV capsid protein well (KD: 60.0 μM).</p>Fórmula:C17H17FN4OS2Cor e Forma:SolidPeso molecular:376.47Tenofovir 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:403.28PXYC12
CAS:<p>PXYC12 inhibits Mtb RpsA, key in trans-translation; binds RpsA-CTD (Kd 2.67μM) and RpsA-CTD Δ438A (Kd 4.67μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38HCV-IN-36
CAS:<p>HCV-IN-36: oral HCV inhibitor, EC50 0.016 μM, CC50 8.78 μM, potent antiviral.</p>Fórmula:C30H36ClN5Cor e Forma:SolidPeso molecular:502.09Derquantel
CAS:<p>nicotinic acetylcholine receptor antagonist</p>Fórmula:C28H37N3O4Pureza:98%Cor e Forma:SolidPeso molecular:479.61FLDP-5
CAS:<p>FLDP-5: BBB-penetrant curcuminoid, induces ROS, DNA damage, S phase arrest, suppresses tumors in LN-18 cells.</p>Fórmula:C21H21NO5Cor e Forma:SolidPeso molecular:367.4SSJ-183
CAS:<p>SSJ-183 is a low-toxicity and orally available and anti-malarial drug with an IC50 = 7.6 nM against P. falciparum and no lethality at doses up to 2000 mg/kg po.</p>Fórmula:C25H22N4OPureza:99.71% - 99.83%Cor e Forma:SolidPeso molecular:394.47TDRL-551
CAS:TDRL-551 is a novel and potent replication protein A (RPA) inhibitor (IC50=18 µM) with potential anticancer activity.TDRL-551 inhibits RPA-DNA interaction andFórmula:C25H23ClIN3O4Pureza:98.09%Cor e Forma:SolidPeso molecular:591.83Z060228
CAS:Z060228 is a potent anti-HBV agent, halts HBV DNA replication, and disrupts Cp149 self-assembly.Fórmula:C20H15ClF4N2O2Pureza:98%Cor e Forma:SolidPeso molecular:426.79HIV-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:550.63SDH-IN-5
CAS:<p>SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibiting</p>Fórmula:C16H19F2N3O2Cor e Forma:SolidPeso molecular:323.34DHDPS-IN-1
CAS:<p>DHDPS-IN-1 (compound 8), a DHDPS inhibitor with 39 μM IC50, has potential in antibacterial and herbicidal applications.</p>Fórmula:C13H11NO5SCor e Forma:SolidPeso molecular:293.3BAY-707
CAS:<p>BAY-707: tolerable in mice, no anticancer efficacy; potent, selective MTH1 inhibitor, IC50 = 2.3 nM; good PK profile.</p>Fórmula:C15H20N4O2Pureza:98%Cor e Forma:SolidPeso molecular:288.34Antiparasitic agent-6
CAS:<p>Compound 5b: antiparasitic against L. infantum (IC50 = 3.89 μM), cytotoxic to HepG2 cells (CC50 = 13.64 μM).</p>Fórmula:C19H15N3O3Cor e Forma:SolidPeso molecular:333.34Bentysrepinine
CAS:Bentysrepinine, a novel anti-HBV agent, inhibits DNA-HBV and cccDNA activities for the treatment of hepatitis B virus (HBV)-infected hepatitis.Fórmula:C29H35N3O4Pureza:98%Cor e Forma:SolidPeso molecular:489.61Urease-IN-8
CAS:<p>Urease-IN-8 (Compound 5e) functions as a competitive inhibitor of urease, with an IC50 value of 3.51 μM and a Ki of 3.11 μM.</p>Fórmula:C23H18N4OSCor e Forma:SolidPeso molecular:398.48Antibacterial agent 48
CAS:<p>Antibacterial agent 48 is an antimicrobial agent that reduces the MIC of the antimicrobial agent Ceftazidime.</p>Fórmula:C13H18N5NaO7SCor e Forma:SolidPeso molecular:411.36Olanexidine Hydrochloride semihydrate
CAS:<p>Olanexidine is a monobiguanide compound with the activity of bactericidal.</p>Fórmula:C17H31Cl4N5OPureza:98%Cor e Forma:SolidPeso molecular:463.27Antifungal agent 74
CAS:<p>Antifungal agent 74 (compound 3c), is a potent substance that exhibits excellent fungicidal activity against C.</p>Fórmula:C4HCl3N4SCor e Forma:SolidPeso molecular:243.5Inarigivir
CAS:Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.Fórmula:C20H26N7O10PSPureza:98%Cor e Forma:SolidPeso molecular:587.5BMVC2
CAS:<p>BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer.</p>Fórmula:C28H25I2N3Cor e Forma:SolidPeso molecular:657.33PSI-7409 tetrasodium
CAS:<p>PSI-7409 tetrasodium, a sofosbuvir metabolite, inhibits GT 1b, 2a, 3a, 4a NS5B polymerases with IC50s of 1.6, 2.8, 0.7, 2.6 μM.</p>Fórmula:C10H16FN2Na4O14P3Pureza:98%Cor e Forma:SolidPeso molecular:592.117Fenpropimorph
CAS:<p>Fenpropimorph is used as a small molecule fungicide.</p>Fórmula:C20H33NOCor e Forma:SolidPeso molecular:303.48Sulfamethomidine
CAS:<p>Sulfamethomidine has antibacterial activity [1].</p>Fórmula:C12H14N4O3SCor e Forma:SolidPeso molecular:294.33SARS-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:463.78Reverse 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:343.45BPH-715
CAS:<p>BPH-715 inhibits the liver-stage growth of P. falciparum with an IC50 of 10 μM for P. falciparum exoerythrocytic forms in HepG2 cells.</p>Fórmula:C17H31NO7P2Pureza:98.91%Cor e Forma:SolidPeso molecular:423.38SQ109
CAS:<p>SQ109 (NSC-722041) is an effective inhibitor of the trypomastigote form of the parasite (IC50 = 50 nM). SQ109 is an antitubercular agent and targets MmpL3.</p>Fórmula:C22H38N2Pureza:99.70% - 99.91%Cor e Forma:SolidPeso molecular:330.55Antitubercular agent-24
CAS:<p>Compound 1: Antitubercular, fights M. tuberculosis H37Rv, IC50 - extracellular 0.83 μM, intracellular 0.17 μM.</p>Fórmula:C18H19N3O2S2Cor e Forma:SolidPeso molecular:373.49Adenallene
CAS:<p>Adenallene inhibits replication and cytopathic effects of HIV in vitro.</p>Fórmula:C9H9N5OPureza:98%Cor e Forma:SolidPeso molecular:203.2BA-53038B
CAS:BA-53038B is an HBV core protein allosteric modulator (CpAM), binding to the HAP pocket and modulating HBV capsid assembly in a distinct manner (EC50: 3.32 μM).Fórmula:C14H16ClNOCor e Forma:SolidPeso molecular:249.74SARS-CoV MPro-IN-1
CAS:<p>MProinhibitor 11b blocks SARS-CoV-2 main protease (IC50=0.04 μM), cuts viral yield and RNA in Vero E6 cells (EC50=0.72 μM).</p>Fórmula:C25H25FN4O4Cor e Forma:SolidPeso molecular:464.49Lupulon
CAS:<p>Lupulon has a role as an apoptosis inducer, antimicrobial agent, angiogenesis inhibitor, and antineoplastic agent.</p>Fórmula:C26H38O4Cor e Forma:SolidPeso molecular:414.583CPLro-IN-2
CAS:<p>3CPLro-IN-2: Potent oral SARS-CoV-2 3CLpro inhibitor, IC50: 1.55 μM, Ki: 6.09 μM, targets vital COVID-19 protein.</p>Fórmula:C32H24BrNO2Cor e Forma:SolidPeso molecular:534.44SARS-CoV-2-IN-18
CAS:<p>SARS-CoV-2-IN-18 (Compound 26) is a potent inhibitor of SARS-CoV-2 3C-like protease (IC50 = 45 nM) [1].</p>Fórmula:C20H14N2O3Cor e Forma:SolidPeso molecular:330.34GlyRS-IN-1
CAS:GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.Fórmula:C12H17N7O7SCor e Forma:SolidPeso molecular:403.37Influenza virus-IN-3
CAS:<p>Influenza virus-IN-3 inhibits H5N1, H5N2, H5N6, H5N8 with low toxicity; targets neuraminidase.</p>Fórmula:C25H32N2O4SCor e Forma:SolidPeso molecular:456.6Antibacterial agent 72
CAS:<p>Antibacterial agent 72 has an antibacterial effect by selectively acting on bacterial membranes.</p>Fórmula:C19H21BrN4SCor e Forma:SolidPeso molecular:417.379-OxoOTrE
CAS:<p>9-OxoOTrE, made by oxidizing 9-HpOTrE, has antimicrobial effects on plant pathogens like bacteria and fungi.</p>Fórmula:C18H28O3Cor e Forma:SolidPeso molecular:292.41GSK983
CAS:<p>GSK983 inhibits DHODH to halt cell growth and dengue virus replication, acting as a broad-spectrum antiviral.</p>Fórmula:C18H16ClN3OPureza:98%Cor e Forma:SolidPeso molecular:325.79HIV-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:508.64L 739594
CAS:<p>L 739594 is an inhibitor of HIV-1 protease.</p>Fórmula:C31H47N3O6Pureza:98%Cor e Forma:SolidPeso molecular:557.72Glucocorticoid receptor modulator 1
CAS:<p>Glucocorticoid receptor modulator 1 is a orally NF-κB and AP-1 inhibitor, inflammatory factors IL-6, IL-1β, TNF-α, and MMP-13, alleviating skin inflammation.</p>Fórmula:C24H23ClN2O4SPureza:99.79%Cor e Forma:SolidPeso molecular:470.97CWHM-1008
CAS:CWHM-1008: Oral antimalarial, EC50 - 46 nM (3D7 strain), 21 nM (Dd2 resistant).Fórmula:C22H26F3N3OCor e Forma:SolidPeso molecular:405.46Vps34-IN-2
CAS:<p>Vps34-IN-2 is a potent and selective Vps34 inhibitor (IC50s: 2 and 82 nM on the Vps34 enzymatic assay and the GFP-FYVE cellular assay, respectively).</p>Fórmula:C18H25F3N4O3Pureza:98%Cor e Forma:SolidPeso molecular:402.41BMS-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:447.42NS2B/NS3-IN-3 hydrochloride
CAS:<p>NS2B/NS3-IN-3 hydrochloride is a Flavivirus NS2B-NS3 protease inhibitor [1].</p>Fórmula:C19H22ClN3O2Pureza:98%Cor e Forma:SolidPeso molecular:359.85Antileishmanial agent-14
CAS:<p>Antileishmanial agent-14, a sulfuretin analog, exhibits potential activity against Leishmania donovani promastigotes (IC 50 = 4.1 μM) and inhibits infection by</p>Fórmula:C23H26ClNO5Pureza:98%Cor e Forma:SolidPeso molecular:431.91Antimalarial agent 19
CAS:<p>Compound 6e, an antimalarial, targets P. falciparum K1 (EC50 0.3 µM) and P. berghei (EC50 15.3 µM); has high solubility and stability.</p>Fórmula:C22H33Cl2N5SPureza:98%Cor e Forma:SolidPeso molecular:470.5SARS-CoV-2-IN-41
CAS:<p>SARS-CoV-2-IN-41 (compound 2) is a potent inhibitor of SARS-CoV-2 3CL protease, exhibiting an IC50 of 0.022 µM and demonstrating antiviral efficacy [1].</p>Fórmula:C22H30F3N5O4S2Pureza:98%Cor e Forma:SolidPeso molecular:549.63Antileishmanial agent-15
CAS:<p>Antileishmanial agent-15 (compound 13c) exhibits potent activity against L.</p>Fórmula:C28H39N5O4Pureza:98%Cor e Forma:SolidPeso molecular:509.64Antiparasitic agent-4
CAS:<p>Compound 4q: Antiparasitic; IC50: 8.51 μM (L. infantum), 2.20 μM (T. cruzi); HepG2 cytotoxicity: CC50 18.97 μM.</p>Fórmula:C16H13N3O2Cor e Forma:SolidPeso molecular:279.29MAC173979
CAS:<p>MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.</p>Fórmula:C9H5Cl2NO3Pureza:98%Cor e Forma:SolidPeso molecular:246.05CM03
CAS:<p>CM03 is a cell-selective G-quadruplex ligand with anti-cancer activity, stabilizing G4 genes, useful in pancreatic cancer research.</p>Fórmula:C34H44N6O6Pureza:98.65%Cor e Forma:SolidPeso molecular:632.75
