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(2.968 produtos)
- Antibiótico(922 produtos)
- Antifecção(23 produtos)
- DHFR(33 produtos)
- Síntese de DNA/RNA(711 produtos)
- HBV(177 produtos)
- HIV Protease(451 produtos)
- HSV(91 produtos)
- Integrase(2 produtos)
- Ribossomo(13 produtos)
Exibir 2 mais subcategorias
Foram encontrados 5863 produtos de "Microbiologia/Virologia"
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CA-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:376.355M038
CAS:5M038, a novel inhibitor of HIV envelope-mediated fusion, strongly inhibits gp41-mediated membrane fusion.Fórmula:C17H8F6N4Pureza:98%Cor e Forma:SolidPeso molecular:382.26KKJ00626
CAS:<p>KKJ00626, an inhibitor of HBV virus, inhibits HBV replication in transfected Huh7 cells.</p>Fórmula:C7H8N4SPureza:98%Cor e Forma:SolidPeso molecular:180.236BrW
CAS:<p>6BrW is an analog of tryptophan effector.</p>Fórmula:C11H11BrN2O2Pureza:98%Cor e Forma:SolidPeso molecular:283.12BMVC2
CAS:<p>BMVC2 (o-BMVC), a carbazole derivative of BMVC, is a G-quadruplex (G4) stabilizer.</p>Fórmula:C28H25I2N3Cor e Forma:SolidPeso molecular:657.33Deoxypheganomycin D
CAS:<p>Deoxypheganomycin D is a specific mycobacteria inhibitor.</p>Fórmula:C30H47N9O11Pureza:98%Cor e Forma:SolidPeso molecular:709.75Acyclovir alaninate
CAS:<p>Acyclovir alanine is a pro-drug of Acyclovir. Acyclovir works by decreasing the production of DNA of the virus and it shows very low cytotoxicity.</p>Fórmula:C11H16N6O4Cor e Forma:SolidPeso molecular:296.28L-708906
CAS:<p>L-708906 is the Human Immunodeficiency Virus Type 1 inhibitor.</p>Fórmula:C24H20O6Pureza:98%Cor e Forma:SolidPeso molecular:404.41BPH-651
CAS:<p>BPH-651 is a CrtM inhibitor.</p>Fórmula:C19H21NOCor e Forma:SolidPeso molecular:279.38PSI-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:592.117Dihydropteroate synthase-IN-1
CAS:<p>"Dihydropteroate synthase-IN-1 (5g) inhibits DHPS and cytochrome P450, useful as radiographic diagnostic material."</p>Fórmula:C19H23N5O4S2Cor e Forma:SolidPeso molecular:449.55ICI-56780
CAS:<p>ICI-56780, a antimalarial agent, displays blood schizonticidal activity against P.berghei.</p>Fórmula:C23H25NO5Cor e Forma:SolidPeso molecular:395.45ITX-4520
CAS:<p>ITX-4520 novel highly potent, orally bioavailable inhibitor of hepatitis C virus (HCV) entry.</p>Fórmula:C24H23F2N3OSCor e Forma:SolidPeso molecular:439.52Ornidazole 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:201.18Lincophenicol
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:338.45Rosaramicin
CAS:<p>Rosaramicin, a lipid-soluble basic macrolide, is an antibacterial substance similar to erythromycin but with a better activity against Gram-negative bacteria.</p>Fórmula:C31H51NO9Pureza:98%Cor e Forma:SolidPeso molecular:581.74RO-9187
CAS:<p>RO-9187 is an effective HCV virus replication inhibitor(IC50: 171 nM).</p>Fórmula:C9H12N6O5Pureza:98%Cor e Forma:SolidPeso molecular:284.23Canocapavir
CAS:Canocapavir (ZM-H1505R) is an HBV coat protein modulator with antiviral activity for the treatment of hepatitis B virus.Fórmula:C27H21BrFN5O3Pureza:98.4% - 98.40%Cor e Forma:SolidPeso molecular:562.39BMH-23
CAS:<p>BMH-23 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Fórmula:C15H15N3Pureza:98%Cor e Forma:SolidPeso molecular:237.3Symetine
CAS:Symetine（L 16726） is a small molecule compound with antiparasitic activity that can be used to study amoebic liver abscesses in guinea pigs.Fórmula:C30H48N2O2Pureza:99.79%Cor e Forma:SolidPeso molecular:468.71WRR-483
CAS:<p>WRR-483, a cysteine protease inhibitor similar to K-11777, has trypanocidal properties and potential against Chagas' disease.</p>Fórmula:C29H41N7O4SCor e Forma:SolidPeso molecular:583.75PNU288034
CAS:<p>PNU288034 is a potent oxazolidinone antibiotic with antimicrobial activity for the prevention and treatment of Gramnegative infections.</p>Fórmula:C16H19F2N3O5SPureza:98.41%Cor e Forma:SolidPeso molecular:403.4TDRL-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:591.83Ipconazole [ISO]
CAS:<p>Ipconazole, a cyclopentanol with 1,2,4-triazolylmethyl, 4-chlorobenzyl & isopropyl groups, is a fungicide that targets seed diseases.</p>Fórmula:C18H24ClN3OCor e Forma:SolidPeso molecular:333.86KFU-127
<p>KFU-127: broad-spectrum antimicrobial; targets bacterial/fungal biofilms; toxic to eukaryotic cells.</p>Fórmula:C34H43BrN2O3Cor e Forma:SolidPeso molecular:607.62MMV687807
CAS:<p>MMV687807: potent anthelmintic, IC50 0.15 μM, CC50 1.69 μM against T. gondii.</p>Fórmula:C15H8ClF6NO2Cor e Forma:SolidPeso molecular:383.67PD 140248
CAS:<p>PD 140248, a broad-spectrum 7-pyrrolidinyl fluoronaphthyridines, has been demonstrated to have excellent in vitro activity against gram-positive organisms.</p>Fórmula:C21H20ClF3N4O3Cor e Forma:SolidPeso molecular:468.86Benzoxonium chloride
CAS:<p>Benzoxonium chloride used in Thio-Ben for cutaneous leishmaniasis treatment with cryotherapy.</p>Fórmula:C23H42ClNO2Cor e Forma:SolidPeso molecular:400.04Stampidine
CAS:<p>Stampidine prevents HIV-1, effective against resistant strains at subnanomolar levels.</p>Fórmula:C20H23BrN3O8PPureza:98%Cor e Forma:SolidPeso molecular:544.29GA-O-06
<p>GA-O-06: 18β-Glycyrrhetinic acid derivative with powerful antimicrobial effects on Gram-positive bacteria and anti-inflammatory properties.</p>Fórmula:C37H46FNO6Cor e Forma:SolidPeso molecular:619.76HIV-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:427.43Edelfosine
CAS:<p>inhibits phosphatidylinositol phospholipase C</p>Fórmula:C27H58NO6PPureza:98%Cor e Forma:SolidPeso molecular:523.73Antituberculosis agent-2
CAS:<p>Compound 8d: treats MDR and sensitive tuberculosis, low toxicity, good oral bioavailability, stable in humans/mice; MIC: 0.454-1.757 μg/mL.</p>Fórmula:C19H17NO4Cor e Forma:SolidPeso molecular:323.34FR-182024
CAS:<p>FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.</p>Fórmula:C18H16N4O4S3Cor e Forma:SolidPeso molecular:448.54Fenpropimorph
CAS:<p>Fenpropimorph is used as a small molecule fungicide.</p>Fórmula:C20H33NOCor e Forma:SolidPeso molecular:303.48(5S,8R)-HBV-IN-10
CAS:<p>'(5S,8R)-HBV-IN-10 is an EC50 0.1-1 μM HBsAg inhibitor, isomer of compound 6 from patent WO2021204258A1.</p>Fórmula:C23H24FN7OCor e Forma:SolidPeso molecular:433.48Mtb-cyt-bd oxidase-IN-3
<p>Mtb-cyt-bd oxidase-IN-3 inhibits M. tuberculosis growth, IC50 0.36 μM, MIC 32 μM, for TB research.</p>Fórmula:C26H35NO2Cor e Forma:SolidPeso molecular:393.56Sulfamethomidine
CAS:<p>Sulfamethomidine has antibacterial activity [1].</p>Fórmula:C12H14N4O3SCor e Forma:SolidPeso molecular:294.33Fungicide4
CAS:<p>Fungicide4 exhibits the high activity against the P. infestans strain.</p>Fórmula:C14H11N3OCor e Forma:SolidPeso molecular:237.26Ceftobiprole medocaril sodium
CAS:<p>Ceftobiprole medocaril sodium (BAL5788) is a prodrug of broad-spectrum cephalosporin active against MRSA, VRSA, and resistant streptococci.</p>Fórmula:C26H25N8NaO11S2Cor e Forma:SolidPeso molecular:712.644-Piperidinecarboxamide
CAS:<p>4-Piperidinecarboxamide is a mycobacterial aspartyl-tRNA synthetase (AspS) inhibitor and a potential anti-tuberculosis (TB) agent [1].</p>Fórmula:C16H15Cl2N3O2SCor e Forma:SolidPeso molecular:384.28HCV-IN-35
CAS:<p>HCV-IN-35 is a potent inhibitor of HCV and shows potential for infectious disease research.</p>Fórmula:C30H36ClN5Cor e Forma:SolidPeso molecular:502.09PC58538
CAS:<p>PC58538 is an inhibitor of FtsZ protein, a important role in the division machinery of bacterial cells.</p>Fórmula:C24H25NO3Cor e Forma:SolidPeso molecular:375.46HIV-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:242.28Antibacterial agent 124
CAS:<p>Antibacterial agent 124 inhibits Sa ProRS with an IC50 of 0.18 μM.</p>Fórmula:C16H17ClFN3O2Cor e Forma:SolidPeso molecular:337.78HBV-IN-29
CAS:<p>HBV-IN-29 (ex8), a flavone derivative, inhibits cccDNA in HBV research.</p>Fórmula:C22H19ClO6Cor e Forma:SolidPeso molecular:414.84Inarigivir
CAS:Inarigivir (ORI-9020) is a dinucleotide that can significantly reduce liver HBV DNA.Fórmula:C20H26N7O10PSPureza:98%Cor e Forma:SolidPeso molecular:587.5BHBM
CAS:<p>BHBM, an acylhydrazone antifungal, halts C. neoformans growth (MIC80 = 1 μg/ml) by blocking glucosylceramide synthesis.</p>Fórmula:C15H13BrN2O2Cor e Forma:SolidPeso molecular:333.18HIV-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:491.61Anti-Influenza agent 4
CAS:<p>Anti-Influenza agent 4 selectively inhibits A/Parma (EC50: 62 nM) and A/Roma (EC50: 150 nM) influenza strains.</p>Fórmula:C19H18N2O5SPureza:98.94% - 98.95%Cor e Forma:SolidPeso molecular:386.42Anti-infective agent 3
CAS:<p>Antiprotozoal and antimycobacterial compound 3l; IC50: P. falciparum 0.47 μM, T. brucei 0.13 μM; MIC against M. smegmatis 4 μg/mL.</p>Fórmula:C14H7ClN2O2Cor e Forma:SolidPeso molecular:270.67Metallo-β-lactamase-IN-8
CAS:<p>Metallo-β-lactamase-IN-8 (compound 17) is a potent, reversible and competitive broad-spectrum metallo-β-lactamases (MβLs) inhibitor with antibacterial activity.</p>Fórmula:C13H11ClN2O4SCor e Forma:SolidPeso molecular:326.76DPC-963
CAS:<p>DPC-963 is a RNA-directed DNA polymerase inhibitor.</p>Fórmula:C14H9F5N2OCor e Forma:SolidPeso molecular:316.23SARS-CoV-2 nsp3-IN-2
CAS:<p>SARS-CoV-2 nsp3-IN-2: Mac1 inhibitor, IC50=180μM, hinders virus replication.</p>Fórmula:C10H12N4O2Cor e Forma:SolidPeso molecular:220.23RNPA1000
CAS:<p>RNPA1000 is an attractive antimicrobial development candidate and RnpA inhibitor.</p>Fórmula:C23H18BrN3O3Pureza:98%Cor e Forma:SolidPeso molecular:464.31Fozivudine tidoxil
CAS:<p>Fozivudine tidoxil, a reverse transcriptase inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C35H64N5O8PSCor e Forma:SolidPeso molecular:745.95HIV-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:424.47SARS-CoV-2 nsp13-IN-3
CAS:<p>SARS-CoV-2 nsp13-IN-3 (Compound C3) is a small molecule inhibitor of SARS-CoV-2 non-structural protein 13 (nsp13) that acts on nsp13 ssDNA+ATPase (IC50: 32 μM).</p>Fórmula:C24H27N7OCor e Forma:SolidPeso molecular:429.52Chitin synthase inhibitor 10
CAS:<p>Chitin Synthase Inhibitor 10: potent antifungal with 0.11 mM IC50, effective against resistant C. albicans and C. neoformans. Used in IFI research.</p>Fórmula:C24H23Br2N3O6Cor e Forma:SolidPeso molecular:609.26IDD388
CAS:IDD388 is a selective and potent aldose reductase (ALR2) inhibitor with antitumor activity that inhibits the ALR1 receptor.Fórmula:C16H12BrClFNO4Pureza:99.56%Cor e Forma:SolidPeso molecular:416.63TBI-166
CAS:<p>TBI-166, an oral riminophenazine, treats tuberculosis with fewer side effects than Clofazimine.</p>Fórmula:C32H30F3N5O3Cor e Forma:SolidPeso molecular:589.61SARS-CoV-2 3CLpro-IN-1
CAS:<p>SARS-CoV-2 3CLpro-IN-1 is a potent inhibitor of the key enzyme 3CL pro in coronaviruses, promising for antiviral drug R&D.</p>Fórmula:C27H30ClN3O3SCor e Forma:SolidPeso molecular:512.06CBR-6672
CAS:<p>CBR-6672, a potent anti-tuberculosis agent; type II NADH dehydrogenase inhibitor; MIC: 0.14 μM.</p>Fórmula:C17H20FN3O2SCor e Forma:SolidPeso molecular:349.42SQ109
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:330.55SARS-CoV-2-IN-16
CAS:<p>SARS-CoV-2-IN-16 strongly inhibits NPro, with EC50 of 3.69 μM and Kd of 7.82 μM, suggesting effective binding and antiviral properties.</p>Fórmula:C17H20N2O2Cor e Forma:SolidPeso molecular:284.35Antileishmanial agent-8
CAS:<p>Compound 18: Antileishmanial, IC50=5.64 μM for L. donovani, low toxicity in L-6 cells, IC50=73.9 μM.</p>Fórmula:C18H16O4Cor e Forma:SolidPeso molecular:296.32HIV-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:357.83LabMol-301
CAS:<p>LabMol-301 blocks NS5 RdRp/NS2B-NS3pro (IC50: 0.8/7.4µM), protects cells from ZIKV death.</p>Fórmula:C18H16N6Cor e Forma:SolidPeso molecular:316.36SARS-CoV-2-IN-31
CAS:<p>SARS-CoV-2-IN-31: COVID-19 inhibitor, IC50: 28.84-38.36 μM, useful in cancer studies.</p>Fórmula:C29H28N4O2Cor e Forma:SolidPeso molecular:464.56MDRTB-IN-1
CAS:<p>MDRTB-IN-1 (5aα) is an antibiotic which is against Mycobacterium tuberculosis H37Rv(MIC90 :10.5 μM).</p>Fórmula:C15H18N2O3Pureza:98%Cor e Forma:SolidPeso molecular:274.32Crisnatol mesylate
CAS:<p>Crisnatol, a potent and selective DNA intercalator, has potential anticancer activity.</p>Fórmula:C24H27NO5SCor e Forma:SolidPeso molecular:441.54Bentysrepinine
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:489.61SPR41
<p>SPR41 inhibits SARS-CoV-2 main protease (K i : 0.184µM) and is antiviral with some cytotoxicity.</p>Fórmula:C27H37N3O5Cor e Forma:SolidPeso molecular:483.6C16-K-cBB1
<p>C16-K-cBB1: potent, selective MRSA killer; MIC 1µg/mL, low hemolysis, works in 120 min at 12.5µg/mL.</p>Fórmula:C33H58ClN5O5SCor e Forma:SolidPeso molecular:672.36Laburnetin
CAS:<p>Laburnetin: an isoflavone antibacterial, combats fungi/S. vesicarium, boosts MRSA methicillin susceptibility, used in pest control.</p>Fórmula:C20H18O6Cor e Forma:SolidPeso molecular:354.35Antifungal agent 68
CAS:<p>Antifungal agent 68 (compound 10) effectively combats fungal infections caused by Candida and Cryptococcus gattii through the inhibition of ergosterol</p>Fórmula:C23H27ClN2O3Cor e Forma:SolidPeso molecular:414.93Antitrypanosomal agent 11
<p>Antitrypanosomal Agent 11 is a chemical compound effective against Trypanosoma cruzi, exhibiting an inhibition concentration (IC 50) of 0.23 μM.</p>Fórmula:C16H10F6N6OCor e Forma:SolidPeso molecular:416.28S-1360
CAS:<p>S-1360 is an inhibitor of HIV-1 integrase.</p>Fórmula:C16H12FN3O3Pureza:98%Cor e Forma:SolidPeso molecular:313.28Antitumor agent-85
<p>Antitumor agent-85 stabilizes G4-DNA with potent anti-tumor effects.</p>Fórmula:C24H33N7Cor e Forma:SolidPeso molecular:419.57RmlA-IN-1
CAS:<p>RmlA-IN-1 inhibits RmlA enzyme with 0.073 μM IC50, affecting l-Rhamnose synthesis and bacterial wall permeability.</p>Fórmula:C18H18N4O4SCor e Forma:SolidPeso molecular:386.42Antifungal agent 32
CAS:<p>Antifungal 32 (1a) strongly inhibits Candida albicans growth, filamentation, biofilm, and adhesion.</p>Fórmula:C25H28N2OCor e Forma:SolidPeso molecular:372.5HCV-IN-33
CAS:<p>HCV-IN-33 (Compound (S)-3i) is an inhibitor of HCV entry.</p>Fórmula:C31H36ClN5Cor e Forma:SolidPeso molecular:514.1HIV-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:541.09Antimicrobial agent-1
CAS:<p>Antimicrobial Agent-1 (compound 6C) shows strong activity (MIC = 2 μg/mL) against TolC mutant E.</p>Fórmula:C22H21N3O2SCor e Forma:SolidPeso molecular:391.49As-358 hydrochloride
CAS:<p>As-358 (hydrochloride) shows well in vivo safety as well as inhibits Ebola virus and Marburg virus with IC 50 values of 9.1 μM and 18.1 μM [1].</p>Fórmula:C18H32ClNO2Cor e Forma:SolidPeso molecular:329.91Antiviral 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:763.82ERCC1-XPF-IN-1
CAS:<p>ERCC1-XPF-IN-1: potent ERCC1-XPF inhibitor (IC50: 0.49 μM), hampers CPD removal, boosts UV toxicity, hinders DNA repair.</p>Fórmula:C28H32ClN5O2Cor e Forma:SolidPeso molecular:506.04Antistaphylococcal agent 1
CAS:<p>Antistaphylococcal agent 1 is an antistaphylococcal therapeutic agent.</p>Fórmula:C22H16N6O2Cor e Forma:SolidPeso molecular:396.4Enisamium iodide
CAS:<p>Enisamium iodide is used as an antiviral agent.</p>Fórmula:C14H15IN2OCor e Forma:SolidPeso molecular:354.19Antiviral agent 19
CAS:<p>Antiviral agent 19 (Compound 3) is a selective inhibitor of Zika virus (EC50: 1.3 μM) with low cytotoxicity.</p>Fórmula:C29H35NO5Cor e Forma:SolidPeso molecular:477.59Antibacterial agent 64
CAS:<p>Potent antibacterial, YycG inhibitor with 6.1 µM IC50. Synergistic with ampicillin against biofilm bacteria.</p>Fórmula:C29H20ClN3O6S2Cor e Forma:SolidPeso molecular:606.07Influenza virus-IN-4
CAS:<p>Influenza virus-IN-4 (compound 11e) is a potent inhibitor of influenza virus neuraminidase, acting on H5N1 (IC50: 3.4 μM), H5N2 (IC50: 0.094 μM), H5N6 (IC50: 0.</p>Fórmula:C23H31FN2O4Cor e Forma:SolidPeso molecular:418.5Mt KARI-IN-5
CAS:<p>Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.</p>Fórmula:C14H10N4O5S3Cor e Forma:SolidPeso molecular:410.45RMI 10874
CAS:<p>RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.</p>Fórmula:C21H26N2O4Pureza:98%Cor e Forma:SolidPeso molecular:370.44DLC27-14
CAS:<p>DLC27-14 is an HIV-1 Nef specific protein disorder catalyzer.</p>Fórmula:C25H25NO4Cor e Forma:SolidPeso molecular:403.47Tromantadine
CAS:Tromantadine is an amantadine derivative with antiherpetic activity (inhibits HSV-1 and HSV-2 replication).Fórmula:C16H28N2O2Pureza:98%Cor e Forma:SolidPeso molecular:280.41Neuraminidase-IN-8
CAS:<p>Neuraminidase-IN-8 (Compound 6d) is a powerful inhibitor of neuraminidase, exhibiting a low half-maximal inhibitory concentration (IC50) of 0.027 μM and</p>Fórmula:C18H16FN3O3SCor e Forma:SolidPeso molecular:373.4Neuraminidase-IN-3
CAS:<p>Neuraminidase-IN-3 inhibits flu NA: H1N1 IC50=0.73nM, H5N1=0.26nM, H5N8=0.63nM.</p>Fórmula:C27H32N2O4SCor e Forma:SolidPeso molecular:480.62
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