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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L-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:279.38Furaprofen
CAS:<p>Furaprofen is an HCV inhibitor with anti-inflammatory activity that inhibits carrageenan-induced paw edema in rats.</p>Fórmula:C17H14O3Pureza:98.49% - 99.52%Cor e Forma:SolidPeso molecular:266.29FabH-IN-1
CAS:<p>FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.</p>Fórmula:C17H16N2OSCor e Forma:SolidPeso molecular:296.39MK-4882
CAS:<p>MK-4882 is an effective inhibitor of HCV NS5A.</p>Fórmula:C42H50N8O7Pureza:98%Cor e Forma:SolidPeso molecular:778.9Cefbuperazone Sodium
CAS:Cefbuperazone Sodium is a penicillin-binding protein inhibitor. It is used as antibacterials.Fórmula:C22H29N9NaO9S2Pureza:98%Cor e Forma:SolidPeso molecular:650.64IDD388
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:416.63CGI-17341
CAS:CGI-17341, an oral 5-nitroimidazole antimicrobial, blocks drug-sensitive and resistant tuberculosis at 0.1-0.3 µg/ml.Fórmula:C7H9N3O3Cor e Forma:SolidPeso molecular:183.16(R)-Gyramide A hydrochloride
CAS:<p>(R)-Gyramide A HCl inhibits DNA gyrase in bacteria (IC50: 875 μM), with MIC 10-80 μM against P. aeruginosa & E. coli, sparing topoisomerase IV.</p>Fórmula:C21H28ClFN2O3SCor e Forma:SolidPeso molecular:442.97Cefmenoxime
CAS:<p>Cefmenoxime: IV/IM cephalosporin antibiotic, resists beta-lactamase, targets Enterobacteriaceae, gram-positive/negative bacteria.</p>Fórmula:C16H17N9O5S3Pureza:98%Cor e Forma:Almost White Or Almost Yellow Crystalline PowderPeso molecular:511.558Nucleoside-Analog-2
CAS:<p>Nucleoside-Analog-2 is a 4'-Azidocytidine analogue, used to against Hepatitis C virus (HCV) replication.</p>Fórmula:C9H11N5O6Pureza:98%Cor e Forma:SolidPeso molecular:285.21L 738372
CAS:<p>L 738372 is a non-nucleoside inhibitor of HIV-1 reverse transcriptase.</p>Fórmula:C18H15N3OCor e Forma:SolidPeso molecular:289.33SARS-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:463.78Homocarbonyltopsentin
CAS:<p>Homocarbonyltopsentin: Small molecule, binds TSL2 pentaloops, enhances SMN2 E7 splicing, EC50 16 μM.</p>Fórmula:C21H14N4O3Pureza:98%Cor e Forma:SolidPeso molecular:370.36Reverse 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:343.45Taribavirin
CAS:<p>Taribavirin: oral drug targeting HCV in liver, spares RBCs to reduce risk of anemia.</p>Fórmula:C8H13N5O4Pureza:98%Cor e Forma:SolidPeso molecular:243.22HIV-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:416.3AFK-108
CAS:<p>AFK-108 is a fungicide agent.</p>Fórmula:C21H26Cl2N2OPureza:98%Cor e Forma:SolidPeso molecular:393.35Flomoxef sodium
CAS:<p>Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.</p>Fórmula:C15H17F2N6NaO7S2Pureza:97.88%Cor e Forma:SolidPeso molecular:518.44Albitiazolium bromide
CAS:<p>Albitiazolium bromide is an antimalarial compound disrupting phosphatidylcholine biosynthesis in Plasmodium, transported via NPP and cation carriers.</p>Fórmula:C24H42BrN2O2S2Pureza:99.743%Cor e Forma:SolidPeso molecular:534.64Netzahualcoyone
CAS:<p>Netzahualcoyone inhibited the respiration of intact cells of B. subtilis but had no effect on the respiration of E. coli.</p>Fórmula:C30H36O6Pureza:98%Cor e Forma:SolidPeso molecular:492.6Xenalamine
CAS:<p>Xenalamine is a synthetic compound of antiviral.</p>Fórmula:C23H21NO4Pureza:98%Cor e Forma:SolidPeso molecular:375.42Nitracrine
CAS:<p>Nitracrine: a 1-nitroacridine, hypoxia-selective, anti-tumor agent; inhibits RNA synthesis, binds DNA reversibly and forms covalent adducts.</p>Fórmula:C18H20N4O2Pureza:98%Cor e Forma:SolidPeso molecular:324.38LmCPB-IN-1
CAS:<p>LmCPB-IN-1, compound 35, is a reversible inhibitor of LmCPB with strong binding (pKi 9.7).</p>Fórmula:C18H30N6O2Cor e Forma:SolidPeso molecular:362.47Neuraminidase-IN-5
CAS:<p>Neuraminidase-IN-5: potent NA inhibitor, IC50=0.02μM, potential anti-influenza, dihydrofurocoumarin derivative.</p>Fórmula:C19H11NO7Cor e Forma:SolidPeso molecular:365.29YM-53601
CAS:<p>YM-53601 is an SQS inhibitor that inhibits adipogenic biosynthesis and lipid secretion in rodents.YM-53601 is a cholesterol-lowering agent that inhibits FDFT1.</p>Fórmula:C21H22ClFN2OPureza:99.65%Cor e Forma:SolidPeso molecular:372.86BMVC
CAS:<p>BMVC is a potent G-quadruplex (G4) stabilizer and a selective telomerase inhibitor (IC50: ~0.2 μM) with anticancer activities.</p>Fórmula:C28H25I2N3Cor e Forma:SolidPeso molecular:657.33Miloxacin
CAS:<p>Miloxacin is an antibiotic active against gram-negative bacteria.</p>Fórmula:C12H9NO6Pureza:98%Cor e Forma:SolidPeso molecular:263.20RSV-IN-4
CAS:<p>RSV-IN-4 is a dual inhibitor for RSV and IAV with an EC50 of 11.76 μM.</p>Fórmula:C18H18N2O2SCor e Forma:SolidPeso molecular:326.41FadD32 Inhibitor-1
CAS:<p>FadD32 inhibitor -1 has anti-tuberculosis activity and is an effective FadD32 inhibitor.</p>Fórmula:C24H20ClN3OPureza:98%Cor e Forma:SolidPeso molecular:401.89Ribocil B
CAS:<p>Ribocil-B is the active S-isomer of ribocil which can inhibit flavin mononucleotide (FMN,KD of 6.6 nM).</p>Fórmula:C19H22N6OSPureza:98%Cor e Forma:SolidPeso molecular:382.48Ametoctradin
CAS:<p>Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.</p>Fórmula:C15H25N5Pureza:99.65%Cor e Forma:SolidPeso molecular:275.39PNU288034
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:403.4SSJ-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:394.47Antibacterial agent 98
CAS:<p>Compound g37, an oral antibacterial, inhibits Gyrase B ATPase and S. aureus DNA super-helix without causing MRSA resistance.</p>Fórmula:C17H13N5O3S2Cor e Forma:SolidPeso molecular:399.45Antimalarial agent 8
CAS:<p>Compound 7e: novel oral antimalarial, effective against P. falciparum in vitro and in vivo (40 mg/kg).</p>Fórmula:C22H21Cl3N4OCor e Forma:SolidPeso molecular:463.79Z060228
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:426.79Influenza 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:417.37HIV-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:416.44Piposulfan
CAS:Piposulfan, a water-insoluble alkylating agent, is used as an antineoplastic and anti-tumor agent.Fórmula:C12H22N2O8S2Cor e Forma:SolidPeso molecular:386.44APOBEC3G-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:253.25LasR-IN-4
CAS:<p>LasR-IN-4 is a potent inhibitor of LasR which inhibits Pseudomonas aeruginosa and its biofilm formation, pyocyanin production, and rhamnolipids production [1].</p>Fórmula:C18H20N4Cor e Forma:SolidPeso molecular:292.38HCV-IN-3
CAS:<p>HCV-IN-3 is a hepatitis C virus (HCV) NS3/4a protein inhibitor (IC50: 20 μM; Kd: 29 μM).</p>Fórmula:C13H11F2NOPureza:98%Cor e Forma:SolidPeso molecular:235.23GSK983
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:508.64Zidebactam sodium salt
CAS:Zidebactam sodium salt is a potent inhibitor of β-lactamase, and also is an inhibitor of penicillin-binding protein2 (PBP2)(IC50 of 0.26 μg/mL).Fórmula:C13H21N5NaO7SPureza:98%Cor e Forma:SolidPeso molecular:414.39G0507
CAS:G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.Fórmula:C18H15N3O3SCor e Forma:SolidPeso molecular:353.39NB-598 hydrochloride
CAS:<p>NB-598 hydrochloride is a competitive squalene epoxidase (SE) inhibitor.</p>Fórmula:C27H32ClNOS2Pureza:98%Cor e Forma:SolidPeso molecular:486.13Phen-DC3
CAS:<p>Phen-DC3 is a G-quadruplex (G4) specific ligand which can inhibit FANCJ and DinG helicases (IC50s of 65±6 and 50±10 nM, respectively).</p>Fórmula:C34H26N6O2Pureza:98%Cor e Forma:SolidPeso molecular:550.61Synthalin sulfate
CAS:<p>Synthalin sulfate is a NMDA receptor antagonist.</p>Fórmula:C12H30N6O4SPureza:98%Cor e Forma:SolidPeso molecular:354.47Antifungal agent 2
CAS:Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.Fórmula:C19H11Br2F3N4O2Pureza:98%Cor e Forma:SolidPeso molecular:544.12BMS-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:447.42RSV/IAV-IN-3
CAS:<p>RSV/IAV-IN-3 is a dual inhibitor of RSV (EC50: 2.92μM) and IAV (EC50:1.90μM), blocking virus replication post-entry.</p>Fórmula:C19H19BrN2O3SCor e Forma:SolidPeso molecular:435.3341F5
CAS:<p>41F5: Anti-fungal with MIC50 0.4-0.8 μM and IC50 0.87 μM against Histoplasma; 62x more selective for yeast vs host cells.</p>Fórmula:C21H22N2OSCor e Forma:SolidPeso molecular:350.48MMV008138
CAS:<p>MMV008138 inhibits the growth of P. falciparum Dd2 strain (IC50 of 250 nM).</p>Fórmula:C18H14Cl2N2O2Cor e Forma:SolidPeso molecular:361.22BDM91514
CAS:<p>BDM91514 enhances antibiotic efficacy by inhibiting AcrB, effectively curbing the proliferation of E.</p>Fórmula:C13H19Cl3N6OCor e Forma:SolidPeso molecular:381.69BPH-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:423.38Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Fórmula:C12H12N2O3Pureza:98%Cor e Forma:SolidPeso molecular:232.24SARS-CoV-2 nsp13-IN-5
CAS:<p>SARS-CoV-2 nsp13-IN-5 inhibits nsp13, affects ssDNA+/-ATPase (IC50: 50/55 μM), useful for COVID-19 research.</p>Fórmula:C28H30N4O4SCor e Forma:SolidPeso molecular:518.63Antitubercular agent-21
CAS:<p>Antitubercular agent-21 (Compound 15) has low toxicity, MIC of 0.4 μg/mL against M. tuberculosis, but is less effective on other microbes.</p>Fórmula:C15H22N6OSCor e Forma:SolidPeso molecular:334.44GNF6702
CAS:<p>GNF6702 inhibits kinetoplastid proteasome, treating leishmaniasis, Chagas, and trypanosomiasis in mice.</p>Fórmula:C22H16FN7O2Cor e Forma:SolidPeso molecular:429.41HCV-IN-37
CAS:<p>HCV-IN-37: potent HCV inhibitor, stable in rat plasma post-oral dose (15 mg/kg), blocks virus entry phase.</p>Fórmula:C31H35F2N5Cor e Forma:SolidPeso molecular:515.64SAMT-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:266.32M2 ion channel blocker
CAS:<p>M2 ion channel blocker ,Antiviral agent, is capable of inhibiting and blocking the activity of M2 ion channel.</p>Fórmula:C18H27N3O2Pureza:98%Cor e Forma:SolidPeso molecular:317.43Biclotymol
CAS:<p>Biclotymol is used in the study about infectious oropharyngeal diseases.</p>Fórmula:C21H26Cl2O2Pureza:98.56%Cor e Forma:SolidPeso molecular:381.34BA38017
CAS:<p>BA38017 is a potent assembly modulator of HBV core protein that inhibits the replication of HBV (EC50 = 0.20 μM) [1].</p>Fórmula:C15H11ClFNO3Cor e Forma:SolidPeso molecular:307.7NSC666715
CAS:<p>NSC666715 is the strand-displacement activity of DNA polymerase inhibitor.</p>Fórmula:C15H13Cl2N5O2S2Pureza:98%Cor e Forma:SolidPeso molecular:430.33(Rac)-ACT-451840
CAS:<p>(Rac)-ACT-451840 is an isomer of ACT-451840 exhibiting antimalarial activity against Plasmodium falciparum NF54.</p>Fórmula:C47H54N6O3Pureza:99.25%Cor e Forma:SolidPeso molecular:750.97Valnivudine
CAS:<p>Valnivudine, oral BCNA antiviral, targets herpes zoster; transforms into CF-1743 in body.</p>Fórmula:C27H35N3O6Pureza:98%Cor e Forma:SolidPeso molecular:497.58Quinoprazine
CAS:<p>Quinoprazine: inhibits Vaccinia virus (IC50=10μM), antimalarial vs Plasmodium berghei, reduces PrPSc, antiprion.</p>Fórmula:C25H26N4Cor e Forma:SolidPeso molecular:382.5Antitubercular agent-31
CAS:<p>Antitubercular agent-31 is an antitubercular agent that inhibits M. tuberculosisH37Rv (MIC: 0.03 μM) and also inhibits DprE1 (IC50: 1.1 μM).</p>Fórmula:C20H24F2N4O5S2Cor e Forma:SolidPeso molecular:502.56Silicon Phthalocyanine 4
CAS:<p>Silicon Phthalocyanine 4 is a drug with anti-cutaneous neoplasms activity.</p>Fórmula:C39H35N9O2Si2Cor e Forma:SolidPeso molecular:717.93Halofuginone hydrobromide
CAS:<p>Halofuginone specifically inhibits collagen type I and MMP-2 gene expression, which may result in the suppression of angiogenesis and tumor cell growth.</p>Fórmula:C16H17BrClN3O3·HBrPureza:97.01% - 99.73%Cor e Forma:SolidPeso molecular:495.59Influenza virus-IN-2
CAS:<p>Influenza virus-IN-2 (compound 19) has anti-influenza A virus activities that is a potent inhibitor of influenza virus with an CC 50 of 150.85 μM and EC 50 of 2</p>Fórmula:C17H17NO5Cor e Forma:SolidPeso molecular:315.32Fuberidazole
CAS:<p>Fuberidazole is an antifungal agent.</p>Fórmula:C11H8N2OPureza:98.95%Peso molecular:184.19Tuberculosis inhibitor 1
CAS:<p>Tuberculosis inhibitor 1 is a potent and non-cytotoxic inhibitor of trypanosoma brucei growth (EC50: 5 nM).</p>Fórmula:C34H37N5O3Pureza:98%Cor e Forma:SolidPeso molecular:563.69JNJ-9676
CAS:<p>JNJ-9676 is an orally active inhibitor of the coronavirus membrane protein, thereby blocking viral assembly and release.coronavirus and SARS-CoV.</p>Fórmula:C28H21F2N5O2Pureza:99.83%Cor e Forma:SoildPeso molecular:497.52,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid
CAS:<p>2,3-Dehydro-2-Deoxy-N-Acetylneuraminic Acid is a pan-sialidase (neuraminidase, NEU) inhibitor with inhibitory activity and against various influenza viruses.</p>Fórmula:C11H17NO8Cor e Forma:SolidPeso molecular:291.26α-Artemether
CAS:<p>alpha-Artemether is a Quinghaosu derivative with antifungal and antimalarial activity.</p>Fórmula:C16H26O5Pureza:98%Cor e Forma:SolidPeso molecular:298.372-Keto-D-galactose
CAS:<p>2-Keto-D-galactose inhibits DNA synthesis and inhibits the proliferation of in vitro grown Ehrlich ascites tumor cells.</p>Fórmula:C6H10O6Pureza:98%Cor e Forma:SolidPeso molecular:178.14Clevudine triphosphate
CAS:<p>Clevudine triphosphate is a TTP analog that is able to inhibit protein priming independently of the deoxynucleoside triphosphate substrate.</p>Fórmula:C10H16FN2O14P3Pureza:98%Cor e Forma:SolidPeso molecular:500.16NS2B/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:431.91KIN1400
CAS:<p>KIN1400 activates IRF3, boosts antiviral immunity, stimulates IFNbeta, and inhibits WNV, DV, and HCV.</p>Fórmula:C24H17F2N3O2SPureza:98%Cor e Forma:SolidPeso molecular:449.47SARS-CoV-2 Mpro-IN-9
CAS:<p>SARS-CoV-2 Mpro-IN-9 (compound c7), a nonpeptidic, noncovalent inhibitor of SARS-CoV-2 main protease (Mpro), exhibits potent inhibitory action (IC50 = 0.085 μM</p>Fórmula:C20H14N2O4Pureza:99.74% - 99.89%Cor e Forma:SolidPeso molecular:346.34Linogliride
CAS:Linogliride: a guanidine derivative, inhibits insulin release, and enhances glucose tolerance by blocking ATP-sensitive K+ channels in pancreatic beta cells.Fórmula:C16H22N4OPureza:98%Cor e Forma:SolidPeso molecular:286.37Antifungal agent 65
CAS:<p>Compound 5d (Antifungal Agent 65) exhibits potent fungicidal activity against Fusarium oxysporum f.sp.</p>Fórmula:C29H29N3O2S2Cor e Forma:SolidPeso molecular:515.69RR-11a analog
CAS:<p>RR-11a (aza-peptide) inhibits asparaginyl endopeptidase: IC50 - 4.5 nM (T. Vaginalis, I. ricinus), 31 nM (S. mansoni).</p>Fórmula:C22H29N5O8Pureza:98.80%Cor e Forma:SolidPeso molecular:491.49Erythromycin Gluceptate
CAS:<p>Erythromycin Gluceptate is an inhibitor of protein translation and mammalian mRNA splicing. It inhibits growth of gram negative and gram positiove bacteria.</p>Fórmula:C44H81NO21Cor e Forma:SolidPeso molecular:960.11Thiambutosine
CAS:<p>Thiambutosine exhibits inhibitory activity against Mycobacterium leprae and mushroom tyrosinase, making it suitable for infection studies.</p>Fórmula:C19H25N3OSPureza:99.95%Cor e Forma:SolidPeso molecular:343.49HBV-IN-22
CAS:<p>HBV-IN-22 (Compound LC5f) is an HBV DNA replication inhibitor that acts on both wild-type HBV (IC50: 0.71 μM) and drug-resistant HBV (IC50: 0.84 μM).</p>Fórmula:C26H29N3O2S2Cor e Forma:SolidPeso molecular:479.66PXYC2
CAS:<p>PXYC2 is an RpsA-CTD antagonist; Kd: 6.35 μM for RpsA-CTD, 5.11 μM for RpsA-CTD Δ438A; vital in trans-translation.</p>Fórmula:C7H6N4O3SCor e Forma:SolidPeso molecular:226.21Antileishmanial agent-12
CAS:<p>Compound 5a: potent anti-leishmanial, IC50 - L. brazilensis 14.9μM, L. infantum 21.3μM; antiprotozoal against T. cruzi 9.3μM.</p>Fórmula:C25H21N3O4Cor e Forma:SolidPeso molecular:427.45Anti-parasitic agent 3
CAS:<p>Anti-parasitic agent 3 is an anti-parasitic agent active against drug-resistant parasites.</p>Fórmula:C21H22FN5O3Pureza:98%Cor e Forma:SolidPeso molecular:411.43Benzylurea
CAS:<p>Benzylurea (AI3-61350) competitively inhibits dehydrogenase/cytokinin oxidase.</p>Fórmula:C8H10N2OPureza:98%Cor e Forma:SolidPeso molecular:150.18HIV-1 inhibitor-43
CAS:<p>HIV-1 Inhibitor-43 suppresses HIV-1, with EC50: 21.3 nM (Y188L), 6.2 nM (K103N-Y181C), <0.7 nM (K103N/Y181C), and lowers HIV RNA/p24 protein.</p>Fórmula:C24H21ClN2O4SCor e Forma:SolidPeso molecular:468.95Antitubercular agent-36
CAS:<p>Antitubercular agent-36 inhibits Mycobacterium tuberculosis with MIC90 of 1.25 μg/mL, used in TB research.</p>Fórmula:C18H17N3O3Cor e Forma:SolidPeso molecular:323.35JFN05510
CAS:<p>Compound: 3'-O-tert-BDMS-5'-O-DMT-N2-IBG 2'-CE phosphoramidite; has anticancer properties and activates enzymes.</p>Fórmula:C50H68N7O9PSiCor e Forma:SolidPeso molecular:970.18BO3482
CAS:<p>BO3482 is an antimicrobial compound and can inhibit the growth of methicillin-resistant Staphylococci (MIC90: 6.25 mg/mL).</p>Fórmula:C14H20N2NaO5S2Pureza:98%Cor e Forma:SolidPeso molecular:383.43
