Antibacteriano
Os inibidores antibacterianos são compostos que visam as células bacterianas, inibindo seu crescimento ou matando-as diretamente. Esses inibidores são essenciais no desenvolvimento de tratamentos para infecções bacterianas e são amplamente utilizados na pesquisa para estudar a fisiologia bacteriana, os mecanismos de resistência e a eficácia de novos agentes antibacterianos. Na CymitQuimica, oferecemos uma variedade de inibidores antibacterianos para apoiar sua pesquisa em microbiologia, doenças infecciosas e desenvolvimento de medicamentos.
Foram encontrados 3365 produtos de "Antibacteriano"
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Urease-IN-16
CAS:Urease-IN-16, with an IC50 of 132 µmol/L, is a urease inhibitor that coordinates with nickel atoms through the oxygen atoms of either carbonyl or boronic acid groups. This compound holds significant potential as an additive in the development of efficient fertilizers and medical applications.Fórmula:C14H17BN2O4SCor e Forma:SolidPeso molecular:320.17Mycobacterium Tuberculosis-IN-6
CAS:Mycobacterium Tuberculosis-IN-6 (compound b1) is an inhibitor of the enoyl reductase InhA from Mycobacterium tuberculosis, with an IC50 value of 7.74 μM. It is useful in antibacterial research.Fórmula:C19H20FNOCor e Forma:SolidPeso molecular:297.367Ibafloxacine
CAS:Ibafloxacine (R835) is a fluoroquinolone antibiotic that is used exclusively in veterinary applications and shows zero good bacteriostatic effect againstFórmula:C15H14FNO3Pureza:97.67%Cor e Forma:SolidPeso molecular:275.27LpxA-IN-1
CAS:LpxA-IN-1, a novel UDP-N-acetylglucosamine acyltransferase (LpxA) inhibitor exhibiting potent activity (IC 50 2 nM), effectively targets Pseudomonas aeruginosaFórmula:C21H11D7F3N5O3Cor e Forma:SolidPeso molecular:452.44Antimicrobial agent-29
CAS:Antimicrobial Agent-29 (Compound C35) influences the interaction between human hemoglobin and the Staphylococcus aureus IsdB hemophore. This compound facilitates the identification of IsdB:Hb PPI inhibitors [1].Fórmula:C19H14N4O4SCor e Forma:SolidPeso molecular:394.4Fostriecin (free base)
CAS:Fostriecin inhibits PP2A/PP4 (IC50s = 3.2/3 nM), weakly affects topoisomerase II/PP1 (IC50s = 40/131 μM), doesn't inhibit PP2B, and may modify epigenetics.Fórmula:C19H27O9PCor e Forma:SolidPeso molecular:430.39MtTMPK-IN-9
MtTMPK-IN-9 moderately inhibits MtbTMPK (IC50: 48 μM), has submicromolar Mycobacterium activity, and is non-toxic, aiding tuberculosis research.Fórmula:C25H26N6O7Cor e Forma:SolidPeso molecular:522.51Meclocycline
CAS:Meclocycline: a tetracycline antibiotic, inhibits LDH, reduces cell toxicity from mutant huntingtin, doesn't change protein levels in PC12 cells.Fórmula:C22H21ClN2O8Cor e Forma:SolidPeso molecular:476.86Antibacterial agent 81
CAS:Antibacterial agent 81 blocks DNA transcription, targets S. aureus (MIC 12.5μM) & M. smegmatis (MIC 7.8μM). Used in infection research.Fórmula:C33H28N2O8Cor e Forma:SolidPeso molecular:580.58Anti-MRSA agent 6
Anti-MRSA agent 6 (compound 3q6) is a potent anti-methicillin-resistant Staphylococcus aureus (anti-MRSA) agent with low cytoxicity for MCF-7, A549 cells [1].Fórmula:C16H11F2N3Cor e Forma:SolidPeso molecular:283.28Metallo-β-lactamase-IN-14
CAS:Metallo-β-lactamase-IN-14 (Compound 17e) serves as an inhibitor of Metallo-β-Lactamase, displaying inhibitory activity against VIM-1 and VIM-2. This compound also exhibits antibacterial effects on Gram-negative (GN) bacteria and P. aeruginosa [1].Fórmula:C20H22N8O2S2Cor e Forma:SolidPeso molecular:470.57Deprodone
CAS:Deprodone is an active compound that inhibits key processes such as bacterial cell wall synthesis by interacting with hydrolase and transferase proteins of methicillin-resistant Staphylococcus aureus (MRSA). It is applied in the research of MRSA infections, inflammatory skin diseases, intestinal disorders, and fatty acid metabolism disorders.Fórmula:C21H28O4Cor e Forma:SolidPeso molecular:344.44Cilastatin ammonium salt
CAS:Cilastatin ammonium salt is an antibiotic that is particularly effective against Gram-positive cocci, with a half-life of 3-4 hours.Fórmula:C16H29N3O5SCor e Forma:SolidPeso molecular:375.48DNA Gyrase-IN-1
DNA Gyrase-IN-1: potent, selective promoter inhibitor. IC50: 2.6 μM, inhibits Mtb, MIC: 0.49 μM. Useful for tuberculosis research.Fórmula:C24H24FN7O6Cor e Forma:SolidPeso molecular:525.49GT-055
GT-055 (LCB18-055) is a novel inhibitor of broad-spectrum β-lactamase.Fórmula:C13H20F3N5O8SCor e Forma:SolidPeso molecular:463.39Antibacterial agent 172
CAS:Antibacterial Agent 172 (Compound 6a), a Clostridioides difficile (Cd) SpoVD inhibitor with an IC50 value of 89 nM, effectively inhibits the sporulation of Clostridioides difficile. It is useful for research on bacterial infections [1].Fórmula:C21H21N9O5S2Cor e Forma:SolidPeso molecular:543.58Pyrromycin
CAS:Pyrromycin is a monosaccharide anthracycline which can be used to inhibit cellular RNA synthesis.Fórmula:C30H35NO11Cor e Forma:SolidPeso molecular:585.60Gougerotin
CAS:Gougerotin is an inhibitor of protein synthesis.Fórmula:C16H25N7O8Cor e Forma:SolidPeso molecular:443.41844-TFM
844-TFM, a NBTI DNA gyrase blocker, IC50: 1.5 μM, kills Mycobacterium abscessus.Fórmula:C24H25F3N4O2Cor e Forma:SolidPeso molecular:458.48OPC-167832
CAS:OPC-167832: oral dprE1 inhibitor, IC50 0.258 μM, anti-tuberculosis, for Mycobacterium tuberculosis research.Fórmula:C21H20ClF3N2O4Cor e Forma:SolidPeso molecular:456.84
