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 2957 produtos de "Antibacteriano"
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MMV676584
CAS:<p>MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .</p>Fórmula:C12H8ClFN2OS2Cor e Forma:SolidPeso molecular:314.792-Hydroxydocosanoic acid
CAS:<p>2-Hydroxydocosanoic acid exhibits antioxidant, cholinesterase inhibitory, and antimicrobial properties [1].</p>Fórmula:C22H44O3Cor e Forma:SolidPeso molecular:356.58Antitubercular agent-17
CAS:<p>Compound 8a: Antitubercular with MIC of 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective effects.</p>Fórmula:C14H12BrN5OCor e Forma:SolidPeso molecular:346.18Anserinone B
CAS:<p>Anserinone B: Antifungal, antibacterial; inhibits S.fimicola (50%), A. furfuraceus (37%); cytotoxic to human tumor cells (GI50=4.4 µg/mL).</p>Fórmula:C11H14O4Cor e Forma:SolidPeso molecular:210.23ANT431
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:285.3GA-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:619.76Phosphoglycolohydroxamic acid
CAS:<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Fórmula:C2H6NO6PCor e Forma:SolidPeso molecular:171.05PXYC13
CAS:<p>PXYC13 inhibits Mtb RpsA essential for trans-translation with Kd of 7.61 μM; less effective on RpsA-CTD Δ438A (Kd 8.50 μM).</p>Fórmula:C15H15N5O2SCor e Forma:SolidPeso molecular:329.38Antituberculosis 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:323.34W13
CAS:<p>W13 is a potent inhibitor of MsbA and is an ATPase stimulator (EC50: 5.5 μM).</p>Fórmula:C30H34N4O3Cor e Forma:SolidPeso molecular:498.62Urease-IN-5
<p>Urease-IN-5: urease inhibitor, IC50 1.473 µM, low cytotoxicity, IC50 17.78 µg/mL on P. vulgaris.</p>Fórmula:C16H20N2O3SCor e Forma:SolidPeso molecular:320.41PXYD3
CAS:<p>PXYD3 inhibits RpsA-CTD (Kd: 5.66 μM) & RpsA-CTD Δ438A (Kd: 6.91 μM) crucial in Mtb translocation.</p>Fórmula:C25H21NO5Cor e Forma:SolidPeso molecular:415.44FR-182024
CAS:<p>FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.</p>Fórmula:C18H16N4O4S3Cor e Forma:SolidPeso molecular:448.54Ebselen oxide
CAS:<p>Ebselen oxide (EB-2) is a HER2 inhibitor with antibacterial and antifungal activity and has shown cytoprotective effects against HN2 in vitro.</p>Fórmula:C13H9NO2SePureza:98%Cor e Forma:SolidPeso molecular:290.18Antitubercular agent 34
CAS:<p>Compound 42g: potent antitubercular, MIC 90 of 1.25 µg/mL, resists liver metabolism.</p>Fórmula:C19H14N4O2SCor e Forma:SolidPeso molecular:362.41Penamecillin
CAS:<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Fórmula:C19H22N2O6SCor e Forma:SolidPeso molecular:406.45Marasmic acid
CAS:<p>Marasmic acid is a bioactive antifungal.</p>Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.3Mtb-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:393.56Antibacterial agent 74
CAS:<p>Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].</p>Fórmula:C16H20N2O3Cor e Forma:SolidPeso molecular:288.34Mtb-cyt-bd oxidase-IN-6
CAS:<p>Mtb-cyt-bd oxidase-IN-6, a potent inhibitor of Mycobacterium tuberculosis (Mtb) cytochrome bd (cyt-bd) oxidase (MtbCyt-bd Oxidase), exhibits an inhibitory</p>Fórmula:C20H27NOCor e Forma:SolidPeso molecular:297.4314α-Demethylase/DNA Gyrase-IN-2
CAS:<p>14α-Demethylase/DNA Gyrase-IN-2 (Compound 6a) is a potent inhibitor of 14α-Demethylase/DNA Gyrase with antibacterial activity.</p>Fórmula:C24H22N4O4Cor e Forma:SolidPeso molecular:430.46Metallo-β-lactamase-IN-3
CAS:<p>Metallo-β-lactamase-IN-3 (compound 35) is a potent metallo-β-lactamases (MBL) inhibitor that has the potential to restore the activity of current β-lactam</p>Fórmula:C10H11NO3SCor e Forma:SolidPeso molecular:225.26Antitubercular agent-18
CAS:<p>Antitubercular agent-18 (9a) MIC: 2 μg/ml for H37Rv, Spec 192, 210; 128 μg/ml for Spec 800. Selective antimycobacterial.</p>Fórmula:C14H12BrN5OCor e Forma:SolidPeso molecular:346.18Ceftobiprole 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:712.64PknB-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:390.52DNA Gyrase-IN-4
CAS:<p>DNA Gyrase-IN-4 inhibits DNA cyclooxygenase (IC50: 0.13 μM) and is effective against Salmonella and E. coli.</p>Fórmula:C22H15Cl2NO4SCor e Forma:SolidPeso molecular:460.334-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:384.28PC58538
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:375.46Salifluor
CAS:<p>Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.</p>Fórmula:C22H24F3NO3Cor e Forma:SolidPeso molecular:407.43PqsR/LasR-IN-3
CAS:<p>PqsR/LasR-IN-3 (Compound 7a) inhibits hERG with the IC 50 of 109.01 μM which is also a PqsR and LasR systems inhibitor in P. aeruginosa [1].</p>Fórmula:C14H17NO5SCor e Forma:SolidPeso molecular:311.35Antibacterial 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:417.39Antibacterial agent 19
CAS:<p>Antibacterial agent 19 targets K. pneumoniae and multi-resistant S. aureus with MICs: 0.022 and 0.045 mg/mL.</p>Fórmula:C16H16F2N2O4Cor e Forma:SolidPeso molecular:338.31Anti-inflammatory agent 14
CAS:<p>Anti-inflammatory agent 14 (compound 28) has a MIC 50 of 2 μM for Mtb H37Rv. Anti-inflammatory agent 14 is also an anti-inflammatory agent [1].</p>Fórmula:C16H16N2O2SCor e Forma:SolidPeso molecular:300.38Metallo-β-lactamase-IN-5
CAS:<p>Metallo-β-lactamase-IN-5 (compound 5c) is a powerful inhibitor of metallo-β-lactamases (MBLs).</p>Fórmula:C19H16N4O3Cor e Forma:SolidPeso molecular:348.36Mtb-cyt-bd oxidase-IN-7
<p>Mtb-cyt-bd oxidase-IN-7 inhibits Cyt-bd with 4.17 μM affinity and has anti-tuberculosis properties.</p>Fórmula:C18H14F3NO2Cor e Forma:SolidPeso molecular:333.3Antifungal agent 37
CAS:<p>Antifungal agent 37 is a heterocyclic disulfide that exhibits antifungal activity [1].</p>Fórmula:C7H10N2S2Cor e Forma:SolidPeso molecular:186.3Topoisomerase IV inhibitor 2
CAS:<p>Compound 5d, a potent TOPO IV inhibitor (IC50: 0.35 μM), also inhibits DNA gyrase (IC50: 0.55 μM) and has antibacterial activity.</p>Fórmula:C33H30FN7O6SPureza:98%Cor e Forma:SolidPeso molecular:671.7B 669
CAS:<p>B 669 has antibacterial activity.</p>Fórmula:C30H28N4Cor e Forma:SolidPeso molecular:444.57Anti-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:270.67Thiamphenicol 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:449.73Caspofungin
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:1093.31Antibacterial agent 65
CAS:<p>Antibacterial agent 65 is a potential antimicrobial agent and antioxidant agent.</p>Fórmula:C17H16O3Cor e Forma:SolidPeso molecular:268.31Antimicrobial agent-6
<p>Antimicrobial agent-6: MIC 4-8 μg/mL for gram+ & gram- bacteria, anti-inflammatory.</p>Fórmula:C40H64N16Cor e Forma:SolidPeso molecular:769.04c-di-AMP
CAS:<p>c-di-AMP (Cyclic diadenylate) is a STING agonist. It binds to the transmembrane protein STING thereby activating the TBK3-IRF3 signaling pathway.</p>Fórmula:C20H24N10O12P2Pureza:98%Cor e Forma:SolidPeso molecular:658.41Metallo-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:326.76GlcN-6-P Synthase-IN-1
CAS:<p>'GlcN-6-P Synthase-IN-1, IC50 3.47 μM, inhibits GlcN-6-P synthase & CYP3A4. Has antimicrobial activity and CNS penetration.'</p>Fórmula:C20H21N7SCor e Forma:SolidPeso molecular:391.49Antibacterial 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:606.07SMR000071098
CAS:<p>SMR000071098 is an inhibitor of Fe-S cluster-dependent aconitase. SMR000071098 interacts with Suf proteins to inhibit iron-sulfur (Fe-S) cluster assembly.</p>Fórmula:C17H12N2O2Cor e Forma:SolidPeso molecular:276.29Anti-infective agent 1
CAS:<p>Compound 3a: potent, selective antiprotozoal/antimycobacterial. IC50: P. falciparum 10.95 μM, T. brucei 0.06 μM. MIC against M. smegmatis: 8 μg/mL.</p>Fórmula:C16H10O2Cor e Forma:SolidPeso molecular:234.25Antiproliferative agent-17
CAS:<p>Antiproliferative Agent-17 exhibits both antimicrobial properties against Gram-positive bacteria and anticancer activity [1].</p>Fórmula:C26H28N2OSCor e Forma:SolidPeso molecular:416.58Topoisomerase IV inhibitor 1
CAS:<p>Compound 7d: Inhibits TOPO IV (IC50: 0.23 μM), DNA gyrase (IC50: 0.43 μM), antibacterial against S. aureus (MIC: 0.972 μM), E. coli (MIC: 0.608 μM).</p>Fórmula:C34H32FN7O6SPureza:98%Cor e Forma:SolidPeso molecular:685.72ACP1b
CAS:<p>ACP1b is an activator of ClpP protease.</p>Fórmula:C18H18ClF3N2O3S2Cor e Forma:SolidPeso molecular:466.93TBI-166
CAS:<p>TBI-166, an oral riminophenazine, treats tuberculosis with fewer side effects than Clofazimine.</p>Fórmula:C32H30F3N5O3Cor e Forma:SolidPeso molecular:589.61OYYF-175
CAS:<p>OYYF-175: potent antimicrobial antifolate; targets multi-drug resistant Gram-Negative bacteria; DHFR inhibitor with 2.36 nM IC50 against E. coli.</p>Fórmula:C17H14FN5Cor e Forma:SolidPeso molecular:307.33Polyketide synthase 13-IN-2
CAS:<p>Comp 42 is a potent PKS13 inhibitor in M. tuberculosis with MIC of 0.25 μg/mL.</p>Fórmula:C22H21NO5Cor e Forma:SolidPeso molecular:379.41SARS-CoV-2 3CLpro-IN-3
CAS:<p>SARS-CoV-2 3CLpro-IN-3 is a SARS CoV-2 3CLpro inhibitor that exhibits antiviral, antibacterial, and antifungal effects.</p>Fórmula:C23H21BrN6O2SCor e Forma:SolidPeso molecular:525.42CBR-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:349.42MurA-IN-2
CAS:<p>MurA-IN-2: potent MurA inhibitor, IC50 of 39μM, chloroacetamide with aliphatic amine; has antibacterial properties.</p>Fórmula:C12H20ClNOCor e Forma:SolidPeso molecular:229.75Arasertaconazole
CAS:<p>Arasertaconazole, a sterol-14-alpha demethylation inhibitor, is used potentially for the treatment of vulvovaginal candcanidiasis.</p>Fórmula:C20H15Cl3N2OSCor e Forma:SolidPeso molecular:437.77TMV-IN-1
CAS:<p>TMV-IN-1: a chalcone inhibits TMV with EC50s of 70.7 and 60.8 μg/mL, applicable in infection and tumor studies.</p>Fórmula:C28H26O4Cor e Forma:SolidPeso molecular:426.5DNA Gyrase-IN-5
CAS:<p>DNA Gyrase-IN-5 is a potent inhibitor of DNA gyrase (IC50: 0.10 μM) and has an antibacterial effect on both wild-type and drug-resistant strains.</p>Fórmula:C25H15BrClN5Cor e Forma:SolidPeso molecular:500.78BTZ-N3
CAS:<p>BTZ-N3 is an effective and selective anti-tuberculosis drug candidate.</p>Fórmula:C17H16F3N5O3SCor e Forma:SolidPeso molecular:427.4Salazopyridazine
CAS:<p>Salazopyridazine is an antibacterial agent that inhibits ulcerative colitis. salazopyridazine can be used in the study of rheumatic diseases.</p>Fórmula:C18H15N5O6SCor e Forma:SolidPeso molecular:429.41P516-0475
CAS:<p>P516-0475, a novel inducer, enhances Streptococcus quorum sensing by blocking PepO, stabilizing SHP pheromones.</p>Fórmula:C15H17N5O3Cor e Forma:SolidPeso molecular:315.33Methdilazine Hydrochloride
CAS:<p>Methdilazine Hydrochloride (Bristaline) is a histamine H1 receptor antagonist for dermatologic conditions and relief of itching by allergies or rhinitis.</p>Fórmula:C18H21ClN2SCor e Forma:Light-Tan Crystalline Powder 4 8-6 (Ntp 1992)Peso molecular:332.89Antibacterial agent 121
CAS:<p>Antibacterial agent 121 exhibits anti-TB and anti-inflammatory properties.</p>Fórmula:C18H22N2O3SCor e Forma:SolidPeso molecular:346.44Cefepime chloride
CAS:<p>Cefepime chloride, a broad-spectrum cephalosporin, combats Gram-positive/negative bacteria and can induce neurotoxicity.</p>Fórmula:C19H25ClN6O5S2Cor e Forma:SolidPeso molecular:517.02BPH-1086
CAS:<p>BPH-1086 inhibits IspH, which with RPS1 binds mRNA or integrates into bacterial ribosomes.</p>Fórmula:C4H8O7P2Cor e Forma:SolidPeso molecular:230.05Antibacterial agent 97
CAS:<p>Antibacterial agent 97 is potent; MIC: 16 μg/mL for E. coli and S. aureus.</p>Fórmula:C19H23N5SCor e Forma:SolidPeso molecular:353.48Type II topoisomerase inhibitor 1
CAS:<p>Potent E. coli DNA gyrase inhibitor (IC50: 1.7 nM), targets Asp73; weak topoisomerase IV inhibitor (IC50: 0.98 μM).</p>Fórmula:C18H15N3O4Cor e Forma:SolidPeso molecular:337.33MurA-IN-3
CAS:<p>MurA-IN-3, a reversible pyrrolidinedione-based MurA inhibitor, exhibits an IC50 of 4.5 μM against MurA and demonstrates antibacterial activity [1].</p>Fórmula:C27H23ClN2O5SCor e Forma:SolidPeso molecular:523Antitubercular agent-26
CAS:<p>Compound 32: oral antitubercular, acts on M. tuberculosis, IC50 ~0.50μM, stable, low cardiotoxicity, non-genotoxic.</p>Fórmula:C22H23N5O3S2Cor e Forma:SolidPeso molecular:469.58Antitubercular agent-14
CAS:<p>Antitubercular agent-14 (Compound 1) shows antitubercular activity. The MIC value of Antitubercular agent-14 against M. tuberculosis is 0.3 μg/mL [1].</p>Fórmula:C20H27ClN2Cor e Forma:SolidPeso molecular:330.89Anticandidal agent-1
CAS:<p>Compound C2 is a broad-spectrum anticandidal, blocking biofilm and filament growth with MIC50 of 13.51μg/mL (C. glabrata) and 8.65μg/mL (C. albicans).</p>Fórmula:C19H22O5Cor e Forma:SolidPeso molecular:330.38Berteroin
CAS:<p>Berteroin, found in cruciferous veggies like rucola and mustard, may act as an antioxidant, reducing inflammation and androgen receptors in cancer.</p>Fórmula:C7H13NS2Cor e Forma:SolidPeso molecular:175.31ATD-3169
CAS:<p>ATD-3169 is a ROS generator with antibacterial activity.</p>Fórmula:C15H14O3Pureza:98%Cor e Forma:SolidPeso molecular:242.27Antimicrobial agent-3
CAS:<p>Antimicrobial agent-3 (Compound U10) is an antimicrobial agent that is used against bacterial, fungal, and tubercular infections [1].</p>Fórmula:C14H11N3OSCor e Forma:SolidPeso molecular:269.32Metallo-β-lactamase-IN-4
CAS:<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent inhibitor of metallo-β-lactamases (MBL) with IC 50 values of 0.5 μM, 2.1 μM, and 3.3 μM for VIM-1, NDM-1 and</p>Fórmula:C10H14N4O3S2Cor e Forma:SolidPeso molecular:302.37Antibacterial agent 122
CAS:<p>Thiourea derivative 122 is a low-toxicity antibacterial used in tuberculosis research with anti-mycobacterial properties.</p>Fórmula:C15H14N2O3SCor e Forma:SolidPeso molecular:302.35Cadrofloxacin
CAS:<p>Cadrofloxacin (Caderofloxacin, CS-940) is a novel fluoroquinolone antimicrobial agent.</p>Fórmula:C19H20F3N3O4Cor e Forma:SolidPeso molecular:411.38C16-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:672.36Metallo-β-lactamase-IN-2
CAS:<p>Metallo-β-lactamase-IN-4 (compound 40) is a potent metallo-β-lactamases (MBL) inhibitor with IC 50 values of 0.1 μM for VIM-1, 1.3 μM for NDM-1 and 5.0 μM for</p>Fórmula:C9H9Cl2NOSCor e Forma:SolidPeso molecular:250.14Metallo-β-lactamase-IN-6
CAS:<p>Metallo-β-lactamase-IN-6 is a highly effective inhibitor of VIM-Type metallo-β-lactamase, demonstrating IC 50 values of 0.56 μM, 29.50 μM, and 5.78 μM for VIM-2</p>Fórmula:C10H9N3O2Cor e Forma:SolidPeso molecular:203.2CL-55
CAS:<p>CL-55 is a novel inhibitor of T3SS.</p>Fórmula:C19H17F2N3O4SCor e Forma:SolidPeso molecular:421.42Mt KARI-IN-2
CAS:<p>Mt KARI-IN-2, an inhibitor for Mtb KARI (Ki: 2.02 μM) and Mtb H37Rv (MIC: 0.78 μM), has low cytotoxicity (HEK IC50: >86 μg/mL).</p>Fórmula:C14H11N5O4S2Cor e Forma:SolidPeso molecular:377.4LpxC-IN-9
CAS:<p>LpxC-IN-9 (compound 19) is a potent inhibitor of LpxC and exhibits antibacterial and hypotensive activity.</p>Fórmula:C23H25N5O3SCor e Forma:SolidPeso molecular:451.54Antibacterial agent 104
CAS:<p>Antibacterial agent 104 is an effective antibacterial agent with significant antibacterial effects in vitro and good anti-MRSA effects in vivo.</p>Fórmula:C28H39NO4SCor e Forma:SolidPeso molecular:485.68Antibacterial agent 105
CAS:<p>Compound 17, a phenanthrolinic quinolone, fights M. tuberculosis (MIC 90: 2.64 μM) and various bacteria (MIC 90: 0.70-44.70 μM).</p>Fórmula:C14H9N3O5Cor e Forma:SolidPeso molecular:299.24Antibacterial agent 95
CAS:<p>Antibacterial 95, a quinoline-derived antituberculotic, shows 0.3 μM MIC against Mycobacterium tuberculosis H37Rv and inhibits its growth in macrophages.</p>Fórmula:C19H16ClNO3Cor e Forma:SolidPeso molecular:341.79Metallo-β-lactamase-IN-9
CAS:<p>Metallo-β-lactamase-IN-9 (Compound 23) serves as a broad-spectrum inhibitor of metallo-beta-lactamases (MBL), exhibiting inhibition constants (IC50) of 35 nM</p>Fórmula:C13H12N6O3SCor e Forma:SolidPeso molecular:332.34FabG1-IN-1
CAS:<p>FabG1-IN-1 (Compound 29) is a potent inhibitor of MabA (FabG1) (IC50: 38 μM).</p>Fórmula:C14H8Cl2INO3Cor e Forma:SolidPeso molecular:436.03VIM-2-IN-1
CAS:<p>VIM-2-IN-1 (compound 1dj) is a β-lactamase inhibitor with antibacterial activity. IC50: 48 μM) and New Delhi Metal (NDM-1) (IC50: 231 μM).</p>Fórmula:C12H13IN4O4SCor e Forma:SolidPeso molecular:436.23Antimycobacterial agent-1
CAS:<p>Compound 33: antimycobacterial, MIC 1 μg/ml vs M. tuberculosis H37Ra, low toxicity (IC50 143.2 μg/ml in Vero cells).</p>Fórmula:C18H12N4O5SCor e Forma:SolidPeso molecular:396.38RmlA-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:386.42Antistaphylococcal agent 2
CAS:<p>Antistaphylococcal agent 2 is an anti-staphylococcal therapeutic agent.</p>Fórmula:C23H21N5O5Cor e Forma:SolidPeso molecular:447.44Sch 25393
CAS:Sch 25393 is an antibacterial agent in vitro.Fórmula:C12H14F3NO4SPureza:98%Cor e Forma:SolidPeso molecular:325.3Undecylprodigiosin
CAS:<p>Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.</p>Fórmula:C25H35N3OCor e Forma:SolidPeso molecular:393.56Antitubercular agent-27
CAS:<p>Antitubercular agent-27: IC50=3.2 μM, MIC=7.8 μM, IC90=7.0 μM; effective against resistant Mycobacterium tuberculosis, low toxicity.</p>Fórmula:C14H8BrN3O3Cor e Forma:SolidPeso molecular:346.14Norstictic acid
CAS:<p>Norstictic acid: a potent, selective transcription regulator with anticancer, antioxidant, and antimicrobial properties.</p>Fórmula:C18H12O9Cor e Forma:SolidPeso molecular:372.28MtTMPK-IN-6
CAS:<p>MtTMPK-IN-6 inhibits M. tuberculosis thymidylate kinase with IC50 of 29 μM, promising for TB research.</p>Fórmula:C23H25N3O3Cor e Forma:SolidPeso molecular:391.46
