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 2949 produtos de "Antibacteriano"
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AHR-9294
CAS:<p>AHR-9294 is a novel inhibitor of H, K-ATPase. It also antagonizes gastric HCl secretion in vivo.</p>Fórmula:C22H24N2O3Cor e Forma:SolidPeso molecular:364.44Closthioamide
CAS:<p>Closthioamide is a potent inhibitor of bacterial DNA gyrase and highly active against MRSA, Ec, VRE, and Mv (MICs: 0.58 μM, 9.00 μM, 0.58 μM and 72.03 μM).</p>Fórmula:C29H38N6O2S6Pureza:98%Cor e Forma:SolidPeso molecular:695.04Antiproliferative 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:685.72Bederocin
CAS:<p>Bederocin (REP8839), a METS inhibitor, has strong activity against S. aureus, S. pyogenes, and Gram-positive bacteria.</p>Fórmula:C20H21BrFN3OSPureza:98%Cor e Forma:SolidPeso molecular:450.37ACP1b
CAS:<p>ACP1b is an activator of ClpP protease.</p>Fórmula:C18H18ClF3N2O3S2Cor e Forma:SolidPeso molecular:466.9310-Thiofolic acid
CAS:<p>10-Thiofolic acid is a potential antibacterial, antineoplastic.</p>Fórmula:C19H18N6O6SCor e Forma:SolidPeso molecular:458.45TBI-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:307.33BPH-651
CAS:<p>BPH-651 is a CrtM inhibitor.</p>Fórmula:C19H21NOCor e Forma:SolidPeso molecular:279.38Polyketide 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:349.42Neoarsphenamine
CAS:<p>Neoarsphenamine is an antisyphilitic still used for infections occasionally.</p>Fórmula:C13H14As2N2NaO4SPureza:98%Cor e Forma:SolidPeso molecular:467.16DuP 105
CAS:<p>DuP 105 is an oral oxazolidinone, a novel synthetic antimicrobial compound effective against gram-positive bacteria.</p>Fórmula:C13H16N2O4SPureza:99.82%Cor e Forma:SolidPeso molecular:296.34MurA-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:229.75CAY10784
CAS:<p>CAY10784(STAT3-IN-17) is a STAT3 inhibitor with antiproliferative and antitumor activities. CAY10784 showed antibacterial activity against Clostridium difficile</p>Fórmula:C11H6F3N3O3SPureza:99.74%Cor e Forma:SolidPeso molecular:317.24Lascufloxacin HCl
CAS:<p>Lascufloxacin (KRP-AM-1977) is a strong antibiotic, most effective against gram-positive bacteria, with limited cross-resistance.</p>Fórmula:C21H25ClF3N3O4Pureza:98%Cor e Forma:SolidPeso molecular:475.89Arasertaconazole
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:332.89BoNT-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:400.43Antibacterial agent 121
CAS:<p>Antibacterial agent 121 exhibits anti-TB and anti-inflammatory properties.</p>Fórmula:C18H22N2O3SCor e Forma:SolidPeso molecular:346.44NSC-79887
CAS:<p>NSC-79887 is a nucleoside hydrolase (NH) inhibitor.</p>Fórmula:C14H16ClNO4Pureza:98%Cor e Forma:SolidPeso molecular:297.73Cefepime 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:337.33C562-1101
CAS:<p>C562-1101 is a novel potent botulinum neurotoxin serotype E (BoNT/E) inhibitor.</p>Fórmula:C22H27N3O5SPureza:98%Cor e Forma:SolidPeso molecular:445.53Deoxypheganomycin D
CAS:<p>Deoxypheganomycin D is a specific mycobacteria inhibitor.</p>Fórmula:C30H47N9O11Pureza:98%Cor e Forma:SolidPeso molecular:709.75MurA-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:330.38Ceftibuten
CAS:<p>Ceftibuten is a third-generation cephalosporin antibiotic.</p>Fórmula:C15H14N4O6S2Pureza:98%Cor e Forma:SolidPeso molecular:410.42Tuberculosis 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:563.69Berteroin
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:242.27Valnivudine
CAS:<p>Valnivudine, oral BCNA antiviral, targets herpes zoster; transforms into CF-1743 in body.</p>Fórmula:C27H35N3O6Pureza:98%Cor e Forma:SolidPeso molecular:497.58Anti-inflammatory agent 11
CAS:<p>Potent anti-inflammatory compound 16 combats tuberculosis, inhibiting Mtb H37Rv and M299 (MICs: 1.3, 6.9 μM) and reduces NO, TNF-α, IL-1β production.</p>Fórmula:C14H14N4OSCor e Forma:SolidPeso molecular:286.35Antimycobacterial agent-3
CAS:<p>Antimycobacterial agent-3: low toxicity, fights MTB H37Rv and drug-resistant strains (MIC 0.029-0.110 μM).</p>Fórmula:C21H15F6N5O4SCor e Forma:SolidPeso molecular:547.43Antimicrobial 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:269.32Biclotymol
CAS:<p>Biclotymol is used in the study about infectious oropharyngeal diseases.</p>Fórmula:C21H26Cl2O2Pureza:98.56%Cor e Forma:SolidPeso molecular:381.34Antibacterial agent 115
CAS:<p>Antibacterial agent 115 is an antibacterial and anti-inflammatory agent that is active when taken orally.</p>Fórmula:C35H48N2O3Cor e Forma:SolidPeso molecular:544.77Metallo-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:302.35Antibacterial agent 125
CAS:<p>Antibacterial agent 125 shows strong activity against Gram-positive pathogens; MICs: 0.25-8 μM; used in antimicrobial resistance research.</p>Fórmula:C15H11ClN2OPureza:98.45%Cor e Forma:SoildPeso molecular:270.71ML344
CAS:<p>ML344 is a CqsS/LuxQ agonist probe that acts as an inducer of light production without autoinducers.</p>Fórmula:C13H19N5Pureza:98%Cor e Forma:SolidPeso molecular:245.32Cadrofloxacin
CAS:<p>Cadrofloxacin (Caderofloxacin, CS-940) is a novel fluoroquinolone antimicrobial agent.</p>Fórmula:C19H20F3N3O4Cor e Forma:SolidPeso molecular:411.38Antibacterial agent 106
CAS:<p>Compound 106 is an orally active antibacterial with biofilm-fighting properties, kills 99.7% of MRSA in macrophages.</p>Fórmula:C20H24N6SCor e Forma:SolidPeso molecular:380.51C16-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:250.14Grepafloxacin Hydrochloride
CAS:<p>Grepafloxacin Hydrochloride is an antimicrobial agent, oral broad-spectrum fluoroquinolone. It is used to treat bacterial infections.</p>Fórmula:C19H23ClFN3O3Cor e Forma:SolidPeso molecular:395.86Metallo-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:377.4Antibacterial agent 72
CAS:<p>Antibacterial agent 72 has an antibacterial effect by selectively acting on bacterial membranes.</p>Fórmula:C19H21BrN4SCor e Forma:SolidPeso molecular:417.37LpxC-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:485.68WCK-5153
CAS:<p>WCK-5153 是 β-Lactamase 的增强剂和 PBP2 的抑制剂，对铜绿假单胞菌具有抗菌活性。 WCK-5153 可用于治疗由高度耐药的革兰氏阴性病原体引起的严重感染的研究。</p>Fórmula:C12H19N5O7SPureza:99.81%Cor e Forma:SolidPeso molecular:377.37Antibacterial 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:299.24Liriodenine methiodide
CAS:<p>Liriodenine methiodide shows antibacterial and antifungal activity against several microorganisms.</p>Fórmula:C18H12INO3Pureza:98%Cor e Forma:SolidPeso molecular:417.2Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Fórmula:C12H12N2O3Pureza:98%Cor e Forma:SolidPeso molecular:232.24Antibacterial 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:341.79L-erythro-Chloramphenicol
CAS:<p>L-erythro-Chloramphenicol functions as a potent inhibitor of electron transport.</p>Fórmula:C11H12Cl2N2O5Pureza:98%Cor e Forma:SolidPeso molecular:323.13MAC173979
CAS:<p>MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.</p>Fórmula:C9H5Cl2NO3Pureza:98%Cor e Forma:SolidPeso molecular:246.05Mab Aspartate Decarboxylase-IN-1
CAS:<p>Mab Aspartate Decarboxylase-IN-1 is a potent inhibitor of aspartate decarboxylase (PanD) (IC50 = 56.3 μM) with antibacterial activity [1].</p>Fórmula:C16H11N3O3Cor e Forma:SolidPeso molecular:293.28Metallo-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:332.34ThrRS-IN-1
CAS:<p>ThrRS-IN-1 inhibits Salmonella ThrRS with IC50 1.4μM, Kd 1.36μM, targets tRNA/L-threonine sites, has strong antibacterial effects.</p>Fórmula:C16H18Cl2N4O3Cor e Forma:SolidPeso molecular:385.25FabG1-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:396.38MmpL3-IN-3
CAS:<p>MmpL3-IN-3 (Compound 12), an MmpL3 inhibitor, exhibits potent anti-tuberculosis activity with a minimum inhibitory concentration (MIC) of 0.1 μM against H37Rv</p>Fórmula:C26H33ClN2SiCor e Forma:SolidPeso molecular:437.09RmlA-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:447.44Synthalin sulfate
CAS:<p>Synthalin sulfate is a NMDA receptor antagonist.</p>Fórmula:C12H30N6O4SPureza:98%Cor e Forma:SolidPeso molecular:354.47Sch 25393
CAS:<p>Sch 25393 is an antibacterial agent in vitro.</p>Fórmula:C12H14F3NO4SPureza:98%Cor e Forma:SolidPeso molecular:325.3Antitubercular agent-19
CAS:<p>Antitubercular agent-19: effective against MTB H37Rv/MDR strains (MIC <0.016μg/ml), low cytotoxicity, high acute toxicity in BALB/c mice.</p>Fórmula:C24H20F6N4O3SCor e Forma:SolidPeso molecular:558.5Sarafloxacin
CAS:<p>Sarafloxacin (A56620) has antibacterial activities against Gram-positive and Gram-negative bacteria.</p>Fórmula:C20H17F2N3O3Pureza:98.07% - 98.94%Cor e Forma:SolidPeso molecular:385.36Acibenzolar-S-methyl
CAS:<p>Acibenzolar-S-methyl, a fungicide, boosts plant defenses by upregulating W-box genes like CAD1, NPR1, PR2.</p>Fórmula:C8H6N2OS2Pureza:99.64% - 99.86%Cor e Forma:Beige Fine PowderPeso molecular:210.28Dihydropteroate 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:449.55VU0420373
CAS:<p>VU0420373 activates HssRS at EC50 10.7 μM, induces heme synthesis, toxic to S. aureus.</p>Fórmula:C15H11FN2OCor e Forma:SolidPeso molecular:254.26Besifloxacin
CAS:<p>Besifloxacin is the fourth generation of fluoroquinolones, which can be used to treat bacterial conjunctivitis</p>Fórmula:C19H21ClFN3O3Pureza:98%Cor e Forma:SolidPeso molecular:393.84Ornidazole 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:201.18Furalazine
CAS:<p>Furalazine: antimicrobial, treats cholera, more effective than chloramphenicol in shortening stool culture positivity.</p>Fórmula:C9H7N5O3Pureza:98%Cor e Forma:SolidPeso molecular:233.18Undecylprodigiosin
CAS:<p>Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.</p>Fórmula:C25H35N3OCor e Forma:SolidPeso molecular:393.56FadD32 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:401.89Oxaquin
CAS:<p>Oxaquin, a water-soluble injectable prodrug, converts to active MCB3681 post-IV to fight Gram-positive bacteria.</p>Fórmula:C31H33F2N4O11PPureza:98%Cor e Forma:SolidPeso molecular:706.58Antitubercular 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:372.28G0507
CAS:<p>G0507, a potent pyrrolopyrimidinedione, blocks E. coli growth by activating σE stress and targeting LolCDE ABC Transporter.</p>Fórmula:C18H15N3O3SCor e Forma:SolidPeso molecular:353.39MtTMPK-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:391.46Dealanylalahopcin
CAS:<p>Dealanylalahopcin is a procollagen prolyl-4-hydroxylase inhibitor.</p>Fórmula:C6H10N2O5Cor e Forma:SolidPeso molecular:190.15Ppc-1
CAS:<p>Ppc-1 inhibits Porphyromonas gingivalis, uncouples mitochondria, and blocks IL-2, with anti-obesity, antibacterial, anti-inflammatory effects.</p>Fórmula:C21H25NO4Pureza:98%Cor e Forma:SolidPeso molecular:355.43Zidebactam sodium salt
CAS:<p>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).</p>Fórmula:C13H21N5NaO7SPureza:98%Cor e Forma:SolidPeso molecular:414.39Antimicrobial 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:391.49PC170942 Sodium
CAS:<p>PC170942 Sodium is a water-soluble bacterial cytokinesis inhibitor that acts by inhibiting FtsZ.</p>Fórmula:C24H24ClNO2SPureza:98%Cor e Forma:SolidPeso molecular:425.97Mtb-cyt-bd oxidase-IN-4
<p>Mtb-cyt-bd oxidase inhibitor; IC50=0.25μM; MIC=8μM against Mycobacterium tuberculosis; for TB research.</p>Fórmula:C25H32FNOCor e Forma:SolidPeso molecular:381.532,6-Dichlorodiphenylamine
CAS:<p>2,6-Dichlorodiphenylamine shows activity against Candida albicans infections. 2,6-Dichlorodiphenylamine elevated the MIC by 4-fold of diclofenac sodium (DFNa).</p>Fórmula:C12H9Cl2NPureza:99.81%Cor e Forma:Off White To Cream Coloured Crystalline SolidPeso molecular:238.11Quinuronium Sulfate
CAS:<p>Quinuronium sulfate treats Babesia in calves; doesn't stop carrier state; may lead to hepatic fat degeneration, not GSH depletion.</p>Fórmula:C22H23N4O5SCor e Forma:SolidPeso molecular:455.51(-)-Pinocembrin
CAS:<p>(-)-Pinocembrin: Anti-tuberculosis (IC50: 1.11 mg/mL dormant, 1.21 mg/mL active), antiproliferative (IC50: 1.88-11 mg/mL on various cell lines).</p>Fórmula:C15H12O4Cor e Forma:SolidPeso molecular:256.25A 65281
CAS:<p>A 65281: antibacterial isothiazoloquinolone, inhibits P4-unknotting, induces DNA breakage via topoisomerase II.</p>Fórmula:C17H16F2N4O2SPureza:98%Cor e Forma:SolidPeso molecular:378.4Antistaphylococcal agent 1
CAS:<p>Antistaphylococcal agent 1 is an antistaphylococcal therapeutic agent.</p>Fórmula:C22H16N6O2Cor e Forma:SolidPeso molecular:396.4CBR-3465
CAS:<p>CBR-3465 is an inhibitor of mycobacterium tuberculosis (Mtb) type II NADH dehydrogenase. The MIC of CBR-3465 against Mtb is 0.16 μM [1].</p>Fórmula:C16H18FN3O2SCor e Forma:SolidPeso molecular:335.4Mt KARI-IN-4
CAS:<p>Mt KARI-IN-4 inhibits Mtb KARI with Ki of 5.48μM, has MIC of 0.78μM against H37Rv, and IC50 >72μg/mL, low cytotoxicity.</p>Fórmula:C13H8FN5O3S2Cor e Forma:SolidPeso molecular:365.36Antibacterial 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:399.45A 65282
CAS:<p>A 65282: antibacterial isothiazoloquinolone, inhibits P4-unknotting, causes DNA breaks via topoisomerase II.</p>Fórmula:C17H16F2N4O2SPureza:98%Cor e Forma:SolidPeso molecular:378.4Finafloxacin hydrochloride
CAS:<p>"Finafloxacin is a fluoroquinolone antimicrobial agent optimized for maximum effectiveness in mildly acidic conditions."</p>Fórmula:C20H20ClFN4O4Cor e Forma:SolidPeso molecular:434.85Netzahualcoyone
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:492.6TXA6101
CAS:<p>TXA6101: FtsZ inhibitor, blocks bacterial division, MIC 1 μg/mL against MRSA, effective on TXA707-resistant mutants. Potential anti-Gram-negative agent.</p>Fórmula:C18H10BrF5N2O3Cor e Forma:SolidPeso molecular:477.18Laburnetin
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:354.35GlyRS-IN-1
CAS:<p>GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.</p>Fórmula:C12H17N7O7SCor e Forma:SolidPeso molecular:403.37SQ109
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:330.55Lalistat 1
CAS:<p>Lalistat 1 inhibits LAL (IC50=68 nM) and H. influenzae IgA1 protease; useful in Niemann-Pick C research.</p>Fórmula:C12H18N4O3SPureza:99.87%Cor e Forma:SolidPeso molecular:298.36Diethyl butylmalonate
CAS:<p>Diethyl butylmalonate shows toxicity to T. pyriformis, with a log(IGC50 -1 ) of 0.557 [1].</p>Fórmula:C11H20O4Cor e Forma:SolidPeso molecular:216.27SARS-CoV-2 3CLpro-IN-4
CAS:<p>SARS-CoV-2 3CLpro-IN-4 (Compound 5g) is a multifunctional inhibitor of SARS CoV-2 3CLpro, exhibiting antiviral, antibacterial, and antifungal activities.</p>Fórmula:C22H19ClN6OSCor e Forma:SolidPeso molecular:450.94Levofloxacin sodium
CAS:<p>Levofloxacin sodium: synthetic antibacterial, stops DNA replication by inhibiting bacterial DNA gyrase.</p>Fórmula:C18H20FN3NaO4Pureza:98%Cor e Forma:SolidPeso molecular:384.363RNPA1000
CAS:<p>RNPA1000 is an attractive antimicrobial development candidate and RnpA inhibitor.</p>Fórmula:C23H18BrN3O3Pureza:98%Cor e Forma:SolidPeso molecular:464.31Dodicin
CAS:<p>Dodicin is a potent disinfectant exhibiting broad-spectrum antimicrobial activity [1].</p>Fórmula:C18H39N3O2Cor e Forma:SolidPeso molecular:329.52Antibacterial agent 73
CAS:<p>Compound 7a: antitubercular (MIC 0.65 μg/mL Mtb), antibacterial, antifungal; cytotoxic (IC50 8.20 μM MCF-7).</p>Fórmula:C15H17FN2OCor e Forma:SolidPeso molecular:260.31Rufloxacin hydrochloride
CAS:<p>Rufloxacin HCl (MF-934 HCl): a fluoroquinolone that inhibits topoisomerase and B-cell differentiation.</p>Fórmula:C17H19ClFN3O3SPureza:99.80%Cor e Forma:SolidPeso molecular:399.867β-Lactamase-IN-1
CAS:β-Lactamase-IN-1 (4-(1,3-dihydroxypropan-2-yl)-6-methoxypyrido[2,3-b]pyrazin-3-one) is a β-Lactamase inhibitor and targets the infection of NeisseriaFórmula:C11H13N3O4Pureza:99.89%Cor e Forma:SolidPeso molecular:251.24Antibacterial agent 96
CAS:<p>Compound 4k is potent against drug-susceptible and resistant M. tuberculosis but toxic to HepG2 and Vero cells.</p>Fórmula:C18H15Cl2NO2Cor e Forma:SolidPeso molecular:348.22Lupulon
CAS:<p>Lupulon has a role as an apoptosis inducer, antimicrobial agent, angiogenesis inhibitor, and antineoplastic agent.</p>Fórmula:C26H38O4Cor e Forma:SolidPeso molecular:414.58BRD0539
CAS:<p>BRD0539 is a cell-permeable spCas9 inhibitor that blocks the binding of spCas9 to DNA and inhibits Streptococcus pyogenes Cas9 (SpCas9).</p>Fórmula:C25H25FN2O3SPureza:98.03%Cor e Forma:SolidPeso molecular:452.54CGI-17341
CAS:<p>CGI-17341, an oral 5-nitroimidazole antimicrobial, blocks drug-sensitive and resistant tuberculosis at 0.1-0.3 µg/ml.</p>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:442.97Olanexidine Hydrochloride semihydrate
CAS:<p>Olanexidine is a monobiguanide compound with the activity of bactericidal.</p>Fórmula:C17H31Cl4N5OPureza:98%Cor e Forma:SolidPeso molecular:463.27Antimicrobial agent-4
CAS:<p>Antimicrobial agent-4 (6a) has potent activity against pathogens; binds target enzyme with 10.0 kcal/mol affinity.</p>Fórmula:C22H16ClN5O2SCor e Forma:SolidPeso molecular:449.91FabH-IN-1
CAS:<p>FabH-IN-1, a broad-spectrum antibiotic and antioxidant, inhibits bacterial FabH enzyme.</p>Fórmula:C17H16N2OSCor e Forma:SolidPeso molecular:296.39Urease-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:398.48Antitubercular 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:334.44S.pombe lumazine synthase-IN-1
CAS:<p>S.pombe lumazine synthase-IN-1 inhibits lumazine synthases: Ki of 243μM for S.pombe, 9.6μM for M.tuberculosis.</p>Fórmula:C14H13N3O6Cor e Forma:SolidPeso molecular:319.27Infliximab
CAS:<p>Infliximab is a chimeric monoclonal antibody that inhibits TNF-α. Infliximab can be used to treat Crohn's disease and rheumatoid arthritis. Cost-effective and quality-assured.</p>Pureza:98% - 99.70%Cor e Forma:LiquidPeso molecular:149 kDaAntibacterial agent 123
CAS:<p>Antibacterial Agent 123 (Compound 111) serves as an effective membrane-disrupting agent targeting antibiotic-resistant Gram-positive bacteria [1].</p>Fórmula:C17H8F9N3OCor e Forma:SolidPeso molecular:441.25DprE1-IN-1
CAS:<p>DprE1-IN-1: Potent, oral DprE1 inhibitor; stable in hepatocytes, low toxicity, anti-bacilli in macrophages, -1.29 log10 CFU.</p>Fórmula:C19H21N3O6S2Cor e Forma:SolidPeso molecular:451.52Mycobactin-IN-1
CAS:<p>Mycobactin-IN-1, a pyrazoline analogue, inhibits MbtA, key in mycobactin synthesis, targeting mycobacteria.</p>Fórmula:C15H13ClN2OCor e Forma:SolidPeso molecular:272.73Sulfisoxazole diethanolamine
CAS:<p>Sulfisoxazole diethanolamine: a sulfonamide antibacterial, endothelin receptors A and B antagonist, inhibits breast cancer exosomes.</p>Fórmula:C15H24N4O5SCor e Forma:SolidPeso molecular:372.44Antitubercular 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:373.49MDRTB-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:274.32Antitubercular agent-39
CAS:<p>Antitubercular agent-39 (Compound P1) is a potent agent effective against both drug-resistant strains and drug-susceptible clinical isolates of tuberculosis,</p>Fórmula:C26H30N4O2Cor e Forma:SolidPeso molecular:430.54Piperic acid
CAS:<p>Piperic acid is a powerful antioxidant and has potent antibacterial properties</p>Fórmula:C12H10O4Cor e Forma:SolidPeso molecular:218.21β-Lactamase-IN-7
CAS:<p>β-Lactamase-IN-7 (compound 14) effectively inhibit Klebsiella pneumoniae that is a potent inhibitor of VIM-Type metallo-β-lactamase with Ki values of 1.26 μM</p>Fórmula:C16H15N3S2Cor e Forma:SolidPeso molecular:313.443-Fucosyllactose
CAS:<p>3-Fucosyllactose, a key fucosylated oligosaccharide in human milk, offers prebiotic and immune benefits.</p>Fórmula:C18H32O15Cor e Forma:SolidPeso molecular:488.44PXYD4
CAS:<p>PXYD4 antagonizes RpsA, key in Mtb translocation, binding RpsA-CTD (Kd 3.24 μM) & RpsA-CTD Δ438A (Kd 1.64 μM).</p>Fórmula:C25H21NO5Cor e Forma:SolidPeso molecular:415.44FPI-1602
CAS:<p>FPI-1602 is a β-lactamase inhibitor with strong antimicrobial activity against Pseudomonas aeruginosa, Escherichia coli, and Enterobacter species [1].</p>Fórmula:C11H17N5O7SCor e Forma:SolidPeso molecular:363.35PC190723
CAS:<p>PC190723 is an inhibitor of the bacterial cytosolic protein FtsZ with antimicrobial activity against Staphylococcus spp.</p>Fórmula:C14H8ClF2N3O2SPureza:97.64%Cor e Forma:SolidPeso molecular:355.75Oxyphenbutazone monohydrate
CAS:<p>Oxyphenbutazone monohydrate: Phenylbutazone derivative, anti-inflammatory, non-selective COX inhibitor, kills dormant M. tuberculosis.</p>Fórmula:C19H22N2O4Cor e Forma:SolidPeso molecular:342.39Antimicrobial agent-8
<p>Antimicrobial agent-8: potent against Gram+ & Gram-, 2-8 μg/mL MIC, anti-inflammatory action.</p>Fórmula:C39H54N16Cor e Forma:SolidPeso molecular:746.95Antibacterial agent 131
<p>Antibacterial agent 131 is a compound with antibacterial properties.</p>Fórmula:C24H17ClN4OSPureza:99.06%Cor e Forma:SolidPeso molecular:444.94DNA Gyrase-IN-2
CAS:<p>DNA Gyrase-IN-2 inhibits E. coli (IC50: 3.29-10.49 μM) and M. tuberculosis (IC50: 4.41-5.61 μM) COX, has antibacterial properties.</p>Fórmula:C24H24N8OS2Cor e Forma:SolidPeso molecular:504.63Antimicrobial agent-22
CAS:<p>Antimicrobial agent-22 (THI 6c) constitutes a broad-spectrum, multi-target antibacterial with notable rapid bactericidal efficacy and effective anti-biofilm</p>Fórmula:C15H16N4OSPureza:97.86%Cor e Forma:SolidPeso molecular:300.38PknB-IN-2
CAS:<p>PknB-IN-2 (Compound 10) is an inhibitor of Mycobacterium tuberculosis protein kinase B (PknB) (IC50: 12.1 μM).</p>Fórmula:C28H32N2O4Cor e Forma:SolidPeso molecular:460.56VP-4509
CAS:<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Fórmula:C14H16N2O5SCor e Forma:SolidPeso molecular:324.35Anti-inflammatory agent 15
CAS:<p>Compound 29, anti-inflammatory and antimycobacterial, halts Mtb H37Rv and M299 growth; MIC50 at 2.3 and 7.8 μM. Blocks iNOS, TNF-α, IL-1β.</p>Fórmula:C17H20N2SCor e Forma:SolidPeso molecular:284.4213(S)-HpOTrE
CAS:<p>13(S)-HpOTrE, a fatty acid from soy LO-2 action on α-linolenic acid, forms in soybeans (9:1 ratio). It generates plant defense signals against pests.</p>Fórmula:C18H30O4Cor e Forma:SolidPeso molecular:310.43Urease-IN-4
<p>Urease-IN-4 inhibits urease (IC50: 1.64 µM), targets P. vulgaris (IC50: 15.27 µg/mL), and is low in cytotoxicity.</p>Fórmula:C16H20N2O3SCor e Forma:SolidPeso molecular:320.41MtInhA-IN-1
<p>MtInhA-IN-1: an oral selective MtInhA inhibitor, IC50 0.23 μM, effective against M. tuberculosis with MIC 0.4 μM.</p>Fórmula:C21H22BrN3Cor e Forma:SolidPeso molecular:396.32Sulfamethomidine
CAS:<p>Sulfamethomidine has antibacterial activity [1].</p>Fórmula:C12H14N4O3SCor e Forma:SolidPeso molecular:294.33(±)-Hydnocarpin
CAS:<p>(±)-Hydnocarpin, a flavonolignan, demonstrates inhibitory activity against S.</p>Fórmula:C25H20O9Cor e Forma:SolidPeso molecular:464.42Sulfasymazine
CAS:Sulfasymazine is a sulfonamide drug.Fórmula:C13H17N5O2SPureza:98%Cor e Forma:SolidPeso molecular:307.37Mycobactin-IN-2
CAS:<p>Mycobactin-IN-2 inhibits mycobactin production by targeting salicyl-AMP ligase (MbtA), a crucial enzyme in its pathway.</p>Fórmula:C15H13BrN2OCor e Forma:SolidPeso molecular:317.18DHDPS-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:293.3Urease-IN-7
CAS:<p>Urease-IN-7 (Compound 5k) acts as a competitive inhibitor of the enzyme urease, exhibiting an IC50 value of 3.33 μM and a K_i of 3.62 μM.</p>Fórmula:C16H10BrFN4SCor e Forma:SolidPeso molecular:389.24Antibacterial agent 26
CAS:<p>Antibacterial agent 26 is an antimicrobial compound that is a potent DHFR inhibitor (S. aureus DHFR Ki of 0.020 nM).</p>Fórmula:C19H17N5O2Pureza:98.86%Cor e Forma:SolidPeso molecular:347.37(R,R)-BAY-Y 3118
CAS:<p>(R,R)-BAY-Y 3118, the R-enantiomer of BAY-Y 3118, exhibits weak bactericidal activity.</p>Fórmula:C20H21ClFN3O3Cor e Forma:SolidPeso molecular:405.85Ranitidine bismuth citrate
CAS:<p>Ranitidine bismuth citrate, oral H2 blocker, IC50 3.3 µM, targets SARS-CoV-2 cells, treats H. pylori; MIC90 16 ng/L.</p>Fórmula:C19H27BiN4O10SCor e Forma:SolidPeso molecular:712.48Cefmenoxime
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:511.558PXYC1
CAS:<p>PXYC1 binds Mtb RpsA-CTD (Kd 0.81 μM) & RpsA-CTD Δ438A (Kd 0.31 μM), hindering trans-translation.</p>Fórmula:C9H10N4O3SCor e Forma:SolidPeso molecular:254.27Amiprilose
CAS:<p>Amiprilose is an Immunopotentiator.</p>Fórmula:C14H27NO6Pureza:99.82% - >99.99%Cor e Forma:SolidPeso molecular:305.37Antibacterial 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:411.36MmpL3-IN-1
CAS:<p>MmpL3-IN-1 (compound 32) inhibits MmpL3 with <0.016 μg/mL MIC against M. tuberculosis, aiding drug-resistant TB research.</p>Fórmula:C20H21F2N3OCor e Forma:SolidPeso molecular:357.4MMV688844
CAS:<p>MMV688844 inhibits M. abscessus DNA cyclooxygenase (IC50: 2μM) and has MIC50 of 12μM on strain bamboo; useful in antimicrobial studies.</p>Fórmula:C23H25ClN4O2Cor e Forma:SolidPeso molecular:424.92PNU288034
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:403.4Ribocil-C Racemate
CAS:<p>Ribocil-C Racemate is a racemic mix and selective inhibitor of E. coli riboflavin riboswitches affecting vitamin B2 synthesis.</p>Fórmula:C21H21N7OSPureza:98%Cor e Forma:SolidPeso molecular:419.5MmpL3-IN-2
CAS:<p>MmpL3-IN-2, an inhibitor targeting MmpL3, exhibits low cytotoxicity and moderate metabolic stability, making it suitable for tuberculosis research [1].</p>Fórmula:C27H30N2Cor e Forma:SolidPeso molecular:382.54Mtb-cyt-bd oxidase-IN-1
<p>Mtb-cyt-bd oxidase-IN-1, a Mycobacterium tuberculosis inhibitor, IC50: 0.13 μM, useful for TB research.</p>Fórmula:C26H35NO2Cor e Forma:SolidPeso molecular:393.56Antibacterial agent 111
CAS:<p>Compound 3: potent against B. cereus & K. pneumonia; MICs: 3.90 & 0.49 μg/mL; targets tyrosyl-tRNA synthetase.</p>Fórmula:C18H12N6SCor e Forma:SolidPeso molecular:344.39ZTB23(R)
CAS:<p>ZTB23(R) is the first potent and selective inhibitor of Mycobacterium tuberculosis Zmp1.</p>Fórmula:C20H15NO5S2Pureza:98%Cor e Forma:SolidPeso molecular:413.478-Deazahomofolic acid
CAS:<p>8-Deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Fórmula:C21H22N6O6Pureza:98%Cor e Forma:SolidPeso molecular:454.44Antimicrobial agent-14
CAS:<p>Antimicrobial agent-14, a benzyl thiophene sulfonamide, has a 200 μM MIC against Campylobacter coli ATCC33559.</p>Fórmula:C9H8ClNO3S2Pureza:98.45%Cor e Forma:SolidPeso molecular:277.75PNU-101603
CAS:<p>PNU-101603, a Sutezolid metabolite, effective against TB including drug-resistant strains, works solo or with SQ109.</p>Fórmula:C16H20FN3O4SCor e Forma:SolidPeso molecular:369.41BDM91514
CAS:<p>BDM91514 enhances antibiotic efficacy by inhibiting AcrB, effectively curbing the proliferation of E.</p>Fórmula:C13H19Cl3N6OCor e Forma:SolidPeso molecular:381.69Megazol
CAS:<p>Megazol treats protozoan infections like Chagas and sleeping sickness; it's a potent nitroimidazole drug.</p>Fórmula:C6H6N6O2SPureza:98%Cor e Forma:SolidPeso molecular:226.22Antitubercular agent-33
CAS:<p>Antitubercular agent-33 is a 2-aminothiazole derivative with potent anti-tubercular activity against Mycobacterium tuberculosis ( Mtb ) [1].</p>Fórmula:C15H10N4O3SCor e Forma:SolidPeso molecular:326.33B 746
CAS:<p>B 746 is an antibacterial for leprosy, Mycobacterium avium, and drug-resistant tuberculosis.</p>Fórmula:C26H20Cl2N4Cor e Forma:SolidPeso molecular:459.37V-06-018
CAS:<p>V-06-018 is a quorum-sensing modulator. It also acts as a LasR antagonist.</p>Fórmula:C18H27NO2Pureza:98%Cor e Forma:SolidPeso molecular:289.41YKAs3003
CAS:<p>YKAs3003 inhibits KAS III with MICs 128-256 μg/mL against multiple bacteria.</p>Fórmula:C13H17NO2Pureza:98%Cor e Forma:SolidPeso molecular:219.28NC00075159
CAS:<p>NC00075159 is an opener of human KCNQ4 (Kv7.4) potassium channel.</p>Fórmula:C15H16N2O3S2Pureza:98%Cor e Forma:SolidPeso molecular:336.43GA-O-02
<p>GA-O-02, an 18β-Glycyrrhetinic acid derivative, inhibits NO/cytokines and fights Gram-positive bacteria; potent anti-inflammatory/antimicrobial.</p>Fórmula:C37H46ClNO6Cor e Forma:SolidPeso molecular:636.22Pracinostat dihydrochloride
CAS:<p>Pracinostat dihydrochloride is a highly effective histone deacetylase (HDAC) inhibitor with IC₅₀ values ranging from 40 to 140 nM, utilized in cancer research. Additionally, it inhibits metallo-β-lactamase domain-containing protein 2 (MBLAC2) hydrolase activity with an EC₅₀ of less than 10 nM.</p>Fórmula:C20H32Cl2N4O2Cor e Forma:SolidPeso molecular:431.40Diazaborine
CAS:<p>Diazaborine disrupts large ribosome formation by inhibiting rRNA maturation and AAA-ATPase Drg1, leading to rapid protein redistribution.</p>Fórmula:C14H13BN2O3SPureza:98%Cor e Forma:SolidPeso molecular:300.14Chlorhexidine-d8 HCl
CAS:<p>Chlorhexidine-d8: internal standard for GC/LC-MS, antimicrobial, inhibits MRSA/MSSA/MRSP/MSSP, affects E. faecium/C. albicans, destabilizes cell walls.</p>Fórmula:C22H24D8Cl4N10Cor e Forma:SolidPeso molecular:586.4168Sulfoxone sodium
CAS:<p>Sulfoxone sodium ( Adesulfone Sodium) is an anti-leprosy drug.</p>Fórmula:C14H16N2NaO6S3Cor e Forma:SolidPeso molecular:427.46Chelator 1a
CAS:<p>Chelator 1a has antifungal activity, inhibiting Aspergillus and Candida, and can be used to study fungal infections and cancer.</p>Fórmula:C16H12BrN3OSCor e Forma:SolidPeso molecular:374.26Miloxacin
CAS:<p>Miloxacin is an antibiotic active against gram-negative bacteria.</p>Fórmula:C12H9NO6Pureza:98%Cor e Forma:SolidPeso molecular:263.20
