Antibacteriano
Los inhibidores antibacterianos son compuestos que atacan las células bacterianas, inhibiendo su crecimiento o matándolas directamente. Estos inhibidores son esenciales en el desarrollo de tratamientos para infecciones bacterianas y se utilizan ampliamente en la investigación para estudiar la fisiología bacteriana, los mecanismos de resistencia y la eficacia de nuevos agentes antibacterianos. En CymitQuimica, ofrecemos una gama de inhibidores antibacterianos para apoyar su investigación en microbiología, enfermedades infecciosas y desarrollo de medicamentos.
Se han encontrado 2959 productos de "Antibacteriano"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
KB-5246
CAS:<p>KB-5246, displays antibacterial activities.is a tetracyclic quinolone.</p>Fórmula:C18H17ClFN3O4SPureza:98%Forma y color:SolidPeso molecular:425.86PknB-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:C28H32N2O4Forma y color:SolidPeso molecular:460.56Anti-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:C17H20N2SForma y color:SolidPeso molecular:284.42Anticancer agent 34
CAS:<p>Anticancer agent 34, a sulfonylurea, inhibits Mycobacterium, E. coli, C. albicans (MIC 0.039-0.156 mg/ml), and A549, PC3 cancers (IC50 8.4, 7.8 μg/ml).</p>Fórmula:C17H14BrN3O3S2Forma y color:SolidPeso molecular:452.3513(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:C18H30O4Forma y color:SolidPeso molecular:310.43CRS400393
CAS:<p>CRS400393: Anti-tuberculosis drug, MIC - M. abs.: 0.03μg/mL, M. avium: 2μg/mL, M. intracellulare: ≤0.12 μg/mL, M. tuberculosis: ≤0.12 μg/mL.</p>Fórmula:C18H20Cl2N2OSPureza:98%Forma y color:SolidPeso molecular:383.34Urease-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:C16H20N2O3SForma y color:SolidPeso molecular:320.41BPH-1358 free base
CAS:<p>BPH-1358 inhibits UPPS (IC50: 110 nM) and FPPS (IC50: 1.8 µM), effective against S. aureus (MIC ~250 ng/mL).</p>Fórmula:C32H28N6O2Pureza:98%Forma y color:SolidPeso molecular:528.6Urease-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:C16H10BrFN4SForma y color: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%Forma y color:SolidPeso molecular:347.37UGM-IN-3
CAS:<p>UGM-IN-3 inhibits UGM (Kd=66 μM) and M. tuberculosis growth (MIC=6.2 μg/mL).</p>Fórmula:C18H16INO2Forma y color:SolidPeso molecular:405.23MMV676584
CAS:<p>MMV676584 has anti-tuberculosis avtivity. MMV676584 is a novel drug candidate for eumycetoma .</p>Fórmula:C12H8ClFN2OS2Forma y color:SolidPeso molecular:314.79MmpL3-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:C20H21F2N3OForma y color: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:C23H25ClN4O2Forma y color:SolidPeso molecular:424.92MmpL3-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:C27H30N2Forma y color:SolidPeso molecular:382.54Antibacterial 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:C18H12N6SForma y color:SolidPeso molecular:344.39Syncytial Virus Inhibitor-1
CAS:<p>Syncytial Virus Inhibitor-1: Potent, oral RSV fusion blocker (EC50: 0.002-0.004 μM for Long, A2, B strains).</p>Fórmula:C23H26N4O3SPureza:98%Forma y color:SolidPeso molecular:438.54WX-081
CAS:<p>WX-081 is an anti-TB drug effective against DS-TB (MIC: 0.083 μg/ml) and MDR-TB strains (MIC: 0.11 μg/ml) with hERG inhibition (IC50: 1.89 μM).</p>Fórmula:C34H33ClN2O2Forma y color:SolidPeso molecular:537.09DHFR-IN-1
CAS:<p>DHFR-IN-1: selective DHFR blocker, IC50 40.71 nM, antifungal, strong against Gram-positive/negative bacteria, synergizes with Levofloxacin (FIC=0.249).</p>Fórmula:C22H22N6O4S2Forma y color:SolidPeso molecular:498.58PNU-101603
CAS:<p>PNU-101603, a Sutezolid metabolite, effective against TB including drug-resistant strains, works solo or with SQ109.</p>Fórmula:C16H20FN3O4SForma y color:SolidPeso molecular:369.41Antibacterial agent 141
CAS:<p>Compound B14 (Antibacterial agent 141) exhibits antibacterial activity against the plant pathogens Xoo, Xac, Psa, and Cmm, with an EC50 value of 1.28 μM.</p>Fórmula:C23H27ClN2O3Forma y color:SolidPeso molecular:414.93LasR-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:C18H20N4Forma y color:SolidPeso molecular:292.38OX11
CAS:<p>OX11 is a selective inhibitor of S. pneumoniae, P. aeruginosa and E. coli bacteria.</p>Fórmula:C17H10Cl2N4O3S2Forma y color:SolidPeso molecular:453.32Pracinostat 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:C20H32Cl2N4O2Forma y color:SolidPeso molecular:431.40Chlorhexidine-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:C22H24D8Cl4N10Forma y color:SolidPeso molecular:586.4168Antibacterial agent 101
CAS:<p>Antibacterial agent 101 exhibited antibacterial and antifungal effects (MIC=4-32 μg/mL).</p>Fórmula:C28H29BrN2OForma y color:SolidPeso molecular:489.45BDM91514
CAS:<p>BDM91514 enhances antibiotic efficacy by inhibiting AcrB, effectively curbing the proliferation of E.</p>Fórmula:C13H19Cl3N6OForma y color:SolidPeso molecular:381.69Tenuazonic acid
CAS:<p>Tenuazonic acid, a nonhost-selective mycotoxin from Alternaria alternate, inhibits PSII by blocking electron transport at D1 protein.</p>Fórmula:C10H15NO3Pureza:98%Forma y color:SolidPeso molecular:197.23Aztreonam lysine
CAS:<p>Aztreonam lysine is an inhaled anti-pseudomonal treatment for people who have pulmonary Pseudomonas aeruginosa infection with cystic fibrosis (CF).</p>Fórmula:C19H31N7O10S2Pureza:98%Forma y color:SolidPeso molecular:581.62Cefroxadine
CAS:<p>Cefroxadine: an oral cephalosporin antibiotic, broad-spectrum, bactericidal, effective for acute uncomplicated cystitis.</p>Fórmula:C16H19N3O5SPureza:98%Forma y color:SolidPeso molecular:365.4AV-1101
CAS:<p>AV-1101, a cytokine production inhibitor, is used potentially for the treatment of HIV infection.</p>Fórmula:C19H20N2O4Pureza:98%Forma y color:SolidPeso molecular:340.37Salifluor
CAS:<p>Salifluor is a broad spectrum antimicrobial agent that has been investigated for its abilities to inhibit dental plaque formation.</p>Fórmula:C22H24F3NO3Forma y color:SolidPeso molecular:407.43Elsamitrucin
CAS:<p>Elsamitrucin, a heterocyclic antibiotic, disrupts DNA replication by intercalating into G-C sequences and inhibiting topoisomerases.</p>Fórmula:C33H35NO13Forma y color:SolidPeso molecular:653.63Flomoxef 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%Forma y color:SolidPeso molecular:518.44Antitubercular 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:C20H24F2N4O5S2Forma y color:SolidPeso molecular:502.56Gln-AMS
CAS:<p>Gln-AMS is an inhibitor of aminoacyl-tRNA synthetases (AARS). It specifically binds to the A-domain located within the NRPS enzymes.</p>Fórmula:C15H22N8O8SPureza:98%Forma y color:SolidPeso molecular:474.45Antibacterial agent 100
CAS:<p>Compound 7c: Antibacterial/fungal, effective on S. aureus, C. albicans (MIC 4 μg/mL), C. neoformans (MIC 8 μg/mL).</p>Fórmula:C28H29BrN2Forma y color:SolidPeso molecular:473.458CAY10711
CAS:<p>CAY10711: potent bactericide for Gram-positive/negative bacteria including MRSA, inhibits biofilms, synergizes with kanamycin, low mammalian toxicity.</p>Fórmula:C41H54N6S2Forma y color:SolidPeso molecular:695.04DNA Gyrase-IN-3
CAS:<p>DNA Gyrase-IN-3 inhibits E. coli DNA gyrase B with IC50 5.41-15.64 μM; shows anti-TB and antibacterial properties.</p>Fórmula:C18H20N6OS2Forma y color:SolidPeso molecular:400.52iMAC2
CAS:<p>iMAC2, a potent MAC (Membrane Attack Complex) inhibitor, exhibits an IC50 of 28 nM and an LD50 of 15,000 nM, demonstrating significant efficacy in inhibiting</p>Fórmula:C19H20Br2FN3Forma y color:SolidPeso molecular:469.19Ribocil 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%Forma y color:SolidPeso molecular:382.48BM635
CAS:<p>BM635 is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).</p>Fórmula:C25H29FN2OForma y color:SolidPeso molecular:392.51KDOAM-25
CAS:<p>KDOAM-25, a potent KDM5 inhibitor, enhances H3K4 methylation, hampers MM1S cell growth; IC50: 71 nM (5A), 19 nM (5B), 69 nM (5C/D).</p>Fórmula:C15H25N5O2Pureza:98%Forma y color:SolidPeso molecular:307.39Mequindox
CAS:<p>Mequindox is an antimicrobial agent [1]. Mequindox, as an inhibitor of DNA synthesis, induces genotoxicity and carcinogenicity in mice [2].</p>Fórmula:C11H10N2O3Forma y color:SolidPeso molecular:218.21Trimetrexate
CAS:Trimetrexate is an effective competitive inhibitor of bacterial, protozoan, and mammalian dihydrofolate reductase.Fórmula:C19H23N5O3Pureza:98%Forma y color:SolidPeso molecular:369.42PXYC2
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:C7H6N4O3SForma y color:SolidPeso molecular:226.21Sakyomicin A
CAS:<p>Sakyomicin A is an inhibitor of reverse transcriptase.</p>Fórmula:C25H26O10Forma y color:SolidPeso molecular:486.47TH-Z93
CAS:<p>TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.</p>Fórmula:C12H22N2O7P2Pureza:98.37%Forma y color:SolidPeso molecular:368.26Benzylurea
CAS:<p>Benzylurea (AI3-61350) competitively inhibits dehydrogenase/cytokinin oxidase.</p>Fórmula:C8H10N2OPureza:98%Forma y color:SolidPeso molecular:150.18Lexithromycin
CAS:<p>Lexithromycin is an erythromycin A derivative. It has antibacterial activity.</p>Fórmula:C38H70N2O13Pureza:98%Forma y color:SolidPeso molecular:762.97NSC10010 hydrochloride
CAS:<p>NSC10010 inhibits gammaherpesvirus B-lymphomas by activating NF-κB and c-Myc pathways.</p>Fórmula:C31H42Cl2N4O2Pureza:98%Forma y color:SolidPeso molecular:573.60Naftoxate
CAS:<p>Naftoxate is an antimicotic. It is effective against both gram-positive and gram-negative bacteria as well as yeasts and other fungi in plant cell culture.</p>Fórmula:C19H14N2OS2Pureza:98%Forma y color:SolidPeso molecular:350.46PC58538
CAS:<p>PC58538 is an inhibitor of FtsZ protein, a important role in the division machinery of bacterial cells.</p>Fórmula:C24H25NO3Forma y color:SolidPeso molecular:375.46FtsZ-IN-1
CAS:<p>FtsZ-IN-1: potent quinoline-based FtsZ inhibitor; targets Gram-positive bacteria, minimal hemolysis, resists drug resistance.</p>Fórmula:C26H32IN3Forma y color:SolidPeso molecular:513.467Metioprim
CAS:<p>Metioprim is a competitive bacterial dihydrofolate reductases inhibitor.</p>Fórmula:C14H18N4O2SPureza:98%Forma y color:SolidPeso molecular:306.38Antitubercular agent-25
CAS:<p>Compound 28: Antitubercular with extracellular IC50 0.42 μM, intracellular 0.20 μM against M. tuberculosis, metabolically stable.</p>Fórmula:C18H16N4O3S2Forma y color:SolidPeso molecular:400.47ORM-3819
CAS:<p>ORM-3819 is a potent and selective PDE III inhibitor. ORM-3819 promotes cardiac contractility through Ca(2+) sensitization.</p>Fórmula:C19H19N5O5Pureza:98%Forma y color:SolidPeso molecular:397.38(S)-Tedizolid
CAS:<p>(S)-Tedizolid is the S-enantiomer of Tedizolid. Tedizolid is a novel oxazolidinone with activity against Gram-positive pathogens.</p>Fórmula:C17H15FN6O3Pureza:98%Forma y color:SolidPeso molecular:370.34Amiprilose
CAS:<p>Amiprilose is an Immunopotentiator.</p>Fórmula:C14H27NO6Pureza:99.82% - >99.99%Forma y color:SolidPeso molecular:305.37Dextrorotation nimorazole phosphate ester
CAS:<p>Dextrorotation nimorazole phosphate ester: new, efficient, well-tolerated antibacterial and antiparasitic fourth-gen nitroimidazole.</p>Fórmula:C11H19N4O7PForma y color:SolidPeso molecular:350.26InhA-IN-3
CAS:<p>InhA-IN-3 (TU13) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.</p>Fórmula:C14H12ClN3O2SPureza:99.48%Forma y color:SolidPeso molecular:321.78InhA-IN-4
CAS:<p>InhA-IN-4 (TU14) is a Mycobacterium tuberculosis InhA (enoyl ACP reductase) inhibitor for the study of Mycobacterium tuberculosis infection.</p>Fórmula:C14H12BrN3O2SPureza:>99.99%Forma y color:SolidPeso molecular:366.23Sulfoxone sodium
CAS:<p>Sulfoxone sodium ( Adesulfone Sodium) is an anti-leprosy drug.</p>Fórmula:C14H16N2NaO6S3Forma y color:SolidPeso molecular:427.46Sarafloxacin
CAS:<p>Sarafloxacin (A56620) has antibacterial activities against Gram-positive and Gram-negative bacteria.</p>Fórmula:C20H17F2N3O3Pureza:98.07% - 98.94%Forma y color:SolidPeso molecular:385.36Dapabutan
CAS:<p>Dapabutan is an antimicrobial agent active against Gram-positive bacteria.</p>Fórmula:C19H40N2O2Forma y color:SolidPeso molecular:328.53Diazaborine
CAS:<p>Diazaborine disrupts large ribosome formation by inhibiting rRNA maturation and AAA-ATPase Drg1, leading to rapid protein redistribution.</p>Fórmula:C14H13BN2O3SPureza:98%Forma y color:SolidPeso molecular:300.14GA-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:C37H46ClNO6Forma y color:SolidPeso molecular:636.22Antimicrobial 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%Forma y color:SolidPeso molecular:300.38NC00075159
CAS:<p>NC00075159 is an opener of human KCNQ4 (Kv7.4) potassium channel.</p>Fórmula:C15H16N2O3S2Pureza:98%Forma y color:SolidPeso molecular:336.43V-06-018
CAS:V-06-018 is a quorum-sensing modulator. It also acts as a LasR antagonist.Fórmula:C18H27NO2Pureza:98%Forma y color:SolidPeso molecular:289.41Sulfasymazine
CAS:Sulfasymazine is a sulfonamide drug.Fórmula:C13H17N5O2SPureza:98%Forma y color:SolidPeso molecular:307.37B 746
CAS:<p>B 746 is an antibacterial for leprosy, Mycobacterium avium, and drug-resistant tuberculosis.</p>Fórmula:C26H20Cl2N4Forma y color:SolidPeso molecular:459.37Antitubercular agent-33
CAS:<p>Antitubercular agent-33 is a 2-aminothiazole derivative with potent anti-tubercular activity against Mycobacterium tuberculosis ( Mtb ) [1].</p>Fórmula:C15H10N4O3SForma y color:SolidPeso molecular:326.33Megazol
CAS:<p>Megazol treats protozoan infections like Chagas and sleeping sickness; it's a potent nitroimidazole drug.</p>Fórmula:C6H6N6O2SPureza:98%Forma y color:SolidPeso molecular:226.22Methylisothiazolinone
CAS:<p>Methylisothiazolinone (MI) is a powerful synthetic biocide and preservative within the group of isothiazolinones.</p>Fórmula:C4H5NOSPureza:99.78%Forma y color:Colorless Prisms LiquidPeso molecular:115.158-Deazahomofolic acid
CAS:<p>8-Deazahomofolic acid is a potential thymidylate synthase (TS) inhibitor and other folate related enzymes inhibitor.</p>Fórmula:C21H22N6O6Pureza:98%Forma y color:SolidPeso molecular:454.44BPH-1358
CAS:<p>BPH-1358 (NSC-50460) inhibits FPPS and UPPS (IC50: 1.8 μM, 110 nM), active against S. aureus (MIC ~250 ng/mL).</p>Fórmula:C32H30Cl2N6O2Pureza:99.74%Forma y color:SolidPeso molecular:601.532,6-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%Forma y color:Off White To Cream Coloured Crystalline SolidPeso molecular:238.11Mtb-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:C26H35NO2Forma y color:SolidPeso molecular:393.56Ribocil-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%Forma y color:SolidPeso molecular:419.5Vebufloxacin
CAS:<p>Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and Pseudomonas</p>Fórmula:C19H22FN3O3Pureza:98%Forma y color:SolidPeso molecular:359.39PNU288034
CAS:<p>PNU288034 is a potent oxazolidinone antibiotic with antimicrobial activity for the prevention and treatment of Gramnegative infections.</p>Fórmula:C16H19F2N3O5SPureza:98.41%Forma y color:SolidPeso molecular:403.4Afabicin
CAS:<p>Afabicin is an antibiotic targeting Staphylococcus aureus. treat acute bacterial skin and skin structure infections.the prodrug of Debio1452.</p>Fórmula:C23H24N3O7PPureza:98%Forma y color:SolidPeso molecular:485.43WCK-4234 sodium
CAS:<p>WCK-4234 sodium inhibits β-lactamase A, C, D & OXA carbapenemases, useful against MDR infections.</p>Fórmula:C7H8N3NaO5SPureza:97.01%Forma y color:SolidPeso molecular:269.21Antibacterial agent 48
CAS:<p>Antibacterial agent 48 is an antimicrobial agent that reduces the MIC of the antimicrobial agent Ceftazidime.</p>Fórmula:C13H18N5NaO7SForma y color:SolidPeso molecular:411.36PXYC1
CAS:<p>PXYC1 binds Mtb RpsA-CTD (Kd 0.81 μM) & RpsA-CTD Δ438A (Kd 0.31 μM), hindering trans-translation.</p>Fórmula:C9H10N4O3SForma y color:SolidPeso molecular:254.27Cefmenoxime
CAS:<p>Cefmenoxime: IV/IM cephalosporin antibiotic, resists beta-lactamase, targets Enterobacteriaceae, gram-positive/negative bacteria.</p>Fórmula:C16H17N9O5S3Pureza:98%Forma y color:Almost White Or Almost Yellow Crystalline PowderPeso molecular:511.558Ranitidine 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:C19H27BiN4O10SForma y color:SolidPeso molecular:712.48Sulfametrole
CAS:<p>Sulfametrole: oral, potent antibacterial for HIV, severe pneumonia, UTIs research.</p>Fórmula:C9H10N4O3S2Forma y color:SolidPeso molecular:286.33(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:C20H21ClFN3O3Forma y color:SolidPeso molecular:405.85DHDPS-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:C13H11NO5SForma y color:SolidPeso molecular:293.3Mycobactin-IN-2
CAS:<p>Mycobactin-IN-2 inhibits mycobactin production by targeting salicyl-AMP ligase (MbtA), a crucial enzyme in its pathway.</p>Fórmula:C15H13BrN2OForma y color:SolidPeso molecular:317.18Tuberculosis inhibitor 3
CAS:<p>Tuberculosis inhibitor 3 is a highly potent and oral anti-tuberculosis drug against both drug-sensitive and drug-resistant Mycobacterium , H37RV & MDR-TB.</p>Fórmula:C21H22F6N4O3SPureza:98.8%Forma y color:SolidPeso molecular:524.48(±)-Hydnocarpin
CAS:<p>(±)-Hydnocarpin, a flavonolignan, demonstrates inhibitory activity against S.</p>Fórmula:C25H20O9Forma y color:SolidPeso molecular:464.42Antitubercular 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:C15H22N6OSForma y color:SolidPeso molecular:334.44Sulfamethomidine
CAS:<p>Sulfamethomidine has antibacterial activity [1].</p>Fórmula:C12H14N4O3SForma y color:SolidPeso molecular:294.33Thiambutosine
CAS:<p>Thiambutosine exhibits inhibitory activity against Mycobacterium leprae and mushroom tyrosinase, making it suitable for infection studies.</p>Fórmula:C19H25N3OSPureza:99.95%Forma y color:SolidPeso molecular:343.49VP-4509
CAS:<p>VP-4509: Anti-MRSA, MIC 49.3 μM; combats Pseudomonas aeruginosa.</p>Fórmula:C14H16N2O5SForma y color:SolidPeso molecular:324.35Metallo-β-lactamase-IN-5
CAS:<p>Metallo-β-lactamase-IN-5 (compound 5c) is a powerful inhibitor of metallo-β-lactamases (MBLs).</p>Fórmula:C19H16N4O3Forma y color:SolidPeso molecular:348.36Oxyphenbutazone monohydrate
CAS:<p>Oxyphenbutazone monohydrate: Phenylbutazone derivative, anti-inflammatory, non-selective COX inhibitor, kills dormant M. tuberculosis.</p>Fórmula:C19H22N2O4Forma y color:SolidPeso molecular:342.39
