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 3386 produtos de "Antibacteriano"
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FtsZ-IN-2
CAS:FtsZ-IN-2, a bacterial FtsZ inhibitor, hampers GTPase; has anti-MRSA/MSSA effects with 2 μg/ml MIC.Fórmula:C30H35N5SCor e Forma:SolidPeso molecular:497.7CP-67015
CAS:CP 67015 has an inhibitory effect on the function of topoisomerase, and is a direct mutagen in mammalian cells, which has effects on gene and chromosome levels.Fórmula:C17H12F2N2O3Cor e Forma:SolidPeso molecular:330.293-Chlorogentisyl alcohol
CAS:3-Chlorogentisyl alcohol: E. coli β-glucuronidase inhibitor (IC50=0.74µM, Ki=0.58µM), antiproliferative, for anti-cancer/inflammatory research.Fórmula:C7H7ClO3Cor e Forma:SolidPeso molecular:174.58Afabicin disodium
CAS:Afabicin (Debio 1450), a Debio1452 precursor, targets Staphylococcus by inhibiting lipid synthesis.Fórmula:C23H22N3Na2O7PCor e Forma:SolidPeso molecular:529.396BioA-IN-13
CAS:BioA-IN-13 is a highly effective inhibitor of the Mycobacterium tuberculosis BioA enzyme, displaying potent cell permeability and whole-cell activity [1].Fórmula:C19H16N2O4SCor e Forma:SolidPeso molecular:368.41Dermadin
CAS:Dermadin is an antibacterial and can be used in paper mill systems to inhibit the growth of Aerobacter aerogenes which is known to produce slime in such system.Fórmula:C9H9NO3Cor e Forma:SolidPeso molecular:179.175DprE1-IN-4
CAS:DprE1-IN-4: Potent DprE1 inhibitor (IC50: 0.90 μg/mL), good pharmacokinetics, kills TB bacteria in mice.Fórmula:C20H21N3O5SCor e Forma:SolidPeso molecular:415.46Mt KARI-IN-5
CAS:Mt KARI-IN-5 inhibits MtbKARI with Ki 4.72 μM, has MIC 1.56 μM against MtbH37Rv, and is low in cytotoxicity with IC50 >64 μg/mL in HEK.Fórmula:C14H10N4O5S3Cor e Forma:SolidPeso molecular:410.45Antitubercular agent-12
CAS:Compound 2c, an effective antitubercular, MIC 1.439 μg/mL, low toxicity with CC50 57.34 μg/mL.Fórmula:C13H7BrN4O5Cor e Forma:SolidPeso molecular:379.12Antitubercular agent-28
CAS:Antitubercular agent-28 targets resistant Mycobacterium tuberculosis; MIC: 4.5 μM, IC50: 1.5 μM, IC90: 2.5 μM; low cytotoxicity.Fórmula:C17H14N4O2Cor e Forma:SolidPeso molecular:306.32Mycobacterial Zmp1-IN-1
Zmp1-IN-1: An inhibitor of mycobacterial Zmp1 with dose-dependent anti-tuberculosis effects.Fórmula:C26H27N3O7SCor e Forma:SolidPeso molecular:525.57Sudoterb HCl
CAS:Sudoterb has anti-tubercular activity.Fórmula:C29H30Cl2F3N5OPureza:98%Cor e Forma:SolidPeso molecular:592.48Octenidine saccharin
CAS:Octenidine saccharin is a Dental Plaque InhibitorFórmula:C50H72N6O6S2Cor e Forma:SolidPeso molecular:917.27Carbazomycin B
CAS:Carbazomycin B, a Streptomyces metabolite, combats fungi, bacteria, P. falciparum, C. albicans, and some cancer cells; inhibits 5-LO (IC50=1.5µM).Fórmula:C15H15NO2Cor e Forma:SolidPeso molecular:241.29Avidinorubicin
CAS:Avidinorubicin is a novel anthracycline with platelet aggregation inhibitory activity.Fórmula:C60H86N4O22Cor e Forma:SolidPeso molecular:1215.34β-Carboline-1-carboxylic acid
CAS:β-Carboline-1-carboxylic acid is an alkaloid that has been found in P.Fórmula:C12H8N2O2Cor e Forma:SolidPeso molecular:212.2BO3482
CAS:BO3482 is an antimicrobial compound and can inhibit the growth of methicillin-resistant Staphylococci (MIC90: 6.25 mg/mL).Fórmula:C14H20N2NaO5S2Pureza:98%Cor e Forma:SolidPeso molecular:383.43Capreomycin free base
CAS:Capreomycin, a polypeptide antibiotic from S. capreolus, combats M. tuberculosis (MIC 10 µg/ml), hindering protein synthesis at 30S/50S ribosomes.Fórmula:C50H88N28O15Cor e Forma:SolidPeso molecular:1321.43Anti-MRSA agent 1
CAS:Anti-MRSA agent 1 is an MRSA inhibitor with an MIC value of 0.5 μg/mL and is effective in alleviating the effects of MRSA resistance.Fórmula:C26H29N7O4SCor e Forma:SolidPeso molecular:535.62Antofloxacin Hydrochloride
CAS:Antofloxacin Hydrochloride: Fluoroquinolone for AECB, AP, cystitis, folliculitis treatment.Fórmula:C18H22ClFN4O4Pureza:98%Cor e Forma:SolidPeso molecular:412.84MtTMPK-IN-4
CAS:MtTMPK-IN-4, a para-piperidine, blocks MtTMPK in tuberculosis with 6.1 μM IC50 and also inhibits tyrosinase.Fórmula:C23H25N3O3Cor e Forma:SolidPeso molecular:391.46Ro 24-6392
CAS:Ro 24-6392, an ester co-drug of ciprofloxacin and desacetylcefotaxime, combats various aerobic bacteria.Fórmula:C31H31FN8O8S2Pureza:98%Cor e Forma:SolidPeso molecular:726.76Erythromycin Gluceptate
CAS:Erythromycin Gluceptate is an inhibitor of protein translation and mammalian mRNA splicing. It inhibits growth of gram negative and gram positiove bacteria.Fórmula:C44H81NO21Cor e Forma:SolidPeso molecular:960.11L-573655
CAS:L-573655, an antibacterial agents, targets lipid A biosynthesis in gram-negative bacteria.Fórmula:C10H10N2O3Pureza:98%Cor e Forma:SolidPeso molecular:206.2Chaetoglobosin C
CAS:Chaetoglobosin C (Compound 4), an anthraquinone-chromone derivative of Chaetomium globosum KMITL-N0802, exhibits anti-tuberculosis activity [1].Fórmula:C32H36N2O5Cor e Forma:SolidPeso molecular:528.64Leu-AMS
CAS:Leu-AMS, a leucine analogue with 22.34 nM IC50, inhibits LRS and bacterial growth without affecting mTORC1.Fórmula:C16H25N7O7SPureza:98%Cor e Forma:SolidPeso molecular:459.48Texaline
CAS:Texaline is an agent of the antitubercular.Fórmula:C15H10N2O3Pureza:98%Cor e Forma:SolidPeso molecular:266.25Kumbicin C
CAS:Kumbicin C inhibits the growth of NS-1 mouse myeloma cells (IC50 = 0.74 μg/ml) and the growth of the Gram-positive bacteria B. subtilis (MIC = 1.6 μg/ml).Fórmula:C28H24N2O3Cor e Forma:SolidPeso molecular:436.5Omeprazole Sodium
CAS:Omeprazole Sodium is a proton pump inhibitor(PPI) and suppresses gastric acid secretion.Fórmula:C17H18N3NaO3SPureza:99.84%Cor e Forma:Clear In WaterPeso molecular:367.4Lascufloxacin
CAS:Lascufloxacin: potent, oral fluoroquinolone antibiotic for respiratory infections, effective against quinolone-resistant strains.Fórmula:C21H24F3N3O4Pureza:98%Cor e Forma:SolidPeso molecular:439.43MAC-0547630
CAS:MAC-0547630 potent and selective inhibitor of UppS.Fórmula:C19H21FN4Pureza:98%Cor e Forma:SolidPeso molecular:324.4CD 1530
CAS:CD 1530 is an ARγ agonist (Kd:150 nM) with potential anticancer activity for the study of oral carcinogenesis.Fórmula:C27H26O3Pureza:98.13%Cor e Forma:SolidPeso molecular:398.49Antitubercular agent-36
CAS:Antitubercular agent-36 inhibits Mycobacterium tuberculosis with MIC90 of 1.25 μg/mL, used in TB research.Fórmula:C18H17N3O3Cor e Forma:SolidPeso molecular:323.35Antitubercular agent-37
CAS:Antitubercular Agent-37 exhibits antimycobacterial properties and functions as an antibacterial agent with an MIC (minimum inhibitory concentration) value of 0.Fórmula:C22H22N8O2Cor e Forma:SolidPeso molecular:430.46Erythromycin hydrochloride
CAS:Erythromycin hydrochloride is an inhibitor of protein translation and mammalian mRNA splicing. It inhibits growth of gram negative and gram positiove bacteria.Fórmula:C37H68ClNO13Cor e Forma:SolidPeso molecular:770.39Ethambutol, (R,R)-
CAS:Ethambutol, (R,R), treats tuberculosis, often combined with other drugs; may also target Mycobacterium avium and kansasii.Fórmula:C10H24N2O2Cor e Forma:SolidPeso molecular:204.31L 652813
CAS:L 652813 is one kind of quaternary heterocyclylamino beta-lactam.Fórmula:C24H22N6NaO5S2Cor e Forma:SolidPeso molecular:561.59UNC10201652
CAS:UNC10201652 inhibits intestinal L1-specific β-glucuronidases; effective against E. coli (IC50: 0.117 μM).Fórmula:C20H25N7OSCor e Forma:SolidPeso molecular:411.52Ro 14-9578
CAS:Ro 14-9578 is anantibacterial agent in the class of tricyclic quinolone.Fórmula:C16H13NO5Pureza:98%Cor e Forma:SolidPeso molecular:299.28Methenamine mandelate
CAS:Methenamine mandelate-loaded nanoparticles can induce DNA damage and apoptosis of cancer cells.Fórmula:C14H20N4O3Cor e Forma:SolidPeso molecular:292.33Antimycobacterial agent-2
CAS:Antimycobacterial agent-2 has MIC99 0.8 μM vs M.tb H37Rv; cytotoxic with IC50 48.1 μM on CHO cells.Fórmula:C31H50O5Cor e Forma:SolidPeso molecular:502.73Antibacterial agent 117
CAS:Triazole-derived Antibacterial 117 inhibits R. prowazekii MetAP1 with a 15 μM IC50 and rickettsial growth.Fórmula:C9H9ClN4SCor e Forma:SolidPeso molecular:240.71Antitubercular agent-20
CAS:Antitubercular agent-20 is an orally active antitubercular agent. agent-20 showed low cytotoxicity and good tolerability in BALB/c mice.Fórmula:C25H22F6N4O3SCor e Forma:SolidPeso molecular:572.52VP-4556
CAS:VP-4556 is a potent anti-MRSA compound with >95% inhibition at 8 μg/mL MIC.Fórmula:C12H12N2O4SCor e Forma:SolidPeso molecular:280.3Anti-inflammatory agent 11
CAS: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.Fórmula:C14H14N4OSCor e Forma:SolidPeso molecular:286.35D-Homoserine lactone
CAS:D-homoserine lactone is an enantiomer of L-homoserine lactone and an inhibitor of serine hydroxymethyltransferase (SHMT; Ki= 11 mM for the rabbit enzyme).1Fórmula:C4H7NO2Cor e Forma:SolidPeso molecular:101.1PNU-176798
CAS:PNU-176798 is an agent with antimicrobial.Fórmula:C16H13FN4O3SPureza:98%Cor e Forma:SolidPeso molecular:360.36KB-5246
CAS:KB-5246, displays antibacterial activities.is a tetracyclic quinolone.Fórmula:C18H17ClFN3O4SPureza:98%Cor e Forma:SolidPeso molecular:425.86Anticancer agent 34
CAS: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).Fórmula:C17H14BrN3O3S2Cor e Forma:SolidPeso molecular:452.35KSK213
CAS:KSK213: Strongly inhibits C. trachomatis (EC50=60 nM); non-toxic to commensals/host cells at 25 μM.Fórmula:C28H25N3O2SCor e Forma:SolidPeso molecular:467.58GNLPT-IN-1
CAS:GNLPT-IN-1 is an inhibitor of gram-negative lipoprotein trafficking.Fórmula:C20H21N3O2Cor e Forma:SolidPeso molecular:335.4trans-Cephalosporin
CAS:Trans-substituted cephalosporin is an efficient inhibitor of NDM-1, demonstrating an IC50 value of 0.13 μM.Fórmula:C16H14N2O4S3Cor e Forma:SolidPeso molecular:394.49Phevamine A
CAS:Phevamine A (PHVA) is a suppressor of plant immune responses.Fórmula:C22H39N7O2Pureza:98%Cor e Forma:SolidPeso molecular:433.59BPH-1358 free base
CAS:BPH-1358 inhibits UPPS (IC50: 110 nM) and FPPS (IC50: 1.8 µM), effective against S. aureus (MIC ~250 ng/mL).Fórmula:C32H28N6O2Pureza:98%Cor e Forma:SolidPeso molecular:528.6UGM-IN-3
CAS:UGM-IN-3 inhibits UGM (Kd=66 μM) and M. tuberculosis growth (MIC=6.2 μg/mL).Fórmula:C18H16INO2Cor e Forma:SolidPeso molecular:405.23Syncytial Virus Inhibitor-1
CAS:Syncytial Virus Inhibitor-1: Potent, oral RSV fusion blocker (EC50: 0.002-0.004 μM for Long, A2, B strains).Fórmula:C23H26N4O3SPureza:98%Cor e Forma:SolidPeso molecular:438.54WX-081
CAS: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).Fórmula:C34H33ClN2O2Cor e Forma:SolidPeso molecular:537.09DHFR-IN-1
CAS:DHFR-IN-1: selective DHFR blocker, IC50 40.71 nM, antifungal, strong against Gram-positive/negative bacteria, synergizes with Levofloxacin (FIC=0.249).Fórmula:C22H22N6O4S2Cor e Forma:SolidPeso molecular:498.58SW203668 (trifluoroacetate salt)
CAS:SW203668: Irreversible stearoyl-CoA desaturase blocker; IC50=54 nM; cytotoxic to CYP4F11-positive cancer cells; IC50=22-116 nM.Fórmula:C24H20F3N3O4SCor e Forma:SolidPeso molecular:503.495'-Hydroxy-staurosporine
CAS:5'-Hydroxy-staurosporine is an AMPK inhibitor with selective toxicity toward human colon tumor cells.Fórmula:C28H26N4O4Cor e Forma:SolidPeso molecular:482.53Antibacterial agent 141
CAS: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.Fórmula:C23H27ClN2O3Cor e Forma:SolidPeso molecular:414.93Cefonicid (free base)
CAS:Cefonicid: second-gen cephalosporin, IV/IM, treats UTIs, respiratory, bone, and soft tissue infections by blocking cell wall formation.Fórmula:C18H18N6O8S3Cor e Forma:SolidPeso molecular:542.57LasR-IN-4
CAS:LasR-IN-4 is a potent inhibitor of LasR which inhibits Pseudomonas aeruginosa and its biofilm formation, pyocyanin production, and rhamnolipids production [1].Fórmula:C18H20N4Cor e Forma:SolidPeso molecular:292.38OX11
CAS:OX11 is a selective inhibitor of S. pneumoniae, P. aeruginosa and E. coli bacteria.Fórmula:C17H10Cl2N4O3S2Cor e Forma:SolidPeso molecular:453.32Levomecol
CAS:Levomecol: Streptomyces-made antibiotic with Chloramphenicol & Methyluracil, halts bacterial growth by blocking protein synthesis.Fórmula:C16H18Cl2N4O7Pureza:98%Cor e Forma:SolidPeso molecular:449.24Antibacterial agent 101
CAS:Antibacterial agent 101 exhibited antibacterial and antifungal effects (MIC=4-32 μg/mL).Fórmula:C28H29BrN2OCor e Forma:SolidPeso molecular:489.45Tenuazonic acid
CAS:Tenuazonic acid, a nonhost-selective mycotoxin from Alternaria alternate, inhibits PSII by blocking electron transport at D1 protein.Fórmula:C10H15NO3Pureza:98%Cor e Forma:SolidPeso molecular:197.23AFN-1252 tosylate
CAS:AFN-1252 tosylate is an enoyl-ACP Reductase inhibitor.Fórmula:C29H29N3O6SPureza:98%Cor e Forma:SolidPeso molecular:547.62Aztreonam lysine
CAS:Aztreonam lysine is an inhaled anti-pseudomonal treatment for people who have pulmonary Pseudomonas aeruginosa infection with cystic fibrosis (CF).Fórmula:C19H31N7O10S2Pureza:98%Cor e Forma:SolidPeso molecular:581.62Epiroprim
CAS:Epiroprim (Ro11-8958) is a selective dihydrofolate reductase (DHFR) inhibitor with antibacterial activity, inhibiting Staphylococcus and Streptococcus.Fórmula:C19H23N5O2Pureza:99.68% - >99.99%Cor e Forma:SolidPeso molecular:353.42Cefroxadine
CAS:Cefroxadine: an oral cephalosporin antibiotic, broad-spectrum, bactericidal, effective for acute uncomplicated cystitis.Fórmula:C16H19N3O5SPureza:98%Cor e Forma:SolidPeso molecular:365.4TL8-506
CAS:TL8-506 is a selective and potent TLR8 agonist that induces cytokine and chemokine production.TL8-506 alleviates inflammatory and autoimmune diseases.Fórmula:C20H17N3O2Pureza:95% - 99.97%Cor e Forma:SolidPeso molecular:331.37AV-1101
CAS:AV-1101, a cytokine production inhibitor, is used potentially for the treatment of HIV infection.Fórmula:C19H20N2O4Pureza:98%Cor e Forma:SolidPeso molecular:340.37BoNT-IN-33
CAS:BoNT-IN-33 is a potent inhibitor of Botulinum neurotoxin/A light chain (BoNT/A LC).Fórmula:C25H26N4OCor e Forma:SolidPeso molecular:398.5Elsamitrucin
CAS:Elsamitrucin, a heterocyclic antibiotic, disrupts DNA replication by intercalating into G-C sequences and inhibiting topoisomerases.Fórmula:C33H35NO13Cor e Forma:SolidPeso molecular:653.63MenA-IN-1
MenA IN-1 inhibits MTB's MenA enzyme; IC50=13µM, GIC50=8µM, helps fight tuberculosis spread.Fórmula:C29H36N2O2Cor e Forma:SolidPeso molecular:444.61Flomoxef sodium
CAS:Flomoxef sodium, an antibiotic belonging to the oxacephem group, exhibits excellent activity against a broad spectrum of Gram-positive bacteria.Fórmula:C15H17F2N6NaO7S2Pureza:99.28%Cor e Forma:SolidPeso molecular:518.44Antitubercular agent-31
CAS:Antitubercular agent-31 is an antitubercular agent that inhibits M. tuberculosisH37Rv (MIC: 0.03 μM) and also inhibits DprE1 (IC50: 1.1 μM).Fórmula:C20H24F2N4O5S2Cor e Forma:SolidPeso molecular:502.56Gln-AMS
CAS:Gln-AMS is an inhibitor of aminoacyl-tRNA synthetases (AARS). It specifically binds to the A-domain located within the NRPS enzymes.Fórmula:C15H22N8O8SPureza:98%Cor e Forma:SolidPeso molecular:474.45Antibacterial agent 100
CAS:Compound 7c: Antibacterial/fungal, effective on S. aureus, C. albicans (MIC 4 μg/mL), C. neoformans (MIC 8 μg/mL).Fórmula:C28H29BrN2Cor e Forma:SolidPeso molecular:473.458CAY10711
CAS:CAY10711: potent bactericide for Gram-positive/negative bacteria including MRSA, inhibits biofilms, synergizes with kanamycin, low mammalian toxicity.Fórmula:C41H54N6S2Cor e Forma:SolidPeso molecular:695.04SARS-CoV-2 3CLpro-IN-4
CAS:SARS-CoV-2 3CLpro-IN-4 (Compound 5g) is a multifunctional inhibitor of SARS CoV-2 3CLpro, exhibiting antiviral, antibacterial, and antifungal activities.Fórmula:C22H19ClN6OSCor e Forma:SolidPeso molecular:450.94Closthioamide
CAS: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).Fórmula:C29H38N6O2S6Pureza:98%Cor e Forma:SolidPeso molecular:695.04DNA Gyrase-IN-3
CAS:DNA Gyrase-IN-3 inhibits E. coli DNA gyrase B with IC50 5.41-15.64 μM; shows anti-TB and antibacterial properties.Fórmula:C18H20N6OS2Cor e Forma:SolidPeso molecular:400.52iMAC2
CAS: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 inhibitingFórmula:C19H20Br2FN3Cor e Forma:SolidPeso molecular:469.19Ribocil B
CAS:Ribocil-B is the active S-isomer of ribocil which can inhibit flavin mononucleotide (FMN,KD of 6.6 nM).Fórmula:C19H22N6OSPureza:98%Cor e Forma:SolidPeso molecular:382.48Antibacterial agent 123
CAS:Antibacterial Agent 123 (Compound 111) serves as an effective membrane-disrupting agent targeting antibiotic-resistant Gram-positive bacteria [1].Fórmula:C17H8F9N3OCor e Forma:SolidPeso molecular:441.25BM635
CAS:BM635 is an MmpL3 inhibitor with outstanding anti-mycobacterial activity (MIC50: 0.12 μM against M. tuberculosis H37Rv).Fórmula:C25H29FN2OCor e Forma:SolidPeso molecular:392.51DprE1-IN-1
CAS:DprE1-IN-1: Potent, oral DprE1 inhibitor; stable in hepatocytes, low toxicity, anti-bacilli in macrophages, -1.29 log10 CFU.Fórmula:C19H21N3O6S2Cor e Forma:SolidPeso molecular:451.52Antimicrobial Compound 1
CAS:Antimicrobial Compound 1: Alkyl pyridinium, 12C tail, 4-carboxyl head, effective against B. subtilis & E. coli.Fórmula:C18H30BrNO2Pureza:>99.99%Cor e Forma:SolidPeso molecular:372.34Ref: TM-T10337
1mg129,00€5mg301,00€10mg411,00€25mg623,00€50mg837,00€100mg1.099,00€200mg1.485,00€1mL*10mM (DMSO)360,00€Thiambutosine
CAS:Thiambutosine exhibits inhibitory activity against Mycobacterium leprae and mushroom tyrosinase, making it suitable for infection studies.Fórmula:C19H25N3OSPureza:99.95%Cor e Forma:SolidPeso molecular:343.49Mequindox
CAS:Mequindox is an antimicrobial agent [1]. Mequindox, as an inhibitor of DNA synthesis, induces genotoxicity and carcinogenicity in mice [2].Fórmula:C11H10N2O3Cor e Forma:SolidPeso molecular:218.21Trimetrexate
CAS:Trimetrexate is an effective competitive inhibitor of bacterial, protozoan, and mammalian dihydrofolate reductase.Fórmula:C19H23N5O3Pureza:98%Cor e Forma:SolidPeso molecular:369.42CAI-1
CAS:CAI-1 is a vibrio cholerae quorum-sensing autoinducer.Fórmula:C13H26O2Cor e Forma:SolidPeso molecular:214.34(3R,4R)-A2-32-01
CAS:(3R,4R)-A2-32-01 is the (R,R)-enantiomer of A2-32-01 and has potential antibacterial activity.Fórmula:C19H27NO2Pureza:98.19%Cor e Forma:SolidPeso molecular:301.42PXYC2
CAS:PXYC2 is an RpsA-CTD antagonist; Kd: 6.35 μM for RpsA-CTD, 5.11 μM for RpsA-CTD Δ438A; vital in trans-translation.Fórmula:C7H6N4O3SCor e Forma:SolidPeso molecular:226.21Bederocin
CAS:Bederocin (REP8839), a METS inhibitor, has strong activity against S. aureus, S. pyogenes, and Gram-positive bacteria.Fórmula:C20H21BrFN3OSPureza:98%Cor e Forma:SolidPeso molecular:450.37Sakyomicin A
CAS:Sakyomicin A is an inhibitor of reverse transcriptase.Fórmula:C25H26O10Cor e Forma:SolidPeso molecular:486.47TH-Z93
CAS:TH-Z93 is a potent FPPS inhibitor (IC50:90 nM) and a lipophilic bisphosphonate.Fórmula:C12H22N2O7P2Pureza:98.37%Cor e Forma:SolidPeso molecular:368.26Benzylurea
CAS:Benzylurea (AI3-61350) competitively inhibits dehydrogenase/cytokinin oxidase.Fórmula:C8H10N2OPureza:98%Cor e Forma:SolidPeso molecular:150.18
