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 2959 produtos de "Antibacteriano"
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Ceftezole
CAS:<p>Ceftezole: alpha-glucosidase inhibitor, anti-diabetic, broad-spectrum antibiotic for gram-positive/negative bacteria.</p>Fórmula:C13H12N8O4S3Pureza:98%Cor e Forma:SolidPeso molecular:440.48Saccharin sodium hydrate
CAS:<p>Saccharin sodium salt hydrate, a sweetener for foods and diabetic diets, has been probed for carcinogenicity.</p>Fórmula:C7H6NNaO4SCor e Forma:Colorless Crystal Or Slightly White Crystalline PowderPeso molecular:223.18Chloramphenicol palmitate
CAS:<p>Chloramphenicol palmitate is a broad-spectrum antibiotic effective against various bacteria and used for bacterial selection in gene studies.</p>Fórmula:C27H42Cl2N2O6Pureza:99.89%Cor e Forma:Crystals Very Slightly Sol In WaterPeso molecular:561.54PPM1A-IN-1
CAS:<p>PPM1A-IN-1 (Compound IV-4) is an inhibitor of the PP2C Ser/Thr protein phosphatase Mg2+/Mn2+-dependent 1A. It exhibits antibacterial activity against Mycobacterium tuberculosis.</p>Fórmula:C16H15BrFNO2Cor e Forma:SolidPeso molecular:352.2Lapyrium
CAS:<p>Lapyrium, a biocide/antistatic cationic surfactant in personal care, also treats waste-water/corrosion as chloride salt.</p>Fórmula:C21H35N2O3Pureza:98%Cor e Forma:SolidPeso molecular:363.51Tetra-N-acetyl Kanamycin A
CAS:Produto Controlado<p>Applications Protected Kanamycin A (K137500). Antibiotic complex produced by Streptomyces kanamyceticus Okami & Umezawa from Japanese soil. Comprised of three components, kanamycin A, the major component, and kanamycins B and C, two minor congeners. Antibacterial.<br>References Ito, et al.: J. Antibiot., 17, 189 (1964), Toda, S., et al.: J. Antibiot., 30, 1002 (1977), Claes, P.J., et al.: Anal. Profiles Drug. Subs., 6, 259 (1977),<br></p>Fórmula:C26H44N4O15Cor e Forma:NeatPeso molecular:652.65Tridehydro Pirlimycin-d5
CAS:Produto ControladoFórmula:C17H20D5ClN2O5SCor e Forma:NeatPeso molecular:409.94Polyquaternium-1
CAS:<p>Polyquaternium-1: a mild eye-safe preservative that inhibits microbes in multi-dose ophthalmic meds.</p>Fórmula:C22H48Cl3N3O6Pureza:95%Cor e Forma:SolidPeso molecular:556.99Norvancomycin hydrochloride
CAS:<p>Norvancomycin hydrochloride (Desmethyl-vancomycin hydrochloride) is used as a treatment for endocarditis, osteomyelitis, pneumonia, sepsis, or soft tissue</p>Fórmula:C65H74Cl3N9O24Pureza:95.29% - 99.02%Cor e Forma:SolidPeso molecular:1471.69ThrRS-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:385.25Antibacterial agent 72
CAS:<p>Antibacterial agent 72 has an antibacterial effect by selectively acting on bacterial membranes.</p>Fórmula:C19H21BrN4SCor e Forma:SolidPeso molecular:417.37Mab 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:293.28MAC173979
CAS:<p>MAC173979 inhibits E. coli de novo PABA biosynthesis and growth.</p>Fórmula:C9H5Cl2NO3Pureza:98%Cor e Forma:SolidPeso molecular:246.05Fumaramidmycin
CAS:<p>Fumaramidmycin is an antibiotic that is produced by Streptomyces kurssanovii NR-7GG1.</p>Fórmula:C12H12N2O3Pureza:98%Cor e Forma:SolidPeso molecular:232.24Anserinone 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:210.23Mtb-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:333.3Benzoxonium chloride
CAS:<p>Benzoxonium chloride used in Thio-Ben for cutaneous leishmaniasis treatment with cryotherapy.</p>Fórmula:C23H42ClNO2Cor e Forma:SolidPeso molecular:400.04PD 140248
CAS:<p>PD 140248, a broad-spectrum 7-pyrrolidinyl fluoronaphthyridines, has been demonstrated to have excellent in vitro activity against gram-positive organisms.</p>Fórmula:C21H20ClF3N4O3Cor e Forma:SolidPeso molecular:468.86HadAB-IN-1
CAS:<p>HadAB-IN-1: potent TB research chemical; IC50 = 0.03μM; inhibits HadAB, affecting Mtb mycolic acid synthesis.</p>Fórmula:C19H17BrClN3O3SCor e Forma:SolidPeso molecular:482.78Antifungal agent 37
CAS:<p>Antifungal agent 37 is a heterocyclic disulfide that exhibits antifungal activity [1].</p>Fórmula:C7H10N2S2Cor e Forma:SolidPeso molecular:186.3DNA 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:460.33PknB-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:390.52Anthrarobin
CAS:<p>Anthrarobin is an antipsoriatic.</p>Fórmula:C14H10O3Pureza:98%Cor e Forma:SolidPeso molecular:226.23ANT431
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:285.3Ceftobiprole 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:712.64YXL-13
CAS:<p>YXL-13 suppresses Pseudomonas aeruginosa, hampers virulence and biofilms, and reduces drug resistance with an IC50 of 3.686 μM.</p>Fórmula:C13H15BrN2O4Cor e Forma:SolidPeso molecular:343.17F-17
CAS:<p>F-17 inhibits biofilm, elastase, pyocyanin, and motility, binds to LasR/PqsR, and is non-cytotoxic.</p>Fórmula:C17H15BrO4Cor e Forma:SolidPeso molecular:363.2Antitubercular 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:346.18BK 218
CAS:<p>BK 218: New cephalosporin, treats S. pneumoniae, H. influenzae, M. catarrhalis; less effective on penicillin-resistant strains; oral/IV use.</p>Fórmula:C15H14ClN7NaO5S2Cor e Forma:SolidPeso molecular:494.88Topoisomerase 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:671.7Metallo-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:225.26B 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:449.7314α-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:430.46Caspofungin
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:268.31GA-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:619.76Antimicrobial 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:326.76PqsR/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:311.35GlcN-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:391.49KFU-127
<p>KFU-127: broad-spectrum antimicrobial; targets bacterial/fungal biofilms; toxic to eukaryotic cells.</p>Fórmula:C34H43BrN2O3Cor e Forma:SolidPeso molecular:607.62Ipconazole [ISO]
CAS:<p>Ipconazole, a cyclopentanol with 1,2,4-triazolylmethyl, 4-chlorobenzyl & isopropyl groups, is a fungicide that targets seed diseases.</p>Fórmula:C18H24ClN3OCor e Forma:SolidPeso molecular:333.86Mtb-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:297.43Antibacterial agent 74
CAS:<p>Antibacterial agent 74 (compound 36) has anti-Salmonella activity [1].</p>Fórmula:C16H20N2O3Cor e Forma:SolidPeso molecular:288.34Phosphoglycolohydroxamic acid
CAS:<p>Phosphoglycolohydroxamic acid inhibits aldolase/triose-phosphate isomerase; used in antibacterial/antifungal research.</p>Fórmula:C2H6NO6PCor e Forma:SolidPeso molecular:171.05Anti-infective agent 2
CAS:<p>Compound 3k is antiprotozoal/antimycobacterial, with IC50s: P. falciparum 0.07 μM, T. brucei 2.20 μM; MIC: M. smegmatis 32 μg/mL.</p>Fórmula:C15H8ClNO2Cor e Forma:SolidPeso molecular:269.68PXYC13
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:329.38Antibacterial 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:234.25Metallo-β-lactamase-IN-7
CAS:<p>Metallo-β-lactamase-IN-7 is a potent inhibitor of VIM -Type metallo-β-lactamase with IC 50 s of 0.019 μM, 13.64 μM, 0.38 μM for VIM-2, VIM-1 and VIM-5,</p>Fórmula:C12H10N4O2SCor e Forma:SolidPeso molecular:274.3Mtb-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:393.56Trimetrexate glucuronate
CAS:<p>Trimetrexate glucuronate, a folic acid foe, blocks DNA/RNA synthesis by inhibiting purine and thymidylic acid production, may fight tumors.</p>Fórmula:C25H33N5O10Cor e Forma:SolidPeso molecular:563.564MtInhA-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:396.32Antituberculosis 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:498.62CI-898 HCl
CAS:<p>CI-898 HCl: lipophilic antifolate, DHFR inhibitor, effective on methotrexate-resistant cancers, synergizes with other drugs in advanced P338 leukemia.</p>Fórmula:C19H26Cl3N5O3Cor e Forma:SolidPeso molecular:478.8Marasmic acid
CAS:<p>Marasmic acid is a bioactive antifungal.</p>Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.3Antiproliferative agent-17
CAS:Antiproliferative Agent-17 exhibits both antimicrobial properties against Gram-positive bacteria and anticancer activity [1].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:685.72Penamecillin
CAS:<p>Penamecillin (Wy 20788) is an orally active antibacterial agent.</p>Fórmula:C19H22N2O6SCor e Forma:SolidPeso molecular:406.45Antibacterial agent 114
CAS:<p>Compound 1: Potent antibacterial, MIC 625-1250μM for P.aeruginosa to S.aureus.</p>Fórmula:C19H14N4OCor e Forma:SolidPeso molecular:314.34ACP1b
CAS:<p>ACP1b is an activator of ClpP protease.</p>Fórmula:C18H18ClF3N2O3S2Cor e Forma:SolidPeso molecular:466.93Urease-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:320.41Antitubercular 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:362.41TBI-166
CAS:<p>TBI-166, an oral riminophenazine, treats tuberculosis with fewer side effects than Clofazimine.</p>Fórmula:C32H30F3N5O3Cor e Forma:SolidPeso molecular:589.61PXYD3
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:415.44Aditoprime
CAS:<p>Aditoprime inhibits bacterial growth by blocking DHFR, effective against L.casei and E.coli with IC50 of 520/47 nM.</p>Fórmula:C15H21N5O2Cor e Forma:SolidPeso molecular:303.36OYYF-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:307.33Antimicrobial agent-5
<p>Antimicrobial agent-5: potent, selective for Gram-negative/positive bacteria, blocks LPS-CD14/TLR4, anti-inflammatory.</p>Fórmula:C32H48N16Cor e Forma:SolidPeso molecular:656.83Ebselen 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:290.18Polyketide 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:SARS-CoV-2 3CLpro-IN-3 is a SARS CoV-2 3CLpro inhibitor that exhibits antiviral, antibacterial, and antifungal effects.Fórmula:C23H21BrN6O2SCor e Forma:SolidPeso molecular:525.42FR-182024
CAS:<p>FR-182024 is a novel cephem derivative, it has potent anti-Helicobacter pylori activity.</p>Fórmula:C18H16N4O4S3Cor e Forma:SolidPeso molecular:448.54CBR-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:349.42Antibacterial 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:270.71PRRSV/CD163-IN-1
CAS:<p>PRRSV/CD163-IN-1 blocks PRRSV GP2a/GP4 and CD163-SRCR5, aiding PRRS research.</p>Fórmula:C25H24FN5O5S2Cor e Forma:SolidPeso molecular:557.62Antitubercular agent-32
CAS:<p>Antitubercular agent-32, a Benzothiazinone, inhibits DprE1 in tuberculosis, stable and water-soluble, IC50: 3.9 μM.</p>Fórmula:C22H28N4O5S2Cor e Forma:SolidPeso molecular:492.61MurA-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:229.75Cyclamidomycin
CAS:<p>Cyclamidomycin is an antibiotic. It also functions as an inhibitor of nucleoside diphosphokinase of Escherichia coli.</p>Fórmula:C7H10N2OCor e Forma:SolidPeso molecular:138.17DuP 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:296.34Pralurbactam
CAS:<p>Pralurbactam is a β-Lactamase inhibitor utilized in the research of bacterial infections.</p>Fórmula:C10H18N6O8SCor e Forma:SolidPeso molecular:382.35Arasertaconazole
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:437.77Bederocin
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:450.37TMV-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:346.444,4'-Dicyanostilbene
CAS:<p>4,4'-Dicyanostilbene: potent anti-Dd2 malaria, EC50=27nM; effective vs. MRSA.</p>Fórmula:C16H10N2Cor e Forma:SolidPeso molecular:230.26Cefepime 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 89
CAS:<p>Antibacterial agent 89 blocks bacterial transcription and clostridial cytotoxins, inhibiting β'CH-σ interactions.</p>Fórmula:C21H10Cl2F3NO5SCor e Forma:SolidPeso molecular:516.27Antibacterial 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:337.33
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