Antibiótico
Os inibidores de antibióticos são substâncias que interferem na atividade dos antibióticos, frequentemente utilizados para estudar os mecanismos de resistência a antibióticos ou para aumentar a eficácia dos antibióticos existentes. Esses inibidores desempenham um papel crítico na compreensão de como as bactérias evitam o tratamento com antibióticos e no desenvolvimento de estratégias para superar a resistência. Na CymitQuimica, oferecemos uma variedade de inibidores de antibióticos para apoiar sua pesquisa em resistência antimicrobiana, farmacologia e inovação terapêutica.
Foram encontrados 932 produtos de "Antibiótico"
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CRS-3123
CAS:CRS-3123, a methionyl-tRNA synthetase inhibitor, is used potentially for the treatment of enteric infections.Fórmula:C19H19Br2N3O2SPureza:98%Cor e Forma:SolidPeso molecular:513.25Methacycline
CAS:<p>Methacycline, a tetracycline antibiotic, inhibits bacterial protein synthesis and effectively suppresses epithelial-mesenchymal transition (EMT). It blocks EMT in vitro and inhibits fibrogenesis in vivo without directly affecting the TGF-β1Smad signaling pathway. As an antimicrobial agent, Methacycline holds potential for research in pulmonary fibrosis.</p>Fórmula:C22H22N2O8Cor e Forma:SolidPeso molecular:442.42DRF-8417
CAS:<p>DRF-8417 is an oxazolidinone antibiotic, active against both Gram-positive bacteria and fastidious Gram-negative bacteria. The MIC50 and MIC90 values of DRF-8417 for Gram-positive pathogens range between 0.06-1 mg/L.</p>Fórmula:C15H17N3O5SCor e Forma:SolidPeso molecular:351.38Bleomycin Free Base
CAS:<p>Bleomycin Free Base, a glycopeptide antibiotic, halts DNA function and treats solid tumors.</p>Fórmula:C55H84N17O21S3Cor e Forma:SolidPeso molecular:1415.55MLEB-22043
<p>MLEB-22043 is a synthetic siderophore-monocyclic β-lactam conjugate which enters bacteria through TonB-dependent transport proteins utilizing its siderophore component, subsequently exerting antibacterial activity via its β-lactam portion. This compound acts as a broad-spectrum antibiotic, exhibiting significant inhibitory activity against pathogens such as Klebsiella pneumoniae, Escherichia coli, Acinetobacter baumannii, and Pseudomonas aeruginosa.</p>Fórmula:C25H25N9O11S2Cor e Forma:SolidPeso molecular:691.65Pibrozelesin
CAS:Pibrozelesin, a water-soluble duocarmycin B2 derivative, binds AT-rich DNA, blocking replication and inducing cell death.Fórmula:C32H36BrN5O8Cor e Forma:SolidPeso molecular:698.56Nikkomycin Z
CAS:Nikkomycin Z (Nikkomycin Z from Streptomyces tendae) is a competitive chitin synthase inhibitor.It inhibitor of the growth of filamentous fungi, insects,Fórmula:C20H25N5O10Pureza:98%Cor e Forma:SolidPeso molecular:495.44Spicamycin
CAS:Spicamycin can be used as a potent inducer of differentiation of human myeloid leukemia cells (HL-60) and murine myeloid leukemia cells (M1).Fórmula:C30H51N7O7Cor e Forma:SolidPeso molecular:621.77Ceftolozane TFA
CAS:<p>Ceftolozane TFA is a cephalosporin class antibiotic (antibiotic) designed to inhibit Gram-negative bacterial infections. Additionally, it can be utilized in the synthesis of novel antibiotics (antibiotic) that are more efficacious and safer.</p>Fórmula:C25H31F3N12O10S2Cor e Forma:SolidPeso molecular:780.71Mal-PEG4-VA-PBD
CAS:Mal-PEG4-VA-PBD is a drug-linker conjugate for Antibody-Drug Conjugates (ADCs), comprising the antitumor antibiotic Pyrrolobenzodiazepine (PBD), connectedFórmula:C68H79N9O17Pureza:98%Cor e Forma:SolidPeso molecular:1294.41Mucidin
CAS:<p>Mucidin is an antifungal antibiotic that inhibits electron transfer reactions within the mitochondrial respiratory chain's cytochrome bc1 complex.</p>Fórmula:C16H18O3Peso molecular:258.31Acetomycin
CAS:<p>Acetomycin, a γ-lactone from S. ramulosus, halts HCT-8 colon and L1210 leukemia cell growth.</p>Fórmula:C10H14O5Cor e Forma:SolidPeso molecular:214.22Saroaspidin B
CAS:<p>Saroaspidin B is a dimeric form of a biphenyl triphenol, characterized as an antibiotic compound.</p>Fórmula:C25H32O8Cor e Forma:SolidPeso molecular:460.52Clavicoronic acid
CAS:Clavicoronic acid, a β-lactamase inhibitor, boosts penicillin antibiotics against resistant bacteria.Fórmula:C15H18O4Cor e Forma:SolidPeso molecular:262.3Streptonigrin (racemate)
CAS:Streptonigrin: aminoquinone antibiotic; antitumor, antibacterial; blocks β-Catenin/Tcf, cytotoxic; alters hamster chromosomes; (-)-isomer, CAS#3930-19-6.Fórmula:C25H22N4O8Cor e Forma:SolidPeso molecular:506.46Myxothiazol
CAS:Myxothiazol blocks mitochondrial complex III and triggers SESN2, a gene important for stress response.Fórmula:C25H33N3O3S2Cor e Forma:SolidPeso molecular:487.68Anti-MRSA agent 19
CAS:<p>Anti-MRSA agent 19 (Compound 1) is an antibiotic that exhibits activity against Staphylococcus aureus. It is active against 40 clinical isolates from the CDC, representing diverse bacterial species with various resistance factors, including resistance to vancomycin, aminoglycoside/tetracycline, and oxazolidinone (median MIC=4 μg/mL).</p>Fórmula:C15H10Cl3NO4Cor e Forma:SolidPeso molecular:374.6Kinamycin B
CAS:Kinamycin B is an antibacterial agent with anticancer activity.Fórmula:C20H16N2O8Pureza:98%Cor e Forma:SolidPeso molecular:412.35Cefamandole lithium
CAS:<p>Cefamandole (lithium), a second-generation broad-spectrum cephalosporin antibiotic, exhibits antimicrobial activity. Upon metabolism in the body, it releases free NMTT, which can lead to hypoprothrombinemia.</p>Fórmula:C18H17LiN6O5S2Cor e Forma:SolidPeso molecular:468.44Antifungal agent 113
CAS:Antifungalagent 113 (compound 9a) serves as an effective antifungal and antibacterial agent. It exhibits strong inhibitory activity against both S. aureus and methicillin-resistant S. aureus.Fórmula:C23H20O5Cor e Forma:SolidPeso molecular:376.40Ganaplacide hydrochloride
CAS:Ganaplacide hydrochloride (KAF156 HCl) is an orally administered imidazopyrimidine antimalarial agent that inhibits Plasmodium PI4K activity.Fórmula:C22H24ClF2N5OPureza:93.97%Cor e Forma:SoildPeso molecular:447.91Saptomycin E
CAS:<p>Saptomycin E is an antitumor antibiotic.</p>Fórmula:C33H35NO9Cor e Forma:SolidPeso molecular:589.63Chitin synthase inhibitor 1
Potent, selective CHS inhibitor with 0.12 mM IC50; effective against drug-resistant fungi.Fórmula:C22H20ClN3O3Cor e Forma:SolidPeso molecular:409.87Imidocarb dihydrochloride monohydrate
Imidocarb dihydrochloride monohydrate is an effective antiprotozoal agent against the parasite B. bovis (IC50: 87 μg/ml).Fórmula:C19H24Cl2N6O2Cor e Forma:SolidPeso molecular:439.34Sinefungin
CAS:Sinefungin (Adenosyl-Ornithine) is an effective inhibitor of virion mRNA(guanine-7-)-methyltransferase, mRNA(nucleoside-2'-)-methyltransferase, and viralFórmula:C15H23N7O5Pureza:98.12%Cor e Forma:SolidPeso molecular:381.39Swainsonine
CAS:<p>Swainsonine (Tridolgosir) is an alkaloid isolated from Astragalus membranaceus and is a potent and reversible inhibitor of alpha-mannosidase. swainsonine has antitumour activity and induces apoptosis and cell cycle arrest in the G2/M phase.</p>Fórmula:C8H15NO3Pureza:98%Cor e Forma:Lyophilized PowderPeso molecular:173.21Nortopixantrone
CAS:<p>Nortopixantrone(BBR 3438) is a novel 9-azacyclophenanthracene pyrazole that shows antitumor activity in a human prostate cancer model.</p>Fórmula:C20H24N6O2Pureza:>99.99%Cor e Forma:SolidPeso molecular:380.44Erythromycylamine
CAS:Erythromycylamine is a useful organic compound for research related to life sciences. The catalog number is T64443 and the CAS number is 26116-56-3.Fórmula:C37H70N2O12Cor e Forma:SolidPeso molecular:734.969Formycin A
CAS:Formycin A shows antitumor and antiviral activities. Formycin A , a purine nucleoside antibiotic, is a potent human immunodeficiency virus type 1 (HIV-1) inhibitor with an EC50 of 10 μM.Fórmula:C10H13N5O4Pureza:98%Cor e Forma:SolidPeso molecular:267.24A 53868A
CAS:<p>A 53868A is an antibiotic, it is isolated from Streptomyces luridus.</p>Fórmula:C11H22N3O5PPureza:98%Cor e Forma:SolidPeso molecular:307.287PKUMDL-LTQ-301
CAS:PKUMDL-LTQ-301 is a potent inhibitor of HipA toxin. PKUMDL-LTQ-301 also inhibits E. coli persistence.Fórmula:C30H28N2O4Pureza:98%Cor e Forma:SolidPeso molecular:480.55DprE1-IN-8
CAS:<p>DprE1-IN-8 is a potent inhibitor of DprE1, exhibiting an IC50 of less than 0.75 μM.</p>Fórmula:C19H12F3N5O4SPureza:98%Cor e Forma:SolidPeso molecular:463.39Ref: TM-T79628
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