Antibiotiques
Les antibiotiques sont des composés conçus pour détruire ou inhiber la croissance de divers microorganismes, jouant un rôle crucial dans le traitement des infections et la prévention de la propagation des maladies. Cette catégorie offre une gamme diversifiée d'ingrédients actifs spécifiquement destinés à la recherche dans le domaine biochimique. Ces composés sont des outils essentiels pour étudier les mécanismes bactériens, les modèles de résistance et le développement de nouveaux agents thérapeutiques. Les chercheurs peuvent explorer une large variété d'antibiotiques pour comprendre leurs effets, optimiser leur utilisation et développer de nouveaux traitements pour combattre les menaces microbiennes émergentes. La disponibilité d'un spectre aussi large d'antibiotiques soutient la recherche avancée et l'innovation en microbiologie et en sciences pharmaceutiques.
Sous-catégories appartenant à la catégorie "Antibiotiques"
- Antibiotiques macrolides(26 produits)
- Antibiotiques stéroïdiens(31 produits)
- Antibiotiques de type tétracycline(20 produits)
- antibiotiques β-lactames(11 produits)
4097 produits trouvés pour "Antibiotiques"
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Borrelidin
CAS :<p>Borrelidin is a potent antibiotic of the polyketide class, which is isolated from various Streptomyces species. Its mode of action is characterized by its inhibition of threonyl-tRNA synthetase, effectively disrupting protein synthesis within bacteria. Additionally, Borrelidin is known for its unique anti-angiogenic properties, which result from the inhibition of endothelial cell proliferation, making it a compound of interest in cancer research.</p>Degré de pureté :Min. 95%Cefodizime
CAS :<p>Cefodizime is a third-generation cephalosporin antibiotic, which is derived from the fungus Acremonium. It exerts its bactericidal effects by inhibiting bacterial cell wall synthesis. This action is achieved through binding to penicillin-binding proteins (PBPs), leading to the interruption of peptidoglycan cross-linking essential for the bacterial cell wall integrity. The breakdown of cell wall synthesis results in the lysis and death of the bacterial cell.</p>Degré de pureté :Min. 95%Porfiromycin
CAS :<p>Porfiromycin is an antineoplastic antibiotic with action on DNA alkylation and cross-linking and is used for research on cancer treatment, particularly for hypoxic tumors.</p>Formule :C16H20N4O5Degré de pureté :Min. 95 Area-%Couleur et forme :PowderMasse moléculaire :348.35 g/mol25-Desacetyl rifapentin
CAS :<p>25-Desacetyl rifapentin is a derivative of rifapentin, an antibiotic belonging to the rifamycin class, sourced from the bacterial species *Amycolatopsis rifamycinica*. This compound functions by inhibiting bacterial DNA-dependent RNA polymerase, which is crucial for transcription in susceptible bacterial strains. By inhibiting this enzyme, 25-Desacetyl rifapentin effectively hampers RNA synthesis, ultimately leading to bacterial cell death.</p>Formule :C45H62N4O11Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :834.99 g/mol7-Descarbamoyl 17-amino geldanamycin
CAS :7-Descarbamoyl 17-amino geldanamycin is a semi-synthetic derivative of the benzoquinone ansamycin antibiotic geldanamycin, which is naturally produced by the bacterium *Streptomyces hygroscopicus*. As an inhibitor of the Heat Shock Protein 90 (Hsp90), it targets this molecular chaperone crucial for the stability and function of numerous oncoproteins. By inhibiting Hsp90, 7-Descarbamoyl 17-amino geldanamycin disrupts protein folding processes, leading to the degradation of client proteins and subsequent disruption of cell signaling pathways involved in tumor growth and survival.Formule :C27H38N2O7Degré de pureté :Min. 95%Masse moléculaire :502.6 g/molSitafloxacin
CAS :<p>Sitafloxacin is an antibacterial agent belonging to the fluoroquinolone class of antibiotics, which is synthetically derived from chemical processes involving fluorinated quinolones. Its mode of action involves the inhibition of bacterial DNA gyrase and topoisomerase IV, enzymes crucial for bacterial DNA replication and transcription. By interfering with these enzymes, Sitafloxacin effectively hampers bacterial DNA synthesis, leading to the eventual demise of the bacterial cell.</p>Formule :C19H18ClF2N3O3Degré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :409.81 g/molMptpB-IN-1
CAS :MptpB-IN-1: orally active, potent MptpB inhibitor; reduces drug-resistant tuberculosis.Formule :C17H11Cl2NO4Couleur et forme :SolidMasse moléculaire :364.18Chitin synthase inhibitor 4
CAS :<p>Chitin synthase inhibitor 4: a CHS inhibitor with antimicrobial properties, potential fungicide.</p>Formule :C20H15FN4ODegré de pureté :99.74%Couleur et forme :SolidMasse moléculaire :346.36Basacv
CAS :Basacv is a bisacridinyl peptidic analog of triostin A.Formule :C54H60N10O10S2Couleur et forme :SolidMasse moléculaire :1073.25S 863390
CAS :S 863390 is a renin inhibitor.Formule :C37H52N6O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :644.85Alalevonadifloxacin HCl
CAS :<p>Alalevonadifloxacin HCl is a novel l-alanine ester prodrug of levonadifloxacin.</p>Formule :C22H27ClFN3O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :467.92Lincophenicol
CAS :Lincophenicol is an Escherichia coli ribosomal peptidyltransferase-catalyzed puromycin reaction inhibitor.Formule :C18H27N3O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :365.42RMI 10874
CAS :RMI 10874 is a tilorone analogue. Tilorone is an orally bioavailable antiviral agent.Formule :C21H26N2O4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :370.44Rosaramicin
CAS :Rosaramicin, a lipid-soluble basic macrolide, is an antibacterial substance similar to erythromycin but with a better activity against Gram-negative bacteria.Formule :C31H51NO9Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :581.74Albitiazolium bromide
CAS :<p>Albitiazolium bromide is an antimalarial compound disrupting phosphatidylcholine biosynthesis in Plasmodium, transported via NPP and cation carriers.</p>Formule :C24H42BrN2O2S2Degré de pureté :99.743%Couleur et forme :SolidMasse moléculaire :534.64Vidarabine phosphate
CAS :Vidarabine phosphate is an adenosine monophosphate analog.Formule :C10H14N5O7PDegré de pureté :99.75%Couleur et forme :White Crystalline PowderMasse moléculaire :347.22Tunicamine
CAS :Tunicamine is a reversible polyprenol-phosphate inhibitor.Formule :C11H21NO9Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :311.29AFK-108
CAS :<p>AFK-108 is a fungicide agent.</p>Formule :C21H26Cl2N2ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :393.35FR900098 (sodium salt)
CAS :<p>FR900098, a fosmidomycin derivative, has potent antimalarial effects, targeting DOXP reductoisomerase and eradicating P. vinckei in mice at >10 mg/kg.</p>Formule :C5H12NNaO5PCouleur et forme :SolidMasse moléculaire :220.117Ferric citrate
CAS :Ferric citrate as a source of iron used in cell culture applications can provide iron with a less toxic form compared to free iron salts.Formule :C6H8FeO7Couleur et forme :Limit Its Spread To The Environment It Is Used In Medicine In Making Blueprints And As A FeedMasse moléculaire :247.968Lipoxamycin hemisulfate
CAS :<p>Lipoxamycin hemisulfate (Lipoxamycin) is an inhibitor of serine palmitoyltransferase (IC50 = 21 nM) with antifungal activity.</p>Formule :C38H74N4O14SDegré de pureté :99.14% - 99.93%Couleur et forme :SolidMasse moléculaire :843.08LY 186826
CAS :<p>LY 186826 is an antibacterial agent with bicyclic pyrazolidinone properties.</p>Formule :C15H16N6O6SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :408.39Amcinafal
CAS :<p>Amcinafal is an active diol,and used against virus replication and interferon production.</p>Formule :C26H35FO6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :462.55Riodoxol
CAS :Riodoxol is an antiviral agent that effectively affects the reproduction and maturation of viruses.Formule :C6H3I3O2Couleur et forme :SolidMasse moléculaire :487.8Chitin synthase inhibitor 2
CAS :Chitin synthase inhibitor 2 (2b) has an IC50 of 0.09 mM, K i 0.12 mM, shows in vitro antimicrobial activity and boosts fluconazole/polyoxin B.Formule :C20H19N3O3Couleur et forme :SolidMasse moléculaire :349.38PD 117588
CAS :PD 117588: Broad-spectrum quinolone; combats Gram-positive and most Gram-negative bacteria, barring P. aeruginosa. More potent than imipenem or ceftazidime.Formule :C20H23F2N3O3Couleur et forme :SolidMasse moléculaire :391.41Pafuramidine maleate
CAS :Pafuramidine is an orally bioavailable prodrug of formamidine which was developed for the treatment of human African trypanosomiasis.Formule :C24H24N4O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :480.16Pyrrofolic acid
CAS :Pyrrofolic acid shows high anti-folate biological activity for S. faecalis.Formule :C23H21N7O7Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :507.46Xenalamine
CAS :Xenalamine is a synthetic compound of antiviral.Formule :C23H21NO4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :375.42Saquayamycin B
CAS :Saquayamycin B, a glycoside, targets Gram-positive bacteria and both adriamycin-sensitive and -resistant P388 leukemia cells.Formule :C43H48O16Couleur et forme :SolidMasse moléculaire :820.83Phenosulfazole
CAS :Phenosulfazole is a potent antiviral agent which has the potential for the research of poliomyelitis virus [1].Formule :C9H8N2O3S2Couleur et forme :SolidMasse moléculaire :256.3Exeporfinium chloride
CAS :Exeporfinium chloride(XF-73) is an antimicrobial agent that can weaken bacterial cell walls.Formule :C44H50Cl2N6O2Couleur et forme :SolidMasse moléculaire :765.81Pyrazofurin
CAS :Pyrazofurin, a pyrimidine analogue, blocks cell growth and DNA synthesis by targeting UMP synthase & orotate-phosphoribosyltransferase (IC50: 0.06-0.37 μM).Formule :C9H13N3O6Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :259.22Epirubicin
CAS :Epirubicin, a doxorubicin derivative, is an antineoplastic, inhibits topoisomerase, DNA/RNA synthesis, and Foxp3, reducing T cell activity.Formule :C27H29NO11Couleur et forme :SolidMasse moléculaire :543.52Linogliride fumarate
CAS :Linogliride fumarate, a guanidine derivative, stimulates insulin release by blocking ATP-sensitive K+ channels, enhancing glucose tolerance.Formule :C20H26N4O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :402.451Pentachloropseudilin
CAS :Pentachloropseudilin inhibits Myosin-1 and speeds up TGF-β receptor turnover, suppressing TGF-β activity.Formule :C10H4Cl5NODegré de pureté :98.14%Couleur et forme :SolidMasse moléculaire :331.41CRK12-IN-1
CAS :CRK12-IN-1: strong inhibitor of CRK12, kills T.b. brucei & T. congolense (EC50s: 1.3 & 18 nM).Formule :C20H26F2N4O3S2Degré de pureté :99.72%Couleur et forme :SolidMasse moléculaire :472.57Abimtrelvir
CAS :Abimtrelvir exhibited antiviral activity.Formule :C24H17ClF3N7O2Couleur et forme :SolidMasse moléculaire :527.89Roridin E
CAS :Roridin E blocks FGFR3, IGF-1R, PDGFRβ, TrkB (IC50s: 0.4–1.4 μM), kills breast cancer cells (IC50: 0.02-0.05 nM), and halts other cancer cells (<0.01 μM).Formule :C29H38O8Couleur et forme :SolidMasse moléculaire :514.61Verticillin A
CAS :Verticillin A, an apoptosis inducer, inhibits Leiomyosarcoma and Malignant peripheral nerve sheath tumor growth.Formule :C30H28N6O6S4Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :696.84Niclosamide monohydrate
CAS :<p>Niclosamide Monohydrate is used for the treatment of most tapeworm infections by inhibiting DNA replication.</p>Formule :C13H10Cl2N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :345.14DDD01035881
CAS :DDD01035881 is a anti-malarial drug that blocks parasite-to-mosquito transmission by targeting the Plasmodium vesicle membrane protein Pfs16.Formule :C14H14BrNO4S2Degré de pureté :99.78%Couleur et forme :SolidMasse moléculaire :404.3SSJ-183
CAS :SSJ-183 is a low-toxicity and orally available and anti-malarial drug with an IC50 = 7.6 nM against P. falciparum and no lethality at doses up to 2000 mg/kg po.Formule :C25H22N4ODegré de pureté :99.71% - 99.83%Couleur et forme :SolidMasse moléculaire :394.474-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid
CAS :<p>4-((4-((4-Aminophenyl)sulfonyl)phenyl)amino)-4-oxobutanoic acid is a sulfonamide compound that can be used as an anti infective agent [1].</p>Formule :C16H16N2O5SCouleur et forme :SolidMasse moléculaire :348.37SQ109
CAS :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.Formule :C22H38N2Degré de pureté :99.70% - 99.91%Couleur et forme :SolidMasse moléculaire :330.55BRD-8000.3
CAS :BRD-8000.3 is a narrow-spectrum antimycobacterial targeting EfpA, inhibiting lipid transport in drug-tolerant Mtb and useful in structural and functional.Formule :C19H21BrN4ODegré de pureté :99.78% - 99.78%Couleur et forme :SolidMasse moléculaire :401.3Linogliride
CAS :Linogliride: a guanidine derivative, inhibits insulin release, and enhances glucose tolerance by blocking ATP-sensitive K+ channels in pancreatic beta cells.Formule :C16H22N4ODegré de pureté :98%Couleur et forme :SolidMasse moléculaire :286.37Ormetoprim
CAS :Ormetoprim (Ro 5-9754), an antibiotic approved for use in the United States, is used to prevent the spread of disease in freshwater aquaculture.Formule :C14H18N4O2Degré de pureté :99.92%Couleur et forme :SolidMasse moléculaire :274.32Antiviral agent 18
CAS :Compound 5, an antiviral agent, effectively targets murine norovirus, with potential in infectious disease and oncology research.Formule :C11H13ClN4O4Couleur et forme :SolidMasse moléculaire :300.7Acyclovir monophosphate
CAS :<p>Acyclovir monophosphate, a strong anti-HSV agent, inhibits viral DNA polymerase, blocking DNA synthesis and chain elongation.</p>Formule :C8H12N5O6PCouleur et forme :SolidMasse moléculaire :305.18
