Antimicrobiens
Les antimicrobiens sont des agents qui détruisent ou inhibent la croissance des microorganismes, y compris les bactéries, les virus, les champignons et les parasites. Ces composés sont essentiels dans la prévention et le traitement des infections, jouant un rôle crucial en médecine, en agriculture et dans l'industrie alimentaire. Chez CymitQuimica, nous proposons une vaste gamme d'antimicrobiens de haute qualité et pureté, adaptés à diverses applications scientifiques et industrielles. Notre catalogue comprend des antibiotiques, des antifongiques, des antiviraux et des désinfectants, tous conçus pour répondre aux besoins de la recherche et du développement, ainsi qu'aux applications cliniques et de production. Avec nos produits, les professionnels peuvent garantir l'efficacité et la sécurité dans le contrôle des infections et la protection de la santé publique.
Sous-catégories appartenant à la catégorie "Antimicrobiens"
- Antibiotiques(4.111 produits)
- Antifongiques(835 produits)
- Antiparasitaires(704 produits)
- Antiviraux(762 produits)
2422 produits trouvés pour "Antimicrobiens"
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Erythromycin B
CAS :<p>Erythromycin B is a semisynthetic macrolide antibiotic, which is derived from the actinomycete *Saccharopolyspora erythraea*. Its mode of action involves inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. This interference with protein synthesis effectively hampers bacterial growth, making it a potent bacteriostatic agent.</p>Formule :C37H67NO12Degré de pureté :90%NmrMasse moléculaire :717.93 g/molBombinin-like peptide (blp-1)
CAS :<p>Bombinin-like peptide (blp-1) is an antimicrobial peptide, which is derived from the skin secretion of certain amphibians, specifically the *Bombina* species of frogs. This peptide functions by disrupting microbial cell membranes, leading to cell lysis and death. Its ability to compromise the integrity of the cell membrane makes it effective against a range of pathogenic microorganisms, including bacteria and fungi.</p>Formule :C115H194N34O33Degré de pureté :Min. 95%Masse moléculaire :2,581 g/molCefteram
CAS :<p>Cefteram is a third-generation cephalosporin antibiotic, which is synthesized through chemical processes starting from cephalosporin C, a compound derived from the fungus Acremonium. As a cephalosporin, it functions by inhibiting bacterial cell wall synthesis. This is achieved through the binding to penicillin-binding proteins (PBPs), which are critical in the formation of the bacterial cell wall. By disrupting this process, Cefteram leads to the lysis and death of the bacteria.</p>Formule :C16H17N9O5S2Degré de pureté :Min. 95%Couleur et forme :White To Off-White SolidMasse moléculaire :479.5 g/molTCA1
CAS :<p>TCA1 is a synthetic small molecule, which is specifically derived from complex organic synthesis processes, designed to target bacterial metabolic pathways. It operates primarily by inhibiting essential enzymatic functions, thereby disrupting normal metabolic activity within bacterial cells. This inhibitory action results in weakened or halted protein synthesis, directly affecting bacterial growth and proliferation.</p>Formule :C16H13N3O4S2Degré de pureté :Min. 95%Masse moléculaire :375.4 g/molMacrolactin Z
CAS :<p>Please enquire for more information about Macrolactin Z including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formule :C29H40O8Degré de pureté :Min. 95%Masse moléculaire :516.6 g/molPotassium clavulanate - 1:1 mixture with cellulose, Antibiotic for Culture Media Use Only
CAS :<p>Potassium clavulanate is a beta-lactamase inhibitor and an antibacterial agent. The presence of potassium clavulanate in culture media inhibits the activity of beta-lactamases, which are enzymes that confer resistance to penicillin and other beta-lactam antibiotics. It also has been shown to be active against bacterial infections such as tuberculosis, sepsis, and pneumonia, where it can inhibit the growth of bacteria by interfering with their ability to form cell walls.</p>Formule :C8H8KNO5Degré de pureté :Min. 95.0 Area-%Masse moléculaire :237.25 g/molSulbactam Related Compound A
CAS :<p>Sulbactam Related Compound A is a chemical compound often used in pharmaceutical research and development. It is typically derived from the synthetic modification of existing antibiotics to explore new potential therapeutic benefits. The compound functions as a beta-lactamase inhibitor, which is of significant interest to researchers due to its potential to enhance the efficacy of beta-lactam antibiotics. By inhibiting the action of bacterial beta-lactamase enzymes, it permits these antibiotics to remain effective against resistant strains of bacteria.</p>Formule :C5H11NO4SDegré de pureté :Min. 95%Masse moléculaire :181.21 g/mol25-O-Deacetyl rifabutin
CAS :<p>25-O-Deacetyl rifabutin is an antibiotic derivative, which is sourced from the semi-synthetic modification of rifabutin, a compound originally derived from the fermentation of the bacterium Amycolatopsis mediterranei. This derivative works by inhibiting bacterial RNA synthesis. It achieves this by specifically targeting the DNA-dependent RNA polymerase enzyme, which is essential for bacterial transcription. The mechanism involves binding to the beta-subunit of the polymerase, thereby blocking the elongation of the RNA chain, which ultimately leads to the death of the bacterial cell.</p>Formule :C44H60N4O10Degré de pureté :Min. 95%Couleur et forme :Purple PowderMasse moléculaire :804.97 g/molNarasin
CAS :<p>Narasin is an ionophore antibiotic, which is a fermentation product derived from certain strains of the bacterium *Streptomyces aureofaciens*. It functions by disrupting the ion gradients across cell membranes, specifically facilitating the transport of sodium and potassium ions. This action interferes with the energy metabolism of certain pathogenic microorganisms, rendering them unable to proliferate effectively.</p>Formule :C43H72O11Degré de pureté :Min. 95%Masse moléculaire :765.03 g/mol1-Ethyl-6-fluoro-7-(piperazin-1-yl)quinolin-4(1H)-one
CAS :<p>1-Ethyl-6-fluoro-7-(piperazin-1-yl)quinolin-4(1H)-one is a fluoroquinolone antibiotic, which is a synthetic derivative sourced from the quinolone family. This compound functions by targeting bacterial DNA gyrase and topoisomerase IV, which are crucial enzymes involved in the replication and transcription of bacterial DNA. By inhibiting these enzymes, the antibiotic effectively disrupts DNA replication in susceptible bacterial strains, leading to cell death.</p>Formule :C15H18FN3ODegré de pureté :Min. 95%Masse moléculaire :275.32 g/molOmomycin
CAS :<p>Omomycin is a novel antibiotic, specifically a macrolide, which is derived from microbial sources, primarily soil-dwelling actinomycetes. Its mode of action involves inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. This interaction prevents the translocation of peptides during translation, thereby halting bacterial growth and proliferation.</p>Formule :C29H39NO4Degré de pureté :Min. 95%Masse moléculaire :465.6 g/molSparsomycin
CAS :<p>Sparsomycin is an antibiotic compound, which is a secondary metabolite isolated from Streptomyces species. Its mode of action involves the inhibition of protein synthesis by targeting the large subunit of the ribosome, specifically binding to the 50S subunit in bacterial ribosomes and the 60S subunit in eukaryotic ribosomes. This binding interferes with peptide bond formation, thereby disrupting the translational process essential for protein synthesis.</p>Formule :C13H19N3O5S2Degré de pureté :Min. 95%Masse moléculaire :361.4 g/molAminosidine
CAS :<p>Aminosidine is a nucleoside analogue that inhibits the HIV-1 reverse transcriptase and the integrase, which are enzymes involved in viral DNA synthesis. Aminosidine is active against Leishmania spp., but not against bacteria. Aminosidine has been shown to be effective in experimental models of human bowel disease and in patients with inflammatory bowel disease. It was also found to be active against wild-type strains of human immunodeficiency virus type 1, but not resistant mutants. The mechanism of action is the inhibition of cellular mitochondrial membrane potential.</p>Degré de pureté :Min. 95%Trovafloxacin mesylate
CAS :<p>Trovafloxacin mesylate is a synthetic antibiotic belonging to the fluoroquinolone class, which is derived from chemical synthesis processes rather than natural sources. The mode of action of trovafloxacin mesylate involves the inhibition of bacterial enzymes DNA gyrase and topoisomerase IV. These enzymes are essential for DNA replication, repair, and transcription within the bacterial cell. By inhibiting these enzymes, trovafloxacin mesylate disrupts bacterial DNA processes, leading to cell death and exerting its antibacterial effects.</p>Formule :C21H19F3N4O6SDegré de pureté :Min. 95%Masse moléculaire :512.46 g/molAztreonam-d6
CAS :<p>Aztreonam-d6 is an isotopically labeled antibiotic, which is a synthetic monobactam derived from bacterial fermentation processes with deuterium enrichment. With a beta-lactam structure, Aztreonam-d6 acts by inhibiting bacterial cell wall synthesis, specifically targeting the penicillin-binding protein 3 (PBP3) in Gram-negative bacteria. This action disrupts cell wall construction, leading to cell lysis and death, making it an effective option against certain resistant bacterial strains.</p>Formule :C13H17N5O8S2Degré de pureté :Min. 95%Masse moléculaire :441.5 g/mol7-Descarbamoyl 17-amino geldanamycin
CAS :<p>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.</p>Formule :C27H38N2O7Degré de pureté :Min. 95%Masse moléculaire :502.6 g/molBRD-K98645985
CAS :<p>BRD-K98645985 is a synthetic biochemical reagent, likely developed through chemical synthesis or natural product isolation. It functions as a modulator of specific biochemical pathways, potentially acting as an enzyme inhibitor, receptor agonist, or antagonist. This compound interacts with targeted proteins or cellular mechanisms, altering physiological responses or signaling cascades. The precise mode of action often involves binding to active sites, thereby influencing molecular conformation and activity.</p>Formule :C33H43N5O4Degré de pureté :Min. 95%Masse moléculaire :573.7 g/molOxysanguinarine
CAS :<p>Oxysanguinarine is an alkaloid compound, which is derived from the plant species of the Papaveraceae family. As a benzophenanthridine alkaloid, it is predominantly extracted from plants such as Sanguinaria canadensis. Its mode of action involves disrupting microbial cell membranes and interfering with enzyme systems, leading to antimicrobial and antifungal effects. This compound exhibits potential in inhibiting the growth of various pathogens, making it a subject of interest in pharmaceutical and microbiological research. Applications of oxysanguinarine extend to studying its efficacy in antimicrobial treatments, exploring its potential as a natural pesticide, and investigating its role in traditional medicine. Due to its complex biochemical interactions, ongoing research aims to better understand its mechanisms and potential therapeutic uses.</p>Formule :C20H13NO5Degré de pureté :Min. 95%Masse moléculaire :347.3 g/mol(S)-4-(((R)-6-(2-Chloro-4-fluorophenyl)-5-(methoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxyli c acid
CAS :<p>(S)-4-(((R)-6-(2-Chloro-4-fluorophenyl)-5-(methoxycarbonyl)-2-(thiazol-2-yl)-3,6-dihydropyrimidin-4-yl)methyl)morpholine-3-carboxylic acid is a selective chemical inhibitor, derived from synthetic organic chemistry methodologies. This compound is engineered for precise interaction with a target protein, modulating cellular pathways involved in disease progression. Its unique structure, including the chlorofluorophenyl and thiazolyl moieties, confers high binding affinity and specificity, making it a valuable tool in biochemical research.</p>Formule :C21H20ClFN4O5SDegré de pureté :Min. 95%Masse moléculaire :494.9 g/molSARS-CoV-IN-1
CAS :<p>SARS-CoV-IN-1 is a small-molecule inhibitor, which is a synthetic compound designed to interfere with viral replication. This compound is sourced through rigorous combinatorial chemistry methods, enabling the precise targeting of viral enzymes. SARS-CoV-IN-1 specifically inhibits the activity of the SARS-CoV-2 main protease (Mpro), an essential enzyme responsible for processing viral polyproteins into functional units necessary for virus replication.</p>Formule :C23H16ClFEN3ODegré de pureté :Min. 95%Masse moléculaire :441.69 g/mol
