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(4.126 produits)
- Antifongiques(874 produits)
- Antiparasitaires(699 produits)
- Antiviraux(764 produits)
2423 produits trouvés pour "Antimicrobiens"
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LTAS-IN-1
CAS :<p>LTAS-IN-1 is a synthetic chemical compound designed as an advanced inhibitor, which is developed through a series of intricate chemical synthesis processes. The mode of action of LTAS-IN-1 involves the selective inhibition of specific enzyme targets, effectively modulating their biological pathways. This selective inhibition allows researchers to investigate the compound's effects on various cellular and molecular processes.</p>Formule :C24H17N3O5Degré de pureté :Min. 95%Masse moléculaire :427.4 g/molCauloside A
CAS :Cauloside A is a steroidal saponin, a type of glycoside compound, which is primarily isolated from the plant Caulophyllum robustum or related species. Saponins are known for their diverse biological activities and the ability to interact with cell membranes due to their amphipathic nature, allowing them to disrupt lipid bilayers.Formule :C35H56O8Degré de pureté :Min. 95%Masse moléculaire :604.8 g/molAldicarb d3
CAS :<p>Aldicarb d3 is an isotopically labeled compound, categorized as a carbamate pesticide, which is derived from chemical synthesis using deuterium labeling. Its mode of action involves the inhibition of acetylcholinesterase, an enzyme essential for nerve function, leading to the disruption of neurological processes in pest organisms.</p>Formule :C7H14N2O2SDegré de pureté :Min. 95%Masse moléculaire :193.28 g/molNocardicin G
CAS :<p>Nocardicin G is a monocyclic β-lactam antibiotic, which is sourced from certain strains of the soil-dwelling actinobacterium *Nocardia*. This organism is known for its ability to synthesize various bioactive compounds. The mode of action of Nocardicin G involves inhibiting bacterial cell wall synthesis by targeting penicillin-binding proteins, resulting in the bactericidal effect against susceptible bacterial strains. This compound specifically disrupts the formation of the peptidoglycan layer, which is essential for bacterial integrity and survival.</p>Formule :C19H19N3O6Degré de pureté :Min. 95%Masse moléculaire :385.4 g/molMagainin 2
CAS :<p>Magainin 2 is an antimicrobial peptide, which is derived from the skin of the African clawed frog, *Xenopus laevis*. This peptide is renowned for its membrane-disrupting mode of action, where it integrates into lipid bilayers of microbial cell membranes, ultimately leading to disruption and cell lysis. The mode of action is primarily through the formation of pores in the membrane, causing a loss of cellular contents and death of the microbial cell.</p>Formule :C114H180N30O29SDegré de pureté :Min. 95%Masse moléculaire :2,466.9 g/molLipoxamycin (hemisulfate)
CAS :<p>Lipoxamycin (hemisulfate) is a complex polyketide acting as an antimicrobial and antitumor agent, derived from a specific strain of soil-derived Actinomycetes. Its mode of action centers on the disruption of protein synthesis, specifically targeting tumor cells by inhibiting key enzymes required for cell growth and replication. The compound's structure, featuring multiple heterocyclic rings and functional groups, allows it to effectively bind to its molecular targets, inducing apoptosis in malignant cells.</p>Formule :C38H74N4O14SDegré de pureté :Min. 95%Masse moléculaire :843.1 g/molNalidixic acid ethyl ester
CAS :Nalidixic acid ethyl ester is a chemical compound that functions as a pro-drug antibacterial agent, specifically belonging to the quinolone class of antibiotics. It is synthesized from nalidixic acid, which is derived from the older synthetic derivative class of naphthyridines. Nalidixic acid ethyl ester exhibits its antibacterial properties through the inhibition of DNA gyrase and topoisomerase IV. These are essential enzymes for bacterial DNA replication, transcription, and repair, leading to the disruption of DNA synthesis in susceptible bacterial cells.Formule :C14H16N2O3Degré de pureté :Min. 95%Masse moléculaire :260.29 g/mol4-Epianhydrotetracycline hydrochloride
CAS :<p>4-Epianhydrotetracycline hydrochloride is a chemically modified antibiotic derivative, originating from the structural transformation of tetracycline. It is derived through epimerization and dehydration processes, which alter the parent compound's structure.</p>Formule :C22H23ClN2O7Degré de pureté :Min. 95%Masse moléculaire :462.9 g/molKanamycin A
CAS :<p>Inhibitor of protein synthesis; aminoglycoside</p>Formule :C18H36N4O11Degré de pureté :Min. 95%Couleur et forme :White Clear LiquidMasse moléculaire :484.5 g/mol8-epiAtazanavir
CAS :<p>8-epiAtazanavir is a stereoisomer of the antiretroviral drug Atazanavir, which is derived from synthetic sources. It acts as an HIV-1 protease inhibitor, where it binds to the active site of the viral protease enzyme, thereby preventing the cleavage of precursor proteins required for the maturation of infectious viral particles. This interference with viral replication is achieved by the structural mimicry of the natural substrate of the protease, allowing it to competitively inhibit the enzyme's activity.</p>Formule :C38H52N6O7Degré de pureté :Min. 95%Masse moléculaire :704.38975Clindamycin 3,4-isopropylidene
CAS :<p>Clindamycin 3,4-isopropylidene is a semi-synthetic antibiotic derivative of clindamycin, which is derived from the bacterial species Streptomyces lincolnensis. This compound is synthesized through chemical modification, specifically forming an isopropylidene group at positions 3 and 4 of the clindamycin molecule. The inclusion of the isopropylidene moiety alters its physicochemical properties, potentially enhancing its stability or spectrum of activity.</p>Formule :C21H37ClN2O5SDegré de pureté :Min. 95%Masse moléculaire :465 g/molCefmetazole lactone
CAS :<p>Cefmetazole lactone is an antibiotic, classified as a cephalosporin, which is a type of β-lactam antimicrobial compound. It is derived from the Cephalosporium fungus, known for its progenitor antimicrobial properties. As a second-generation cephalosporin, cefmetazole lactone operates by inhibiting bacterial cell wall synthesis, essentially interfering with the transpeptidation process of peptidoglycan, a critical component of the bacterial cell wall. This disruption leads to cell lysis and eventual bacterial death, mainly affecting Gram-positive and some Gram-negative bacteria.</p>Formule :C13H13N3O5S2Degré de pureté :Min. 95%Masse moléculaire :355.40 g/molTCMDC-135051
CAS :<p>TCMDC-135051 is a synthetic ligand, which is derived from advanced combinatorial chemistry techniques. It operates as a potent modulator of specific receptor sites by selectively binding and altering their physiological activity. The source of TCMDC-135051's activity is its molecular architecture, designed to target epitopes with high affinity and precision. This targeted action makes TCMDC-135051 a valuable tool for probing cellular pathways and mechanisms, providing insights into complex biological processes.</p>Formule :C29H33N3O3Degré de pureté :Min. 95%Masse moléculaire :471.6 g/molSofosbuvir impurity N
CAS :<p>Sofosbuvir impurity N is a chemical impurity found as a byproduct in the synthesis of sofosbuvir, a nucleotide analog used as an antiviral drug. Its origin is directly linked to the complex chemical processes involved in producing the active pharmaceutical ingredient. This impurity is specifically identified and analyzed to ensure the purity and efficacy of the sofosbuvir drug. Impurities like these are of significant interest in pharmaceutical development, as they provide insights into the synthetic pathways and potential degradation products.</p>Formule :C20H25FN3O9PDegré de pureté :Min. 95%Masse moléculaire :501.4 g/molLincomycin B hydrochloride
CAS :<p>Inhibitor of protein synthesis; lincosamide</p>Formule :C17H33ClN2O6SDegré de pureté :Min. 95%Masse moléculaire :428.97 g/molColistin A
CAS :Colistin A is an antimicrobial peptide, which is a type of polymyxin antibiotic derived from the bacterium *Paenibacillus polymyxa*. It exerts its bactericidal effect by interacting electrostatically with the lipopolysaccharides and phospholipids in the outer membrane of Gram-negative bacteria. This action disrupts the bacterial cell membrane, leading to increased permeability and cell death.Formule :C53H100N16O13Degré de pureté :Min. 95%Masse moléculaire :1,169.5 g/mol1-Anthroylnitrile
CAS :<p>1-Anthroylnitrile is a chemical compound, specifically an organic aromatic compound known as a polycyclic aromatic nitrile, which is synthesized from anthracene via nitrile substitution at the 1-position. With its aromatic structure, 1-Anthroylnitrile exhibits unique photophysical properties, functioning as a significant fluorescent probe due to its strong absorption and emission in the UV-visible spectrum.</p>Formule :C16H9NODegré de pureté :Min. 95%Masse moléculaire :231.25 g/mol(R)-Ambrisentan
CAS :<p>(R)-Ambrisentan is an endothelin receptor antagonist, which is a pharmacological agent derived synthetically to target and inhibit specific cellular pathways. It is primarily utilized in the treatment of pulmonary arterial hypertension (PAH), where it plays a crucial role in modulating vascular function. The mode of action of (R)-Ambrisentan involves selective antagonism of the endothelin type A (ETA) receptors, which are responsible for vasoconstriction and proliferation of vascular smooth muscle cells. By blocking these receptors, it mitigates the effects of endothelin, a potent vasoconstrictor, thus reducing blood pressure and improving blood flow in pulmonary arteries.</p>Formule :C22H22N2O4Degré de pureté :Min. 95%Masse moléculaire :378.40 g/molFlufenacet-methylsulfone
CAS :<p>Flufenacet-methylsulfone is an herbicidal derivative, which is sourced from the modification of flufenacet metabolites. It operates by inhibiting the biosynthesis of very-long-chain fatty acids, which are crucial components in the formation of cell membranes within target plant species. This biochemical intervention disrupts normal cell division and elongation in weeds, ultimately inhibiting their growth and establishment.</p>Formule :C12H16FNO3SDegré de pureté :Min. 95%Masse moléculaire :273.33 g/molMagnoloside A
CAS :<p>Magnoloside A is a bioactive compound, which is a natural product derived from the bark of the Magnolia plant. This compound is part of a group of phenolic glycosides that is extracted using advanced phytochemical techniques. Its mode of action primarily involves the inhibition of pro-inflammatory cytokines and modulation of various signaling pathways involved in inflammation and oxidative stress.</p>Formule :C29H36O15Degré de pureté :Min. 95%Masse moléculaire :624.6 g/mol
