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(4.115 produits)
- Antifongiques(841 produits)
- Antiparasitaires(704 produits)
- Antiviraux(763 produits)
2422 produits trouvés pour "Antimicrobiens"
Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
Metalaxyl-hydroxymethyl
CAS :<p>Metalaxyl-hydroxymethyl is a systemic fungicide, which is synthesized chemically. With its unique mechanism of action as an acylalanine fungicide, it targets and disrupts RNA synthesis specifically in oomycetes—a group of fungus-like organisms. This disruption inhibits the growth and spread of pathogenic fungi.</p>Formule :C15H21NO5Degré de pureté :Min. 95%Masse moléculaire :295.33 g/molTigecycline mesylate
CAS :<p>Tigecycline mesylate is a novel glycylcycline antibiotic, which is a derivative of the tetracycline class of antibiotics. It is a semi-synthetic product derived from minocycline, exhibiting a broad spectrum of antibacterial activity. Tigecycline mesylate functions through the inhibition of bacterial protein synthesis. It achieves this by binding to the 30S ribosomal subunit, thereby preventing the incorporation of amino acid residues into elongating peptide chains, a crucial step in protein production.</p>Formule :C30H43N5O11SDegré de pureté :Min. 95%Masse moléculaire :681.8 g/molTenatoprazole sodium
CAS :<p>Tenatoprazole sodium is a proton pump inhibitor, which is a synthetic pharmaceutical compound designed to selectively inhibit the hydrogen-potassium ATPase enzyme in the gastric parietal cells. This enzyme is essential for the final step of gastric acid production. Originating from organic chemical synthesis processes, Tenatoprazole sodium features a unique imidazopyridine structure, distinguishing it from other members of the proton pump inhibitor class such as omeprazole, which belongs to the benzimidazole family.</p>Formule :C16H18N4NaO3SDegré de pureté :Min. 95%Masse moléculaire :369.4 g/molPSI-352938
CAS :<p>Please enquire for more information about PSI-352938 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formule :C16H23FN5O6PDegré de pureté :Min. 95%Masse moléculaire :431.36 g/molArbekacin sulfate
CAS :<p>Inhibitor of DNA replication; aminoglycoside class</p>Formule :C22H44N6O10·xH2SO4Degré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :650.7 g/mol4-(4,5-Dihydroxy-3-methoxy-6-methyloxan-2-yl)oxy-2,5,7-trihydroxy-3-methoxy-2-methyl-3,4-dihydrotetracene-1,6,11-trione
CAS :<p>4-(4,5-Dihydroxy-3-methoxy-6-methyloxan-2-yl)oxy-2,5,7-trihydroxy-3-methoxy-2-methyl-3,4-dihydrotetracene-1,6,11-trione is an anthraquinone derivative, which is a specialized organic compound. This compound is typically derived from complex synthetic processes involving multi-step organic reactions starting from anthraquinone precursors. Its mode of action primarily involves the disruption of microbial cell walls and the inhibition of essential enzymatic pathways that are critical for microbial replication and survival.</p>Formule :C27H28O12Degré de pureté :Min. 95%Masse moléculaire :544.5 g/mol3-Descyano fludioxonil 3-carboxylic acid
CAS :<p>3-Descyano fludioxonil 3-carboxylic acid is a synthetic compound, which is derived from chemical modification of fludioxonil, a well-known fungicide. The compound acts by disrupting fungal cell osmoregulation through inhibition of the protein kinase pathway. This disruption inhibits spore germination and mycelial growth, contributing to its antifungal properties.</p>Formule :C12H7F2NO4Degré de pureté :Min. 95%Masse moléculaire :267.18 g/mol2-Sec-butyl-1-(decyloxy)-4-tritylbenzene
CAS :<p>2-Sec-butyl-1-(decyloxy)-4-tritylbenzene is a synthetic organic compound, typically utilized in chemical research and development. It is sourced through a series of organic synthesis reactions, involving alkylation, etherification, and aromatic substitution, primarily in a controlled laboratory environment.</p>Formule :C39H48ODegré de pureté :Min. 95%Masse moléculaire :532.8 g/molAlamifovir
CAS :<p>Alamifovir is an antiviral agent, which is synthetically derived. The mode of action of Alamifovir involves the inhibition of viral replication within host cells by targeting specific viral enzymes crucial for the replication process. This interference with the viral life cycle diminishes the ability of the virus to propagate and spread within the host organism.</p>Formule :C19H20F6N5O5PSDegré de pureté :Min. 95%Masse moléculaire :575.42 g/molVancomycin aglycon
CAS :<p>Vancomycin aglycon is a glycopeptide antibiotic, which is a derivative of vancomycin. It is sourced from the fermentation products of certain Amycolatopsis species, a genus of actinobacteria. The mode of action of vancomycin aglycon involves the inhibition of bacterial cell wall synthesis. It specifically binds to the D-Ala-D-Ala terminus of nascent peptidoglycan chains, thereby preventing the cross-linking that is crucial for maintaining cell wall integrity.</p>Formule :C53H52Cl2N8O17Degré de pureté :Min. 95%Masse moléculaire :1,143.93 g/molCefadroxil monohydrate, Antibiotic for Culture Media Use Only
CAS :<p>Cefadroxil is a broad-spectrum bactericidal antibiotic that belongs to the cephalosporin family. It is a semi-synthetic penicillin and inhibits bacterial cell wall synthesis through binding to one or more of the penicillin-binding proteins (PBPs). Cefadroxil monohydrate is used as an antibiotic for culture media and has been proven to be effective against methicillin-resistant Staphylococcus aureus (MRSA). In addition, the drug has been shown to have no significant effect on blood tests or microscopic studies.</p>Formule :C16H19N3O6SDegré de pureté :Min. 97.0 Area-%Masse moléculaire :381.40 g/molMoxifloxacin
CAS :<p>Moxifloxacin is a synthetic broad-spectrum antibiotic, which is derived from the fluoroquinolones class. It functions by inhibiting bacterial topoisomerase II (DNA gyrase) and topoisomerase IV, enzymes critical for DNA replication, transcription, repair, and recombination. The inhibition of these enzymes results in DNA breakage, thereby leading to bacterial cell death.</p>Formule :C21H24FN3O4Degré de pureté :Min. 95%Masse moléculaire :401.4 g/molMGB-BP-3
CAS :<p>MGB-BP-3 is a synthetic antimicrobial agent, which is derived from natural DNA-binding minor groove binder (MGB) compounds. Its structure is based on distamycin, known for targeting the minor groove of DNA. MGB-BP-3 operates by binding to specific sequences within the DNA minor groove, thereby interfering with the replication and transcription processes of bacterial cells. This binding disrupts the DNA function and inhibits the growth and proliferation of bacterial pathogens.</p>Formule :C36H37N7O4Degré de pureté :Min. 95%Masse moléculaire :631.7 g/molSecorapamycin B
CAS :<p>Secorapamycin B is a secondary metabolite, which is a macrolide lactam produced by the actinobacterium species Amycolatopsis. This compound is characterized by its unique structural features, including a polyketide backbone, which is biosynthesized via modular polyketide synthases. The mode of action for Secorapamycin B involves binding to FK-binding proteins (FKBP), inhibiting calcineurin function, and subsequently suppressing T-cell activation.</p>Formule :C51H81NO14Degré de pureté :Min. 95%Masse moléculaire :932.20 g/molClindamycin sulfoxide
CAS :<p>Clindamycin sulfoxide is a potent metabolite of the lincosamide antibiotic clindamycin, which is derived from the fermentation product of *Streptomyces lincolnensis*. This compound acts by inhibiting bacterial protein synthesis through binding to the 50S ribosomal subunit, thereby interfering with the translocation steps in protein elongation. The mechanism effectively suppresses the growth of a broad range of Gram-positive bacteria, including *Staphylococcus aureus*, *Streptococcus pneumoniae*, and anaerobic microorganisms.</p>Formule :C18H33ClN2O6SDegré de pureté :Min. 95%Masse moléculaire :440.98 g/molThiamethoxam-urea
CAS :<p>Thiamethoxam-urea is an advanced agrochemical formulation, which is a synthetic compound derived from the integration of the neonicotinoid insecticide thiamethoxam and the stabilizing agent urea. This product is engineered from laboratory synthesis, where chemical reactions enable the effective combination of these components to ensure optimal stability and efficacy. The mode of action of Thiamethoxam-urea involves neurotoxic interference within the central nervous system of target organisms, primarily acting as an agonist at nicotinic acetylcholine receptors in insects. This disrupts neural transmission, leading to paralysis and eventual death of the pest.</p>Formule :C8H10ClN3O2SDegré de pureté :Min. 95%Masse moléculaire :247.7 g/mol6-Chloro didesacetyl famciclovir
CAS :<p>6-Chloro didesacetyl famciclovir is a synthetic antiviral compound, which is derived from famciclovir, with specific modifications to enhance its biochemical properties. It is a chlorinated analog resulting from structural alterations to famciclovir, a prodrug of the antiviral agent penciclovir.</p>Formule :C10H14ClN5O2Degré de pureté :Min. 95%Masse moléculaire :271.7 g/molValidamycin D
CAS :<p>Validamycin D is an antifungal antibiotic produced by the fermentation of certain Streptomyces species. This compound acts by inhibiting the synthesis of trehalose, a crucial component in the cell structure and stress response of fungi. By disrupting trehalose production, Validamycin D effectively impairs the growth and viability of fungal cells, making it a potent agent in the management of fungal pathogens.</p>Formule :C20H35NO13Degré de pureté :Min. 95%Masse moléculaire :497.5 g/molBonducellpin D
CAS :<p>Bonducellpin D is an experimental bioactive compound derived from the seeds of Caesalpinia bonduc, a tropical plant species known for its rich phytochemical composition. This product is of natural botanical origin, harnessed through advanced extraction and purification techniques to ensure its high purity and activity.</p>Formule :C22H28O7Degré de pureté :Min. 95%Masse moléculaire :404.5 g/molRiamilovir
CAS :<p>Riamilovir is an antiviral agent, which is synthesized chemically, designed to combat the replication of specific viruses. It acts as a nucleoside analogue, interfering with viral nucleic acid synthesis. By incorporating itself into the viral RNA, it effectively hampers the ability of the virus to replicate its genetic material, thereby inhibiting its proliferation within the host.</p>Formule :C5H4N6O3SDegré de pureté :Min. 95%Masse moléculaire :228.19 g/mol
