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"
Trier par
Degré de pureté (%)
0
100
|
0
|
50
|
90
|
95
|
100
Pyraziflumid
CAS :Pyraziflumid is a fungicide, which is chemically synthesized with a specific mode of action as a succinate dehydrogenase inhibitor (SDHI). This compound is designed to target mitochondrial complex II, disrupting critical energy production within fungal cells. The inhibition of succinate dehydrogenase prevents the fungi from efficiently undergoing respiration, ultimately leading to cell death.Formule :C18H10F5N3ODegré de pureté :Min. 95%Masse moléculaire :379.3 g/molMinocycline hydrochloride dihydrate
CAS :<p>Minocycline hydrochloride dihydrate is a broad-spectrum antibiotic, which is a synthetic derivative of tetracycline. It is sourced from chemical synthesis processes and possesses potent antimicrobial properties. The mode of action involves inhibiting bacterial protein synthesis by binding to the 30S ribosomal subunit, thereby preventing the addition of amino acids to the growing peptide chain. This mechanism effectively disrupts bacterial growth and replication.</p>Formule :C23H32ClN3O9Degré de pureté :Min. 95%Masse moléculaire :530 g/molFenamiphos-sulfoxide d3 (S-methyl d3)
CAS :<p>Fenamiphos-sulfoxide d3 (S-methyl d3) is a deuterated, labeled pesticide intermediate, which is often utilized in advanced laboratory settings for precise analytical studies. This compound is synthesized as a stable isotope-labeled analog, enabling researchers to conduct sophisticated mass spectrometric analyses. Its mode of action involves serving as a reference or tracer in studies concerning the metabolism and degradation of fenamiphos, a well-known organophosphate pesticide.</p>Formule :C13H22NO4PSDegré de pureté :Min. 95%Masse moléculaire :322.38 g/molCarbazomycin D
CAS :<p>Carbazomycin D is a bioactive product classified as an antibiotic, which is derived from the bacterium Streptomyces. These actinomycetes are well-known for their ability to produce a wide range of secondary metabolites with antimicrobial properties. The mode of action of Carbazomycin D involves the inhibition of bacterial cell wall synthesis, effectively disrupting the growth and replication of gram-positive bacteria.</p>Formule :C17H19NO3Degré de pureté :Min. 95%Masse moléculaire :285.34 g/molAqabamycin B
CAS :Aqabamycin B is a novel antibiotic compound, which is derived from marine microorganisms. This secondary metabolite is isolated from a marine sponge-associated bacterium, showcasing the rich potential of oceanic sources for discovering new antimicrobial agents. The mode of action of Aqabamycin B involves inhibition of bacterial cell wall synthesis, disrupting the structural integrity and leading to cell lysis. Its efficacy extends predominantly to combatting multi-drug resistant bacterial strains.Formule :C16H10N2O6Degré de pureté :Min. 95%Masse moléculaire :326.26 g/mol(R)-(+)-Pantoprazole
CAS :<p>(R)-(+)-Pantoprazole is a proton pump inhibitor (PPI), which is derived from benzimidazole compounds. Its mode of action involves the selective and irreversible inhibition of the H+/K+ ATPase enzyme system, commonly known as the proton pump, located on the gastric parietal cells. By binding covalently to this enzyme, (R)-(+)-Pantoprazole effectively reduces gastric acid secretion, leading to an increase in gastric pH.</p>Formule :C16H15F2N3O4SDegré de pureté :Min. 95%Masse moléculaire :383.4 g/molBPH-1358
CAS :<p>BPH-1358 is a novel synthetic inhibitor, which is derived from a series of advanced chemoinformatics-based design strategies. It functions through the targeted binding to specific cell surface receptors involved in the modulation of immune responses. By blocking these receptors, BPH-1358 effectively alters signaling pathways that are crucial for immune activation and inflammatory responses.</p>Formule :C32H28N6O2Degré de pureté :Min. 95%Masse moléculaire :528.6 g/molFamciclovir-d4
CAS :<p>Famciclovir-d4 is a deuterium-labeled antiviral nucleoside analog, which is a synthetic derivative of the guanine analog famciclovir. This compound is sourced through advanced chemical synthesis where deuterium atoms replace specific hydrogen atoms, providing an isotopic label that aids in the tracking and analysis of the pharmaceutical compound within biological systems.</p>Formule :C14H19N5O4Degré de pureté :Min. 95%Masse moléculaire :325.36 g/molAqabamycin C
CAS :Aqabamycin C is an antibiotic compound, which is derived from marine bacteria, specifically, the actinomycete strain found in marine environments. Its mode of action involves the disruption of bacterial cell wall synthesis, making it particularly effective against certain gram-negative bacteria. This antibiotic selectively inhibits pathogens by interfering with their essential cellular processes.Formule :C16H10N2O5Degré de pureté :Min. 95%Masse moléculaire :310.26 g/molClindamycin-2,4-diphosphate
CAS :<p>Clindamycin-2,4-diphosphate is a phosphorylated derivative of the antibiotic clindamycin, which is a semi-synthetic lincosamide antibiotic originally derived from Streptomyces lincolnensis. Its mode of action involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, thereby preventing peptide chain elongation during translation. This mechanism effectively disrupts protein production in susceptible bacteria, leading to their growth inhibition or death.</p>Formule :C18H35ClN2O11P2SDegré de pureté :Min. 95%Masse moléculaire :584.94 g/molTebufenozide-1-hydroxyethyl
CAS :<p>Tebufenozide-1-hydroxyethyl is an insect growth regulator, which is a synthetic chemical derived from a modified benzoic acid structure. Its mode of action involves mimicking the molting hormone ecdysone, which disrupts the normal development process of insects by inducing premature molting. This specific interference targets lepidopteran larvae, leading to incomplete development and eventual death, thereby controlling pest populations effectively without harming non-target organisms.</p>Formule :C22H28N2O3Degré de pureté :Min. 95%Masse moléculaire :368.5 g/molThiabendazole NH d6
CAS :Thiabendazole NH d6 is a deuterated derivative of Thiabendazole, which is an antifungal agent and pesticide. It is derived from synthetic sources, specifically designed by incorporating deuterium atoms into the molecular structure. This subtle isotopic modification enhances its utility in research settings, particularly in studies related to pharmacokinetics and metabolic profiling. The mode of action of Thiabendazole involves the inhibition of the enzyme fumarate reductase, interfering with the energy metabolism of fungal and parasitic organisms. Additionally, it disrupts microtubule formation, preventing cell division and growth.Formule :C10H7N3SDegré de pureté :Min. 95%Masse moléculaire :207.29 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/molCladospirone bisepoxide
CAS :Cladospirone bisepoxide is a naturally occurring bioactive compound, classified specifically as a fungal metabolite, which is derived from species within the Cladosporium genus. The compound exhibits a complex bisepoxide structure, contributing to its unique chemical properties. Its mode of action involves disrupting microbial cellular processes, displaying potent antimicrobial activity by interfering with the synthesis and functioning of vital cellular components in targeted microorganisms.Formule :C20H14O7Degré de pureté :Min. 95%Masse moléculaire :366.3 g/molButafenacil
CAS :<p>Butafenacil is a herbicide, which is a chemical formulation sourced from synthetic compounds. It acts by inhibiting protoporphyrinogen oxidase (PPO), an enzyme critical in the biosynthesis of chlorophyll. This inhibition disrupts the photosynthetic process, leading to the accumulation of reactive oxygen species that cause cell membrane damage and ultimately result in plant death.</p>Formule :C17H14ClF3N2O6Degré de pureté :Min. 95%Masse moléculaire :434.7 g/molAlbendazole-2-aminosulfoxide
CAS :<p>Albendazole-2-aminosulfoxide is a metabolite of the benzimidazole class of antiparasitic agents, which is derived from the biotransformation of albendazole in the liver. As a potent bioactive compound, its mode of action primarily involves the selective binding to the β-tubulin of parasitic organisms, disrupting the polymerization of microtubules necessary for their cellular structures. This disruption impedes vital processes such as glucose uptake and cellular division, leading to parasite death.</p>Formule :C10H13N3OSDegré de pureté :Min. 95%Masse moléculaire :223.3 g/mol4'-Ethynyl-2'-deoxyadenosine
CAS :<p>4'-Ethynyl-2'-deoxyadenosine is a deoxynucleoside analogue, which is synthesized through chemical processes. This compound acts as an antiviral agent, primarily targeting the viral replication machinery. Its mode of action involves the incorporation into viral DNA by mimicking natural nucleosides, which subsequently inhibits the enzymatic activity of reverse transcriptase. This inhibition disrupts the synthesis of viral DNA, effectively curtailing viral replication.</p>Formule :C12H13N5O3Degré de pureté :Min. 95%Masse moléculaire :275.26 g/molTioconazole
CAS :<p>Tioconazole is an antifungal agent, which is a synthetic derivative of imidazole with broad-spectrum activity against fungi. This compound is chemically synthesized through complex organic reactions to enhance its antimycotic efficacy. Tioconazole functions by inhibiting the synthesis of ergosterol, an essential component of the fungal cell membrane. By disrupting the ergosterol biosynthesis pathway, tioconazole destabilizes the fungal cell membrane, leading to increased permeability and eventual cell death.</p>Formule :C16H13Cl3N2OSDegré de pureté :Min. 95%Masse moléculaire :387.71 g/molClarithromycin - EP
CAS :<p>A macrolide, broad-spectrum antibiotic that targets cytochrome P4503A4 (CYP3A4). Clarithromycin has been used to potentiate the pharmacological effects of some drugs that are metabolised by the cytochrome P450.</p>Formule :C38H69NO13Degré de pureté :Min. 95%Masse moléculaire :747.95 g/molTigecycline, Antibiotic for Culture Media Use Only
CAS :Tigecycline is an antibiotic specifically tailored for use in culture media, which is derived from glycylcycline, a structural analogue of minocycline. Its mode of action involves binding to the 30S ribosomal subunit, thereby inhibiting protein synthesis in a broad spectrum of Gram-positive and Gram-negative bacteria. This action is distinct and not easily circumvented by common resistance mechanisms, such as efflux or ribosomal protection proteins, making tigecycline an effective agent in controlling bacterial contamination during microbiological studies.Formule :C29H39N5O8Degré de pureté :Min. 95 Area-%Masse moléculaire :585.65 g/mol
