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(4.128 produits)
- Antifongiques(901 produits)
- Antiparasitaires(701 produits)
- Antiviraux(765 produits)
2423 produits trouvés pour "Antimicrobiens"
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3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine
CAS :<p>3-(Dichloroacetyl)-2,2,5-trimethyloxazolidine is an oxazolidine derivative, which is a synthetic compound primarily used in the agricultural industry. It is derived through a chemical synthesis process involving the condensation of dichloroacetic acid with trimethyloxazolidine under controlled conditions. This compound functions as a pre-emergent herbicide by inhibiting the biosynthesis of essential enzymes in target plant species.</p>Formule :C8H13Cl2NO2Degré de pureté :Min. 95%Masse moléculaire :226.1 g/molMeldonium
CAS :Produit contrôléMeldonium is a cardiovascular drug, which is a synthetic compound originating from Latvia. It functions by modulating carnitine metabolism, leading to decreased fatty acid oxidation and augmented glucose oxidation. This shift in energy substrate helps to improve energy efficiency, particularly under conditions of ischemia, which can prevent ischemic damage by balancing oxygen supply and demand.Formule :C6H14N2O2Degré de pureté :Min. 95 Area-%Masse moléculaire :146.19 g/molVicriviroc
CAS :<p>Vicriviroc is an investigational pharmaceutical compound, specifically classified as an HIV entry inhibitor. It originates from a synthetic source, designed to target the CCR5 co-receptor on human immune cells. The mode of action involves blocking this co-receptor, thereby preventing the HIV virus from binding and fusing with the host cell membrane. This inhibition effectively obstructs the virus's ability to enter and infect the host cells, particularly those within the chemokine receptor family.</p>Formule :C28H38F3N5O2Degré de pureté :Min. 95%Masse moléculaire :533.63 g/mol9-(Tetrahydro-5-methyl-2-furyl)adenine
CAS :<p>9-(Tetrahydro-5-methyl-2-furyl)adenine is a synthetic cytokinin, which is a type of plant growth regulator. This compound is derived from chemical synthesis, rather than extraction from natural sources. The mode of action involves promoting cell division and differentiation in plant tissues, primarily by enhancing the synthesis of proteins crucial for growth and development.</p>Formule :C10H13N5ODegré de pureté :Min. 95%Masse moléculaire :219.24 g/mol7-(3-Aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid,hydrate,hydrochloride
CAS :7-(3-Aminopyrrolidin-1-yl)-1-(2,4-difluorophenyl)-6-fluoro-4-oxo-1,8-naphthyridine-3-carboxylic acid, hydrate, hydrochloride is a fluoroquinolone antibiotic, which is a synthetic antimicrobial compound. It operates by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes critical for the replication, transcription, and repair processes of bacterial DNA. This disruption in DNA activity leads to cell death, providing its bactericidal effect.Formule :C19H16ClF3N4O3Degré de pureté :Min. 95%Masse moléculaire :440.8 g/molSofosbuvir impurity J
CAS :<p>Sofosbuvir impurity J is a chemical impurity that arises during the synthesis of Sofosbuvir, an antiviral medication primarily used in the treatment of hepatitis C. This impurity is a byproduct produced during the manufacturing process of Sofosbuvir, originating from its chemical synthesis pathway.</p>Formule :C22H30FN4O8PDegré de pureté :Min. 95%Masse moléculaire :528.5 g/molRSV-IN-1
CAS :RSV-IN-1 is a small molecule inhibitor, which is a synthetic compound with potent antiviral activity against Respiratory Syncytial Virus (RSV). Its primary source is chemical synthesis, designed to specifically target and inhibit the function of RSV’s viral polymerase complex. The mode of action involves the interruption of viral RNA synthesis, thereby preventing the replication and proliferation of RSV within host cells.Formule :C20H21N5O4SDegré de pureté :Min. 95%Masse moléculaire :427.5 g/molAzabon
CAS :<p>Azabon is a synthetic terpenoid compound, which is derived from renewable natural sources through a series of hydrogenation and isomerization processes. Its mode of action involves inhibiting specific enzymatic pathways, potentially interfering with cellular processes that are dependent on those enzymes. Primarily, Azabon is investigated for its applications in biochemical research, particularly for its effects on metabolic pathways that involve terpenoid interactions.</p>Formule :C14H20N2O2SDegré de pureté :Min. 95%Masse moléculaire :280.39 g/molAscomycin
CAS :<p>Ascomycin is an immunosuppressive macrolide, which is a product derived from the fermentation of the bacterium *Streptomyces hygroscopicus*. Its mode of action involves binding to the intracellular protein FK506-binding protein (FKBP), inhibiting the calcium-dependent signal transduction pathway that is crucial for T-cell activation. This interference with the immune response is achieved through the inhibition of calcineurin, thus preventing the dephosphorylation and nuclear translocation of nuclear factor of activated T-cells (NF-AT), a necessary step in the activation of genes required for T-cell proliferation.</p>Formule :C43H69NO12Degré de pureté :Min. 95%Masse moléculaire :792.01 g/molIohexol
CAS :<p>Iohexol is a non-ionic, water-soluble radiopaque contrast agent, which is synthesized from iodinated organic compounds. With its high iodine content, Iohexol acts as an excellent medium for absorbing X-rays, thereby enhancing the contrast in radiographic images. The compound’s mode of action involves the attenuation of X-ray beams, with its iodine atoms providing the requisite density to create a contrast between different structures and fluids within the body.</p>Formule :C19H26I3N3O9Degré de pureté :Min. 98 Area-%Masse moléculaire :821.14 g/molMMV008138
CAS :<p>MMV008138 is an antimalarial compound, which is a synthetic chemical entity derived from medicinal chemistry efforts aimed at targeting malaria. The source of MMV008138 is the pharmaceutical research pipeline focused on identifying new antimalarial agents. It operates by inhibiting the Plasmodium falciparum enzyme PfNDH2, an essential component in the parasite’s respiratory chain, disrupting its energy production capabilities and ultimately leading to parasite death.</p>Formule :C18H14Cl2N2O2Degré de pureté :Min. 95%Masse moléculaire :361.2 g/molFilipin III
CAS :<p>Filipin III is a polyene macrolide antibiotic, which is extracted from Streptomyces filipinensis. Known for its unique mode of action, Filipin III interferes with cholesterol-rich membranes by binding to ergosterol and cholesterol. This interaction disrupts the membrane structure, altering membrane permeability and ultimately affecting cell viability.</p>Degré de pureté :Min. 95%Validamycin C
CAS :Validamycin C is an aminoglycoside antifungal antibiotic, which is derived from the soil bacterium Streptomyces hygroscopicus. It functions primarily by inhibiting the synthesis of trehalase, an enzyme crucial for the breakdown of trehalose into glucose monomers. This inhibition disrupts the cellular function of fungi, particularly affecting their osmotic balance and cellular integrity, ultimately leading to the control of fungal growth.Formule :C26H45NO18Degré de pureté :Min. 95%Masse moléculaire :659.6 g/molN-Demethyl rifampin
CAS :<p>N-Demethyl rifampin is a metabolite of rifampin, which is a natural product derivative. Rifampin itself is a well-known antibiotic derived from the bacterium *Amycolatopsis rifamycinica*. N-Demethyl rifampin is formed through the metabolic process where rifampin undergoes demethylation. This transformation occurs primarily in the liver, mediated by the cytochrome P450 enzyme system.</p>Formule :C42H56N4O12Degré de pureté :Min. 95%Masse moléculaire :808.91 g/molPyrasulfotole-desmethyl
CAS :<p>Pyrasulfotole-desmethyl is a metabolite of pyrasulfotole, which is an herbicidal compound derived synthetically. It operates as a 4-hydroxyphenylpyruvate dioxygenase (HPPD) inhibitor, effectively disrupting the biosynthesis of carotenoids. This disruption leads to a depletion in essential pigments necessary for plant growth, ultimately causing chlorosis and plant death.</p>Formule :C13H11F3N2O4SDegré de pureté :Min. 95%Masse moléculaire :348.3 g/molManumycin B
CAS :<p>Manumycin B is a polyketide antibiotic, which is a secondary metabolite isolated from certain Streptomyces species. This compound is known for its complex biosynthetic origin involving iterative cycles of polyketide synthesis, leading to its characteristic structure. The mode of action of Manumycin B primarily involves the inhibition of farnesyltransferase, an enzyme critical for the post-translational modification of various proteins, including the Ras family of GTPases. By hindering this enzyme, Manumycin B disrupts the signaling pathways that are essential for tumor cell growth and proliferation.</p>Formule :C28H34N2O7Degré de pureté :Min. 95%Masse moléculaire :510.6 g/molVancomycin CDP-1
CAS :<p>Vancomycin CDP-1 is a degradation product of vancomycin with no direct therapeutic action but used in research for analytical method development and validation.</p>Formule :C66H74Cl2N8O25Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :1,450.24 g/molRestanza
CAS :<p>Restanza is an antibiotic, which is derived from novel sources to combat resistant bacterial strains. It functions through the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, effectively halting the translation process. This mechanism of action is designed to disrupt the proliferation of bacteria, making it a powerful tool in the fight against various infections.</p>Formule :C42H59N3O10Degré de pureté :Min. 95%Masse moléculaire :765.9 g/mol6-[[(2R)-3,3-Dimethyl-2-oxiranyl]methyl]-7-methoxy-2H-1-benzopyran-2-one
CAS :6-[[(2R)-3,3-Dimethyl-2-oxiranyl]methyl]-7-methoxy-2H-1-benzopyran-2-one is a synthetic anticoagulant compound, which is a derivative of naturally occurring plant metabolites known as coumarins. Coumarins are prevalent in various plant species and are recognized for their diverse biological activities, including anticoagulant properties. Structurally modified to enhance efficacy and specificity, this compound acts by inhibiting vitamin K epoxide reductase, a critical enzyme in the blood coagulation pathway. This results in reduced synthesis of active clotting factors, ultimately decreasing the tendency for blood clot formation.Formule :C15H16O4Degré de pureté :Min. 95%Masse moléculaire :260.28 g/molCarbovir triphosphate triethylamine
CAS :<p>Carbovir triphosphate triethylamine is a nucleotide analog, which is a derivative of nucleoside analogs designed for antiviral applications. It is synthesized through chemical modification of guanosine analogs, resulting in its active triphosphate form. This compound functions as a potent antiretroviral agent by mimicking natural nucleotides and interfering with viral DNA synthesis. The active triphosphate impedes the action of viral reverse transcriptase by incorporating itself into the viral DNA chain, causing premature termination and effectively halting viral replication.</p>Degré de pureté :Min. 95%
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