Antimicrobials
Antimicrobials are agents that destroy or inhibit the growth of microorganisms, including bacteria, viruses, fungi, and parasites. These compounds are essential in the prevention and treatment of infections, playing a crucial role in medicine, agriculture, and the food industry. At CymitQuimica, we offer an extensive range of high-quality, high-purity antimicrobials suitable for various scientific and industrial applications. Our catalog includes antibiotics, antifungals, antivirals, and disinfectants, all designed to meet the needs of research and development, as well as clinical and production applications. With our products, professionals can ensure the effectiveness and safety in infection control and public health protection.
Subcategories of "Antimicrobials"
- Antibiotics(4,110 products)
- Antifungals(835 products)
- Antiparasitics(704 products)
- Antivirals(762 products)
Found 2422 products of "Antimicrobials"
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Acequinocyl-hydroxy
CAS:<p>Acequinocyl-hydroxy is an acaricide, which is a chemical agent used to manage and control mite populations in various agricultural settings. It is derived from a combination of synthetic organic compounds designed specifically to disrupt the normal biological processes of target pests. The mode of action of Acequinocyl-hydroxy involves interference with the mitochondrial electron transport chain of mites, ultimately disrupting cellular respiration and leading to the death of the pest.</p>Formula:C22H30O3Purity:Min. 95%Molecular weight:342.5 g/molFenoprofen sodium salt dihydrate
CAS:<p>Fenoprofen sodium salt dihydrate is a nonsteroidal anti-inflammatory drug (NSAID), which is a synthetic compound derived from propionic acid. It acts by inhibiting the cyclooxygenase (COX) enzymes, COX-1 and COX-2, leading to decreased synthesis of prostaglandins. This reduction in prostaglandin synthesis is responsible for its analgesic, anti-inflammatory, and antipyretic effects.</p>Formula:C15H13NaO3·2H2OPurity:Min. 95%Molecular weight:264.25 g/mol8-Oxo-gtp 8-hydroxy-gtp
CAS:<p>8-Oxo-GTP, also known as 8-Hydroxy-GTP, is a nucleotide analog, which is synthetically derived. It closely resembles the naturally occurring guanosine triphosphate (GTP) but contains a modified 8-hydroxy group, making it a valuable tool for studying oxidative damage and nucleotide modification processes.</p>Formula:C10H16N5O15P3Purity:Min. 95%Molecular weight:539.18 g/molFosravuconazole L-lysine ethanolate
CAS:<p>Fosravuconazole L-lysine ethanolate is an antifungal prodrug, which is a derivative of the widely used antifungal agent ravuconazole. This compound is synthesized through chemical modification to enhance its bioavailability and aqueous solubility, addressing limitations found in its parent compound. Fosravuconazole is designed to undergo in vivo conversion to ravuconazole, its active form, by enzymatic processes within the body.</p>Formula:C31H40F2N7O8PSPurity:Min. 95%Molecular weight:739.7 g/molDDD107498 succinate
CAS:<p>DDD107498 succinate is a potent antimalarial agent, which is a synthetic compound discovered through target-based drug screening. This compound is derived from intensive research initiatives focusing on eliminating malaria by disrupting a unique biochemical pathway in the parasite. It primarily acts by inhibiting the translation elongation factor 2, a critical protein that facilitates protein synthesis within the Plasmodium species responsible for malaria. By targeting this specific mechanism, the compound effectively halts the growth and replication of the parasite within the human bloodstream.</p>Formula:C31H37FN4O6Purity:Min. 95%Molecular weight:580.6 g/molVancomycin hydrochloride from streptomyces orientalis
CAS:<p>Vancomycin hydrochloride is a glycopeptide antibiotic, derived from the bacterium *Streptomyces orientalis*. This compound functions by inhibiting bacterial cell wall synthesis, specifically targeting the D-alanyl-D-alanine termini in peptidoglycan chains. It disrupts transglycosylation and transpeptidation, critical steps in cell wall biosynthesis, ultimately leading to cell lysis.</p>Formula:C66H75Cl2N9O24·HClPurity:Min. 95%Molecular weight:1,485.71 g/molLobucavir
CAS:<p>Lobucavir is an antiviral compound with a mode of action that inhibits viral DNA polymerase. It is used for treating infections caused by herpesviruses and hepatitis B virus.</p>Formula:C11H15N5O3Purity:Min. 95%Molecular weight:265.27 g/molTyrothricin
CAS:<p>Tyrothricin is a peptide antibiotic, which is derived from the bacterium Bacillus brevis. This compound comprises a mixture of polypeptides, primarily gramicidin and tyrocidine, both of which are instrumental in its antimicrobial activity. The mode of action of tyrothricin involves disrupting bacterial cell membranes, leading to cell lysis and death. Gramicidin increases the permeability of the bacterial membrane to ions, while tyrocidine promotes disruption of membrane integrity, which together exert bactericidal and bacteriostatic effects.</p>Formula:C65H85N11O13Purity:Min. 95%Molecular weight:1,228.44 g/molCephradine
CAS:<p>Cephradine is a broad-spectrum antibiotic, which is a synthetic derivative of cephalosporin C, originating from the mold Cephalosporium acremonium. Its mode of action involves interfering with bacterial cell wall synthesis. Cephradine binds to penicillin-binding proteins (PBPs) located inside the bacterial cell wall, inhibiting the final transpeptidation step of peptidoglycan synthesis, which leads to cell lysis and death.</p>Formula:C16H23N3O6SPurity:Min. 95%Molecular weight:385.4 g/molAqabamycin A
CAS:<p>Aqabamycin A is an antibiotic compound, which is derived from marine microorganisms, specifically actinomycetes. These marine bacteria are known for producing a wide array of bioactive compounds, including antibiotics, due to their unique metabolites shaped by the oceanic environment. Aqabamycin A operates by inhibiting bacterial RNA polymerase, thereby disrupting the transcription process essential for bacterial protein synthesis. This specific mode of action targets the growth and replication of bacteria, making it a potent agent against pathogenic strains.</p>Formula:C16H11NO3Purity:Min. 95%Molecular weight:265.26 g/molCefacetrile sodium
CAS:<p>Cefacetrile sodium is a broad-spectrum antibiotic belonging to the cephalosporin class. It is a semi-synthetic derivative sourced from cephalosporin C, a naturally occurring compound derived from the Acremonium fungus. Its mode of action involves the inhibition of bacterial cell wall synthesis. This occurs by binding to penicillin-binding proteins within the bacterial cell membrane, ultimately leading to cell lysis and death due to the inability to synthesize peptidoglycan, a critical component of the bacterial cell wall.</p>Formula:C13H13N3NaO6SPurity:Min. 95%Molecular weight:362.31 g/mol(10E)-3-O-De(a-L-cladinose)-10-dehydro-11-dehydroxy-6-O-methyl-erythromycin
CAS:<p>Erythromycin derivative</p>Formula:C30H53NO9Purity:Min. 95%Molecular weight:571.74 g/molCarbovir monophosphate
CAS:<p>Carbovir monophosphate is an antiviral agent, which is a metabolite derived from the prodrug abacavir. It functions as a nucleotide analog that interferes with viral replication. The source of Carbovir monophosphate is the metabolic conversion of abacavir, an antiretroviral medication used in the treatment of HIV. This conversion occurs primarily in the liver, facilitated by cellular enzymes.</p>Formula:C11H14N5O5PPurity:Min. 95%Molecular weight:327.23 g/molDarunavir-D9
CAS:<p>Darunavir-D9 is a prodrug of darunavir, which is an HIV protease inhibitor. Darunavir-D9 has been shown to be bioequivalent in pharmacokinetic parameters to darunavir given as a tablet. The drug exhibits a low plasma concentration profile and high clearance values. This may be due to rapid absorption and distribution of the drug, with a short elimination half-life. Darunavir-D9 also has little effect on the matrix effect and reproducibility of the reaction monitoring assay, making it an ideal candidate for use in clinical trials.</p>Formula:C27H28D9N3O7SPurity:Min. 95%Molecular weight:556.72 g/molZabofloxacin
CAS:<p>Zabofloxacin is a synthetic fluoroquinolone antibiotic, which is derived from chemical synthesis with a distinct bactericidal mode of action. Its mechanism involves the inhibition of bacterial DNA gyrase and topoisomerase IV, enzymes critical for DNA replication, transcription, and repair. This dual targeting results in potent antibacterial activity against a wide range of Gram-positive and Gram-negative pathogens.</p>Formula:C19H20FN5O4Purity:Min. 95%Molecular weight:401.4 g/molWybutosine
CAS:<p>Modified nucleoside of phenylalanine tRNA</p>Formula:C21H28N6O9Purity:Min. 95%Molecular weight:508.48 g/molCefquinome sulfate
CAS:<p>Cefquinome sulfate is a cephalosporin antibiotic, which is a synthetic, broad-spectrum antimicrobial agent. It is derived from the beta-lactam family, specifically designed to combat Gram-positive and Gram-negative bacterial pathogens. The mode of action involves inhibiting bacterial cell wall synthesis. It achieves this by binding to penicillin-binding proteins (PBPs) within the bacterial cell wall, ultimately leading to cell lysis and death due to the interruption of necessary cell wall components.</p>Formula:C23H26N6O9S3Purity:Min. 95%Color and Shape:White To Light (Or Pale) Yellow To Beige To Light Brown SolidMolecular weight:626.69 g/molMiloxacin
CAS:<p>Miloxacin is an antibacterial agent, which is sourced as a synthetic derivative of quinolone compounds. It exhibits its mode of action through the inhibition of bacterial DNA gyrase and topoisomerase IV, enzymes pivotal for DNA replication, transcription, and repair processes. This interference disrupts bacterial cell division, leading to cell death in susceptible organisms.</p>Formula:C12H9NO6Purity:Min. 95%Molecular weight:263.2 g/molIndaziflam-desindenyl
CAS:<p>Indaziflam-desindenyl is an advanced herbicide, which is a product of synthetic chemistry, specifically designed for controlling the germination and growth of a broad spectrum of weed species. It operates through cellulose biosynthesis inhibition, targeting the cellulose production in plant cell walls, thus preventing proper cell division and development. This mode of action disrupts essential mechanisms in the plant's early growth stages, making it particularly effective as a pre-emergent herbicide.</p>Formula:C5H8FN5Purity:Min. 95%Molecular weight:157.15 g/molDichlobentiazox
CAS:<p>Dichlobentiazox is a fungicide, which is synthesized from synthetic chemical sources with a mode of action that targets specific fungal processes. It works by inhibiting the biosynthesis of essential cellular components in pathogenic fungi, thereby disrupting their growth and ability to proliferate.</p>Formula:C11H6Cl2N2O3S2Purity:Min. 95%Molecular weight:349.2 g/mol
