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(4,115 products)
- Antifungals(837 products)
- Antiparasitics(704 products)
- Antivirals(763 products)
Found 2422 products of "Antimicrobials"
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Mitomycin D
CAS:<p>Mitomycin D is an antibiotic and chemotherapeutic agent known for its ability to inhibit DNA synthesis, making it a potent antitumor agent. It is derived from the bacterium *Streptomyces caespitosus*. Mitomycin D functions as a DNA crosslinking agent by alkylating the DNA strands, which interferes with DNA replication and transcription. This mechanism leads to the cessation of cellular division and ultimately induces apoptosis in rapidly dividing cells.</p>Formula:C15H18N4O5Purity:Min. 95%Molecular weight:334.33 g/molBPH715
CAS:<p>Please enquire for more information about BPH715 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C17H31NO7P2Purity:Min. 95%Molecular weight:423.4 g/molAclacinomycin HCl
CAS:<p>Aclacinomycin HCl is a cytotoxic antibiotic that inhibits the growth of tumor cells. It has been shown to induce apoptosis in human leukemia cells by altering the transmembrane potential and inhibiting cell proliferation. Aclacinomycin HCl also induces DNA damage response, which leads to caspase activities and cell death. This drug is highly selective for tumor cells, with no effect on normal cells. It has been shown to be effective against primary liver cancer in animal models, as well as developmental disorders such as autism spectrum disorder (ASD).</p>Formula:C42H53NO15·HClPurity:Min. 95%Color and Shape:Orange PowderMolecular weight:848.33 g/molSarecycline
CAS:<p>Sarecycline is a tetracycline-class antibiotic, which is derived from naturally occurring tetracycline antibiotics. Its mode of action involves inhibition of bacterial protein synthesis by binding to the 30S ribosomal subunit, thereby preventing the addition of amino acids to nascent peptide chains. This specific mechanism disrupts bacterial growth, making Sarecycline effective against certain strains of bacteria implicated in dermatological conditions.</p>Formula:C24H29N3O8Purity:Min. 95 Area-%Molecular weight:487.5 g/molViolacein
CAS:<p>Violacein is a model system for studying the effects of hydroxyl groups on cell lysis. It is a fatty acid that contains nitrogen atoms and has antimicrobial properties. Violacein has been shown to cause the loss of mitochondrial membrane potential in HL-60 cells, which may be due to its ability to act as a multidrug efflux pump inhibitor. Violacein also exhibits antimicrobial activity against several bacterial strains, including MRSA and methicillin-sensitive Staphylococcus aureus (MSSA). In addition, violacein has been shown to induce cell lysis in vitro via the degradation of proteins and lipids in the cytoplasm.</p>Formula:C20H13N3O3Purity:Min. 95%Color and Shape:PowderMolecular weight:343.3 g/molGatifloxacin hydrate
CAS:<p>Gatifloxacin hydrate is a fluoroquinolone antibiotic, which is synthesized chemically. It exerts its bactericidal effects primarily by inhibiting bacterial DNA gyrase and topoisomerase IV. These enzymes are crucial for bacterial DNA replication, transcription, and repair. By preventing these processes, gatifloxacin effectively halts bacterial cell division, ultimately leading to cell death.</p>Formula:C19H24FN3O5Purity:Min. 95%Molecular weight:393.4 g/molCEF3
CAS:<p>CEF3 is a cephalosporin-based antibacterial agent, which is derived from the fermentation of Streptomyces species. This compound functions by inhibiting bacterial cell wall synthesis, specifically targeting the transpeptidase enzyme involved in the cross-linking of peptidoglycan layers. The disruption of this process results in weakened bacterial cell walls, leading to cell lysis and death, particularly affecting Gram-positive and some Gram-negative bacteria.</p>Formula:C42H74N10O12Purity:Min. 95%Molecular weight:911.1 g/molTebufenozide-hydroxymethyl
CAS:<p>Tebufenozide-hydroxymethyl is an insect growth regulator, which is synthesized chemically to function as an agonist of the molting hormone, ecdysone, in target pest species. It operates by mimicking the effects of ecdysone, leading to premature and lethal molting in lepidopteran larvae. This disruption in the developmental cycle of the insects effectively suppresses their population by preventing them from reaching maturity and reproducing.</p>Formula:C22H28N2O3Purity:Min. 95%Molecular weight:368.5 g/molBleomycin HCl
CAS:<p>Inducer of DNA strand breaks; glycopeptide antibiotic, anti-neoplastic</p>Formula:C50H71N16O21S2R•(HCl)xPurity:Min. 95%Color and Shape:White To Off-White SolidAtazanavir-d5
CAS:<p>Atazanavir-d5 is an isotopically labeled variant of the antiretroviral drug Atazanavir, a non-peptidic HIV-1 protease inhibitor. It is synthesized using stable isotope labeling, specifically deuterium, which replaces five hydrogen atoms. The mechanism of action involves binding to the active site of the HIV-1 protease enzyme, a critical enzyme in the replication cycle of HIV, thereby preventing the cleavage of the viral gag-pol polyprotein precursors into the mature protein components of an infectious viral particle.</p>Formula:C38H52N6O7Purity:Min. 95%Molecular weight:709.9 g/molFormycin A
CAS:<p>Formycin A is a nucleoside analog, which is an antibiotic product derived from certain Streptomyces species. Its mode of action involves mimicking adenosine, one of the four nucleosides in RNA. By doing so, it interferes with the RNA processing of certain microorganisms, ultimately disrupting their ability to synthesize proteins effectively. This interference results in the inhibition of bacterial and parasitic growth.</p>Formula:C10H13N5O4Purity:Min. 95%Molecular weight:267.24 g/molSE 563
CAS:<p>SE 563 is a biocontrol agent, which is an organism-based product derived from natural sources. It is sourced from a specific strain of entomopathogenic nematodes known for their effectiveness in targeting and controlling insect pests. The mode of action involves the nematodes seeking out their insect hosts in the soil, entering through natural openings, and releasing symbiotic bacteria that kill the host from within.</p>Formula:C22H17ClF3NO3Purity:Min. 95%Molecular weight:435.08491Azoxystrobin-d4
CAS:<p>Azoxystrobin-d4 is a deuterated fungicide, which is a synthetic chemical compound designed for use in research, particularly within the field of agrochemical studies. It is a derivative of azoxystrobin, a well-known strobilurin fungicide, and is produced through isotope labeling, where hydrogen atoms are replaced with deuterium. This isotopic substitution does not alter the chemical activity of the compound but assists in analytical studies, such as mass spectrometry, by enabling precise tracking and quantification.</p>Formula:C22H17N3O5Purity:Min. 95%Molecular weight:407.4 g/molViramidine hydrochloride
CAS:<p>Viramidine hydrochloride is an antiviral prodrug with action as a precursor to ribavirin, targeting viral RNA synthesis and is used for research on hepatitis C and other viral infections.</p>Formula:C8H14ClN5O4Purity:Min. 95%Molecular weight:279.68 g/molβ-Cypermethrin
CAS:<p>Beta-cypermethrin is a synthetic pyrethroid insecticide, which is a chemically altered derivative of natural pyrethrins found in chrysanthemum flowers. These pyrethrins are modified to enhance their stability and potency. Beta-cypermethrin acts by targeting the nervous system of insects, specifically by modifying the function of voltage-gated sodium channels. This action leads to prolonged depolarization of the neuron, resulting in paralysis and eventual death of the insect.</p>Formula:C22H19Cl2NO3Purity:Min. 95%Molecular weight:416.3 g/molSporidesmolide
CAS:<p>Sporidesmolide is a cyclic depsipeptide, which is a type of compound characterized by having both ester and amide bonds in its structure. This product is derived from fungal sources, specifically certain species within the genus *Sporidesmium*. The mode of action for sporidesmolide involves disrupting microbial cell membrane integrity, leading to increased permeability and eventual cell death. This activity primarily targets bacteria and fungi, making it an important subject of study for its potential antimicrobial properties.</p>Formula:C34H60N4O8Purity:Min. 95%Molecular weight:652.9 g/molTigemonam
CAS:<p>Tigemonam is a synthetic beta-lactam antibiotic, which is derived from chemical synthesis processes. This compound operates by inhibiting bacterial cell wall synthesis, specifically targeting the penicillin-binding proteins (PBPs). The disruption of the cell wall synthesis ultimately leads to cell lysis and death of the bacteria, making it effective primarily against gram-negative bacterial infections.</p>Formula:C12H15N5O9S2Purity:Min. 95%Molecular weight:437.41 g/molThienamycin
CAS:<p>Thienamycin is a β-lactam antibiotic, which originates from the fermentation of the bacterium *Streptomyces cattleya*. Its mode of action involves inhibiting the synthesis of bacterial cell walls. Thienamycin accomplishes this by binding to penicillin-binding proteins (PBPs) critical for peptidoglycan construction, thereby disrupting cell wall integrity and leading to bacterial lysis.</p>Formula:C11H16N2O4SPurity:80%MinColor and Shape:PowderMolecular weight:272.32 g/molNifursemizone
CAS:<p>Nifursemizone is an antimicrobial agent, which is a synthetic nitrofuran derivative. It is engineered from chemical precursors through targeted synthetic processes designed to maximize its antibacterial properties. The mode of action of Nifursemizone involves the inhibition of bacterial enzymes and interference with nucleic acid synthesis. This action disrupts essential bacterial functions, leading to the inhibition of bacterial growth and eventual cell death.</p>Formula:C8H10N4O4Purity:Min. 95%Molecular weight:226.19 g/molVirginiamycin - Complex of M1+S1
CAS:<p>Virginiamycin - Complex of M1+S1 is an antibiotic compound, which is derived from the actinobacterium Streptomyces virginiae. It functions through the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, thereby obstructing peptide bond formation and impeding microbial growth. The complex is composed of two major components: Virginiamycin M1 and Virginiamycin S1, which synergistically enhance antimicrobial efficacy.</p>Formula:C71H84N10O17Purity:Min. 95%Molecular weight:1,349.48 g/mol
