Antimicrobianos
Los antimicrobianos son agentes que destruyen o inhiben el crecimiento de microorganismos, incluyendo bacterias, virus, hongos y parásitos. Estos compuestos son esenciales en la prevención y tratamiento de infecciones, desempeñando un papel crucial en la medicina, la agricultura y la industria alimentaria. En CymitQuimica, ofrecemos una extensa gama de antimicrobianos de alta calidad y pureza, adecuados para diversas aplicaciones científicas e industriales. Nuestro catálogo incluye antibióticos, antifúngicos, antivirales y desinfectantes, todos diseñados para satisfacer las necesidades de investigación y desarrollo, así como para aplicaciones clínicas y de producción. Con nuestros productos, los profesionales pueden garantizar la eficacia y seguridad en el control de infecciones y en la protección de la salud pública.
Subcategorías de "Antimicrobianos"
- Antibióticos(4.139 productos)
- Antifúngicos(908 productos)
- Antiparasitarios(703 productos)
- Antivirales(767 productos)
Se han encontrado 2430 productos de "Antimicrobianos"
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Sulconazole nitrate
CAS:Sulconazole nitrate is an antifungal agent, which is a synthetic compound derived from imidazole. Its mode of action involves the inhibition of ergosterol synthesis, an essential component of fungal cell membranes, leading to increased membrane permeability and ultimately cell death.Fórmula:C18H16Cl3N3O3SPureza:Min. 95%Peso molecular:460.76 g/molAsukamycin
CAS:Asukamycin is an antibiotic, which is a secondary metabolite derived from the bacterium *Streptomyces nodosus*. Its mode of action involves the inhibition of cell wall synthesis in susceptible bacteria by interfering with peptidoglycan polymerization, which is essential for maintaining bacterial cell integrity. Additionally, asukamycin exhibits the ability to interfere with the biosynthesis of important cellular components in certain pathogens, contributing to its antimicrobial efficacy.Fórmula:C31H34N2O7Pureza:Min. 95%Peso molecular:546.6 g/molChaetoglobosin A - From chaetomium globosum
CAS:Chaetoglobosin A is a mycotoxin, which is a secondary metabolite produced by the fungus Chaetomium globosum. This compound exhibits its mode of action by disrupting the cytoskeletal elements within cells, primarily affecting actin polymerization. This interference leads to alterations in cell morphology and can induce apoptosis in certain cell lines.
Fórmula:C32H36N2O5Pureza:Min. 95%Peso molecular:528.64 g/molTigecycline Impurity 8
Tigecycline Impurity 8 is a chemical impurity associated with Tigecycline, which is a glycylcycline antibiotic. This impurity is typically synthesized or isolated as a part of pharmaceutical development and quality control processes. Its source is inherently linked to the chemical synthesis of Tigecycline, where it may arise as a byproduct or degradation product.Fórmula:C29H37N5O8Pureza:Min. 95%Peso molecular:583.65 g/molPhthivazid
CAS:Phthivazid is an antibiotic, which is a synthetic derivative of isonicotinic acid hydrazide. It functions by inhibiting the synthesis of mycolic acids in the mycobacterium cell wall, which are essential components for the survival of the bacteria. This disruption in the cell wall synthesis results in bactericidal activity against Mycobacterium tuberculosis.Fórmula:C14H13N3O3Pureza:90% MinForma y color:PowderPeso molecular:271.27 g/molPicloxydine digluconate
CAS:Picloxydine digluconate is an antiseptic agent, which is derived from synthetic chemical processes designed to produce highly effective antimicrobial compounds. It operates through the disruption of microbial cell membranes, leading to the leakage of cell contents and subsequent cell death. This mode of action is particularly efficient against a wide spectrum of bacteria, including both Gram-positive and Gram-negative strains, as well as fungi and some viruses.Fórmula:C26H36Cl2N10O7Pureza:Min. 95%Peso molecular:671.5 g/molseco erythromycin
CAS:Seco erythromycin is a derivative of the macrolide antibiotic erythromycin, which originates from the bacterium *Saccharopolyspora erythraea*. As a semi-synthetic compound, it retains the core lactone ring structure of erythromycin, but modifications in its chemical configuration confer distinct properties. Seco erythromycin operates by binding to the 50S subunit of the bacterial ribosome, inhibiting protein synthesis. This action effectively halts bacterial growth by preventing the translocation of peptides and thus impairs protein assembly.Fórmula:C37H69NO14Pureza:Min. 95%Peso molecular:751.94 g/molTrans-tetradecenyl acetate
CAS:Trans-tetradecenyl acetate is a synthetic pheromone, which is an analog of a naturally occurring insect sex pheromone. It is derived from synthetic organic chemistry processes that aim to replicate the molecular structure of pheromones produced by insects. The mode of action involves mimicking the natural pheromone signals used by female insects to attract males. By dispersing trans-tetradecenyl acetate into the environment, it disrupts the mating communication between the sexes, leading to a reduction in successful mating events and, consequently, a decrease in pest population over time.Fórmula:C16H30O2Pureza:Min. 95%Peso molecular:254.41 g/molClindamycin-d3 hydrochloride
CAS:Producto controladoClindamycin-d3 hydrochloride is an isotopically labeled pharmaceutical compound, specifically designed for use in the field of analytical chemistry and pharmacokinetics. It is derived from clindamycin, a known antibiotic sourced from modifications of the naturally occurring compound lincomycin, produced by the actinobacterium Streptomyces lincolnensis. The incorporation of deuterium atoms, replacing hydrogen, allows for its use in sophisticated analytical methods such as mass spectrometry, where it serves to trace the metabolic pathways and to quantify the bioavailability and distribution of clindamycin in biological systems with high precision.Fórmula:C18H30ClD3N2O5S•HClPureza:Min. 95%Peso molecular:464.46 g/molDuocarmycin sa
CAS:Duocarmycin SA is an antitumor antibiotic, which is derived from the natural products of Streptomyces bacteria. This compound exhibits its mode of action through the alkylation of DNA, specifically binding within the minor groove. The alkylation process preferentially targets adenine-thymine-rich regions, leading to irreversible DNA damage and subsequent inhibition of DNA replication. Such interaction results in the induction of apoptosis in rapidly dividing cells.
Fórmula:C25H23N3O7Pureza:Min. 95%Peso molecular:477.5 g/molMethiozolin
CAS:Methiozolin is an herbicide, which is a synthetic compound with a specific mode of action. It targets the cell division process, specifically inhibiting the synthesis of very-long-chain fatty acids in plants. This mode of action makes Methiozolin effective against problematic weed species such as annual bluegrass (Poa annua), which is known for its pervasive growth in turfgrass systems.
Fórmula:C17H17F2NO2SPureza:Min. 95%Peso molecular:337.4 g/molFinafloxacin hydrochloride
CAS:Finafloxacin hydrochloride is an antibiotic, which is a synthetic compound derived from the fluoroquinolone class. Its source is a chemically engineered structure, specifically designed to combat bacterial infections effectively. The mode of action of Finafloxacin hydrochloride involves the inhibition of bacterial DNA gyrase and topoisomerase IV, essential enzymes responsible for DNA replication, transcription, and repair in bacteria. By inhibiting these enzymes, it disrupts bacterial DNA processes, ultimately leading to cell death and resolution of the infection.Fórmula:C20H20ClFN4O4Pureza:Min. 95%Peso molecular:434.85 g/molEgcg octaacetate
CAS:Please enquire for more information about Egcg octaacetate including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C38H34O19Pureza:Min. 95%Peso molecular:794.7 g/molOfloxacin d3 hydrochloride
CAS:Ofloxacin d3 hydrochloride is a deuterated form of the quinolone antibiotic, which is a synthetic derivative designed for research purposes. It is sourced from the fluorinated carboxyquinolone class, where deuterium atoms replace certain hydrogen atoms to study metabolic pathways involving ofloxacin with minimal isotopic interference. Ofloxacin d3 inhibits bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication, transcription, and repair. By stabilizing the transient cleavable complex with DNA, it prevents the ligation of DNA strands, leading to bacterial cell death. This compound is utilized primarily in laboratory settings for studying the pharmacokinetics and biodistribution of quinolones, as well as for elucidating resistance mechanisms in bacterial strains. Its stable isotopic composition makes it ideal for advanced analytical techniques such as mass spectrometry. Through these investigations, insights into drug metabolism, efficacy, and resistance can be gleaned, contributing to the broader understanding of quinolone antibiotic activity.Fórmula:C18H21ClFN3O4Pureza:Min. 95%Peso molecular:400.8 g/molLascufloxacin
CAS:Lascufloxacin is a synthetic fluoroquinolone antibiotic, which is derived from chemical synthesis. Its mode of action involves inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication, transcription, repair, and recombination. By targeting these enzymes, lascufloxacin effectively hampers bacterial cell division and growth, leading to cell death. This mechanism specifically affects Gram-positive and Gram-negative bacterial strains, making it a versatile agent in antibacterial therapy.
Fórmula:C21H24F3N3O4Pureza:Min. 95%Peso molecular:439.4 g/molNaftifine N-Oxide
CAS:Naftifine N-Oxide is an antifungal agent, which is derived from synthetic chemical processes. Its structure is based on the modification of the known antifungal, naftifine, by introducing an N-oxide functional group, which may enhance certain pharmacokinetic properties. As a synthetic derivative, Naftifine N-Oxide is specifically designed to interfere with the biosynthesis of ergosterol, an essential component of fungal cell membranes. By inhibiting squalene epoxidase, an enzyme crucial to the ergosterol pathway, Naftifine N-Oxide effectively disrupts the development and maintenance of the fungal cell membrane, compromising cell integrity and leading to antifungal activity.Fórmula:C21H21NOPureza:Min. 95%Peso molecular:303.4 g/molCeftibuten Hydrate
CAS:Ceftibuten Hydrate is a third-generation cephalosporin antibiotic, which is a synthetic derivative of naturally occurring cephalosporin C, derived from the fungus Acremonium. It functions by inhibiting bacterial cell wall synthesis, leading to cell lysis and death. This bactericidal action is accomplished through the binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, disrupting the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls.Fórmula:C15H14N4O6S2·xH2OPureza:Min. 95%Peso molecular:410.42 g/molN-Nitroso-N-phenylbenzylamine
CAS:N-Nitroso-N-phenylbenzylamine is a nitroso compound, which is synthesized through a chemical reaction involving nitrosation. It arises typically from the interaction of secondary amines and nitrosating agents. This compound functions as a potential mutagen due to its ability to form reactive intermediates that can interact with DNA. These intermediates can lead to modifications in the DNA structure, potentially causing mutations.Fórmula:C13H12N2OPureza:Min. 95%Peso molecular:212.25 g/molErythromycin, Antibiotic for Culture Media Use Only
CAS:Erythromycin, Antibiotic for Culture Media Use Only, is a macrolide antibiotic derived from the bacterium *Saccharopolyspora erythraea*. It functions by inhibiting protein synthesis, specifically targeting the 50S ribosomal subunit in susceptible bacteria. This action results in the prevention of peptide chain elongation, effectively halting bacterial growth and proliferation.Fórmula:C37H67NO13Pureza:Min. 93.0 Area-%Peso molecular:733.93 g/molRef: 3D-E-3250
-Unit-ggA consultar1kgA consultar100gA consultar250gA consultar500gA consultar2500gA consultarCenicriviroc sulfone
CAS:Cenicriviroc sulfone is a small-molecule pharmaceutical compound, which is a synthetic product derived from medicinal chemistry optimization processes. It functions as a dual antagonist of the CCR2 and CCR5 receptors, which are chemokine receptors involved in inflammatory response and HIV entry, respectively. By blocking these receptors, Cenicriviroc sulfone inhibits the signaling pathways that lead to immune cell recruitment and inflammation.
Fórmula:C41H52N4O5SPureza:Min. 95%Peso molecular:712.90 g/mol
