Antimicrobianos
Os antimicrobianos são agentes que destroem ou inibem o crescimento de microrganismos, incluindo bactérias, vírus, fungos e parasitas. Esses compostos são essenciais na prevenção e tratamento de infecções, desempenhando um papel crucial na medicina, agricultura e indústria alimentícia. Na CymitQuimica, oferecemos uma ampla gama de antimicrobianos de alta qualidade e pureza, adequados para diversas aplicações científicas e industriais. Nosso catálogo inclui antibióticos, antifúngicos, antivirais e desinfetantes, todos projetados para atender às necessidades de pesquisa e desenvolvimento, bem como para aplicações clínicas e de produção. Com nossos produtos, os profissionais podem garantir a eficácia e a segurança no controle de infecções e na proteção da saúde pública.
Subcategorias de "Antimicrobianos"
- Antibióticos(4.115 produtos)
- Antifúngicos(841 produtos)
- Antiparasitários(704 produtos)
- Antivíricos(763 produtos)
Foram encontrados 2422 produtos de "Antimicrobianos"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Virginiamycin - 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>Fórmula:C71H84N10O17Pureza:Min. 95%Peso molecular:1,349.48 g/molSARS-CoV-IN-2
CAS:<p>SARS-CoV-IN-2 is a highly specific and potent antiviral inhibitor, which is chemically synthesized to target SARS-CoV-2, the virus responsible for COVID-19. This compound functions by interfering with the viral replication process, specifically targeting the viral 3CL protease enzyme, crucial for viral polyprotein cleavage. By inhibiting this protease, SARS-CoV-IN-2 effectively hampers the replication cycle of the virus, limiting its ability to proliferate within the host cells.</p>Fórmula:C24H18ClFEN3OPureza:Min. 95%Peso molecular:455.72 g/mol(4S)-2-[Carboxy[[[3-(2-chloro-6-fluorophenyl)-5-methylisoxazol-4-yl]carbonyl]amino]methyl]-5,5-dimethylthiazolidine-4-carboxylic aci d disodium salt (penicilloic acids of flucloxacillin disodium salt)
CAS:<p>(4S)-2-[Carboxy[[[3-(2-chloro-6-fluorophenyl)-5-methylisoxazol-4-yl]carbonyl]amino]methyl]-5,5-dimethylthiazolidine-4-carboxylic acid disodium salt, known as the penicilloic acids of flucloxacillin disodium salt, is a β-lactam antibiotic. This compound is derived from the penicillin family and exhibits potent antibacterial properties. The mode of action involves the inhibition of bacterial cell wall synthesis, primarily targeting the transpeptidase enzyme, which plays a crucial role in cross-linking the peptidoglycan layers of the bacterial cell wall. By acylating this enzyme, the penicilloic acids disrupt the integrity of the cell wall, leading to cell lysis and death of the bacteria.</p>Fórmula:C19H17ClFN3Na2O6SPureza:Min. 95%Peso molecular:515.9 g/mol2-Methyl-4-isothiazolin-3-one
CAS:Produto Controlado<p>2-Methyl-4-isothiazolin-3-one or MIT is a powerful antimicrobial and antifungal agent which is widely used in personal care products. It is also used in industrial applications as a preservative and antifouling agent.</p>Fórmula:C4H5NOSPureza:Min. 96%Cor e Forma:Yellow PowderPeso molecular:115.15 g/mol(4E)-1-(3,4-Dichlorophenyl)-4-[(4-ethoxyphenyl)methylidene]pyrazolidine-3,5-dione
CAS:(4E)-1-(3,4-Dichlorophenyl)-4-[(4-ethoxyphenyl)methylidene]pyrazolidine-3,5-dione is a synthetic compound belonging to the class of pyrazolidine diones. This compound is mainly derived from chemical synthesis in a laboratory setting. It acts through its interaction with specific biological pathways, potentially affecting enzyme activity or receptor sites involved in various physiological processes.Fórmula:C18H14Cl2N2O3Pureza:Min. 95%Peso molecular:377.2 g/molNeuraminidase-in-1
CAS:<p>Neuraminidase-in-1 is a chemical compound known as a neuraminidase inhibitor, which is synthetically derived. This inhibitor functions by blocking the activity of the neuraminidase enzyme, a glycoprotein found on the surface of various viruses, including influenza. The enzyme is crucial for the viral life cycle as it facilitates the release of new viral particles from infected host cells. By inhibiting this enzyme, Neuraminidase-in-1 effectively halts the replication and spread of the virus within the host organism.</p>Fórmula:C14H11N3O6Pureza:Min. 95%Peso molecular:317.25 g/molAlamethacin
CAS:<p>Alamethacin is a peptide antibiotic, which is derived from the soil fungus Trichoderma viride. This compound consists of a sequence of amino acids that form a helical structure, enabling its interaction with lipid membranes. Alamethacin functions by inserting itself into cellular membranes and forming voltage-dependent ion channels. As a result, it alters membrane permeability, causing ion imbalance and leading to cell death.</p>Fórmula:C92H150N22O25Pureza:Min. 95%Cor e Forma:SolidPeso molecular:1,964.31 g/moltert-Butyl 4-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-1-yl]piperidine-1-carboxylate
CAS:<p>Tert-Butyl 4-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-1-yl]piperidine-1-carboxylate is a boronic ester compound used primarily in organic synthesis. It is derived from the reaction of a piperidine-based carboxylate with a dioxaborolane moiety, forming a unique structural entity that serves as a versatile building block in molecular modification and drug development.</p>Fórmula:C19H32BN3O4Pureza:Min. 95%Peso molecular:377.3 g/molAcorafloxacin
CAS:<p>Acorafloxacin is a synthetic fluoroquinolone antibiotic, which is derived from the chemical modification of the quinolone core structure. It acts by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes crucial for bacterial DNA replication and transcription. The bactericidal action results from preventing the supercoiling and relaxation of the bacterial DNA, ultimately interrupting essential cellular processes.</p>Fórmula:C21H23F2N3O4Pureza:Min. 95%Peso molecular:419.4 g/molLevofloxacin
CAS:<p>Levofloxacin is a fluoroquinolone antibiotic with a mode of action that inhibits bacterial DNA gyrase and topoisomerase IV. It is used for treating bacterial infections like pneumonia and urinary tract infections.</p>Fórmula:C18H20FN3O4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:361.37 g/mol7-Ethyl-10-(4-amino-1-piperidino)carbonyloxycamptothecin-d3
CAS:<p>7-Ethyl-10-(4-amino-1-piperidino)carbonyloxycamptothecin-d3 is a synthetic chemical compound, which is a deuterated derivative of irinotecan. Deuteration involves the substitution of deuterium for hydrogen atoms, which is often utilized to enhance the metabolic stability and pharmacokinetic properties of compounds in research applications. The compound is derived from camptothecin, a natural alkaloid sourced from the Chinese tree Camptotheca acuminata.</p>Fórmula:C28H30N4O6Pureza:Min. 95%Peso molecular:521.6 g/molPazufloxacin
CAS:<p>Pazufloxacin is an antibacterial agent, which is a synthetic derivative originating from the fluoroquinolone class of compounds. This source categorizes it alongside a group of broad-spectrum antibiotics known for their efficacy against a wide variety of bacterial pathogens. The mode of action of pazufloxacin involves the inhibition of bacterial DNA gyrase and topoisomerase IV. These are essential enzymes for bacterial DNA replication, transcription, repair, and recombination processes. By inhibiting these enzymes, pazufloxacin disrupts the bacterial DNA processes, ultimately leading to cell death.</p>Fórmula:C16H15FN2O4Pureza:Min. 95%Peso molecular:318.3 g/molCefminox Sodium
CAS:<p>Cefminox Sodium is a beta-lactam antibiotic, which is synthesized through chemical modification of naturally occurring compounds. This product is classified as a second-generation cephalosporin, derived from cephalosporin C obtained from the fungus Acremonium. It exerts its mode of action by inhibiting bacterial cell wall synthesis. This occurs through the binding to penicillin-binding proteins, ultimately disrupting the cross-linking of peptidoglycan chains which are essential for bacterial cell wall integrity.</p>Fórmula:C16H20N7O7S3·NaPureza:Min. 95%Peso molecular:541.56 g/molCefodizime
CAS:<p>Cefodizime is a third-generation cephalosporin antibiotic, which is derived from the fungus Acremonium. It exerts its bactericidal effects by inhibiting bacterial cell wall synthesis. This action is achieved through binding to penicillin-binding proteins (PBPs), leading to the interruption of peptidoglycan cross-linking essential for the bacterial cell wall integrity. The breakdown of cell wall synthesis results in the lysis and death of the bacterial cell.</p>Pureza:Min. 95%(±)-Salbutamol
CAS:Produto Controlado<p>(±)-Salbutamol is a racemic mixture of a beta-2 adrenergic agonist, which is synthetically derived. This compound functions primarily by selectively stimulating beta-2 adrenergic receptors, which are predominantly located on the smooth muscle cells lining the airways. The activation of these receptors leads to the relaxation of bronchial muscle tissue, resulting in bronchodilation and improved airflow.</p>Fórmula:C13H21NO3Peso molecular:239.31 g/molAntimicrobial compound 1
CAS:<p>Antimicrobial Compound 1 is a broad-spectrum antimicrobial agent, which is derived from natural sources, specifically from marine bacteria with known potent antimicrobial properties. This compound acts by targeting and disrupting the synthesis of bacterial cell walls, specifically inhibiting peptidoglycan cross-linking, which ultimately leads to cell lysis and death due to osmotic instability. Such a mechanism offers a robust approach to tackling Gram-positive and Gram-negative bacteria.</p>Fórmula:C18H30BrNO2Pureza:Min. 95%Peso molecular:372.3 g/molPC 190723
CAS:<p>PC 190723 is a synthetic chemical compound, which is derived through targeted chemical synthesis processes involving precise organic reactions. Its mode of action involves disrupting cellular division by inhibiting specific protein functions essential for the mitotic process. This molecular interaction results in potent effects on cell division, making it a valuable tool for studying cellular mechanics and developing therapeutic strategies.</p>Fórmula:C14H8ClF2N3O2SPureza:Min. 95%Peso molecular:355.75 g/molPorfiromycin
CAS:<p>Porfiromycin is an antineoplastic antibiotic with action on DNA alkylation and cross-linking and is used for research on cancer treatment, particularly for hypoxic tumors.</p>Fórmula:C16H20N4O5Pureza:Min. 95 Area-%Cor e Forma:PowderPeso molecular:348.35 g/molUrdamycin B
CAS:<p>Urdamycin B is an anthracycline antibiotic, which is derived from the bacterium *Streptomyces fradiae*. This compound acts by intercalating into DNA, disrupting the replication and transcription processes, leading to cell death. Its mode of action involves inhibiting topoisomerase II, an enzyme critical for DNA replication and cell cycle progression. This mechanism impairs cellular proliferation, making it effective against rapidly dividing cells.</p>Fórmula:C37H44O13Pureza:Min. 95%Peso molecular:696.70 g/mol
