Antimicrobianos
Subcategorías de "Antimicrobianos"
- Antibióticos(4.133 productos)
- Antifúngicos(888 productos)
- Antiparasitarios(687 productos)
- Antivirales(764 productos)
Se han encontrado 2437 productos de "Antimicrobianos"
Troleandomycin
CAS:Troleandomycin is a macrolide antibiotic with action on bacterial protein synthesis by binding to the ribosome and is used for treating bacterial infections, particularly respiratory infections.Fórmula:C41H67NO15Pureza:Min. 95 Area-%Forma y color:White Off-White PowderPeso molecular:813.97 g/molNelfinavir mesylate
CAS:Anti-viral; HIV protease inhibitorFórmula:C33H49N3O7S2Forma y color:White PowderPeso molecular:663.89 g/molErtapenem sodium
CAS:Ertapenem sodium is a carbapenem antibiotic with action on bacterial cell wall synthesis and is used for treating severe bacterial infections like intra-abdominal infections and pneumonia.Fórmula:C22H24N3NaO7SPureza:Min. 85 Area-%Forma y color:PowderPeso molecular:497.5 g/molTicarcillin disodium salt, Antibiotic for Culture Media Use Only
CAS:Ticarcillin is a member of the beta-lactam family of antibiotics and has bactericidal activity against Gram-positive and Gram-negative bacteria such as Staphylococcus and Pseudomonas strains. Ticarcillin inhibits cell wall synthesis by binding to penicillin-binding protein (PBP) and blocking transpeptidase. It also has a C-terminal that can inhibit domain I and II beta-lactamases (namely, PEN2). The lactam ring in ticarcillin is cleaved by beta-lactamase, which makes it ineffective, thus ticarcillin is often combined with β-lactamase inhibitors such as clavulanic acid.Fórmula:C15H14N2Na2O6S2Pureza:Min. 87.0 Area-%Peso molecular:428.40 g/molClindamycin-2-phosphate
CAS:Clindamycin-2-phosphate is a lincosamide antibiotic with action on bacterial protein synthesis inhibition and is used for treating serious bacterial infections like skin and respiratory infections.Fórmula:C18H34ClN2O8PSPureza:Min. 95%Forma y color:White PowderPeso molecular:504.96 g/molColistin sulfate
CAS:Colistin is a narrow-spectrum antibiotic efficient mostly against gram-negative bacteria. Colistin interacts with the outer membrane of gram-negative bacteria and induces a transfer of divalent cations of calcium and magnesium from the negatively charged phosphate groups. This causes the disruption of the outer membrane and release of lipopolysaccharides. It is commonly used against Enterobacteriaceae and Aeromonas, and none-fermentative gram-negative bacteria as well as for carbapenem-resistant Acinetobacter strains.Fórmula:C53H102N16O17SPureza:Min. 77 Area-%Forma y color:White PowderPeso molecular:1,266.73 g/molOseltamivir acid
CAS:Inhibitor of viral neuraminidase enzyme, effective against influenza A and B viruses. This antiviral compound inhibits neuraminidase-mediated cleavage of host cell sialic acids, which interact with newly synthesised virions from the host cell. This prevents virion budding from the host, resulting in inhibition of virion release and viral infection overall.Fórmula:C14H24N2O4Pureza:Min. 95 Area-%Forma y color:White PowderPeso molecular:284.35 g/molChloramphenicol D5
CAS:Producto controladoLabeled analogue of Chloramphenicol; interferes with protein synthesisFórmula:C11H7Cl2D5N2O5Pureza:Min. 95%Forma y color:White To Off-White SolidPeso molecular:328.16 g/molPHMB HCl - 20% aqueous solution
CAS:Producto controladoPolyhexamethylene biguanidine, also known as PHMB or polyhexamide, is a highly water soluble and hydrolytically stable polymeric material. The presence of multiple hydrogen bonding and chelation sites within PHMB renders it of potential interest in the field of supramolecular chemistry. PHMB shows activity against both Gram-positive and Gram-negative bacteria and is widely used across several sectors, typically as the hydrochloride salt, in a variety of disinfectant solutions and antiseptics. PHMB is also available as a solid in neat.The polymerization degree is 12~16, and the M.W is about 3200Fórmula:(C8H17N5)n•(HCl)xPureza:19.0 To 21.0%Forma y color:Colorless Clear LiquidVancomycin hydrochloride, Antibiotic for Culture Media Use Only
CAS:Vancomycin hydrochloride is an antibiotic that is used against Gram-positive bacteria, including Staphylococcus aureus. It has been shown to inhibit the growth of bacteria by binding the D-alanyl-D-alanine moiety of the peptidoglycan cell wall precursor, inhibiting the peptidoglycan synthesis and disrupting its cross linking. It also inhibits particle formation when it reacts with human plasma, which can lead to hemolysis and hemagglutination. The absorption spectrum for vancomycin hydrochloride shows maxima at 230, 260, 290, and 320 nm, which are characteristic for this compound. Vancomycin has been used in several studies for treatment of methicillin-resistant Staphylococcus aureus infections.
Fórmula:C66H76Cl3N9O24Peso molecular:1,485.71 g/molRef: 3D-Q-201920
25gA consultar50gA consultar100gA consultar250gA consultar500gA consultar-Unit-ggA consultarBenznidazole
CAS:Benznidazole is an antiprotozoal agent and is used for the treatment of Chagas disease. It generates free radicals that damage the DNA and other cellular components of the parasite.
Fórmula:C12H12N4O3Pureza:Min. 97 Area-%Forma y color:White PowderPeso molecular:260.25 g/molRaltegravir
CAS:Raltegravir is an antiretroviral agent, which is a synthetic integrase inhibitor sourced from pharmaceutical research. Its mode of action involves the inhibition of the HIV-1 integrase enzyme, which is essential for the viral replication process. By blocking the strand transfer step of the integration of viral DNA into the host cell genome, Raltegravir prevents the proliferation of the virus within the host.
Fórmula:C20H21FN6O5Pureza:Min. 98 Area-%Forma y color:White Off-White PowderPeso molecular:444.42 g/molZanamivir hydrate - Bio-X ™
CAS:Potent and selective inhibitor of influenza A and B sialidases. Zanamivir belongs to the class of drugs known as neuraminidase inhibitors. This compound is a sialic acid analogue that occupies viral neuraminidase active site, inhibits enzyme’s hydrolytic activity and cleavage of sialic acid residues from host cell surface glycans. It therefore prevents shedding newly produced virions from infected cell surface and reduces infection of surrounding cells. In in vitro studies with influenza A and B virus isolates, zanamivir inhibited the plaque formation by 50% in canine cells (MDCK) with concentrations between 0.004 and 0.014 μM and 0.02 and 16 μM, respectively. Zanamivir hydrate is part of our Bio-X ™ Range. These products are aimed at life science researchers who need high quality ready to use products for assay development, screening or other R&D work. With a solubility datasheet and convenient vials, all of our Bio-X ™ products are in stock across our global warehouses for rapid delivery and ease of use.Fórmula:C12H22N4O8Pureza:(%) Min. 98%Forma y color:PowderPeso molecular:350.33 g/molPiromidic acid
CAS:Quinolone antibiotic; antimalarialFórmula:C14H16N4O3Pureza:Min. 95%Forma y color:Off-White PowderPeso molecular:288.3 g/molGentamycin sulfate, Antibiotic for Culture Media Use Only
CAS:Gentamycin sulphate is the salt form of the broad-spectrum antibiotic gentamycin (a.k.a. gentamicin). Gentamycin is active against clinically relevant bacteria, such as: Pseudomonas aeruginosa, Klebsiella pneumoniae, Escherichia coli, Serratia marcescens, and is used to fight infections from Staphylococcus, Citrobacter and Enterobacteriaceae species. Gentamycin is a natural mixture of four congeners, one of which is gentamicin C2a. Gentamycin has been included in biomedical implantable materials, such as, bone grafts, to reduce the risk of infection.Fórmula:C21H45N5O11SPeso molecular:575.67 g/molRef: 3D-G-2420
1gA consultar1kgA consultar250gA consultar500gA consultar2500gA consultar-Unit-ggA consultarAclacinomycin A
CAS:Dual inhibitor of topoisomerase I and II
Fórmula:C42H53NO15Pureza:Min. 95%Forma y color:PowderPeso molecular:811.87 g/molGentamicin C1a pentaacetate
CAS:Gentamicin C1a pentaacetate is an aminoglycoside antibiotic derivative, which is synthesized through the acetylation of the hydroxyl groups in gentamicin C1a. This compound is derived from the fermentation products of Micromonospora species, a genus of actinobacteria. Its mode of action is similar to that of standard aminoglycosides, primarily involving the binding to bacterial 30S ribosomal subunits. This binding interferes with protein synthesis by causing misreading of mRNA, ultimately leading to the inhibition of protein production and bacterial cell death.
Fórmula:C29H59N5O17Pureza:Min. 95%Forma y color:Off-White PowderPeso molecular:749.8 g/molCeftriaxone disodium hemiheptahydrate
CAS:Ceftriaxone disodium hemiheptahydrate is a third-generation cephalosporin antibiotic, which is a semisynthetic derivative of cephalosporin C. This compound is sourced from the fungus Acremonium, which is known for its role in deriving crucial β-lactam antibiotics. Ceftriaxone acts by inhibiting bacterial cell wall synthesis, specifically targeting the penicillin-binding proteins (PBPs). This action disrupts peptidoglycan cross-linking, leading to bacterial cell lysis and death.Fórmula:(C18H18N8Na2O7S3)2•(H2O)7Pureza:Min. 94 Area-%Forma y color:White Yellow PowderPeso molecular:1,327.23 g/mol2,4-Diamino-6,7-diisopropylpteridine phosphate salt
CAS:Producto controladoA nucleophilic heterocycleFórmula:C12H21N6O4PPureza:Min. 98 Area-%Peso molecular:344.31 g/molMitomycin C - High Purity
CAS:Mitomycin C is a cytotoxic agent that inhibits DNA synthesis. This product is tested according to USP specification. Mitomycin C has been shown to be effective against resistant mutants and carcinoma cell lines. It also has genotoxic activity and induces statistically significant chromosome aberrations in mammalian cells. Mitomycin C is toxic to the mitochondria, which may be due to its ability to induce mitochondrial membrane potential collapse, leading to apoptosis. Mitomycin C binds to the response element in the genome, causing transcriptional repression of a number of genes involved in cell proliferation, differentiation, or apoptosis. Mitomycin C inhibits squamous carcinoma cells by binding to their DNA and preventing RNA synthesis.Fórmula:C15H18N4O5Pureza:Cas Rn [50-07-7] M. F. C15H18N4O5Forma y color:PowderPeso molecular:334.33 g/mol
