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(4.145 produtos)
- Antifúngicos(912 produtos)
- Antiparasitários(712 produtos)
- Antivíricos(767 produtos)
Foram encontrados 2427 produtos de "Antimicrobianos"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Ticarcillin 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%Cor e Forma: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-%Cor e Forma: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-%Cor e Forma:White PowderPeso molecular:284.35 g/molChloramphenicol D5
CAS:Produto ControladoLabeled analogue of Chloramphenicol; interferes with protein synthesisFórmula:C11H7Cl2D5N2O5Pureza:Min. 95%Cor e Forma:White To Off-White SolidPeso molecular:328.16 g/molPHMB HCl - 20% aqueous solution
CAS:Produto 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%Cor e Forma: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
-Unit-ggA consultar25gA consultar50gA consultar100gA consultar250gA consultar500gA 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-%Cor e Forma: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-%Cor e Forma: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%Cor e Forma:PowderPeso molecular:350.33 g/molPiromidic acid
CAS:Quinolone antibiotic; antimalarialFórmula:C14H16N4O3Pureza:Min. 95%Cor e Forma: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
-Unit-ggA consultar1gA consultar1kgA consultar250gA consultar500gA consultar2500gA consultarAclacinomycin A
CAS:Dual inhibitor of topoisomerase I and II
Fórmula:C42H53NO15Pureza:Min. 95%Cor e Forma: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%Cor e Forma: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-%Cor e Forma:White Yellow PowderPeso molecular:1,327.23 g/mol2,4-Diamino-6,7-diisopropylpteridine phosphate salt
CAS:Produto 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. C15H18N4O5Cor e Forma:PowderPeso molecular:334.33 g/molVirginiamycin - Activity - 50%
CAS:Inhibitor of protein synthesis; streptograminFórmula:C71H84N10O17Cor e Forma:Off-White PowderPeso molecular:1,349.48 g/molLincomycin hydrochloride monohydrate
CAS:Inhibitor of protein synthesis; lincosamideFórmula:C18H34N2O6S·HCl·H2OPureza:Min. 82%Cor e Forma:White Off-White PowderPeso molecular:461.01 g/mol1,6'-Di-HABA kanamycin A
CAS:1,6'-Di-HABA kanamycin A is a derivative of kanamycin A, an aminoglycoside antibiotic used to treat bacterial infections by blocking cell wall synthesis or by inhibiting protein synthesis.Fórmula:C26H50N6O15Pureza:Min. 95 Area-%Cor e Forma:PowderPeso molecular:686.71 g/molJNJ 4796
CAS:JNJ-4796 is an antiviral compound with a mode of action that inhibits hemagglutinin-mediated fusion in influenza A viruses. It is used for preventing and treating influenza infections.Fórmula:C28H27N9O3Pureza:Min. 95%Peso molecular:537.6 g/molCefotetan disodium
CAS:Inhibitor of cell wall synthesis; cephalosporin classFórmula:C17H15N7Na2O8S4Pureza:Min. 85 Area-%Cor e Forma:PowderPeso molecular:619.59 g/molFosamprenavir calcium
Fosamprenavir calcium is an antiretroviral medication, which is derived from the prodrug of amprenavir. It is synthesized through chemical processes to enhance oral bioavailability and improve pharmacokinetic properties. Through its mode of action, fosamprenavir is converted in vivo to amprenavir, which acts as an inhibitor of the HIV-1 protease enzyme. By inhibiting this enzyme, it prevents the cleavage of the Gag-Pol polyprotein, disrupting viral replication and processing, ultimately leading to the production of immature, non-infectious viral particles.Fórmula:C25H34CaN3O9PSPureza:Min. 95%Peso molecular:623.67 g/molLedipasvir
CAS:Anti-viral; inhibitor of NS5A proteinFórmula:C49H54F2N8O6Pureza:Min. 98 Area-%Cor e Forma:Off-White PowderPeso molecular:889.00 g/molAmikacin hydrate, Antibiotic for Culture Media Use Only
CAS:Amikacin hydrate is an aminoglycoside antibiotic, which is derived from kanamycin through a semi-synthetic process. It functions by binding to the 30S subunit of the bacterial ribosome, thereby inhibiting protein synthesis and leading to errors in the translation process. This disruption is bactericidal, effectively eliminating bacterial pathogens.Fórmula:C22H43N5O13·xH2OPureza:Min. 90.0%Peso molecular:585.6 g/molRef: 3D-A-0080
-Unit-ggA consultar1gA consultar5gA consultar10gA consultar25gA consultar2500mgA consultarAmrubicin maleate
CAS:Amrubicin maleate is an anthracycline antibiotic and is used for the treatment of small cell lung cancer. It inhibits topoisomerase II, leading to DNA breaks and cell deathFórmula:C25H25NO9·C4H4O4Pureza:(%) Min. 80%Cor e Forma:PowderPeso molecular:599.54 g/molImidocarb dipropionate
CAS:Imidocarb Dipropionate is an antiprotozoal compound with a mode of action that interferes with the glycolysis of parasites like Babesia. It is used for treating infections such as babesiosis in animals.
Fórmula:C19H20N6O·2C3H6O2Pureza:Min. 99 Area-%Cor e Forma:White PowderPeso molecular:496.56 g/molAtazanavir sulfate
CAS:Anti-viral; HIV protease inhibitor
Fórmula:C38H52N6O7·H2SO4Pureza:Min. 95%Cor e Forma:PowderPeso molecular:802.94 g/molZalcitabine - Bio-X ™
CAS:Zalcitabine (also known as dideoxycytidine or ddC) is a nucleoside analogue reverse transcriptase inhibitor (NRTI) medication used in the treatment of human immunodeficiency virus (HIV) infections. It works by blocking reverse transcriptase, an enzyme essential for replication of the HIV virus, thereby preventing the virus from multiplying and spreading. Zalcitabine is often used in combination with other antiretroviral drugs to effectively treat HIV/AIDS.Fórmula:C9H13N3O3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:211.22 g/molTebipenem pivoxil
CAS:Tebipenem pivoxil is a prodrug of tebipenem with enhanced oral bioavailability and similar action on bacterial cell wall synthesis and is used for treating bacterial infections, particularly in pediatric patients.Fórmula:C22H31N3O6S2Pureza:Min. 95%Peso molecular:497.63 g/molEnduracidin - ca. 8%
CAS:Polypeptide antibiotic used as a feed additiveFórmula:C107H138Cl2N26O31Pureza:7.2 To 8.8%Cor e Forma:Beige PowderPeso molecular:2355.3Midecamycin
CAS:Midecamycin is a macrolide antibiotic with action on bacterial protein synthesis by binding to the 50S ribosomal subunit and is used for treating respiratory tract and skin infections.Fórmula:C41H67NO15Pureza:Min. 95%Cor e Forma:PowderPeso molecular:813.97 g/molGS 331007
CAS:Anti-viral; RNA polymerase inhibitor; sofosbuvir metaboliteFórmula:C10H13FN2O5Pureza:Min. 95%Cor e Forma:Off-White PowderPeso molecular:260.22 g/molCefotetan
CAS:Inhibitor of cell wall synthesis; cephalosporin classFórmula:C17H17N7O8S4Pureza:Min. 96 Area-%Cor e Forma:PowderPeso molecular:575.62 g/molPafuramidine
CAS:Pafuramidine is an antiprotozoal prodrug with action on protozoal DNA synthesis inhibition and is used for treating African sleeping sickness and Pneumocystis pneumonia.Fórmula:C20H20N4O3Pureza:Min. 95%Cor e Forma:PowderPeso molecular:364.4 g/molDelamanid
CAS:Delamanid is a second-line antimicrobial agent, which is a synthetic derivative of the nitro-dihydro-imidazooxazole compound. Delamanid originates from a laboratory synthesis designed to target and inhibit specific components of bacterial cell wall synthesis. The mode of action involves the inhibition of mycolic acid synthesis, which is critical for the maintenance and construction of the cell wall in Mycobacterium tuberculosis. This inhibition disrupts bacterial cell wall integrity, ultimately exerting a bactericidal effect against actively replicating and dormant mycobacterial cells.Fórmula:C25H25F3N4O6Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:534.48 g/molPleconaril
CAS:Anti-viral; capsid inhibitorFórmula:C18H18F3N3O3Pureza:Min. 98 Area-%Cor e Forma:White PowderPeso molecular:381.35 g/molTriflumezopyrim
CAS:Produto ControladoTriflumezopyrim is a mesoionic insecticide with action on nicotinic acetylcholine receptors to block nerve signaling and is used for controlling rice hoppers and leafhoppers in agriculture.Fórmula:C20H13F3N4O2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:398.3 g/mol7-Deazaadenosine
CAS:Antibiotic; RNA and DNA synthesis inhibitor; adenosine analogueFórmula:C11H14N4O4Pureza:Min. 97 Area-%Cor e Forma:Off-White To Light (Or Pale) Brown SolidPeso molecular:266.26 g/molMolnupiravir - Bio-X ™
CAS:Produto ControladoEIDD 2801 is an orally bioavailable prodrug of β-D-N4-hydroxycytidine and was shown to inhibit SARS-CoV-2 replication in human airway epithelial cells. EIDD 2801 was also tested in mice infected with SARS-CoV and MERS-CoV viruses. EIDD 2801 targets the RNA-dependent RNA polymerase (RdRp) and reduces virus titer and improved pulmonary function in experimental animals when used in prophylactic and therapeutic regime.
Fórmula:C13H19N3O7Pureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:329.31 g/molFosfomycin calcium
CAS:Broad-spectrum antibiotic; bacterial cell wall biogenesis inhibitorFórmula:C3H7O4P•CaxPureza:Min. 95%Cor e Forma:White PowderPeso molecular:176.12 g/molCabotegravir
CAS:Anti-viral; HIV integrase inhibitorFórmula:C19H17F2N3O5Pureza:Min. 95%Cor e Forma:White/Off-White SolidPeso molecular:405.35 g/molPosaconazole - Form I
CAS:Posaconazole is an antifungal agent that inhibits the 14-alpha demethylase enzyme which is responsible for the synthesis of the fungal cell wall component, ergosterol. This demethylase enzyme synthesizes ergosterol through converting lanosterol to ergosterol. Therefore Posaconazole prevents the formation of fungal cell walls with the appropriate membrane permeability thus leading to fungal cell lysis. Posaconazole can be used as an antifungal drug to treat opportunistic fungal infections in immunocompromised individuals such as HIV patients. Moreover it is shown to inflict its inhibitory activity against common pathogenic fungus such as Candida and Aspergillus species but also Mucorales and some Fusarium species, which are less common.Fórmula:C37H42F2N8O4Pureza:Min. 95%Peso molecular:700.78 g/molBMS 806
CAS:BMS 806 is an antiretroviral agent and is used for the treatment of HIV. It inhibits the fusion of the HIV virus with the host cell membrane.Fórmula:C22H22N4O4Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:406.43 g/molFlavomycin - 8% premix
CAS:Flavomycin - 8% premix is an antibacterial feed additive with action on bacterial cell wall synthesis and is used for promoting growth and improving feed efficiency in livestock and poultry.Fórmula:C69H107N4O35PPureza:7 To 9%Cor e Forma:PowderPeso molecular:1,583.57 g/molAcetylspiramycin - Mixture of components
CAS:Acetylspiramycin - Mixture of components is a derivative of spiramycin and is used as an antibiotic.Fórmula:C45H76N2O15Cor e Forma:PowderPeso molecular:885.09 g/molRimantadine HCl - Bio-X ™
CAS:Rimantadine is an anti-viral drug that is used for the prevention of influenza A infection. This drug is an RNA synthesis inhibitor and exerts its effects on the viral replication cycle. Although not fully understood, it is said that the M2 gene may play a role in Rimantadine susceptibility.Fórmula:C12H22ClNPureza:Min. 95%Cor e Forma:PowderPeso molecular:215.76 g/molSecnidazole
CAS:Antimicrobial agentFórmula:C7H11N3O3Pureza:Min. 95%Cor e Forma:White PowderPeso molecular:185.18 g/molOrmetoprim - Bio-X ™
CAS:Ormetoprim is an antibacterial drug used in veterinary medicine to treat several bacterial infections in animals. This drug is a dihydrofolate reductase inhibitor and disrupts DNA and RNA synthesis in bacteria.Fórmula:C14H18N4O2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:274.32 g/molLersivirine
CAS:Anti-viral; non-nucleoside reverse transcriptase inhibitorFórmula:C17H18N4O2Pureza:Min. 95%Cor e Forma:SolidPeso molecular:310.14298
