Antimicrobianos

<p>Halauxifen is a synthetic herbicide, which is a product of chemical synthesis used in agricultural practices. Derived from advanced chemical research and development, its primary source is a laboratory setting where it is engineered to exhibit specific properties for plant management.</p>

<p>Metabolite of voriconazole; sterol 14?-demethylase inhibitor</p>

<p>Bacitracin B1 is a polypeptide antibiotic and is used for the treatment of bacterial infections. Its mode of action is similar to bacitracin.</p>

<p>Antibiotic of anthracycline class; DNA synthesis inhibitor</p>

<p>STAADIUMTM GalactoZide II is a targeted inhibitor for β-galactosidase producing bacteria. The antibacterial activity of STAADIUMTM GalactoZide II is triggered by the enzyme β-galactosidase which is produced by E.coli (EHEC), thermophilic lactic acid bacteria, and other coliform bacteria. STAADIUMTM GalactoZide II can help to selectively inhibit the growth of E. coli in complex bacterial cultures and canbe used in microbiome studies, food control, environmental safety, hygiene, and clinical diagnostics. STAADIUMTM GalactoZide II is not compatible with some experimental conditions, e.g. pH indicators such as neutral red, indigo stains, and possibly H2S staining. STAADIUMTM GalactoZide II can be added as an enzyme-specific selective supplement to agar plates and as an enrichment agent to broth culture.</p>

<p>Amphotericin A is a polyene macrolide antibiotic, which is derived primarily from the soil bacterium *Streptomyces nodosus*. This compound functions by binding to ergosterol, an essential component of fungal cell membranes. This binding creates pores in the membrane, increasing its permeability and ultimately leading to cell death. Unlike its more widely used counterpart Amphotericin B, Amphotericin A is less frequently utilized but is critical in the study and understanding of antifungal activity.</p>

<p>Ticarcillin disodium salt is a beta-lactam antibiotic that has in vitro activity against Gram-positive and Gram-negative bacteria. Ticarcillin is active against penicillinase-producing strains of Staphylococcus aureus, Enterobacter aerogenes, Proteus mirabilis, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Serratia marcescens, Streptococcus pyogenes, Streptococcus faecalis, and Streptococcus pneumoniae. Furthermore, it inhibits transpeptidase activity of the cell wall of bacteria which prevents peptidoglycan synthesis. It is bactericidal for many bacteria at low concentrations.</p>

<p>Potassium clavulanate is a beta-lactamase inhibitor and an antibacterial agent. The presence of potassium clavulanate in culture media inhibits the activity of beta-lactamases, which are enzymes that confer resistance to penicillin and other beta-lactam antibiotics. It also has been shown to be active against bacterial infections such as tuberculosis, sepsis, and pneumonia, where it can inhibit the growth of bacteria by interfering with their ability to form cell walls. Potassium clavulanate is also used as an antimicrobial agent for blood culture technique and antimicrobial treatment.</p>

<p>Amicoumacin A is an antibiotic compound, which is derived from the bacterium Bacillus subtilis. This natural source is known for its production of a variety of biologically active compounds that contribute to its utility in numerous scientific contexts. The mode of action of Amicoumacin A involves the inhibition of bacterial protein synthesis by targeting the ribosomal subunit. Specifically, it interferes with the translation process, effectively disrupting the growth and proliferation of susceptible bacterial strains.<br><br>Amicoumacin A is primarily utilized in research settings to study bacterial resistance mechanisms, as well as to explore novel antibacterial therapies. Its application in scientific research extends to examining its potential synergistic effects with other antimicrobial agents, and it serves as a model compound for understanding ribosomal inhibition. The study of Amicoumacin A not only contributes to the broader field of antibiotic development but also offers insights into the molecular interactions that underlie bacterial protein synthesis and antibiotic resistance. This compound's unique properties make it an important subject of investigation for microbiologists and pharmacologists alike, emphasizing its relevance in the ongoing battle against antibiotic-resistant pathogens.</p>

<p>Tobramycin is used to treat severe infections with gram-negative bacteria and it is often applied in combination with beta-lactams. It has similar antimicrobial effects to gentamicin and is effective against all Enterobacteriacae, but more effective than gentamicin against P. aeruginosa, which is why it is often used for gentamicin-resistant strains, especially in the case of cystic fibrosis.</p>

<p>Cefsulodin sodium salt is a beta lactam antibiotic in the third-generation cephalosporin family that inhibits penicillin-binding proteins (PBPs) to disrupt bacterial cell wall synthesis.</p>

<p>ester of Monensin.  Monensin is a polyether antibiotic isolated from Streptomyces cinnamonensis.  It is widely used in ruminant animal feeds.</p>

<p>Please enquire for more information about Cephalexin hydrate, Antibiotic for Culture Media Use Only including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Afabicin is an antibiotic, which is a derivative of the natural product lipiarmycin. It acts by inhibiting the bacterial enzyme DNA-dependent RNA polymerase, crucial for bacterial growth and reproduction. This targeted action disrupts RNA synthesis, effectively halting the proliferation of susceptible bacterial strains.</p>

<p>Fluconazole hydrate is an antifungal medication, which is a synthetic triazole antifungal agent derived from the compound fluconazole. It functions as a powerful inhibitor of the enzyme lanosterol 14α-demethylase, a critical component in the biosynthesis of ergosterol. Ergosterol is an essential component of fungal cell membranes, and its inhibition disrupts membrane synthesis, leading to impaired fungal cell growth and replication.</p>

<p>PF 1022A is a cyclooctadepsipeptide, which is a type of cyclic peptide composed of amino acids and hydroxy acids. It is derived from the fermentation products of the fungus *Mycelia sterilia*, a member of the *Rosellinia* genus. Its mode of action involves disrupting glutamate-gated chloride channels in parasitic nematodes, which leads to paralysis and eventual death of the parasite.</p>

<p>Abacavir sulfate is a pharmaceutical compound classified as a nucleoside reverse transcriptase inhibitor (NRTI), which is derived from synthetic sources. Its mode of action involves the inhibition of the reverse transcriptase enzyme, essential for the replication of HIV. By incorporating itself into the viral DNA chain during replication, Abacavir effectively halts the process, preventing further multiplication of the virus within the host cells.<br><br>This antiretroviral medication is primarily used in the management and treatment of human immunodeficiency virus (HIV-1) infections. Abacavir sulfate is a critical component in highly active antiretroviral therapy (HAART), contributing to the reduction of viral load, enhancing immune function, and improving the long-term clinical outcomes in patients living with HIV. Its application in combination therapies has been instrumental in transforming HIV from a fatal disease into a manageable chronic condition.</p>

<p>Methyl 6-(2,3-dichlorophenyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate is a synthetic organic compound that can be classified as a specialized chemical reagent. It is primarily sourced from chemical synthesis, utilizing a series of controlled reactions involving halogenated aromatic compounds and cyclohexene derivatives.</p>

<p>Perfluorodecanephosphonic acid is a fluorinated organic compound, which is synthesized through the controlled polymerization of fluorinated precursors. It is characterized by its unique perfluorinated alkyl chain and a phosphonic acid group, providing a distinctive combination of hydrophobic and functional properties. Its mode of action involves the strong adsorption onto surfaces through the phosphonic acid moiety, allowing the formation of highly stable self-assembled monolayers (SAMs).</p>