Antimicrobiens

<p>Carumonam is a synthetic monobactam antibiotic, which is derived from chemically modifying aztreonam to enhance its antimicrobial properties. Its source is entirely synthetic, allowing for precise structural modifications to target specific bacterial pathogens. The mode of action involves the inhibition of bacterial cell wall synthesis. Carumonam binds to penicillin-binding proteins (PBPs) on the surface of bacterial cell walls, disrupting the peptidoglycan cross-linking process necessary for cell wall strength and integrity. This action results in bacterial cell lysis and death, making it effective against a range of Gram-negative bacteria.</p>

<p>Gramicidin S hydrochloride is a cyclic peptide antibiotic, which is a derivative of the naturally occurring antibiotic gramicidin S. It is sourced from Bacillus brevis, a type of soil bacterium. This peptide operates through a unique mode of action, whereby it disrupts bacterial cell membranes. By integrating into the lipid bilayer, it increases membrane permeability, leading to leakage of essential ions and molecules, and ultimately causing cell death.</p>

<p>Desoxymycin is an antibiotic product that belongs to the class of aminoglycosides, which is derived from natural sources such as certain species of Streptomyces bacteria. This compound exhibits its mode of action by specifically binding to the bacterial ribosomal RNA, interfering with protein synthesis. As a result, it inhibits the replication and growth of susceptible bacterial strains.</p>

<p>Quinofumelin is a fungicide, which is synthetically derived with a novel mode of action targeting specific biochemical pathways in fungi. Its unique mechanism disrupts crucial cellular processes within pathogenic fungi, thereby halting their growth and spread. This fungicide has been meticulously developed through advanced chemical synthesis to ensure high efficacy and specificity against a broad spectrum of fungal pathogens affecting various crops.</p>

<p>(S)-HPMPA is a nucleotide analogue, which is a chemically synthesized compound designed to mimic nucleotides. It acts as both an antiviral and an antitumor agent, sourced primarily through synthetic chemistry involving the modification of naturally occurring nucleotide structures. The mode of action of (S)-HPMPA involves mimicking natural substrates of various viral polymerases and cellular enzymes, thereby inhibiting viral DNA synthesis and disrupting the replication cycle of DNA viruses. Additionally, it can interfere with certain cellular pathways contributing to its antitumor effects.</p>

<p>Sebuthylazine-2-hydroxy is a selective pre-emergent herbicide, which is a derivative of the sym-triazine compound family synthesized through chemical processes. It functions primarily as a soil-acting agent that inhibits photosynthesis by binding to the D1 protein in the photosystem II complex, thereby disrupting the electron transport chain. This biochemical action effectively curtails the growth of susceptible weed species by preventing their development, particularly annual grasses and broadleaf weeds.</p>

<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>Amicoumacin C is a biological product derived from certain strains of the Bacillus species, specifically fermented by Bacillus subtilis. It is recognized as a potent antibiotic compound, noted for its ability to inhibit bacterial protein synthesis, primarily by interacting with the 30S ribosomal subunit, thereby hindering the translation process.</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>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>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>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>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>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>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>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>

<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>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>