Antimicrobici

Cefotiam is a broad-spectrum cephalosporin antibiotic, which is a beta-lactam compound derived from the mold Acremonium. It functions by inhibiting bacterial cell wall synthesis, particularly by targeting penicillin-binding proteins, which leads to cell lysis and death in susceptible bacteria. This mechanism of action makes it effective against various Gram-positive and Gram-negative bacteria.

6-[(1,1-Dimethylethyl)amino]-1,3,5-triazine-2,4(1H,3H)-dione, commonly known as Terbuthylazine, is a selective systemic herbicide, which is synthesized chemically and primarily sourced from the triazine group of compounds. It operates by inhibiting photosynthesis, specifically interfering with the electron transport in photosystem II. This disruption in the photosynthetic pathway effectively halts the growth of susceptible weed species.

3-(2,4,6-Trimethylphenylsulfonyl)-1,2,4-triazole is a sulfonyl-triazole reagent, which is widely utilized in the field of organic chemistry. This compound is synthetically derived, serving as an important tool in the construction of sulfonyl-protected intermediates and heterocyclic structures. Its mode of action involves acting as a versatile electrophile in conditions favoring nucleophilic attack, facilitating the formation of carbon-nitrogen and carbon-sulfur bonds.

Dioxohongdenafil is a synthetic compound, which is a type of pharmaceutical analog. It is derived from sildenafil, a well-known phosphodiesterase type 5 (PDE5) inhibitor, originally conceptualized through chemical modification of the parent compound. The mode of action of Dioxohongdenafil involves competitive inhibition of the PDE5 enzyme, leading to an increase in cyclic guanosine monophosphate (cGMP) levels. This biochemical alteration results in vasodilation and increased blood flow, mimicking the therapeutic mechanism observed in sildenafil.

Oxfendazole is a benzimidazole anthelmintic with action on microtubule formation in parasitic worms and is used for treating gastrointestinal parasites in livestock.

Thiadiazin is a synthetic compound, belonging to the class of heterocyclic chemical substances, which is primarily derived from chemical synthesis processes involving sulfur, nitrogen, and carbon atoms. It is characterized by a five-membered ring structure containing both sulfur and nitrogen atoms, which contributes to its diverse chemical properties.

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.

Please enquire for more information about Sibofimloc including the price, delivery time and more detailed product information at the technical inquiry form on this page

Please enquire for more information about Rilopirox including the price, delivery time and more detailed product information at the technical inquiry form on this page

Ascomycin is an immunosuppressive macrolide, which is a product derived from the fermentation of the bacterium *Streptomyces hygroscopicus*. Its mode of action involves binding to the intracellular protein FK506-binding protein (FKBP), inhibiting the calcium-dependent signal transduction pathway that is crucial for T-cell activation. This interference with the immune response is achieved through the inhibition of calcineurin, thus preventing the dephosphorylation and nuclear translocation of nuclear factor of activated T-cells (NF-AT), a necessary step in the activation of genes required for T-cell proliferation.

Cefdinir monohydrate is a third-generation cephalosporin antibiotic, which is synthetically derived from cephalosporin C, a compound originally isolated from the fungus Acremonium. This antibiotic works by inhibiting bacterial cell wall synthesis through binding to penicillin-binding proteins (PBPs), which results in the interruption of peptidoglycan cross-linking. Consequently, this action leads to cell lysis and death of the bacterium.

Rifamycin PR-14 is a semi-synthetic antibiotic, which is derived from the naturally occurring antibiotic rifamycin. Originating from a fermentation process involving the bacterium Amycolatopsis mediterranei, rifamycin is modified to create the PR-14 variant to enhance its antibacterial properties and pharmacokinetic profile. This compound functions by inhibiting bacterial DNA-dependent RNA polymerase, effectively halting RNA synthesis and subsequent protein production, leading to bacterial cell death.