Antimicrobici

<p>Minocycline hydrochloride dihydrate is a broad-spectrum antibiotic, which is a synthetic derivative of tetracycline. It is sourced from chemical synthesis processes and possesses potent antimicrobial properties. The mode of action involves inhibiting bacterial protein synthesis by binding to the 30S ribosomal subunit, thereby preventing the addition of amino acids to the growing peptide chain. This mechanism effectively disrupts bacterial growth and replication.</p>

<p>Censavudine is an antiviral compound, which is a synthetic nucleoside analog designed to interfere with viral replication processes. The source of this compound lies in its chemical synthesis, which involves precise structural modifications to resemble natural nucleosides. Its mode of action involves incorporation into viral RNA by the viral polymerase, leading to chain termination. This mechanism effectively hinders the replication of viral genomes, thus preventing the proliferation of the virus within the host organism.</p>

<p>Clenhexerol is a topical antiseptic, which is a chemically synthesized product with broad-spectrum antimicrobial properties. It is derived from chlorhexidine, commonly used in various medical formulations for its efficacy against both Gram-positive and Gram-negative bacteria. Clenhexerol operates through disrupting microbial cell membranes, leading to leakage of cellular components and cell death, making it highly effective in reducing microbial load on skin and mucous membranes.</p>

Beta-cypermethrin is a synthetic pyrethroid insecticide, which is a chemically altered derivative of natural pyrethrins found in chrysanthemum flowers. These pyrethrins are modified to enhance their stability and potency. Beta-cypermethrin acts by targeting the nervous system of insects, specifically by modifying the function of voltage-gated sodium channels. This action leads to prolonged depolarization of the neuron, resulting in paralysis and eventual death of the insect.

<p>Sporidesmolide is a cyclic depsipeptide, which is a type of compound characterized by having both ester and amide bonds in its structure. This product is derived from fungal sources, specifically certain species within the genus *Sporidesmium*. The mode of action for sporidesmolide involves disrupting microbial cell membrane integrity, leading to increased permeability and eventual cell death. This activity primarily targets bacteria and fungi, making it an important subject of study for its potential antimicrobial properties.</p>

Aqabamycin C is an antibiotic compound, which is derived from marine bacteria, specifically, the actinomycete strain found in marine environments. Its mode of action involves the disruption of bacterial cell wall synthesis, making it particularly effective against certain gram-negative bacteria. This antibiotic selectively inhibits pathogens by interfering with their essential cellular processes.

<p>Clindamycin-2,4-diphosphate is a phosphorylated derivative of the antibiotic clindamycin, which is a semi-synthetic lincosamide antibiotic originally derived from Streptomyces lincolnensis. Its mode of action involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, thereby preventing peptide chain elongation during translation. This mechanism effectively disrupts protein production in susceptible bacteria, leading to their growth inhibition or death.</p>

<p>Pantoprazole magnesium is a pharmaceutical compound that belongs to the class of proton pump inhibitors (PPIs). It is derived from the benzimidazole chemical family and synthesized through a chemical process that involves the formation of a magnesium salt of pantoprazole. This compound's mode of action involves the irreversible inhibition of the H+/K+ ATPase enzyme system located on the gastric parietal cell surface. By blocking this enzyme system, pantoprazole magnesium effectively reduces the secretion of gastric acid.</p>

<p>Phenamacril is a synthetic fungicide, which is derived from chemical synthesis processes with a unique mode of action that targets fungal signaling pathways. It operates by inhibiting the myosin-5 ATPase activities within filamentous fungi, disrupting key cellular functions and effectively halting fungal growth.</p>

<p>Thienamycin is a β-lactam antibiotic, which originates from the fermentation of the bacterium *Streptomyces cattleya*. Its mode of action involves inhibiting the synthesis of bacterial cell walls. Thienamycin accomplishes this by binding to penicillin-binding proteins (PBPs) critical for peptidoglycan construction, thereby disrupting cell wall integrity and leading to bacterial lysis.</p>

<p>11-Deoxyfusidic acid is a steroidal antibiotic, which is derived from the fermentation broth of certain strains of fungi, specifically within the Fusidium genus. Its mode of action involves inhibiting bacterial protein synthesis by interacting with elongation factor G (EF-G) on the ribosome, thus disrupting essential processes and impeding bacterial growth.</p>

<p>Cyclosporin L is an immunosuppressive agent, which is a cyclic polypeptide derived from the soil fungus Tolypocladium inflatum. It primarily functions by inhibiting the activity of calcineurin, a key phosphatase involved in the activation of T-cells. This inhibition prevents the transcription of interleukin-2 and other cytokines critical for T-cell proliferation.</p>

4'-Ethynyl-2'-deoxyadenosine is a deoxynucleoside analogue, which is synthesized through chemical processes. This compound acts as an antiviral agent, primarily targeting the viral replication machinery. Its mode of action involves the incorporation into viral DNA by mimicking natural nucleosides, which subsequently inhibits the enzymatic activity of reverse transcriptase. This inhibition disrupts the synthesis of viral DNA, effectively curtailing viral replication.

<p>SARS-CoV-IN-2 is a highly specific and potent antiviral inhibitor, which is chemically synthesized to target SARS-CoV-2, the virus responsible for COVID-19. This compound functions by interfering with the viral replication process, specifically targeting the viral 3CL protease enzyme, crucial for viral polyprotein cleavage. By inhibiting this protease, SARS-CoV-IN-2 effectively hampers the replication cycle of the virus, limiting its ability to proliferate within the host cells.</p>

<p>A macrolide, broad-spectrum antibiotic that targets cytochrome P4503A4 (CYP3A4). Clarithromycin has been used to potentiate the pharmacological effects of some drugs that are metabolised by the cytochrome P450.</p>

<p>Tylosin D is an antibiotic product, which is derived from the bacterium *Streptomyces fradiae*. Its mode of action involves binding to the 50S subunit of the bacterial ribosome, thereby inhibiting protein synthesis essential for bacterial growth and replication. This mechanism is particularly effective against Gram-positive bacteria and mycoplasma species, making it a crucial agent in combatting infections in the veterinary field.</p>

4''-(p-Fluorobenzyl)tylosin A is a semi-synthetic derivative of tylosin, which is a macrolide antibiotic produced by fermentation of the bacterium *Streptomyces fradiae*. This compound demonstrates a modified structure by incorporating a p-Fluorobenzyl group at the 4'' position of tylosin, enhancing its pharmaceutical properties. The mode of action involves binding to the 50S subunit of the bacterial ribosome, thereby inhibiting protein synthesis and exerting its bacteriostatic effects against Gram-positive bacteria.

<p>Methicillin sodium hydrate is a semi-synthetic β-lactam antibiotic, which is a derivative of the naturally occurring antibiotic penicillin. It is sourced from the modification of the penicillin nucleus, specifically designed to resist degradation by the bacterial enzyme penicillinase. This enzyme, produced by certain bacterial strains, can render penicillin ineffective. Methicillin operates by inhibiting the synthesis of bacterial cell walls, specifically binding to penicillin-binding proteins (PBPs). This action disrupts the cross-linking of peptidoglycan chains, a critical component for bacterial cell wall integrity, ultimately leading to cell lysis and death.</p>

<p>(4S)-2-[Carboxy[[[3-(2-chloro-6-fluorophenyl)-5-methylisoxazol-4-yl]carbonyl]amino]methyl]-5,5-dimethylthiazolidine-4-carboxylic acid disodium salt, known as the penicilloic acids of flucloxacillin disodium salt, is a β-lactam antibiotic. This compound is derived from the penicillin family and exhibits potent antibacterial properties. The mode of action involves the inhibition of bacterial cell wall synthesis, primarily targeting the transpeptidase enzyme, which plays a crucial role in cross-linking the peptidoglycan layers of the bacterial cell wall. By acylating this enzyme, the penicilloic acids disrupt the integrity of the cell wall, leading to cell lysis and death of the bacteria.</p>

Atherosperminine is an alkaloid compound, which is a bioactive chemical derived from plants. Specifically, it is sourced from members of the Lauraceae family, such as Atherosperma moschatum. This compound exhibits a range of pharmacological activities that are of significant interest to researchers. The mode of action of atherosperminine involves interactions with various biological pathways, potentially affecting physiological processes and exhibiting therapeutic effects.

<p>Bensulide-oxon is a metabolite derived from the organophosphate pesticide bensulide, which is predominantly used in agricultural settings. It forms as a result of environmental or biological processes that involve the oxidation of bensulide. As a potent acetylcholinesterase (AChE) inhibitor, bensulide-oxon disrupts normal neuronal signaling by preventing the breakdown of the neurotransmitter acetylcholine, leading to an accumulation that affects the nervous systems of target organisms.</p>

<p>LTAS-IN-1 is a synthetic chemical compound designed as an advanced inhibitor, which is developed through a series of intricate chemical synthesis processes. The mode of action of LTAS-IN-1 involves the selective inhibition of specific enzyme targets, effectively modulating their biological pathways. This selective inhibition allows researchers to investigate the compound's effects on various cellular and molecular processes.</p>

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

<p>Acephate d3 is an isotopically labeled organophosphorus insecticide, which is a synthetic chemical compound used primarily for its insecticidal properties. It is derived by incorporating deuterium, a stable hydrogen isotope, into the molecular structure of acephate. The inclusion of deuterium isotopes is instrumental in tracing and studying the biochemical pathways and metabolic degradation of acephate within target organisms and ecosystems.</p>

<p>Tebufloquin is an insecticide, which is a synthetic compound designed to target specific pests. It is derived from chemical synthesis with a mode of action that interferes with critical biological pathways in insects, rendering them unable to survive or reproduce. Tebufloquin works primarily by targeting the nervous system of insects, leading to paralysis and eventual death.</p>

(4E)-1-(3,4-Dichlorophenyl)-4-[(4-ethoxyphenyl)methylidene]pyrazolidine-3,5-dione is a synthetic compound belonging to the class of pyrazolidine diones. This compound is mainly derived from chemical synthesis in a laboratory setting. It acts through its interaction with specific biological pathways, potentially affecting enzyme activity or receptor sites involved in various physiological processes.

<p>Biotinamidocaproate tobramycin amide is a chemical conjugate, serving as an innovative antimicrobial agent derived from the integration of biotin with tobramycin, an aminoglycoside antibiotic. This product embodies the amalgamation of tobramycin’s robust antibacterial properties with biotin’s ability to guide compounds specifically to targets through biotin-avidin interactions.</p>

Deacetylanisomycin is a bacterial metabolite, which is derived from the soil bacterium Streptomyces griseolus. It acts as an inhibitor of protein synthesis by binding to the 60S ribosomal subunit, thus interfering with peptide bond formation during translation. This mode of action is key to its effectiveness in studying the mechanisms of protein synthesis interruption.

<p>Neuraminidase-in-1 is a chemical compound known as a neuraminidase inhibitor, which is synthetically derived. This inhibitor functions by blocking the activity of the neuraminidase enzyme, a glycoprotein found on the surface of various viruses, including influenza. The enzyme is crucial for the viral life cycle as it facilitates the release of new viral particles from infected host cells. By inhibiting this enzyme, Neuraminidase-in-1 effectively halts the replication and spread of the virus within the host organism.</p>

<p>2-(1-Hydroxyethyl)-6-ethylaniline is an organic chemical compound, which is often utilized as an intermediate in the synthesis of dyes, pigments, and other industrial chemicals. This compound is derived from aromatic amines and undergoes specific chemical reactions that enable its functionality in various synthetic processes.</p>

<p>Alamethacin is a peptide antibiotic, which is derived from the soil fungus Trichoderma viride. This compound consists of a sequence of amino acids that form a helical structure, enabling its interaction with lipid membranes. Alamethacin functions by inserting itself into cellular membranes and forming voltage-dependent ion channels. As a result, it alters membrane permeability, causing ion imbalance and leading to cell death.</p>

<p>Gatifloxacin related compound E is a chemical reference standard, which is often used in pharmaceutical and analytical chemistry research for the identification and quantification of impurities. It is generally synthesized or isolated as part of the quality control and validation process for the production of the antibiotic Gatifloxacin. The mode of action of this compound revolves around its structural similarity to Gatifloxacin, which allows it to serve as a benchmark to ensure the accuracy and reliability of high-performance liquid chromatography (HPLC) and other analytical techniques.</p>

<p>Mesosulfuron is a selective herbicide, which is a synthetic chemical compound with a specific mode of action designed to inhibit acetolactate synthase (ALS). This enzyme inhibition disrupts the biosynthesis of essential amino acids such as valine, leucine, and isoleucine, leading to the cessation of cell division and consequent plant growth arrest. The herbicide is primarily utilized in agricultural settings, particularly for post-emergence control of various grass weeds within cereal crops, including wheat and barley. Its application is crucial for managing weed competition that can significantly impact crop yield and quality. Mesosulfuron is absorbed through the foliage and roots of targeted species, providing systemic action that ensures effective control. Its usage is governed by stringent regulations to minimize environmental impact and to manage herbicide resistance through integrated weed management strategies.</p>

<p>Cefepime-d3 sulfate is an isotopically labeled antibiotic, which is derived from the fourth-generation cephalosporin, cefepime. The source of this compound is synthetic, utilizing deuterium to label the parent cefepime molecule, allowing for detailed metabolic and pharmacokinetic studies. With deuterium's stable, non-radioactive nature, it serves as a powerful tool in mass spectrometry-based analyses.</p>

Lincomycin 2-palmitate hydrochloride is a semi-synthetic antibiotic, derived from the natural antibiotic lincomycin through chemical modification. It is sourced from fermentative processes involving the bacterium *Streptomyces lincolnensis*. The compound exerts its action by inhibiting protein synthesis in susceptible bacteria. This occurs through its binding to the 50S subunit of the bacterial ribosome, thereby hindering peptide chain elongation and ultimately arresting bacterial growth.

<p>Oxacillin sodium is a beta-lactam antibiotic with action on bacterial cell wall synthesis and is used for treating infections caused by penicillin-resistant Staphylococcus aureus.</p>

<p>N-Demethylclindamycin is a metabolite of clindamycin, which is a semi-synthetic antibiotic derived from the naturally occurring compound lincomycin. This product is synthesized by enzymatic or chemical processes that remove the N-methyl group from clindamycin's molecular structure, making it an important derivative in the study of antibiotic activity and metabolic pathways.</p>

Hexazinone metabolite A is a chemical compound derived from the degradation of the parent herbicide hexazinone, which is commonly used in agriculture and forestry for broad-spectrum weed control. This metabolite is a result of microbial and environmental processes that modify the original chemical structure, altering its behavior and ecological interactions. With a mode of action involving the disruption of photosynthetic processes, Hexazinone metabolite A impacts plant growth by inhibiting photosystem II, thereby impeding electron transfer required for photosynthesis.

<p>Hypothemycin is a natural product that serves as a potent inhibitor of protein kinases. It is derived from the fungus Hypomyces subiculosus and belongs to the class of resorcylic acid lactones. Its mode of action involves binding covalently to the ATP-binding site of kinases, leading to the inhibition of their activity. This covalent modification is achieved through the formation of a Michael-type addition with a reactive ene-diene functionality within its structure. By targeting these critical enzymes, hypothemycin disrupts key signaling pathways that are essential for cell growth and proliferation.</p>

<p>Capsimycin is an antibiotic product, which is derived from the bacterium Streptomyces. This compound is part of a class of natural products isolated from soil-dwelling actinomycetes, known for their ability to produce a wide array of bioactive molecules. The mode of action of Capsimycin involves the inhibition of cell wall biosynthesis in susceptible bacterial strains. This specific mechanism disrupts the integrity of the bacterial cell wall, ultimately leading to cell lysis and death, making Capsimycin effective against a variety of Gram-positive bacteria.</p>

<p>Cladosporin is a secondary metabolite and natural product, specifically a fungal cyclodepsipeptide, which is isolated from the fungus *Cladosporium cladosporioides*. It exhibits its mode of action by selectively inhibiting the lysyl-tRNA synthetase enzyme in the Plasmodium species, the causative agent of malaria. This inhibition disrupts the protein synthesis pathway crucial for the survival and proliferation of the parasite.</p>

Voxilaprevir is an antiviral compound, which is a product of chemical synthesis with a unique mode of action targeting the Hepatitis C virus (HCV). It acts as a potent inhibitor of the HCV NS3/4A protease, a crucial enzyme required for the viral replication process. By inhibiting this protease, Voxilaprevir disrupts the viral life cycle, preventing replication and aiding in the clearance of the virus from the host.

<p>Tert-Butyl 4-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazol-1-yl]piperidine-1-carboxylate is a boronic ester compound used primarily in organic synthesis. It is derived from the reaction of a piperidine-based carboxylate with a dioxaborolane moiety, forming a unique structural entity that serves as a versatile building block in molecular modification and drug development.</p>

<p>Flutimide is a nonsteroidal antiandrogen, which is synthesized chemically. It functions by competitively inhibiting the binding of androgens, such as testosterone, to androgen receptors. This interferes with the action of androgens at the cellular level, leading to a reduction in the growth effects mediated by these hormones.</p>

Please enquire for more information about PSI-352938 including the price, delivery time and more detailed product information at the technical inquiry form on this page

Acorafloxacin is a synthetic fluoroquinolone antibiotic, which is derived from the chemical modification of the quinolone core structure. It acts by inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes crucial for bacterial DNA replication and transcription. The bactericidal action results from preventing the supercoiling and relaxation of the bacterial DNA, ultimately interrupting essential cellular processes.

<p>3-Descyano fludioxonil 3-carboxylic acid is a synthetic compound, which is derived from chemical modification of fludioxonil, a well-known fungicide. The compound acts by disrupting fungal cell osmoregulation through inhibition of the protein kinase pathway. This disruption inhibits spore germination and mycelial growth, contributing to its antifungal properties.</p>

<p>2-Sec-butyl-1-(decyloxy)-4-tritylbenzene is a synthetic organic compound, typically utilized in chemical research and development. It is sourced through a series of organic synthesis reactions, involving alkylation, etherification, and aromatic substitution, primarily in a controlled laboratory environment.</p>

(E)-Cefotaxime is a third-generation cephalosporin antibiotic, which is derived from the actinomycete mold Acremonium. Its mode of action involves inhibiting bacterial cell wall synthesis by binding to penicillin-binding proteins, leading to cell lysis and death. This mechanism is highly effective against a wide range of Gram-positive and Gram-negative bacteria, including strains resistant to earlier cephalosporins and penicillins.

Cefadroxil is a broad-spectrum bactericidal antibiotic that belongs to the cephalosporin family. It is a semi-synthetic penicillin and inhibits bacterial cell wall synthesis through binding to one or more of the penicillin-binding proteins (PBPs). Cefadroxil monohydrate is used as an antibiotic for culture media and has been proven to be effective against methicillin-resistant Staphylococcus aureus (MRSA). In addition, the drug has been shown to have no significant effect on blood tests or microscopic studies.