Antimicrobianos

<p>Fibracillin is a bioengineered peptide, which is derived from specifically modified bacterial strains with advanced genetic manipulation techniques. Its mode of action involves the stimulation of fibroblast activity through targeted binding to cellular receptors, promoting collagen synthesis and extracellular matrix formation. This action facilitates the regeneration of connective tissues and supports wound healing 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>Malformin C is a cyclic pentapeptide, which is a secondary metabolite derived from certain strains of the fungus Aspergillus. Its mode of action involves disrupting cellular processes by interfering with cell division. Specifically, it is thought to affect mitotic spindle formation, leading to abnormal cell cycle progression.</p>

<p>Rolitetracycline is a semi-synthetic tetracycline antibiotic, which is derived from the natural compound tetracycline. It functions primarily by inhibiting protein synthesis in susceptible bacteria. This is achieved through the binding to the 30S ribosomal subunit, effectively blocking the attachment of aminoacyl-tRNA to the mRNA-ribosome complex, thereby preventing the addition of new amino acids to the nascent peptide chain. As a result, bacterial cell growth is inhibited, leading to bacteriostatic effects.</p>

<p>Tunicamycin V is an antibiotic and nucleoside analog, which is a secondary metabolite derived from various Streptomyces species. It functions predominantly by inhibiting the initial step of N-linked glycosylation, a critical post-translational modification process in eukaryotic cells. This inhibition occurs through the blockage of UDP-N-acetylglucosamine: dolichyl-phosphate N-acetylglucosamine-1-phosphate transferase, thereby preventing the synthesis of dolichol-linked oligosaccharides and ultimately affecting protein folding and quality control mechanisms within the endoplasmic reticulum.</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>

<p>AT-527 is an investigational antiviral compound, which is a nucleoside analog prodrug with a specific mode of action inhibiting viral RNA polymerase. This product is derived from synthetic organic chemistry processes, uniquely designed to interfere with the replication machinery of certain RNA viruses. Upon administration, AT-527 undergoes intracellular conversion to its active triphosphate form, which then incorporates into the viral RNA. This incorporation results in premature chain termination or erroneous RNA synthesis, effectively disrupting the viral replication cycle.</p>

<p>2'-Deoxycoformycin is a potent adenosine deaminase inhibitor, which is derived from the fermentation of Streptomyces antibioticus, a species of actinomycete bacteria. This compound acts by specifically inhibiting the enzyme adenosine deaminase, leading to an accumulation of toxic deoxyadenosine triphosphate in lymphocytes. This buildup hinders DNA synthesis, effectively suppressing the proliferation of lymphoid cells.</p>

<p>Spiromesifen-alcohol-4-hydroxymethyl is a selective miticide, which is a derivative of spiromesifen. This compound is sourced from novel chemical synthesis approaches focusing on the manipulation of chemical structures to improve efficacy and selectivity. The mode of action of Spiromesifen-alcohol-4-hydroxymethyl centers on disrupting the lipid biosynthesis pathway within target mites and whiteflies. By inhibiting acetyl-CoA carboxylase, it leads to impaired energy storage and membrane biosynthesis, ultimately causing the mortality of these pests.</p>

<p>(Z)-Fenpyroximate is a selective acaricide, which is a chemical agent specifically designed to control mite populations. It is derived from the chemical class of pyrazole compounds. The mode of action of (Z)-Fenpyroximate involves the inhibition of the mitochondrial electron transport chain, particularly targeting complex I (NADH: ubiquinone oxidoreductase). This disruption prevents ATP production, leading to mite mortality due to energy starvation.</p>

2-(((5-Methyl-2-thienyl)methylene)amino)-N-phenylbenzamide is a synthetic compound that functions as an enzyme inhibitor, specifically targeting proteins involved in various signaling pathways. This compound is sourced through synthetic organic chemistry whereby it is meticulously crafted to interact with biological molecules at a molecular level. Its mode of action involves binding to the active or allosteric sites of specific enzymes, which can modulate the enzyme's activity. This interaction can lead to the downregulation or inhibition of specific biochemical pathways, making it an invaluable tool in the study of cellular processes.

<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>N-(4-(4-Methylpiperidin-1-yl)-3-(trifluoromethyl)phenyl)-4-(morpholinomethyl)benzamide is a sophisticated chemical compound, classified as a synthetic small molecule. It is synthesized through a series of organic reactions, showcasing the intricate art of modern chemical synthesis and design.</p>

<p>Inhibitor of N-glycosylation in eukaryotes</p>

Metalaxyl-hydroxymethyl is a systemic fungicide, which is synthesized chemically. With its unique mechanism of action as an acylalanine fungicide, it targets and disrupts RNA synthesis specifically in oomycetes—a group of fungus-like organisms. This disruption inhibits the growth and spread of pathogenic fungi.

<p>Avermectin A1b is an antiparasitic compound, which is a macrocyclic lactone isolated from the soil bacterium *Streptomyces avermitilis*. This compound functions primarily by enhancing the release of gamma-aminobutyric acid (GABA) and binding to glutamate-gated chloride channels in nerve and muscle cells of parasites. This interaction leads to an increase in the permeability of cell membranes to chloride ions, resulting in paralysis and death of the parasite.</p>

<p>Tenatoprazole sodium is a proton pump inhibitor, which is a synthetic pharmaceutical compound designed to selectively inhibit the hydrogen-potassium ATPase enzyme in the gastric parietal cells. This enzyme is essential for the final step of gastric acid production. Originating from organic chemical synthesis processes, Tenatoprazole sodium features a unique imidazopyridine structure, distinguishing it from other members of the proton pump inhibitor class such as omeprazole, which belongs to the benzimidazole family.</p>

<p>Inhibitor of DNA replication; aminoglycoside class</p>

Fradimycin B is an aminoglycoside antibiotic, which is derived from the bacterium Streptomyces. It exhibits its mode of action by binding to the bacterial 30S ribosomal subunit, thereby inhibiting protein synthesis. This results in a bactericidal effect, effectively disrupting the growth and proliferation of susceptible bacterial strains.

(E)-Parthenolide is a sesquiterpene lactone, which is a naturally occurring organic compound often extracted from plants such as feverfew (Tanacetum parthenium). This compound exerts its effects primarily through the modulation of NF-kB signaling pathways, which play crucial roles in the regulation of immune responses, cell proliferation, and survival. By inhibiting NF-kB, (E)-Parthenolide can interfere with the expression of genes that promote cell growth and inflammation. This action makes it a compound of interest in cancer research, particularly as a potential therapeutic agent that targets cancer stem cells and reduces chemoresistance. Its applications extend to studying its efficacy in inhibiting tumor growth and inducing apoptosis in various cancer cell lines. Moreover, due to its natural source, (E)-Parthenolide is also being explored for its potential as an anti-inflammatory agent in the treatment of inflammatory conditions.

<p>Oligomycin A is a macrolide antibiotic, which is isolated from the Streptomyces species of bacteria. Its mode of action involves inhibiting ATP synthase by binding to the F_O subunit of the enzyme complex in the mitochondrial membrane. This binding effectively stops the flow of protons across the membrane, which is critical for ATP generation through oxidative phosphorylation.</p>

<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>

<p>Vancomycin aglycon is a glycopeptide antibiotic, which is a derivative of vancomycin. It is sourced from the fermentation products of certain Amycolatopsis species, a genus of actinobacteria. The mode of action of vancomycin aglycon involves the inhibition of bacterial cell wall synthesis. It specifically binds to the D-Ala-D-Ala terminus of nascent peptidoglycan chains, thereby preventing the cross-linking that is crucial for maintaining cell wall integrity.</p>

<p>Tigecycline mesylate is a novel glycylcycline antibiotic, which is a derivative of the tetracycline class of antibiotics. It is a semi-synthetic product derived from minocycline, exhibiting a broad spectrum of antibacterial activity. Tigecycline mesylate functions through the inhibition of bacterial protein synthesis. It achieves this by binding to the 30S ribosomal subunit, thereby preventing the incorporation of amino acid residues into elongating peptide chains, a crucial step in protein production.</p>

<p>MGB-BP-3 is a synthetic antimicrobial agent, which is derived from natural DNA-binding minor groove binder (MGB) compounds. Its structure is based on distamycin, known for targeting the minor groove of DNA. MGB-BP-3 operates by binding to specific sequences within the DNA minor groove, thereby interfering with the replication and transcription processes of bacterial cells. This binding disrupts the DNA function and inhibits the growth and proliferation of bacterial pathogens.</p>

<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</p>

<p>Secorapamycin B is a secondary metabolite, which is a macrolide lactam produced by the actinobacterium species Amycolatopsis. This compound is characterized by its unique structural features, including a polyketide backbone, which is biosynthesized via modular polyketide synthases. The mode of action for Secorapamycin B involves binding to FK-binding proteins (FKBP), inhibiting calcineurin function, and subsequently suppressing T-cell activation.</p>

<p>4-(4,5-Dihydroxy-3-methoxy-6-methyloxan-2-yl)oxy-2,5,7-trihydroxy-3-methoxy-2-methyl-3,4-dihydrotetracene-1,6,11-trione is an anthraquinone derivative, which is a specialized organic compound. This compound is typically derived from complex synthetic processes involving multi-step organic reactions starting from anthraquinone precursors. Its mode of action primarily involves the disruption of microbial cell walls and the inhibition of essential enzymatic pathways that are critical for microbial replication and survival.</p>

<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>

<p>6-Chloro didesacetyl famciclovir is a synthetic antiviral compound, which is derived from famciclovir, with specific modifications to enhance its biochemical properties. It is a chlorinated analog resulting from structural alterations to famciclovir, a prodrug of the antiviral agent penciclovir.</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>

<p>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.</p>

<p>Moxifloxacin is a synthetic broad-spectrum antibiotic, which is derived from the fluoroquinolones class. It functions by inhibiting bacterial topoisomerase II (DNA gyrase) and topoisomerase IV, enzymes critical for DNA replication, transcription, repair, and recombination. The inhibition of these enzymes results in DNA breakage, thereby leading to bacterial cell death.</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>

28-Epirapamycin is a semisynthetic derivative of the macrolide antibiotic rapamycin, which is derived from the bacterium *Streptomyces hygroscopicus*. This compound functions primarily as an mTOR (mechanistic target of rapamycin) inhibitor. The mTOR pathway is crucial for regulating cell growth, proliferation, and survival by integrating signals from nutrients, growth factors, and cellular energy status.

<p>Clindamycin sulfoxide is a potent metabolite of the lincosamide antibiotic clindamycin, which is derived from the fermentation product of *Streptomyces lincolnensis*. This compound acts by inhibiting bacterial protein synthesis through binding to the 50S ribosomal subunit, thereby interfering with the translocation steps in protein elongation. The mechanism effectively suppresses the growth of a broad range of Gram-positive bacteria, including *Staphylococcus aureus*, *Streptococcus pneumoniae*, and anaerobic microorganisms.</p>

<p>Thiamethoxam-urea is an advanced agrochemical formulation, which is a synthetic compound derived from the integration of the neonicotinoid insecticide thiamethoxam and the stabilizing agent urea. This product is engineered from laboratory synthesis, where chemical reactions enable the effective combination of these components to ensure optimal stability and efficacy. The mode of action of Thiamethoxam-urea involves neurotoxic interference within the central nervous system of target organisms, primarily acting as an agonist at nicotinic acetylcholine receptors in insects. This disrupts neural transmission, leading to paralysis and eventual death of the pest.</p>

<p>Gramicidin is an antibiotic, which is derived from soil bacteria of the genus Bacillus, specifically Bacillus brevis. This polypeptide antibiotic exerts its antibacterial effects by disrupting the cell membranes of susceptible bacteria. Gramicidin forms channels in the phospholipid bilayers of bacterial cell membranes, leading to uncontrolled cation fluxes, which ultimately results in cell death. This mechanism is particularly effective against Gram-positive bacteria due to their specific cell wall structure.</p>

<p>Validamycin D is an antifungal antibiotic produced by the fermentation of certain Streptomyces species. This compound acts by inhibiting the synthesis of trehalose, a crucial component in the cell structure and stress response of fungi. By disrupting trehalose production, Validamycin D effectively impairs the growth and viability of fungal cells, making it a potent agent in the management of fungal pathogens.</p>

Bonducellpin D is an experimental bioactive compound derived from the seeds of Caesalpinia bonduc, a tropical plant species known for its rich phytochemical composition. This product is of natural botanical origin, harnessed through advanced extraction and purification techniques to ensure its high purity and activity.

<p>Riamilovir is an antiviral agent, which is synthesized chemically, designed to combat the replication of specific viruses. It acts as a nucleoside analogue, interfering with viral nucleic acid synthesis. By incorporating itself into the viral RNA, it effectively hampers the ability of the virus to replicate its genetic material, thereby inhibiting its proliferation within the host.</p>

<p>Tebuthiuron-N-hydroxymethyl is a derivative herbicide, primarily sourced from synthetic chemical processes. It functions as a broad-spectrum soil-active herbicide with systemic properties. Its mode of action involves the inhibition of photosynthesis by disrupting electron transport in the chloroplasts, thereby stunting plant growth and effectively controlling a wide range of vegetation.</p>

<p>Amidosulfuron-o-desmethyl is a metabolite derivative, which is studied primarily as a secondary product originating from the breakdown of the herbicide amidosulfuron. Synthesized through microbial and environmental degradation processes, it is part of the sulfonylurea class of compounds. The mode of action involves inhibition of the plant enzyme acetolactate synthase (ALS), leading to disrupted synthesis of essential branched-chain amino acids, ultimately affecting plant growth and survival.</p>

<p>Plant growth regulator</p>

<p>Tropodithietic acid is a bioactive compound, which is a potent antibacterial agent derived from certain marine bacteria, including the genus Phaeobacter. This antibiotic is characterized by its ability to disrupt quorum sensing, a mechanism that bacteria use for communication and coordination of group behaviors, including virulence. By interfering with this process, tropodithietic acid impedes bacterial colonization and biofilm formation, effectively inhibiting pathogenic activity.</p>

<p>Tri-O-benzyl FR 900098 is a chemical compound, often referenced in biochemical research contexts. It is a synthetic derivative that originates from complex chemical synthesis, involving multiple benzylation steps to modify the original molecular framework. This structural transformation lends the compound unique chemical properties.</p>

<p>N4-Methyl-5-(3,4,5-trimethoxybenzyl)-pyrimidine-2,4-diamine is a synthetic organic compound, classified as an antimicrobial agent. This compound is developed through chemical synthesis processes, derived from pyrimidine analogs, and is commonly used in medicinal chemistry and pharmacology research. It operates by inhibiting key enzymes involved in the folic acid pathway, crucial for bacterial growth and proliferation. By targeting this pathway, the compound prevents nucleic acid synthesis, ultimately leading to bacterial cell death.</p>

<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>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>Pyrenophorin is a polyketide metabolite, which is derived from certain fungi, specifically from the genus Pyrenophora. This compound demonstrates its biological efficacy through its unique mode of action as an antimicrobial agent, interfering with cellular processes in target microorganisms, leading to their inhibition or death.</p>

<p>Levomekol is a topical antibiotic ointment, which is a synthesized pharmaceutical product with antibacterial and anti-inflammatory properties. It contains chloramphenicol, a broad-spectrum antibiotic, and methyluracil, which promotes tissue repair and regeneration. The mode of action involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit of susceptible microorganisms, effectively curbing bacterial growth and proliferation. Concurrently, methyluracil stimulates leukocyte activity and enhances the healing process by promoting cellular regeneration and collagen production.</p>

<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>

<p>Neticonazole hydrochloride is an antifungal agent, which is a synthetic imidazole derivative with potent antifungal properties. It is synthesized through a multi-step chemical process in a laboratory setting, designed to enhance its efficacy and stability. Its mode of action involves the inhibition of ergosterol synthesis, a critical component of fungal cell membranes. By hindering this pathway, Neticonazole hydrochloride compromises the integrity and function of the fungal cell membrane, ultimately leading to cell death.</p>

<p>Penciclovir diacetate is an antiviral compound, which is synthesized as a prodrug derivative of penciclovir. This compound originates from chemical modification processes designed to improve the pharmacokinetic properties of its active metabolite. Once administered, penciclovir diacetate undergoes in vivo conversion to penciclovir, an active nucleoside analog. The mode of action involves selective inhibition of viral DNA polymerase after being phosphorylated to its triphosphate form, thereby impeding viral DNA synthesis and replication.</p>

<p>Ionomycin is an ionophore compound with a mode of action that facilitates calcium ion transport across cell membranes. It is used in research to study calcium signaling and T-cell activation.</p>

<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.</p>

<p>Triadimenol-tert-butylhydroxy is a systemic fungicide, originating from synthetic chemical processes, characterized by its ability to inhibit fungal sterol biosynthesis. This sterol biosynthesis disruption occurs through the demethylation of lanosterol or 24-methylene dihydrolanosterol, which impedes the production of ergosterol, a crucial component in fungal cell membranes. The inhibition results in disrupted cell membrane integrity and impaired fungal growth, leading to effective control over a range of plant-pathogenic fungi.</p>

<p>HBV-IN-4 is an antiviral compound that serves as a potent and selective inhibitor of hepatitis B virus (HBV). It is derived from chemical synthesis with a focus on targeting the viral replication machinery. The mode of action involves interrupting the HBV lifecycle by inhibiting the functioning of viral polymerase, thereby preventing the synthesis of viral DNA and subsequent viral propagation.</p>

<p>Anti-parasitic; pyruvate ferredoxin oxidoreductase inhibitor</p>

<p>8-Methylpyrido[2,3-d]pyridazin-5(6H)-one is a heterocyclic compound used in the field of medicinal chemistry. This compound is synthesized through complex organic reactions involving pyridazine and pyridine derivatives. As a molecule, its primary mode of action involves interactions with specific biochemical pathways, potentially influencing enzymatic activity or receptor bindings, leading to modulation of biological activities.</p>

<p>Diclobutrazol is a plant growth regulator, a synthetic compound primarily derived from chemical synthesis methods. This compound acts by inhibiting the biosynthesis of gibberellins, which are plant hormones that regulate various aspects of growth and development. The inhibition of gibberellin biosynthesis results in reduced plant elongation, leading to more compact growth forms.</p>

<p>Validamycin E is an antifungal antibiotic, which is a secondary metabolite derived from the actinobacterium Streptomyces hygroscopicus. Its mode of action involves the inhibition of trehalase, an enzyme crucial for the hydrolysis of trehalose into glucose, disrupting essential energy pathways in fungi. By inhibiting trehalase, Validamycin E effectively interferes with the growth and development of fungal pathogens.</p>

<p>Pirlimycin HCl is an antibacterial product, which is a semi-synthetic derivative of the natural antibiotic lincomycin produced by Streptomyces lincolnensis. Its mode of action involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, thereby preventing the elongation of peptide chains. This action is particularly effective against Gram-positive bacteria, including Staphylococcus and Streptococcus species.</p>

<p>Sulfamoyldapsone is a synthetic antimicrobial compound, which is derived from the dapsone family. Its source is primarily synthetic, designed through chemical modifications of the parent compound dapsone, a well-known antibacterial agent. The mode of action of sulfamoyldapsone involves the inhibition of bacterial folic acid synthesis. By targeting dihydropteroate synthase, an enzyme essential for the production of folic acid in microorganisms, the compound effectively interferes with bacterial growth and replication.</p>

Pseudomonic acid F is a naturally occurring secondary metabolite, which is derived from the bacterium *Pseudomonas fluorescens*. Its mode of action involves the inhibition of bacterial protein synthesis by targeting the bacterial isoleucyl-tRNA synthetase enzyme. This inhibition disrupts the addition of isoleucine to the growing polypeptide chain, effectively impeding bacterial growth and proliferation.

<p>ABT-072 is a direct-acting antiviral (DAA) agent, specifically designed as an inhibitor of the hepatitis C virus (HCV) NS5B polymerase. This compound originates from advanced pharmaceutical research and development efforts aimed at targeting viral replication mechanisms. Being an NS5B polymerase inhibitor, ABT-072 functions by interfering with the viral RNA-dependent RNA polymerase. This enzyme plays a critical role in the replication cycle of the hepatitis C virus, facilitating the synthesis of new viral RNA strands. By inhibiting this enzyme, ABT-072 effectively halts viral replication.</p>

<p>CPFX2090 is a sophisticated software platform designed for advanced data analytics and visualization, which is developed by a team of computational scientists utilizing cutting-edge algorithms and machine learning techniques. It operates through a dynamic interface that enables automated data processing, multidimensional analysis, and real-time visualization. The platform's mode of action involves ingesting large datasets, performing parallel computations, and visualizing results with interactive graphical tools.</p>

Imazethapyr-1-hydroxyethyl is a selective, systemic herbicide, which is synthesized through chemical processes. It functions primarily by inhibiting the acetohydroxyacid synthase (AHAS) enzyme, also known as acetolactate synthase (ALS). This enzyme is vital for the biosynthesis of branched-chain amino acids like valine, leucine, and isoleucine, which are essential for plant growth. By hindering this enzyme's action, Imazethapyr-1-hydroxyethyl effectively stunts the growth and development of susceptible plant species.

<p>Vapendavir diphosphate is an antiviral compound, which is a synthesized small molecule with selective activity targeting picornaviruses. This compound is derived from rigorous medicinal chemistry efforts focusing on the inhibition of viral replication. Vapendavir diphosphate functions by binding to a specific site on the viral capsid, thereby inhibiting the uncoating process essential for viral RNA release into the host cell. This mode of action effectively prevents the virus from replicating within the host.</p>

<p>Please enquire for more information about ML303 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Rifamycin PR-3 is an antibiotic, which is derived from bacterial fermentation, specifically from the bacterium Amycolatopsis rifamycinica. It acts by inhibiting DNA-dependent RNA polymerase, thereby blocking RNA synthesis in susceptible bacteria. This inhibition disrupts protein synthesis, ultimately leading to bacterial cell death. Rifamycin PR-3 is primarily used for the treatment of various bacterial infections, particularly those caused by gram-positive bacteria and certain mycobacteria. Its application is crucial in managing diseases such as tuberculosis, where it targets the Mycobacterium tuberculosis. As a member of the rifamycin class of antibiotics, it is also explored for use in treating refractory cases and in combinations to prevent the development of resistance. This compound’s efficacy in penetrating phagocytic cells makes it an important player in addressing intracellular infections. Scientists continue to study its pharmacokinetics and potential for synergistic combinations, which may expand its utility in infectious disease therapy.</p>

<p>BRL 42715 is an antibacterial agent, which is a synthetic compound with a unique mechanism of action. This compound is derived from rational drug design aimed at targeting specific bacterial enzymes critical for cell wall synthesis. By irreversibly inhibiting these enzymes, BRL 42715 disrupts the bacterial cell wall formation, leading to cell lysis and death.</p>

<p>Anhydro erythromycin A is a semi-synthetic derivative of erythromycin A, which has been shown to be an effective inhibitor of bacterial growth, showing higher selectivity for this inhibition. It is a prodrug that is activated by acid catalysis and can be used as a substitute against methicillin-resistant staphylococcus. Anhydro erythromycin A was developed with the goal of increasing its stability and its potency against methicillin-resistant Staphylococcus aureus, which has been shown to be resistant to erythromycin.</p>

<p>Please enquire for more information about Omaciclovir including the price, delivery time and more detailed product information at the technical inquiry form on this page</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>Thiostrepton is a thiopeptide antibiotic with action on bacterial protein synthesis by binding to the ribosome and is used for treating bacterial infections in veterinary medicine and research applications.</p>

<p>Oligomycin is a macrolide antibiotic, which is derived from species of the bacterium Streptomyces. It acts as a potent inhibitor of the mitochondrial ATP synthase complex, specifically targeting the F₀ portion of the enzyme. This interference results in the blockage of proton translocation across the mitochondrial membrane, thereby preventing ATP synthesis. Due to this mode of action, Oligomycin is primarily utilized in biochemical research to study cellular respiration and energy metabolism. It serves as a valuable tool in elucidating the mechanisms of oxidative phosphorylation and the role of ATP in various cellular processes. In addition, its application extends to investigations on mitochondrial dysfunctions and the screening of mitochondrial-targeted drugs.</p>

<p>Ascomycin is an immunosuppressant macrolide lactone, which is derived from the soil bacterium *Streptomyces hygroscopicus*. It functions primarily by inhibiting the T-cell activation pathway. The mechanism involves binding to the immunophilin FKBP-12, forming a complex that inhibits the calcium-dependent phosphatase, calcineurin. This inhibition prevents the dephosphorylation and subsequent translocation of nuclear factor of activated T cells (NFAT), which is crucial for the transcription of interleukin-2 and other cytokines. Consequently, this suppresses the activation and proliferation of T-cells, which are essential components of the adaptive immune response.</p>

<p>(2RS,4S)-2-[[(Phenylacetyl)amino]methyl]-5,5-dimethylthiazolidine-4-carboxylic acid, commonly referred to as penilloic acids, is a hydrolytic degradation product of benzylpenicillin. It is derived through the enzymatic or chemical cleavage of the β-lactam ring of benzylpenicillin, which is a classic β-lactam antibiotic.</p>

<p>Acepromazine hydrochloride is a phenothiazine derivative tranquilizer, which is synthesized chemically. Its mode of action is primarily through antagonism of dopamine receptors in the central nervous system, leading to a sedative effect. Additionally, it exerts peripheral actions, including alpha-adrenergic blockade and diminished release of hypothalamic and hypophyseal hormones, contributing to vasodilation and other physiological effects.</p>

<p>Dicloxacillin sodium salt monohydrate is a beta-lactam antibiotic with action on bacterial cell wall synthesis and is used for treating infections caused by penicillinase-producing bacteria.</p>

<p>Mafoprazine is an experimental psychotropic drug, which is an organic compound synthetically derived from the azapirone family. It functions primarily as a serotonin receptor agonist, specifically targeting the 5-HT1A receptors, while also exhibiting moderate affinity for dopamine and adrenergic receptors. This dual action on neurotransmitter systems is thought to contribute to its therapeutic effects.</p>

<p>Dihydrostreptomycin sesquisulfate is an aminoglycoside antibiotic, which is derived from the bacterium Streptomyces griseus. Its mode of action involves binding to the 30S subunit of the bacterial ribosome, leading to the disruption of protein synthesis. This binding interferes with the initiation complex formation, causing misreading of mRNA and ultimately inhibiting bacterial growth.</p>

<p>L-689502 is a synthetic compound that functions as a selective antagonist for neuropeptide Y1 receptors. It is derived from chemical synthesis processes specifically designed to target and modulate these receptors. As an antagonist, its primary mode of action involves binding to the neuropeptide Y1 receptors and inhibiting their activity, thereby blocking the effects of the naturally occurring ligand, neuropeptide Y (NPY).</p>

<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>