Antimicrobials

<p>Bromophos-methyl-oxon is an organophosphate insecticide and acaricide, which is a synthetic chemical derived from organophosphate compounds. It functions by inhibiting the activity of the enzyme acetylcholinesterase in target organisms. This inhibition leads to the accumulation of acetylcholine at nerve synapses, disrupting normal nerve function and ultimately resulting in the paralysis and death of pests.</p>

<p>Asukamycin is an antibiotic, which is a secondary metabolite derived from the bacterium *Streptomyces nodosus*. Its mode of action involves the inhibition of cell wall synthesis in susceptible bacteria by interfering with peptidoglycan polymerization, which is essential for maintaining bacterial cell integrity. Additionally, asukamycin exhibits the ability to interfere with the biosynthesis of important cellular components in certain pathogens, contributing to its antimicrobial efficacy.</p>

<p>Chaetoglobosin A is a mycotoxin, which is a secondary metabolite produced by the fungus Chaetomium globosum. This compound exhibits its mode of action by disrupting the cytoskeletal elements within cells, primarily affecting actin polymerization. This interference leads to alterations in cell morphology and can induce apoptosis in certain cell lines.</p>

<p>Pantoprazole-d3 is a stable isotope-labeled version of the proton pump inhibitor pantoprazole, which is derived synthetically for scientific research and analytical applications. Isotope labeling involves substituting hydrogen atoms with deuterium, resulting in Pantoprazole-d3 containing three deuterium atoms. This modification preserves the pharmacological profile of the parent compound while enabling precise tracking in biological studies through advanced spectroscopic techniques.</p>

<p>Phthivazid is an antibiotic, which is a synthetic derivative of isonicotinic acid hydrazide. It functions by inhibiting the synthesis of mycolic acids in the mycobacterium cell wall, which are essential components for the survival of the bacteria. This disruption in the cell wall synthesis results in bactericidal activity against Mycobacterium tuberculosis.</p>

<p>Trans-tetradecenyl acetate is a synthetic pheromone, which is an analog of a naturally occurring insect sex pheromone. It is derived from synthetic organic chemistry processes that aim to replicate the molecular structure of pheromones produced by insects. The mode of action involves mimicking the natural pheromone signals used by female insects to attract males. By dispersing trans-tetradecenyl acetate into the environment, it disrupts the mating communication between the sexes, leading to a reduction in successful mating events and, consequently, a decrease in pest population over time.</p>

<p>Duocarmycin SA is an antitumor antibiotic, which is derived from the natural products of Streptomyces bacteria. This compound exhibits its mode of action through the alkylation of DNA, specifically binding within the minor groove. The alkylation process preferentially targets adenine-thymine-rich regions, leading to irreversible DNA damage and subsequent inhibition of DNA replication. Such interaction results in the induction of apoptosis in rapidly dividing cells.</p>

<p>PSI-7409 is a novel antimicrobial compound, which is synthetically derived with a unique mechanism of action. This compound is engineered through a complex synthesis process ensuring high purity and efficacy. PSI-7409 exerts its effects by disrupting bacterial cell wall synthesis, leading to cell lysis and death. Its precise mode of interaction on the molecular level involves inhibition of key enzymatic pathways essential for peptidoglycan assembly, thereby compromising the structural integrity of bacterial cells.</p>

<p>Bromobutide-desbromo is a chemical compound that functions as a selective herbicide. It is derived from synthetic sources and is specifically formulated to interfere with photosynthesis in target plants. The mode of action of bromobutide-desbromo involves inhibiting photosystem II, a crucial component of the photosynthetic electron transport chain in plants. This inhibition disrupts the energy conversion process, leading to a decrease in ATP and NADPH production, which are essential for plant growth.</p>

<p>2,4,5,6-Tetrachlorophenol-13C6 is an isotopically labeled chemical compound, primarily used as a reference standard in analytical chemistry. This compound, derived from its non-labeled counterpart 2,4,5,6-tetrachlorophenol, is synthesized through the incorporation of carbon-13 isotopes. Its primary mode of action involves acting as a stable, traceable marker, facilitating accurate quantification and analysis of environmental samples, particularly in mass spectrometry.</p>

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

<p>Radicinol is a natural compound, which is a dihydroflavonol primarily sourced from plant origins. This compound is biosynthesized in specific plant species and extracted through meticulous biochemical processes to ensure its purity and efficacy. The mode of action of Radicinol involves the modulation of specific cellular pathways, conferring antioxidative and anti-inflammatory properties. It acts by scavenging free radicals and enhancing cellular resilience against oxidative stress.</p>

<p>Lascufloxacin is a synthetic fluoroquinolone antibiotic, which is derived from chemical synthesis. Its mode of action involves inhibiting bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication, transcription, repair, and recombination. By targeting these enzymes, lascufloxacin effectively hampers bacterial cell division and growth, leading to cell death. This mechanism specifically affects Gram-positive and Gram-negative bacterial strains, making it a versatile agent in antibacterial therapy.</p>

<p>Fluxapyroxad-N-desmethyl is a fungicidal metabolite, which is derived from the parent compound fluxapyroxad, a pyridine carboxamide fungicide. The source of this compound is through the biological or chemical transformation of fluxapyroxad, which involves demethylation. Its mode of action involves the inhibition of succinate dehydrogenase, an essential enzyme in the fungal pathogen's mitochondrial electron transport chain. This inhibition results in disruption of energy production within the fungal cells, ultimately leading to their death.</p>

<p>N-Biotinyl-12-aminododecanoyltobramycin amide is a synthetic bioconjugate, which is derived from the aminoglycoside antibiotic tobramycin. This compound is chemically modified by the addition of a biotin moiety linked through a 12-aminododecanoyl spacer. The source of this product is rooted in the conjugation of biotin to tobramycin, allowing for targeted delivery and potential hybrid applications in both therapeutic and diagnostic fields.</p>

<p>Tolnifanide is a fungicidal product, which is a synthetic compound derived from chemical synthesis. It operates by interfering with the normal cellular function of fungi, inhibiting their growth and reproduction. This mode of action involves disrupting key processes within the fungal cells, rendering them unable to thrive in their host environment.</p>

<p>Ofloxacin methyl ester is a chemical compound, which is a derivative utilized in scientific research, particularly in the synthesis of ofloxacin-related compounds. It is a synthetic ester, derived from chemical synthesis involving ofloxacin, a fluoroquinolone antibiotic. The mode of action of ofloxacin methyl ester is based on its role as an intermediate compound. It facilitates the creation of active forms or analogs that can be tested for their pharmacological properties. Although not directly used as a therapeutic agent, it plays a crucial role in the development and modification of molecules for antibacterial applications.</p>

<p>3'-N-Desmethyl-3'-N-formyl azithromycin is a semi-synthetic macrolide antibiotic, derived from the well-known azithromycin. It is created through structural modification, where the 3'-N-demethylated and 3'-N-formyl groups enhance its pharmacokinetic properties and potentially improve its antimicrobial efficacy.</p>

<p>Inhibitor of protein synthesis; streptogramin</p>

<p>Cenicriviroc sulfone is a small-molecule pharmaceutical compound, which is a synthetic product derived from medicinal chemistry optimization processes. It functions as a dual antagonist of the CCR2 and CCR5 receptors, which are chemokine receptors involved in inflammatory response and HIV entry, respectively. By blocking these receptors, Cenicriviroc sulfone inhibits the signaling pathways that lead to immune cell recruitment and inflammation.</p>

<p>Griseoluteic acid is a cyclic lipopeptide that inhibits bacterial growth by binding to the enzyme cyclase, which is involved in the production of cyclic AMP. Griseoluteic acid also inhibits the synthesis of rRNA (ribosomal RNA), which is required for protein synthesis. The compound has been shown to have a high degree of resistance against antibiotic-resistant strains and exhibits a low toxicity profile in vitro. Griseoluteic acid also has an inhibitory effect on hydrogen bonding interactions, which may be due to its ability to inhibit energy metabolism. This compound also exhibits anti-inflammatory properties and has been shown to have neurodevelopmental effects in animal models.</p>

<p>Triazoxide-desoxy is an investigational compound, which is a synthetic derivative of triazoxide, originating from pharmacological research aimed at modulating physiological pathways. This compound acts primarily by influencing ion channel activity at a cellular level, impacting the regulation of potassium channels which are crucial for maintaining cellular homeostasis and signaling.</p>

<p>Ceratotoxin A is a peptide toxin, which is derived from the venom of the female fruit fly *Ceratitis capitata*. This toxin is part of a group of antimicrobial peptides that play a crucial role in the innate immune response of the fly. Ceratotoxin A functions by integrating into the cell membranes of bacteria, leading to membrane disruption and subsequent bacterial cell death.</p>

<p>Abacavir-d4 is a deuterium-labeled analogue of the antiretroviral medication Abacavir. It serves as a critical tool for pharmaceutical research and development. This isotopically labeled compound is synthesized by incorporating four deuterium atoms into the molecular structure of Abacavir, preserving the pharmacokinetic and pharmacodynamic properties of the original molecule while allowing for precise analytical quantification.</p>

<p>Carbovir is a nucleoside reverse transcriptase inhibitor (NRTI), which is derived from carbocyclic nucleosides. Its mode of action involves the selective inhibition of the reverse transcriptase enzyme, an essential component in the replication cycle of retroviruses, such as HIV. By incorporating into the viral DNA chain during synthesis, Carbovir effectively halts chain elongation, thereby impeding the virus's ability to proliferate.</p>

<p>Coumoxystrobin is a fungicide, which is a product of synthetic chemistry with a mode of action that involves the inhibition of mitochondrial respiration. Specifically, it disrupts the electron transport chain by binding to the Qo site in complex III, thereby preventing the transfer of electrons. This action halts ATP production, leading to the death of fungal cells.</p>

<p>Gentamicin C2 pentaacetate (2 : 1 Mixture of C2 and C2a) is an aminoglycoside class antibiotic derivative, primarily derived from the fermentation of Micromonospora species. This product is a semi-synthetic compound, combining two closely related gentamicin components, C2 and C2a, in a specified ratio. Its mode of action involves binding to the 30S subunit of the bacterial ribosome, which disrupts protein synthesis resulting in bactericidal activity against a wide spectrum of Gram-negative and some Gram-positive bacteria.</p>

<p>Aureonitol is a fungal metabolite, which is sourced from specific species of fungi, primarily within the Aspergillus and Penicillium genera. This is a naturally occurring compound that functions as an antibiotic, disrupting the biosynthesis processes within certain microorganisms. It achieves this action by inhibiting key enzymes involved in cell wall formation or by interfering with nucleic acid pathways, thereby impeding the growth and proliferation of bacterial cells.</p>

<p>Licoflavone B is a naturally occurring flavonoid, which is primarily derived from the roots of licorice plants, such as Glycyrrhiza inflata. It functions as a bioactive compound with potential antioxidant and anti-inflammatory activities. The mode of action of Licoflavone B involves the scavenging of free radicals, modulation of signaling pathways, and inhibition of pro-inflammatory mediators. These biological activities render it valuable in research focused on chronic diseases and oxidative stress.</p>

<p>Fluhexafon is an innovative acaricide, which is derived from advanced chemical synthesis. Its mode of action involves disrupting critical biological processes in mites, specifically targeting nerve receptor pathways to inhibit their survival and reproduction. By interfering with the neurotransmission, it effectively reduces mite populations, ensuring healthier crops.</p>

<p>Acetophos is an organophosphate insecticide, which is a synthetic chemical compound derived from phosphoric acid. It functions by inhibiting acetylcholinesterase, an essential enzyme in the nervous systems of insects. This inhibition leads to the accumulation of acetylcholine, causing continuous nerve impulses that result in the paralysis and eventual death of the pest.</p>

<p>Napyradiomycin A is a secondary metabolite, classified as a type of antibiotic, which is derived from marine Streptomyces bacteria. This natural product is of considerable interest due to its unique biosynthetic origin, found specifically in marine ecosystems. Napyradiomycin A exhibits its mode of action primarily through the inhibition of bacterial RNA synthesis. This is achieved by interacting with bacterial enzymes, subsequently halting their reproductive and metabolic processes, which makes it a potent antibacterial agent.</p>

<p>SARS-CoV-IN-3 is a small-molecule inhibitor, which is derived through synthetic organic chemistry targeting SARS-CoV-2. It exhibits its mode of action by specifically inhibiting the viral RNA-dependent RNA polymerase (RdRp) enzyme. This enzyme is crucial for viral RNA synthesis, and by inhibiting its activity, SARS-CoV-IN-3 effectively suppresses viral replication within host cells.</p>

<p>Biotinyl tobramycin amide is a biotinylated form of the antibiotic tobramycin, which is derived from the actinobacterium Streptomyces tenebrarius. It features a tobramycin core, a potent aminoglycoside antibiotic, chemically linked to biotin. This modification allows for the specific attachment to avidin or streptavidin-labeled probes due to the strong biotin-streptavidin interaction, facilitating various labeling and detection techniques in research.</p>

<p>trans-Abacavir dihydrochloride is a synthetic compound classified as a nucleoside analog. It is derived from chemical synthesis and serves as a prodrug that is metabolized in the body to its active form, carbovir triphosphate. Its primary mode of action involves the inhibition of the HIV-1 reverse transcriptase enzyme. This inhibition is achieved through the incorporation of the active metabolite into viral DNA, resulting in chain termination and preventing viral replication.</p>

<p>Anti-fungal; sterol 14α-demethylase inhibitor</p>

<p>DSHS00884 is a CRISPR-associated enzyme, which is a type of gene-editing tool derived from bacterial immune systems. This enzyme functions as a molecular scissor that targets specific DNA sequences and introduces breaks or modifications at defined loci. The mode of action involves recognizing specific guide RNA sequences that direct the enzyme to complementary DNA sites where it executes precise edits. This precision stems from its ability to form base-pair interactions with the targeted DNA, ensuring minimal off-target effects.</p>

<p>Rifampicin is a drug that inhibits protein synthesis in bacteria and is used to treat tuberculosis. Rifampicin binds to the beta subunit of the bacterial RNA polymerase, inhibiting transcription and translation. It has been shown to inhibit the acetylcholine receptor function in rats, which may be related to its antituberculosis activity. Histopathological studies have shown that rifampicin inhibits the growth of human tumors in mice, including lung cancer, breast cancer, and leukemia. The drug is also being studied for its potential use in treating Alzheimer's disease. The pharmacokinetics and oral bioavailability of rifampicin have been studied and Rifampicin has been shown to be an effective anti-tuberculosis drug.</p>

<p>Mecillinam is a beta-lactam antibiotic specifically designed for use in culture media. It is derived from the amidinopenicillin family, featuring a unique ability to interfere with bacterial cell wall synthesis. Its mode of action involves inhibiting penicillin-binding protein 2 (PBP2), an essential enzyme for cell wall elongation and maintenance in Gram-negative bacteria. This targeted inhibition results in the formation of spherical cells and subsequent cell lysis.</p>

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

<p>Thiamphenicol is a semisynthetic derivative of chloramphenicol with action on bacterial protein synthesis inhibition and is used for treating bacterial infections, particularly in veterinary medicine.</p>

<p>Furaprofen is a nonsteroidal anti-inflammatory drug (NSAID), which is a synthetic pharmaceutical compound derived from the carboxylic acid class. Its mode of action involves inhibiting the enzyme cyclooxygenase (COX), which plays a crucial role in the biosynthesis of pro-inflammatory prostaglandins. By blocking COX activity, Furaprofen reduces the formation of these signaling molecules, thereby alleviating inflammation and pain.</p>

<p>Gemifloxacin is an antibacterial agent primarily classified as a fluoroquinolone antibiotic, which is a synthetic compound derived from chemical processes in pharmaceutical manufacturing. Its mechanism of action involves the inhibition of key bacterial enzymes, namely DNA gyrase and topoisomerase IV. These enzymes are crucial for bacterial DNA replication, transcription, repair, and recombination. By obstructing these enzymes, Gemifloxacin effectively inhibits bacterial cell division and growth, leading to the eradication of susceptible bacterial strains.</p>

<p>Lydicamycin is an antibacterial compound, which is a polyketide-derived antibiotic produced by the microorganism Streptomyces. This natural compound functions by inhibiting bacterial protein synthesis, effectively interrupting critical cellular processes within susceptible bacteria. The mode of action primarily focuses on binding to the bacterial ribosome, thereby disrupting protein production and inhibiting bacterial growth.</p>

<p>AT-511 is an antiviral compound, which is derived from organic synthesis processes associated with the development of nucleotide analogs. It acts by targeting the RNA-dependent RNA polymerase, a crucial enzyme in the replication process of RNA viruses. By inhibiting this enzyme, AT-511 effectively halts viral replication, reducing the viral load within the host.</p>

<p>Tuberculosis inhibitor 3 is a synthesized chemical compound designed to target the Mycobacterium tuberculosis bacterium, which is the causative agent of tuberculosis. This inhibitor is derived through advanced chemical synthesis techniques, involving the modification of specific molecular structures to enhance its binding affinity and specificity toward the bacterial cellular targets.</p>

<p>Duocarmycin MA is a cytotoxic compound, which is a derivative of natural products isolated from bacteria of the Streptomyces genus. Its mode of action involves the alkylation of DNA, leading to the cleavage of the DNA helix and ultimately resulting in cell apoptosis. This process is highly selective for adenine-thymine rich regions, allowing it to precisely target and disrupt cancerous cells.</p>

<p>Sulconazole nitrate is an antifungal agent, which is a synthetic compound derived from imidazole. Its mode of action involves the inhibition of ergosterol synthesis, an essential component of fungal cell membranes, leading to increased membrane permeability and ultimately cell death.</p>

<p>Clindamycin-d3 hydrochloride is an isotopically labeled pharmaceutical compound, specifically designed for use in the field of analytical chemistry and pharmacokinetics. It is derived from clindamycin, a known antibiotic sourced from modifications of the naturally occurring compound lincomycin, produced by the actinobacterium Streptomyces lincolnensis. The incorporation of deuterium atoms, replacing hydrogen, allows for its use in sophisticated analytical methods such as mass spectrometry, where it serves to trace the metabolic pathways and to quantify the bioavailability and distribution of clindamycin in biological systems with high precision.</p>

<p>Fosfomycin calcium monohydrate is an antibacterial agent, derived from Streptomyces species. This compound functions as a structural analog of phosphoenolpyruvate, interfering with cell wall synthesis. Specifically, it targets and irreversibly inhibits the enzyme UDP-N-acetylglucosamine enolpyruvyl transferase (MurA), which is critical in the early stages of bacterial cell wall biosynthesis. This inhibition prevents the formation of peptidoglycan, leading to bacterial cell lysis.</p>

<p>Letrozole is a non-steroidal aromatase inhibitor, which is synthesized chemically. This product acts by inhibiting the aromatase enzyme, thus reducing estrogen production in the body. Estrogen plays a critical role in the proliferation of hormone-sensitive breast cancer cells, and by lowering its levels, Letrozole effectively impedes cancer growth.</p>

<p>Naftifine N-Oxide is an antifungal agent, which is derived from synthetic chemical processes. Its structure is based on the modification of the known antifungal, naftifine, by introducing an N-oxide functional group, which may enhance certain pharmacokinetic properties. As a synthetic derivative, Naftifine N-Oxide is specifically designed to interfere with the biosynthesis of ergosterol, an essential component of fungal cell membranes. By inhibiting squalene epoxidase, an enzyme crucial to the ergosterol pathway, Naftifine N-Oxide effectively disrupts the development and maintenance of the fungal cell membrane, compromising cell integrity and leading to antifungal activity.</p>

<p>Ceftibuten Hydrate is a third-generation cephalosporin antibiotic, which is a synthetic derivative of naturally occurring cephalosporin C, derived from the fungus Acremonium. It functions by inhibiting bacterial cell wall synthesis, leading to cell lysis and death. This bactericidal action is accomplished through the binding to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, disrupting the final transpeptidation step of peptidoglycan synthesis in bacterial cell walls.</p>

<p>Propicillin is a broad-spectrum antimicrobial agent that has been shown to be effective against both gram-positive and gram-negative bacteria. Propicillin belongs to the group of nonsteroidal anti-inflammatory drugs. It is a particle that is soluble in water and lipid. Propicillin does not inhibit the growth of Streptococcus species, but does cause cell lysis by attaching to fatty acids on the surface of cells. Propicillin also inhibits microbial infection by inhibiting enzymes involved in fatty acid synthesis. The human serum pharmacokinetics of propicillin have been studied and found to be similar to those of ampicillin, which allows for use as an intravenous drug in humans. The pharmacokinetics, biochemical properties, and cellular mechanisms are complex, but it is known that propicillin binds to bacterial ribosomes and inhibits protein synthesis by binding to the peptidyl transferase centre on the ribosome.</p>

<p>Coronarin D ethyl ether is a diterpenoid compound, which is derived from the plant Hedychium coronarium, also known as white ginger lily. This compound belongs to a class of naturally occurring chemicals with complex polycyclic structures. The source of Coronarin D ethyl ether is the rhizome of Hedychium coronarium, which is part of the Zingiberaceae family. These plants are often studied for their bioactive properties and potential therapeutic applications.</p>

<p>Pyrimorph is a fungicide, which is a synthetic compound with specific activity against oomycete pathogens. It belongs to the chemical class of morpholines. Its mode of action involves the disruption of the biosynthetic pathways essential for the survival and proliferation of oomycetes, leading to their effective inhibition. Pyrimorph specifically targets the biosynthesis of cellulose in the cell walls of these pathogens, inhibiting their capacity to multiply and cause disease.</p>

<p>Clindamycin 4-phosphate is a semi-synthetic antibiotic, which is a derivative of the natural antibiotic lincomycin. It is specifically synthesized from Streptomyces lincolnensis cultures. The mode of action of Clindamycin 4-phosphate involves inhibiting bacterial protein synthesis by binding to the 50S subunit of the bacterial ribosome, thus preventing peptide chain elongation and subsequent bacterial growth.</p>

<p>A2ti-1 is a specialized therapeutic agent, which is derived from recombinant DNA technology with the specific mode of action of targeting and modulating cytokine signaling pathways within the immune system. It is designed to interact with specific cytokine receptors, thereby inhibiting or modulating the downstream signaling cascades that are pivotal in the inflammatory response and immune regulation.</p>

<p>Acetoxypolygodial is a sesquiterpenoid compound, which is a naturally derived product from the roots of the plant Polygonum hydropiper. This compound exhibits its mode of action through its ability to disrupt microbial cell membranes, leading to increased permeability and eventual cell death. Its primary mechanism involves direct interaction with lipid bilayers, causing destabilization.</p>

<p>Artelinic acid is a synthetic antimalarial agent, which is derived from artemisinin, a natural compound sourced from the sweet wormwood plant (Artemisia annua). The mode of action of Artelinic acid involves the generation of free radicals within the Plasmodium parasite, leading to oxidative stress and damage to the parasite’s cellular components, ultimately resulting in parasite death. This mechanism is particularly effective against Plasmodium species, including those strains resistant to other antimalarial drugs.</p>

<p>Puromycin-D3 is a deuterium-labeled antibiotic, which is synthetically derived from the bacterium *Streptomyces alboniger*, with three hydrogen atoms replaced by deuterium. Its mode of action involves the inhibition of protein synthesis by mimicking the aminoacyl end of tRNA, causing premature chain termination during translation on ribosomes. This mechanism specifically targets growing peptides in cells, making it a valuable tool for studying protein synthesis.</p>

<p>(E)-10,11-Didehydro-11-deoxy-6-O-methylerythromycin is a semisynthetic macrolide antibiotic, which is derived from erythromycin, a natural product obtained from the bacterium *Saccharopolyspora erythraea*. This compound functions as an inhibitor of protein synthesis by binding to the 50S ribosomal subunit of bacteria, thus preventing the growth and proliferation of susceptible bacterial strains. The alteration in its chemical structure, notably the methylation at the 6-O position, enhances its stability and improves its pharmacokinetic profile compared to the parent compound, erythromycin.</p>

<p>Telavancin is a lipoglycopeptide antibiotic, which is a semi-synthetic derivative of vancomycin. Its source is derived through modifications of the glycopeptide antibiotic, specifically aimed to enhance antibacterial activity. Telavancin functions by inhibiting cell wall synthesis in Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA). It does this by binding to the D-alanyl-D-alanine terminus of cell wall precursors, disrupting peptidoglycan polymerization and, consequently, cell wall integrity. Additionally, Telavancin increases membrane permeability and disrupts membrane potential, further enhancing its bactericidal activity.</p>

<p>Sisunatovir hydrochloride is an antiviral agent, which is a synthetic compound with a mechanism of action specifically targeting the respiratory syncytial virus (RSV). As a potent inhibitor, Sisunatovir hydrochloride interferes with the viral replication process by binding to a specific protein essential for the virus's ability to replicate within host cells.</p>

<p>6,11-Di-O-methyl erythromycin is a semi-synthetic derivative of erythromycin, which is a macrolide antibiotic originally sourced from the bacterium *Saccharopolyspora erythraea*. This compound is produced through chemical modification of the natural antibiotic to improve its pharmacokinetic properties, such as stability and absorption.</p>

<p>Pivmecillinam hydrochloride is an antibacterial prodrug, which is derived from the source compound mecillinam, a beta-lactam antibiotic. It functions by inhibiting bacterial cell wall synthesis, specifically targeting the penicillin-binding protein 2 (PBP2). This affinity leads to a weakening of the bacterial cell wall, causing cell lysis and death, particularly in gram-negative bacteria.</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>Spiramycin hexanedioate is a macrolide antibiotic, which is derived from the bacterium *Streptomyces ambofaciens*. Its mode of action involves binding to the 50S ribosomal subunit of susceptible bacteria, thereby inhibiting protein synthesis. This interaction results in the interruption of bacterial growth and reproduction, particularly effective against Gram-positive organisms.</p>

<p>Piperacillin-d5 is a stable isotopically labeled antibiotic, which is synthesized chemically to incorporate deuterium atoms. It is derived from the β-lactam group of antibiotics, sharing properties with its non-labeled counterpart, piperacillin. The incorporation of five deuterium atoms allows researchers to use it as a tracer in various pharmacokinetic and metabolic studies without altering its biological activity.</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>Sordarin sodium salt is an antifungal agent, characterized as a semisynthetic derivative produced from the fermentation products of filamentous fungi, specifically belonging to the phylum Ascomycota. This compound exerts its effects by selectively inhibiting fungal protein synthesis. It achieves this by obstructing the function of elongation factor 2 (EF-2), an essential component of fungal ribosomal activity, thereby disrupting the translational elongation step of protein synthesis.</p>

<p>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</p>

<p>Thienamycin p-nitrobenzyl ester, N-methylpyrrolidinone hydrochloride is a synthetic compound commonly utilized in biochemical research, particularly in the study of beta-lactam antibiotics. It is derived through synthetic pathways involving the modification of thienamycin, a naturally occurring beta-lactam antibiotic, to enhance its stability and facilitate its study in various experimental settings. This modification allows for investigation into the structure-activity relationships and potential enhancements of antibiotic function.</p>

<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>Macrosphelide A is a bioactive macrocyclic lactone, which is a secondary metabolite derived from the culture of certain fungal species. It functions primarily through the disruption of cell adhesion processes, which is facilitated by its ability to interfere with the function of specific cell surface receptors. This mode of action underlies its potential as an immunosuppressive agent, where it can inhibit the activities of immune cells by altering cellular communication and adhesion.</p>

<p>Sulbenicillin is a semi-synthetic penicillin antibiotic, which is derived from 6-aminopenicillanic acid, a natural precursor in the biosynthesis of penicillins. With its beta-lactam structure, Sulbenicillin disrupts bacterial cell wall synthesis by inhibiting penicillin-binding proteins, which are essential enzymes in the cross-linking of peptidoglycan layers. This disruption compromises the structural integrity of the bacterial cell wall, resulting in cell lysis and death, particularly in Gram-negative bacteria.</p>

<p>Inhibitor of protein synthesis; lincosamide class</p>

<p>Cyprazine-desisopropyl is a metabolite, which is a derivative form resulting from the biotransformation of cyromazine, an insect growth regulator. Cyromazine is originally sourced as a triazine-class pesticide, commonly used to control insect populations by disrupting their growth processes. Cyprazine-desisopropyl, similarly, impacts the development stages of target insect species.</p>

<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>

<p>Vebufloxacin is an antibacterial agent, which is synthesized as a member of the fluoroquinolone class of antibiotics. This compound is derived from chemical synthesis, specifically designed to target and inhibit bacterial DNA gyrase and topoisomerase IV. These enzymes play crucial roles in DNA replication and transcription, making them ideal targets for disrupting bacterial cell function.</p>

<p>Nifedipine is a pharmaceutical compound belonging to the class of dihydropyridine calcium channel blockers, which is synthetically derived. Its mode of action involves the inhibition of calcium ions entering vascular smooth muscle and cardiac muscle cells, leading to vasodilation. By blocking these channels, it reduces peripheral vascular resistance, thereby decreasing blood pressure and easing cardiac workload.</p>

<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>Showdomycin is an antibiotic, which is derived from the bacterium *Streptomyces showdoensis*. The mode of action of Showdomycin involves its role as a nucleoside analog that disrupts nucleic acid synthesis by incorporating itself into the nucleic acid chains during replication and transcription, thereby impairing cellular functions.</p>

<p>Aqabamycin F is a type of antibiotic compound, which is derived from marine natural sources, specifically from bacteria found in oceanic environments. This product is characterized by its unique molecular structure that offers potent antimicrobial properties. The mode of action of Aqabamycin F involves inhibiting essential bacterial enzymes, thus disrupting the cellular processes necessary for bacteria to survive and proliferate. This mechanism makes it effective against a wide range of bacterial pathogens, contributing to its potential in treating infections that are resistant to conventional antibiotics. Research into Aqabamycin F continues to explore its full spectrum of activity, offering insights into new therapeutic pathways for antibiotic-resistant bacterial infections. Its unique origin and molecular activity position Aqabamycin F as a promising candidate for addressing the growing challenge of antibiotic resistance.</p>

<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>

<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>

<p>Grazoprevir hydrate is a direct-acting antiviral agent used in the treatment of hepatitis C virus (HCV) infections. It is a synthetic compound derived through targeted pharmaceutical synthesis aimed at inhibiting viral replication. This compound operates by selectively inhibiting the NS3/4A protease, an enzyme critically involved in the post-translational processing and replication of the HCV polyprotein. By blocking this protease, grazoprevir effectively disrupts the virus's life cycle, thereby reducing viral load in patients.</p>

<p>BRITE-338733 is an advanced biotechnological product, which is derived from microbial fermentation with high specificity enzymatic action. This product is engineered to efficiently catalyze specific biochemical reactions, thereby facilitating various lab-scale processes.</p>

<p>Bromuconazole is a systemic fungicide, which is a synthetic chemical compound primarily used to protect crops from fungal diseases. It is derived from the triazole class of fungicides, which are known for their ability to inhibit important biochemical processes within fungal cells. The mode of action of Bromuconazole involves the inhibition of the enzyme C14-demethylase, a key component in the biosynthesis of ergosterol. Ergosterol is an essential component of fungal cell membranes, and its disruption leads to impaired cellular function and ultimately the death of the fungal organism.</p>