Antimicrobici
Gli antimicrobici sono agenti che distruggono o inibiscono la crescita di microrganismi, inclusi batteri, virus, funghi e parassiti. Questi composti sono essenziali nella prevenzione e nel trattamento delle infezioni, svolgendo un ruolo cruciale nella medicina, nell'agricoltura e nell'industria alimentare. Presso CymitQuimica offriamo un'ampia gamma di antimicrobici di alta qualità e purezza, adatti a varie applicazioni scientifiche e industriali. Il nostro catalogo comprende antibiotici, antifungini, antivirali e disinfettanti, tutti progettati per soddisfare le esigenze della ricerca e dello sviluppo, nonché per applicazioni cliniche e di produzione. Con i nostri prodotti, i professionisti possono garantire l'efficacia e la sicurezza nel controllo delle infezioni e nella protezione della salute pubblica.
Sottocategorie di "Antimicrobici"
- Antibiotici(4.131 prodotti)
- Antimicotici(909 prodotti)
- Antiparassitari(702 prodotti)
- Antivirali(765 prodotti)
Trovati 2424 prodotti di "Antimicrobici"
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Erythromycin B
CAS:<p>Erythromycin B is a semisynthetic macrolide antibiotic, which is derived from the actinomycete *Saccharopolyspora erythraea*. Its mode of action involves inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. This interference with protein synthesis effectively hampers bacterial growth, making it a potent bacteriostatic agent.</p>Formula:C37H67NO12Purezza:90%NmrPeso molecolare:717.93 g/molClenpenterol d5 hydrochloride
CAS:<p>Clenpenterol d5 hydrochloride is a deuterated chemical compound, which is a stable isotopic variant of the beta-agonist Clenpenterol, commonly used in research and analytical studies. This compound is synthetically derived to enhance specificity and precision in scientific investigations. Deuteration involves the replacement of hydrogen atoms with deuterium, which contributes to the increased stability and differentiation of the isotopes during analysis.</p>Formula:C13H21Cl3N2OPurezza:Min. 95%Peso molecolare:332.7 g/molLascufloxacin
CAS:<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>Formula:C21H24F3N3O4Purezza:Min. 95%Peso molecolare:439.4 g/molIsoflucypram
CAS:<p>Please enquire for more information about Isoflucypram including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C19H21ClF3N3OPurezza:Min. 95%Peso molecolare:399.8 g/mol6-o-Methacrylate
CAS:<p>6-o-Methacrylate is a monomer used in the synthesis of polymers, which is predominantly sourced from petroleum-based feedstocks through chemical synthesis. Its mode of action involves free radical polymerization, a process where the methacrylate group participates in chain reactions to form complex polymer structures. This compound is a key building block in the creation of various copolymers and homopolymers.</p>Formula:C23H30O9Purezza:Min. 95%Peso molecolare:450.5 g/molEtofenprox-carboxy
CAS:Etofenprox-carboxy is an insecticide, which is a synthetic chemical derivative with a unique pyrethroid-like structure. It acts on the nervous system of target insect species by disrupting their neuronal function. This disruption occurs through the stimulation of sodium channels, which, unlike traditional pyrethroids, provides a lower risk to mammals and non-target organisms. It is especially favored for its selective toxicity and reduced environmental persistence.Formula:C25H26O4Purezza:Min. 95%Peso molecolare:390.5 g/molSulbactam Related Compound A
CAS:<p>Sulbactam Related Compound A is a chemical compound often used in pharmaceutical research and development. It is typically derived from the synthetic modification of existing antibiotics to explore new potential therapeutic benefits. The compound functions as a beta-lactamase inhibitor, which is of significant interest to researchers due to its potential to enhance the efficacy of beta-lactam antibiotics. By inhibiting the action of bacterial beta-lactamase enzymes, it permits these antibiotics to remain effective against resistant strains of bacteria.</p>Formula:C5H11NO4SPurezza:Min. 95%Peso molecolare:181.21 g/molRibocil B
CAS:<p>Ribocil B is an analog of riboflavin, functioning as a synthetic antibiotic. It is derived from chemical synthesis, designed to mimic the structure of natural riboflavin analogs which are crucial for bacterial growth. Ribocil B acts by specifically inhibiting riboswitches, a type of non-coding RNA that regulates gene expression in response to small molecules. This inhibition disrupts RNA synthesis in bacteria by targeting the flavin mononucleotide (FMN) riboswitch.</p>Formula:C19H22N6OSPurezza:Min. 95%Peso molecolare:382.5 g/molClofoctol
CAS:<p>Clofoctol is an antibacterial agent, which is derived from synthetic origins, specifically designed for therapeutic applications in bacterial infections. Its mode of action involves inhibiting bacterial protein synthesis, thereby preventing the growth and proliferation of harmful bacteria. This compound is particularly effective against Gram-positive bacteria.</p>Formula:C21H26Cl2OPurezza:Min. 95%Peso molecolare:365.34 g/molHexazinone metabolite D
CAS:<p>Hexazinone metabolite D is a derivative compound that results from the biotransformation of Hexazinone, which is a systemic herbicide. This metabolite originates from the breakdown processes mediated by biological or environmental factors in ecosystems where Hexazinone is applied. Its mode of action involves the inhibition of photosynthesis by targeting photosystem II, ultimately reducing the transfer of electrons, which leads to the disruption of energy production in susceptible plant species.</p>Formula:C10H15N3O3Purezza:Min. 95%Peso molecolare:225.24 g/molOmomycin
CAS:<p>Omomycin is a novel antibiotic, specifically a macrolide, which is derived from microbial sources, primarily soil-dwelling actinomycetes. Its mode of action involves inhibiting bacterial protein synthesis by binding to the 50S ribosomal subunit. This interaction prevents the translocation of peptides during translation, thereby halting bacterial growth and proliferation.</p>Formula:C29H39NO4Purezza:Min. 95%Peso molecolare:465.6 g/molSparsomycin
CAS:<p>Sparsomycin is an antibiotic compound, which is a secondary metabolite isolated from Streptomyces species. Its mode of action involves the inhibition of protein synthesis by targeting the large subunit of the ribosome, specifically binding to the 50S subunit in bacterial ribosomes and the 60S subunit in eukaryotic ribosomes. This binding interferes with peptide bond formation, thereby disrupting the translational process essential for protein synthesis.</p>Formula:C13H19N3O5S2Purezza:Min. 95%Peso molecolare:361.4 g/molBesifloxacin hydrochloride
CAS:Besifloxacin hydrochloride is a fourth-generation fluoroquinolone antibiotic, which is a synthetic derivative of the broad-spectrum quinolone class. Its origin can be traced to laboratory chemical synthesis, tailored specifically to target bacterial infections in ocular applications. The mode of action of besifloxacin involves the inhibition of bacterial enzymes DNA gyrase and topoisomerase IV. These enzymes play crucial roles in bacterial DNA replication, transcription, repair, and recombination. By disrupting these processes, besifloxacin effectively impedes bacterial cell division, leading to the death of the bacterial cells.Formula:C19H21ClFN3O3·HClPurezza:Min. 95%Peso molecolare:430.3 g/molValidamycin B
CAS:Validamycin B is an aminoglycoside antibiotic, which is a type of product derived from the bacterium *Streptomyces hygroscopicus*. Its mode of action involves inhibiting the trehalase enzyme, an essential component for fungal cell viability, thereby disrupting the energy supply within the fungal cells. This disruption leads to impediments in fungal growth and proliferation.Formula:C20H35NO14Purezza:Min. 95%Peso molecolare:513.5 g/mol7-Deazaadenosine, Antibiotic for Culture Media Use Only
CAS:7-Deazaadenosine is a chemical compound used as an antibiotic for culture media, which is a synthetic nucleoside analog derived from adenosine. Its structure is modified by replacing a nitrogen atom in the purine ring with a carbon atom, thus altering its biological interactions. The primary mode of action of 7-Deazaadenosine involves its incorporation into nucleic acids, where it acts as an inhibitor of nucleic acid-processing enzymes. This interference can effectively impede processes like DNA and RNA synthesis.Formula:C11H14N4O4Purezza:Min. 97.0 Area-%Peso molecolare:266.25 g/molRef: 3D-W-203540
1gPrezzo su richiesta100mgPrezzo su richiesta250mgPrezzo su richiesta500mgPrezzo su richiesta2500mgPrezzo su richiesta-Unit-ggPrezzo su richiestaAztreonam-d6
CAS:<p>Aztreonam-d6 is an isotopically labeled antibiotic, which is a synthetic monobactam derived from bacterial fermentation processes with deuterium enrichment. With a beta-lactam structure, Aztreonam-d6 acts by inhibiting bacterial cell wall synthesis, specifically targeting the penicillin-binding protein 3 (PBP3) in Gram-negative bacteria. This action disrupts cell wall construction, leading to cell lysis and death, making it an effective option against certain resistant bacterial strains.</p>Formula:C13H17N5O8S2Purezza:Min. 95%Peso molecolare:441.5 g/molErythromycin, Antibiotic for Culture Media Use Only
CAS:Erythromycin, Antibiotic for Culture Media Use Only, is a macrolide antibiotic derived from the bacterium *Saccharopolyspora erythraea*. It functions by inhibiting protein synthesis, specifically targeting the 50S ribosomal subunit in susceptible bacteria. This action results in the prevention of peptide chain elongation, effectively halting bacterial growth and proliferation.Formula:C37H67NO13Purezza:Min. 93.0 Area-%Peso molecolare:733.93 g/molRef: 3D-E-3250
1kgPrezzo su richiesta100gPrezzo su richiesta250gPrezzo su richiesta500gPrezzo su richiesta2500gPrezzo su richiesta-Unit-ggPrezzo su richiestaCefluprenam
CAS:<p>Cefluprenam is a cephalosporin antibiotic, which is a synthetic derivative of the fungus Cephalosporium. It functions by inhibiting bacterial cell wall synthesis, effectively disrupting the peptidoglycan cross-linking process essential for bacterial structural integrity. This inhibition leads to cell lysis and ultimately bacterial death.</p>Formula:C20H25FN8O6S2Purezza:Min. 95%Peso molecolare:556.60 g/molCefoxitin EP impurity B
Cefoxitin EP impurity B is a chemical reference standard, which is derived from the synthesis and purification processes involved in producing Cefoxitin. As an impurity standard, its primary role is to serve as a benchmark for quality control in pharmaceutical formulations. The mode of action of Cefoxitin EP impurity B involves the structural analysis and quantification of impurity levels, ensuring that the primary pharmaceutical products meet necessary safety and efficacy criteria.Formula:C16H17N3O7S2Purezza:Min. 95%Peso molecolare:427.45 g/molChlortetracycline-13C-d3 hydrochloride
Prodotto controllato<p>Chlortetracycline-13C-d3 hydrochloride is a stable isotope-labeled antibiotic with action on bacterial protein synthesis inhibition and is used for research in bacterial resistance and analytical studies.</p>Formula:C2113CH21D3Cl2N2O8Colore e forma:PowderPeso molecolare:519.35 g/molCenicriviroc sulfone
CAS:<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>Formula:C41H52N4O5SPurezza:Min. 95%Peso molecolare:712.90 g/molClomeprop (free acid)
CAS:<p>Clomeprop (free acid) is a selective herbicide, which is synthesized chemically to target grass species. Its mode of action involves the inhibition of the enzyme acetyl-CoA carboxylase, crucial for fatty acid synthesis. This interferes with lipid production, which is vital for plant growth and development.</p>Formula:C10H10Cl2O3Purezza:Min. 95%Peso molecolare:249.09 g/molEthofumesate-2-hydroxy
CAS:<p>Ethofumesate-2-hydroxy is a selective herbicide, which is a synthetic chemical compound with a specific mode of action. This herbicide primarily originates from chemical synthesis processes designed to interfere with plant growth at a biochemical level. The mode of action of Ethofumesate-2-hydroxy involves the inhibition of lipid synthesis, which disrupts cell membrane formation and hampers weed growth. It effectively targets susceptible weed species by inhibiting essential biochemical pathways, thus leading to their decline or death.</p>Formula:C11H14O5SPurezza:Min. 95%Peso molecolare:258.29 g/molCeratotoxin A
CAS:<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>Formula:C135H243N35O32Purezza:Min. 95%Peso molecolare:2,868.6 g/molOxohongdenafil
CAS:<p>Please enquire for more information about Oxohongdenafil including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C25H32N6O4Purezza:Min. 95%Peso molecolare:480.6 g/mol6,11-Di-O-methyl erythromycin
CAS:<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>Formula:C39H71NO13Purezza:Min. 95%Peso molecolare:761.98 g/molSpiro-oxanthromicin A
CAS:Spiro-oxanthromicin A is a novel antibiotic compound, which is derived from a rare species of actinomycete bacteria. The unique structure of Spiro-oxanthromicin A integrates spiroketal and oxanthrone moieties, facilitating its distinctive antimicrobial properties. It operates by selectively binding to bacterial ribosomal subunits, inhibiting protein synthesis and effectively curbing pathogenic proliferation.Formula:C36H26O10Purezza:Min. 95%Peso molecolare:618.6 g/molFlufenoxystrobin
CAS:<p>Flufenoxystrobin is a synthetic fungicide, which is derived from the strobilurin class of compounds known for their antifungal properties. It operates by inhibiting mitochondrial respiration in fungal cells, specifically blocking the electron transport chain at the Qo site of cytochrome b. This disruption in energy production is lethal to the targeted fungi.</p>Formula:C19H16ClF3O4Purezza:Min. 95%Peso molecolare:400.8 g/molNigericin sodium
CAS:<p>Nigericin transports cations across the membrane of the cell and it is used to study anion transport. It can be used as a buffer to control pH value inside of the cell.</p>Formula:C40H67NaO11Purezza:Min. 95%Peso molecolare:746.94 g/molCoumoxystrobin
CAS:<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>Formula:C26H28O6Purezza:Min. 95%Peso molecolare:436.5 g/molSulfamethazine Sodium Salt
CAS:<p>Sulfamethazine Sodium Salt is a synthetic sulfonamide antibacterial agent derived from sulfanilamide compounds, characterized by its broad-spectrum efficacy against various bacterial pathogens. It operates by interfering with bacterial folic acid synthesis, specifically inhibiting the enzyme dihydropteroate synthase. This action results in the incapacitation of bacterial growth and replication, as folic acid is essential for nucleic acid formation and cell division.</p>Formula:C12H13N4O2S·NaPurezza:Min. 95%Peso molecolare:300.31 g/mol2-Amino-5-(4-hydroxy-3,5-dimethoxybenzyl)pyrimidin-4-ol
CAS:<p>2-Amino-5-(4-hydroxy-3,5-dimethoxybenzyl)pyrimidin-4-ol is a synthetic pyrimidine derivative, which is meticulously engineered through organic synthesis pathways. This compound emerges from a tailored chemical reaction involving the strategic manipulation of a pyrimidine core to incorporate specific functional groups. The unique structural configuration of this molecule allows it to interact with biological macromolecules, primarily through hydrogen bonding and pi-pi interactions, potentially influencing biochemical pathways.</p>Formula:C13H15N3O4Purezza:Min. 95%Peso molecolare:277.28 g/molAbacavir-d4
CAS:Prodotto controllato<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>Formula:C14H14D4N6OPurezza:Min. 95%Peso molecolare:290.36 g/molBonducellpin D
CAS: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.Formula:C22H28O7Purezza:Min. 95%Peso molecolare:404.5 g/molAureonitol
CAS:<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>Formula:C13H18O2Purezza:Min. 95%Peso molecolare:206.28 g/molSyncytial virus inhibitor-1
CAS:<p>Syncytial virus inhibitor-1 is a potent antiviral compound, which is a synthetic small molecule with a specific mode of action targeting respiratory syncytial virus (RSV). This compound is engineered to inhibit the fusion process between the viral envelope and the host cell membrane, thereby preventing the virus from entering and infecting the cells.</p>Formula:C23H26N4O3SPurezza:Min. 95%Peso molecolare:438.5 g/molCadazolid
CAS:<p>Cadazolid is an investigational antibiotic, which is a synthetic oxazolidinone-cephalosporin hybrid, with a novel mechanism of action. It is engineered to disrupt bacterial protein synthesis by binding to the 50S ribosomal subunit, while also exerting strong bactericidal effects. This dual-action approach combines attributes of both linezolid and cephalosporins to target and disrupt essential bacterial processes.</p>Formula:C29H29F2N3O8Purezza:Min. 95%Peso molecolare:585.55 g/molMiconazole
CAS:Anti-fungal; sterol 14α-demethylase inhibitorFormula:C18H14Cl4N2OPurezza:Min. 95 Area-%Colore e forma:White Off-White PowderPeso molecolare:416.13 g/molPirodavir
CAS:Pirodavir is a potent antiviral compound, which is a synthetic molecule developed through pharmaceutical research. It acts by targeting the rhinovirus, the most common viral infectious agent in humans, primarily responsible for the common cold. Pirodavir's mode of action involves binding to the viral capsid, thereby preventing the uncoating process essential for viral replication.Formula:C21H27N3O3Purezza:Min. 95%Peso molecolare:369.46 g/molAlisporivir
CAS:<p>Alisporivir is an investigational antiviral agent, which is a synthetic derivative of cyclosporine A. It originates from the structural modification of naturally occurring cyclosporines, specifically designed to retain potent antiviral activity while minimizing immunosuppressive effects. Its mode of action involves the inhibition of cyclophilin, an essential cellular protein that facilitates the replication of hepatitis C virus (HCV) by interacting with viral proteins. By binding to cyclophilin, alisporivir disrupts this interaction, effectively halting the viral replication process.</p>Formula:C63H113N11O12Purezza:Min. 95%Peso molecolare:1,216.6 g/molThiosildenafil-despiperazine
CAS:<p>Thiosildenafil-despiperazine is a derivative of sildenafil, which is a phosphodiesterase type 5 (PDE5) inhibitor. This compound is synthesized through structural modifications of sildenafil, leading to alterations in its pharmacological profile and potential applications. The source of this derivative involves chemical synthesis techniques to modify the core structure of sildenafil, specifically targeting modifications in the piperazine ring and replacing it with a thioside group to enhance or alter desired effects.</p>Formula:C17H20N4O4S2Purezza:Min. 95%Peso molecolare:408.5 g/mol3,4-Dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine
CAS:3,4-Dihydro-2H,6H-pyrimido[1,2-c][1,3]benzothiazin-6-imine is a chemical compound classified as a heterocyclic organic compound, which is synthesized through chemical processes in the laboratory. This compound belongs to a novel class of molecules with potential pharmacological applications, particularly in the realm of infectious diseases. Its mode of action involves the inhibition of specific enzymatic pathways essential for the survival of certain pathogenic organisms, such as Plasmodium species responsible for malaria.Formula:C11H11N3SPurezza:Min. 95%Peso molecolare:217.29 g/molL-Carnitine fumarate
CAS:<p>L-Carnitine fumarate is a compound that functions as a dietary supplement, which is synthesized by combining L-carnitine, an amino acid derivative naturally found in the body, with fumaric acid. This product is primarily sourced from fermentation or chemical synthesis processes to produce L-carnitine, which is then reacted with fumaric acid to form the fumarate salt. This combination enhances the stability and bioavailability of L-carnitine.</p>Formula:C7H15NO3·C4H4O4Purezza:Min. 95%Peso molecolare:277.27 g/molSPR741
CAS:<p>SPR741 is an antimicrobial potentiator, which is derived from polymyxin B, an antibiotic sourced from the bacterium *Bacillus polymyxa*. Its mode of action involves permeabilizing the outer membrane of Gram-negative bacteria, allowing otherwise impermeable antibiotics to enter the bacterial cell. This potentiation effect significantly enhances the efficacy of co-administered antibiotics against resistant strains.</p>Formula:C44H73N13O13Purezza:Min. 95%Peso molecolare:992.1 g/mol6-(2-Chlorophenoxy)-5-fluoro-4(3H)-pyrimidinone
CAS:<p>6-(2-Chlorophenoxy)-5-fluoro-4(3H)-pyrimidinone is a heterocyclic compound, which is a synthetic derivative developed for biochemical research. This compound is synthesized through a series of organic reactions, involving halogenation and cyclization techniques, typically conducted in a controlled laboratory setting. Its design incorporates specific structural features, such as the chlorophenoxy and fluoro groups, which are strategically positioned to enhance its binding affinity and specificity.</p>Formula:C10H6ClFN2O2Purezza:Min. 95%Peso molecolare:240.62 g/molQuinocarcin
CAS:<p>Quinocarcin is an antitumor antibiotic, which is a potent chemical compound derived from the bacterium Streptomyces. This compound exhibits its mode of action through interaction with DNA, where it induces DNA cross-linking and inhibits DNA replication, ultimately leading to cell death. The mechanism makes it particularly effective as a cytotoxic agent against rapidly dividing cancer cells.</p>Formula:C18H22N2O4Purezza:Min. 95%Peso molecolare:330.4 g/molMagainin 1
CAS:Magainin 1 is a peptide antibiotic, which is sourced from the skin secretions of the African clawed frog, *Xenopus laevis*. It operates through a membranolytic mode of action, whereby it integrates into microbial cell membranes, forming pores and causing cell lysis by disrupting membrane integrity. This mechanism is largely non-specific, making it effective against a broad spectrum of bacteria and fungi.Formula:C112H177N29O28SPurezza:Min. 95%Peso molecolare:2,409.85 g/molTerrelulamide A
CAS:Terrelulamide A is a bioactive compound, specifically a cyclic peptide, which is derived from marine cyanobacteria. The source of Terrelulamide A is primarily marine environments where these cyanobacteria undergo complex biosynthetic processes to produce such metabolites. This compound's mode of action involves the disruption of cellular processes by binding to specific molecular targets that are critical in cell cycle regulation. It exhibits cytotoxic activity, effectively inhibiting cancer cell proliferation through its interaction with those pathways.Formula:C20H26N6O7Purezza:Min. 95%Peso molecolare:462.5 g/molRiamilovir
CAS:<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>Formula:C5H4N6O3SPurezza:Min. 95%Peso molecolare:228.19 g/molBiotinyl tobramycin amide
CAS:<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>Formula:C28H51N7O11SPurezza:Min. 95%Peso molecolare:693.81 g/molTebuthiuron-N-hydroxymethyl
CAS: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.Formula:C9H16N4O2SPurezza:Min. 95%Peso molecolare:244.32 g/molFenamiphos-sulfoxide d3 (S-methyl d3)
CAS:<p>Fenamiphos-sulfoxide d3 (S-methyl d3) is a deuterated, labeled pesticide intermediate, which is often utilized in advanced laboratory settings for precise analytical studies. This compound is synthesized as a stable isotope-labeled analog, enabling researchers to conduct sophisticated mass spectrometric analyses. Its mode of action involves serving as a reference or tracer in studies concerning the metabolism and degradation of fenamiphos, a well-known organophosphate pesticide.</p>Formula:C13H22NO4PSPurezza:Min. 95%Peso molecolare:322.38 g/molCefquinome
CAS:<p>Cefquinome is a broad-spectrum antibiotic, which is a fourth-generation cephalosporin. It is derived from the β-lactam class of antibiotics and is specifically designed for veterinary applications. Its mode of action involves the inhibition of bacterial cell wall synthesis, leading to cell lysis and death. This action is facilitated through the binding of cefquinome to penicillin-binding proteins, which undermines the structural integrity of bacterial cell walls, proving effective against both Gram-positive and Gram-negative bacteria.</p>Formula:C23H24N6O5S2Purezza:Min. 95%Peso molecolare:528.61 g/molDesmethyl doxorubicin oxalate
CAS:<p>Desmethyl doxorubicin oxalate is an anthracycline-type chemotherapeutic agent, which is derived from the naturally occurring antibiotic doxorubicin. This compound comprises a desmethylated form of doxorubicin combined with oxalate. Its mode of action involves intercalating DNA strands and inhibiting topoisomerase II, thereby disrupting DNA replication and transcription. This interference leads to the inhibition of cancer cell proliferation and induces apoptosis.</p>Formula:C26H27NO11Purezza:Min. 95%Peso molecolare:529.49 g/molBPH-1358
CAS:BPH-1358 is a novel synthetic inhibitor, which is derived from a series of advanced chemoinformatics-based design strategies. It functions through the targeted binding to specific cell surface receptors involved in the modulation of immune responses. By blocking these receptors, BPH-1358 effectively alters signaling pathways that are crucial for immune activation and inflammatory responses.Formula:C32H28N6O2Purezza:Min. 95%Peso molecolare:528.6 g/molN,N′-1,2-Ethanediylbis[3-nitrobenzenesulfonamide]
CAS:N,N′-1,2-Ethanediylbis[3-nitrobenzenesulfonamide] is a chemical compound, specifically a bis-sulfonamide derivative. It is synthesized through the reaction of sulfonamide derivatives with ethylenediamine, resulting in a unique structure characterized by its two nitrobenzenesulfonamide groups linked by an ethylene bridge. As a source, it is obtained through synthetic organic chemistry methods involving nitration and sulfonamidation processes.Formula:C14H14N4O8S2Purezza:Min. 95%Peso molecolare:430.4 g/molSARS-CoV-IN-1
CAS:SARS-CoV-IN-1 is a small-molecule inhibitor, which is a synthetic compound designed to interfere with viral replication. This compound is sourced through rigorous combinatorial chemistry methods, enabling the precise targeting of viral enzymes. SARS-CoV-IN-1 specifically inhibits the activity of the SARS-CoV-2 main protease (Mpro), an essential enzyme responsible for processing viral polyproteins into functional units necessary for virus replication.Formula:C23H16ClFEN3OPurezza:Min. 95%Peso molecolare:441.69 g/molAcequinocyl-hydroxy
CAS:<p>Acequinocyl-hydroxy is an acaricide, which is a chemical agent used to manage and control mite populations in various agricultural settings. It is derived from a combination of synthetic organic compounds designed specifically to disrupt the normal biological processes of target pests. The mode of action of Acequinocyl-hydroxy involves interference with the mitochondrial electron transport chain of mites, ultimately disrupting cellular respiration and leading to the death of the pest.</p>Formula:C22H30O3Purezza:Min. 95%Peso molecolare:342.5 g/molRifampicin, Antibiotic for Culture Media Use Only
CAS: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.Formula:C43H58N4O12Purezza:Min. 90.0 Area-%Peso molecolare:822.94 g/molRef: 3D-R-6000
1gPrezzo su richiesta1kgPrezzo su richiesta100gPrezzo su richiesta250gPrezzo su richiesta500gPrezzo su richiesta-Unit-ggPrezzo su richiesta8-Oxo-gtp 8-hydroxy-gtp
CAS:<p>8-Oxo-GTP, also known as 8-Hydroxy-GTP, is a nucleotide analog, which is synthetically derived. It closely resembles the naturally occurring guanosine triphosphate (GTP) but contains a modified 8-hydroxy group, making it a valuable tool for studying oxidative damage and nucleotide modification processes.</p>Formula:C10H16N5O15P3Purezza:Min. 95%Peso molecolare:539.18 g/molThiabendazole NH d6
CAS:Thiabendazole NH d6 is a deuterated derivative of Thiabendazole, which is an antifungal agent and pesticide. It is derived from synthetic sources, specifically designed by incorporating deuterium atoms into the molecular structure. This subtle isotopic modification enhances its utility in research settings, particularly in studies related to pharmacokinetics and metabolic profiling. The mode of action of Thiabendazole involves the inhibition of the enzyme fumarate reductase, interfering with the energy metabolism of fungal and parasitic organisms. Additionally, it disrupts microtubule formation, preventing cell division and growth.Formula:C10H7N3SPurezza:Min. 95%Peso molecolare:207.29 g/molSanfetrinem cilexetil
CAS:<p>Sanfetrinem cilexetil is an oral prodrug, which is derived from trinem antibiotics, a subgroup of β-lactams. It is a synthetic compound developed to enhance the pharmacokinetic properties of its active form, sanfetrinem. Upon oral administration, sanfetrinem cilexetil undergoes hydrolysis in the digestive tract to release the active β-lactam antibiotic, sanfetrinem.</p>Formula:C23H33NO8Purezza:Min. 95%Peso molecolare:451.50 g/molNicotinamide
CAS:Nicotinamide is an amide form of vitamin B3, which is a water-soluble vitamin derived from dietary sources such as meat, fish, and yeast. In cellular biology, it functions as a precursor to nicotinamide adenine dinucleotide (NAD+), a critical coenzyme in redox reactions and energy production within the cells. Nicotinamide facilitates the transfer of electrons in metabolic processes, contributing to ATP production and cellular respiration. Moreover, it plays a pivotal role in DNA repair and cellular signaling through the regulation of sirtuins and poly(ADP-ribose) polymerases (PARPs).Formula:C6H6N2OPurezza:Min. 97.0 Area-%Peso molecolare:122.12 g/molFosmanogepix
CAS:<p>Fosmanogepix is a novel antifungal prodrug, which is derived from manogepix. This product is a synthetic compound, designed to target invasive fungal infections through its unique mechanism of action. The prodrug itself is inactive until metabolized in the body, where it converts into its active form, manogepix. This activation occurs through enzymatic hydrolysis, enabling it to exert its antifungal effects.</p>Formula:C22H21N4O6PPurezza:Min. 95%Colore e forma:PowderPeso molecolare:468.4 g/molCephradine
CAS:<p>Cephradine is a broad-spectrum antibiotic, which is a synthetic derivative of cephalosporin C, originating from the mold Cephalosporium acremonium. Its mode of action involves interfering with bacterial cell wall synthesis. Cephradine binds to penicillin-binding proteins (PBPs) located inside the bacterial cell wall, inhibiting the final transpeptidation step of peptidoglycan synthesis, which leads to cell lysis and death.</p>Formula:C16H23N3O6SPurezza:Min. 95%Peso molecolare:385.4 g/molCefacetrile sodium
CAS:<p>Cefacetrile sodium is a broad-spectrum antibiotic belonging to the cephalosporin class. It is a semi-synthetic derivative sourced from cephalosporin C, a naturally occurring compound derived from the Acremonium fungus. Its mode of action involves the inhibition of bacterial cell wall synthesis. This occurs by binding to penicillin-binding proteins within the bacterial cell membrane, ultimately leading to cell lysis and death due to the inability to synthesize peptidoglycan, a critical component of the bacterial cell wall.</p>Formula:C13H13N3NaO6SPurezza:Min. 95%Peso molecolare:362.31 g/mol(10E)-3-O-De(a-L-cladinose)-10-dehydro-11-dehydroxy-6-O-methyl-erythromycin
CAS:Erythromycin derivativeFormula:C30H53NO9Purezza:Min. 95%Peso molecolare:571.74 g/molCarbovir monophosphate
CAS:<p>Carbovir monophosphate is an antiviral agent, which is a metabolite derived from the prodrug abacavir. It functions as a nucleotide analog that interferes with viral replication. The source of Carbovir monophosphate is the metabolic conversion of abacavir, an antiretroviral medication used in the treatment of HIV. This conversion occurs primarily in the liver, facilitated by cellular enzymes.</p>Formula:C11H14N5O5PPurezza:Min. 95%Peso molecolare:327.23 g/molDarunavir-D9
CAS:Darunavir-D9 is a prodrug of darunavir, which is an HIV protease inhibitor. Darunavir-D9 has been shown to be bioequivalent in pharmacokinetic parameters to darunavir given as a tablet. The drug exhibits a low plasma concentration profile and high clearance values. This may be due to rapid absorption and distribution of the drug, with a short elimination half-life. Darunavir-D9 also has little effect on the matrix effect and reproducibility of the reaction monitoring assay, making it an ideal candidate for use in clinical trials.Formula:C27H28D9N3O7SPurezza:Min. 95%Peso molecolare:556.72 g/molZabofloxacin
CAS:<p>Zabofloxacin is a synthetic fluoroquinolone antibiotic, which is derived from chemical synthesis with a distinct bactericidal mode of action. Its mechanism involves the inhibition of bacterial DNA gyrase and topoisomerase IV, enzymes critical for DNA replication, transcription, and repair. This dual targeting results in potent antibacterial activity against a wide range of Gram-positive and Gram-negative pathogens.</p>Formula:C19H20FN5O4Purezza:Min. 95%Peso molecolare:401.4 g/molAspterric acid
CAS:Plant growth regulatorFormula:C15H22O4Purezza:Min. 95%Peso molecolare:266.33 g/molN'-Desmethyl azithromycin
CAS:<p>N'-Desmethyl azithromycin is a semi-synthetic derivative antibiotic, which is derived from the chemical modification of azithromycin, a macrolide antibiotic sourced originally from the bacterium *Streptomyces erythreus*. It functions primarily by inhibiting bacterial protein synthesis, binding specifically to the 50S ribosomal subunit, which results in the prevention of transpeptidation and translocation processes during translation. This action effectively halts bacterial growth, rendering it bacteriostatic.</p>Formula:C37H70N2O12Purezza:Min. 95%Peso molecolare:734.96 g/molIndaziflam-desindenyl
CAS:Indaziflam-desindenyl is an advanced herbicide, which is a product of synthetic chemistry, specifically designed for controlling the germination and growth of a broad spectrum of weed species. It operates through cellulose biosynthesis inhibition, targeting the cellulose production in plant cell walls, thus preventing proper cell division and development. This mode of action disrupts essential mechanisms in the plant's early growth stages, making it particularly effective as a pre-emergent herbicide.Formula:C5H8FN5Purezza:Min. 95%Peso molecolare:157.15 g/molButafenacil
CAS:<p>Butafenacil is a herbicide, which is a chemical formulation sourced from synthetic compounds. It acts by inhibiting protoporphyrinogen oxidase (PPO), an enzyme critical in the biosynthesis of chlorophyll. This inhibition disrupts the photosynthetic process, leading to the accumulation of reactive oxygen species that cause cell membrane damage and ultimately result in plant death.</p>Formula:C17H14ClF3N2O6Purezza:Min. 95%Peso molecolare:434.7 g/molTuberculosis inhibitor 3
CAS:<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>Formula:C21H22F6N4O3SPurezza:Min. 95%Peso molecolare:524.5 g/molBaumycin C1
CAS:<p>Baumycin C1 is an anthracycline-type antibiotic, which is derived from the bacterium *Streptomyces coeruleorubidus*. The mode of action of Baumycin C1 involves intercalating into DNA strands, thereby disrupting the process of DNA synthesis and replication. This intercalation results in the inhibition of topoisomerase II, an enzyme crucial for DNA unwinding, leading to the generation of double-strand breaks and subsequent interruption of cellular proliferation.</p>Formula:C28H29NO11Purezza:Min. 95%Peso molecolare:555.5 g/molDuocarmycin MA
CAS: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.Formula:C34H31ClN4O5Purezza:Min. 95%Peso molecolare:611.1 g/mol8-Fluoro erythromycin
CAS:<p>8-Fluoro erythromycin is a synthetic derivative of the macrolide antibiotic erythromycin. It is derived from the fermentation of *Streptomyces erythraeus*, a species known for producing erythromycin, which is chemically modified to include a fluorine atom at the eighth position. This modification enhances its pharmacokinetic properties, improving its stability and bioavailability compared to the parent compound.</p>Formula:C37H66FNO13Purezza:Min. 95%Peso molecolare:751.92 g/molWF-3681
CAS:<p>WF-3681 is a chemical compound utilized as an insecticide, which is synthesized from organic compounds through a controlled chemical process. The mode of action for WF-3681 involves the disruption of the neural pathways in target insects, leading to paralysis and eventual death. This mechanism specifically interferes with neurotransmitter functions, ensuring efficacy against a broad range of agricultural pests. The compound's specificity minimizes impacts on non-target organisms and the surrounding environment.</p>Formula:C13H12O5Purezza:Min. 95%Peso molecolare:248.23 g/molA2ti-2
CAS:A2ti-2 is an advanced metallurgical alloy, which is a synthesized product combining high-grade titanium and aluminum elements. It is engineered through a precise metallurgical process that involves controlled alloying at elevated temperatures, optimizing the atomic structure for superior performance traits. The mode of action for A2ti-2 involves its exceptional ability to maintain stability under extreme temperatures, providing resistance to thermal degradation and mechanical stress.Formula:C18H18N4O2SPurezza:Min. 95%Peso molecolare:354.4 g/molFGI 106
CAS:<p>FGI 106 is an antifungal agent, which is derived from natural sources with a mechanism of action involving disruption of fungal cell wall integrity. The compound is isolated from naturally occurring substances, specifically targeting the structural components of the cell walls in various fungal species. By compromising the protective barrier of the cell wall, FGI 106 effectively inhibits fungal growth and proliferation, making it a potent tool against a variety of fungal pathogens.</p>Formula:C28H42Cl4N6Purezza:Min. 95%Peso molecolare:604.5 g/mol2'-O-Acetylspiramycin I
CAS:<p>2'-O-Acetylspiramycin I is a semi-synthetic derivative of spiramycin, which is a macrolide antibiotic originally sourced from the bacterium *Streptomyces ambofaciens*. The modification involves the acetylation at the 2'-hydroxyl group of spiramycin, enhancing certain pharmacokinetic properties.</p>Formula:C45H76N2O15Purezza:Min. 95%Peso molecolare:885.09 g/molUniconazole
CAS:Uniconazole is a synthetic plant growth regulator, which is derived from triazole compounds. It acts as a potent inhibitor of gibberellin biosynthesis, specifically targeting enzymes involved in gibberellin production. By inhibiting gibberellins, uniconazole reduces internode elongation and alters growth patterns, resulting in shorter, more compact plants.Formula:C15H18ClN3OPurezza:Min. 95%Peso molecolare:291.78 g/molSultasin
CAS:<p>Sultasin is a combination antibiotic product, which is derived from the synthesis of sulbactam, a β-lactamase inhibitor, and ampicillin, a β-lactam antibiotic. The mode of action of Sultasin involves the inhibition of bacterial cell wall synthesis. Ampicillin works by attaching to penicillin-binding proteins (PBPs) inside the bacterial cell wall, disrupting the final transpeptidation step of peptidoglycan synthesis, which leads to cell lysis. Sulbactam enhances the efficacy of ampicillin by inhibiting β-lactamase enzymes produced by resistant bacterial strains, thereby preventing the degradation of the antibiotic.</p>Formula:C25H29N3Na2O9S2Purezza:Min. 95%Peso molecolare:625.6 g/molAlbendazole-2-aminosulfoxide
CAS:<p>Albendazole-2-aminosulfoxide is a metabolite of the benzimidazole class of antiparasitic agents, which is derived from the biotransformation of albendazole in the liver. As a potent bioactive compound, its mode of action primarily involves the selective binding to the β-tubulin of parasitic organisms, disrupting the polymerization of microtubules necessary for their cellular structures. This disruption impedes vital processes such as glucose uptake and cellular division, leading to parasite death.</p>Formula:C10H13N3OSPurezza:Min. 95%Peso molecolare:223.3 g/molBO3482
CAS:Please enquire for more information about BO3482 including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C14H20N2NaO5S2Purezza:Min. 95%Peso molecolare:383.4 g/molMitomycin D
CAS:<p>Mitomycin D is an antibiotic and chemotherapeutic agent known for its ability to inhibit DNA synthesis, making it a potent antitumor agent. It is derived from the bacterium *Streptomyces caespitosus*. Mitomycin D functions as a DNA crosslinking agent by alkylating the DNA strands, which interferes with DNA replication and transcription. This mechanism leads to the cessation of cellular division and ultimately induces apoptosis in rapidly dividing cells.</p>Formula:C15H18N4O5Purezza:Min. 95%Peso molecolare:334.33 g/molCycloxydim-sulfone-glutaric acid
CAS:<p>Cycloxydim-sulfone-glutaric acid is a synthesized herbicide, which is a derivative of cycloxydim, a cyclohexanedione compound. It is characterized by its ability to effectively inhibit acetyl-CoA carboxylase, an enzyme crucial in fatty acid biosynthesis within plant systems. The source of this compound is primarily through complex chemical synthesis processes that combine its constituent elements to enhance its stability and efficacy as a herbicide.</p>Formula:C10H16O6SPurezza:Min. 95%Peso molecolare:264.3 g/molAclacinomycin HCl
CAS:<p>Aclacinomycin HCl is a cytotoxic antibiotic that inhibits the growth of tumor cells. It has been shown to induce apoptosis in human leukemia cells by altering the transmembrane potential and inhibiting cell proliferation. Aclacinomycin HCl also induces DNA damage response, which leads to caspase activities and cell death. This drug is highly selective for tumor cells, with no effect on normal cells. It has been shown to be effective against primary liver cancer in animal models, as well as developmental disorders such as autism spectrum disorder (ASD).</p>Formula:C42H53NO15·HClPurezza:Min. 95%Colore e forma:Orange PowderPeso molecolare:848.33 g/molFosfomycin calcium monohydrate
CAS: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.Formula:C3H7CaO5PPurezza:Min. 95%Peso molecolare:194.14 g/molNeticonazole
CAS:<p>Neticonazole is a synthetic antifungal compound, which is derived from pharmaceutical chemical synthesis. It functions primarily as an imidazole derivative, disrupting the synthesis of ergosterol, a crucial component of fungal cell membranes. This interference leads to increased cell membrane permeability, ultimately causing cell lysis and death of the fungal organism.</p>Formula:C17H22N2OSPurezza:Min. 95%Peso molecolare:302.4 g/molAcivicin hydrochloride
CAS:Acivicin hydrochloride is a synthetic compound that acts as a glutamine antagonist, sourced from microbial fermentation processes. It functions primarily through the inhibition of glutamine-utilizing enzymes, such as gamma-glutamyl transferase and carbamoyl phosphate synthetase, which play critical roles in nucleotide biosynthesis and other metabolic pathways. By disrupting these biochemical processes, Acivicin hydrochloride can hinder the proliferation of rapidly dividing cells, displaying potential antitumor properties.Formula:C5H8Cl2N2O3Purezza:Min. 95%Peso molecolare:215.03 g/molGatifloxacin hydrate
CAS:<p>Gatifloxacin hydrate is a fluoroquinolone antibiotic, which is synthesized chemically. It exerts its bactericidal effects primarily by inhibiting bacterial DNA gyrase and topoisomerase IV. These enzymes are crucial for bacterial DNA replication, transcription, and repair. By preventing these processes, gatifloxacin effectively halts bacterial cell division, ultimately leading to cell death.</p>Formula:C19H24FN3O5Purezza:Min. 95%Peso molecolare:393.4 g/molPropicillin
CAS:<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>Formula:C18H22N2O5SPurezza:Min. 95%Peso molecolare:378.4 g/molRef: 3D-AAA55127
5mgPrezzo su richiesta10mgPrezzo su richiesta25mgPrezzo su richiesta50mgPrezzo su richiesta100mgPrezzo su richiestaBleomycin HCl
CAS:<p>Inducer of DNA strand breaks; glycopeptide antibiotic, anti-neoplastic</p>Formula:C50H71N16O21S2R•(HCl)xPurezza:Min. 95%Colore e forma:White To Off-White SolidDimethenamid-oxalamid
CAS:<p>Dimethenamid-oxalamid is a pre-emergent herbicide, which is a synthetic compound developed for agricultural use. It is derived from research focused on improving crop protection through chemical innovation. The mode of action involves inhibiting the synthesis of very long-chain fatty acids (VLCFAs) in weeds, disrupting their cell division and growth processes, ultimately leading to the prevention of weed emergence.</p>Formula:C12H17NO4SPurezza:Min. 95%Peso molecolare:271.33 g/mol7-epi-Clindamycin
CAS:<p>7-epi-Clindamycin is a clindamycin derivative, which is a semisynthetic antibiotic derived from the bacterium *Streptomyces lincolnensis*. Its mode of action involves binding to the 50S subunit of the bacterial ribosome, thereby inhibiting protein synthesis. This results in the suppression of bacterial growth, making it effective against certain Gram-positive bacteria and anaerobic species.</p>Formula:C18H34Cl2N2O5SPurezza:Min. 95%Colore e forma:White To Off-White SolidPeso molecolare:461.44 g/molFaldaprevir
CAS:Hepatitis C virus protease inhibitorFormula:C40H49BrN6O9SPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:869.82 g/molPropiconazole
CAS:<p>Propiconazole is a triazole fungicide with action on fungal cell membranes by inhibiting ergosterol biosynthesis and is used for controlling fungal diseases in crops and turf.</p>Formula:C15H17Cl2N3O2Purezza:Min. 95%Colore e forma:Clear LiquidPeso molecolare:342.22 g/molQuinthiophos
CAS:<p>Quinthiophos is an organophosphate insecticide, which is synthesized chemically. Its mode of action involves the inhibition of the enzyme acetylcholinesterase, which is critical in nerve function. By disrupting this enzyme, quinthiophos causes an accumulation of acetylcholine at the synapses, leading to continual nerve signal transmission, paralysis, and eventual death of the targeted pests.</p>Formula:C17H16NO2PSPurezza:Min. 95%Peso molecolare:329.4 g/mol
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