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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3-Chloro-4-(3-chloro-2-nitrophenyl)pyrrole
CAS:<p>3-Chloro-4-(3-chloro-2-nitrophenyl)pyrrole is a synthetic chemical compound, classified as an organochlorine derivative. This compound originates from the modification of pyrrole structures, which are heterocyclic aromatic compounds. The synthesis involves chlorination and nitration processes to enhance its potential activity and specificity.</p>Formula:C10H6Cl2N2O2Purezza:Min. 95%Peso molecolare:257.07 g/mol14-Chloro daunorubicin
CAS:<p>14-Chloro daunorubicin is a chemotherapeutic agent, which is a synthetic derivative of the naturally occurring anthracycline antibiotic, daunorubicin. This compound is specifically modified to include a chlorine atom at the 14th position, which enhances its pharmacological effectiveness compared to its parent compound. The drug acts primarily by intercalating into DNA, disrupting the function of topoisomerase II, and generating free radicals. These mechanisms collectively inhibit DNA replication and transcription, leading to cell apoptosis, particularly in rapidly dividing cancer cells.</p>Formula:C27H28ClNO10Purezza:Min. 95%Peso molecolare:561.96 g/molClindamycin sulfoxide
CAS:<p>Clindamycin sulfoxide is a potent metabolite of the lincosamide antibiotic clindamycin, which is derived from the fermentation product of *Streptomyces lincolnensis*. This compound acts by inhibiting bacterial protein synthesis through binding to the 50S ribosomal subunit, thereby interfering with the translocation steps in protein elongation. The mechanism effectively suppresses the growth of a broad range of Gram-positive bacteria, including *Staphylococcus aureus*, *Streptococcus pneumoniae*, and anaerobic microorganisms.</p>Formula:C18H33ClN2O6SPurezza:Min. 95%Peso molecolare:440.98 g/molThiamethoxam-urea
CAS:<p>Thiamethoxam-urea is an advanced agrochemical formulation, which is a synthetic compound derived from the integration of the neonicotinoid insecticide thiamethoxam and the stabilizing agent urea. This product is engineered from laboratory synthesis, where chemical reactions enable the effective combination of these components to ensure optimal stability and efficacy. The mode of action of Thiamethoxam-urea involves neurotoxic interference within the central nervous system of target organisms, primarily acting as an agonist at nicotinic acetylcholine receptors in insects. This disrupts neural transmission, leading to paralysis and eventual death of the pest.</p>Formula:C8H10ClN3O2SPurezza:Min. 95%Peso molecolare:247.7 g/molParvodicin C2
CAS:<p>Parvodicin C2 is a natural antibiotic compound, which is derived from the fermentation of specific actinomycete strains. This antibiotic functions through the inhibition of bacterial protein synthesis, specifically targeting the ribosomal subunits and leading to disruption in the peptide chain elongation process. The targeted mode of action allows it to effectively limit the replication and survival of susceptible bacterial strains.</p>Formula:C83H88Cl2N8O29Purezza:Min. 95%Peso molecolare:1,732.5 g/molColistin A
CAS:Colistin A is an antimicrobial peptide, which is a type of polymyxin antibiotic derived from the bacterium *Paenibacillus polymyxa*. It exerts its bactericidal effect by interacting electrostatically with the lipopolysaccharides and phospholipids in the outer membrane of Gram-negative bacteria. This action disrupts the bacterial cell membrane, leading to increased permeability and cell death.Formula:C53H100N16O13Purezza:Min. 95%Peso molecolare:1,169.5 g/molCefminox Sodium
CAS:<p>Cefminox Sodium is a beta-lactam antibiotic, which is synthesized through chemical modification of naturally occurring compounds. This product is classified as a second-generation cephalosporin, derived from cephalosporin C obtained from the fungus Acremonium. It exerts its mode of action by inhibiting bacterial cell wall synthesis. This occurs through the binding to penicillin-binding proteins, ultimately disrupting the cross-linking of peptidoglycan chains which are essential for bacterial cell wall integrity.</p>Formula:C16H20N7O7S3·NaPurezza:Min. 95%Peso molecolare:541.56 g/molFlufenacet-methylsulfone
CAS:<p>Flufenacet-methylsulfone is an herbicidal derivative, which is sourced from the modification of flufenacet metabolites. It operates by inhibiting the biosynthesis of very-long-chain fatty acids, which are crucial components in the formation of cell membranes within target plant species. This biochemical intervention disrupts normal cell division and elongation in weeds, ultimately inhibiting their growth and establishment.</p>Formula:C12H16FNO3SPurezza:Min. 95%Peso molecolare:273.33 g/molCefodizime
CAS:<p>Cefodizime is a third-generation cephalosporin antibiotic, which is derived from the fungus Acremonium. It exerts its bactericidal effects by inhibiting bacterial cell wall synthesis. This action is achieved through binding to penicillin-binding proteins (PBPs), leading to the interruption of peptidoglycan cross-linking essential for the bacterial cell wall integrity. The breakdown of cell wall synthesis results in the lysis and death of the bacterial cell.</p>Purezza:Min. 95%Amidosulfuron-o-desmethyl
CAS:Amidosulfuron-o-desmethyl is a metabolite derivative, which is studied primarily as a secondary product originating from the breakdown of the herbicide amidosulfuron. Synthesized through microbial and environmental degradation processes, it is part of the sulfonylurea class of compounds. The mode of action involves inhibition of the plant enzyme acetolactate synthase (ALS), leading to disrupted synthesis of essential branched-chain amino acids, ultimately affecting plant growth and survival.Formula:C8H13N5O7S2Purezza:Min. 95%Peso molecolare:355.4 g/molTris(4'-carboxy-1,1'-biphenyl)amine
CAS:<p>Tris(4'-carboxy-1,1'-biphenyl)amine is an organic compound commonly employed as a building block in the development of advanced materials. It is synthesized through a series of chemical reactions involving biphenyl and aniline derivatives, ultimately producing a triphenylamine core with carboxylic acid functional groups. The unique molecular architecture allows this compound to participate in various chemical interactions, including π-π stacking and hydrogen bonding, which are pivotal in its applications.</p>Formula:C39H27NO6Purezza:Min. 95%Peso molecolare:605.6 g/molTropodithietic acid
CAS:<p>Tropodithietic acid is a bioactive compound, which is a potent antibacterial agent derived from certain marine bacteria, including the genus Phaeobacter. This antibiotic is characterized by its ability to disrupt quorum sensing, a mechanism that bacteria use for communication and coordination of group behaviors, including virulence. By interfering with this process, tropodithietic acid impedes bacterial colonization and biofilm formation, effectively inhibiting pathogenic activity.</p>Purezza:Min. 95%Porfiromycin
CAS:<p>Porfiromycin is an antineoplastic antibiotic with action on DNA alkylation and cross-linking and is used for research on cancer treatment, particularly for hypoxic tumors.</p>Formula:C16H20N4O5Purezza:Min. 95 Area-%Colore e forma:PowderPeso molecolare:348.35 g/molN4-Methyl-5-(3,4,5-trimethoxybenzyl)-pyrimidine-2,4-diamine
CAS:<p>N4-Methyl-5-(3,4,5-trimethoxybenzyl)-pyrimidine-2,4-diamine is a synthetic organic compound, classified as an antimicrobial agent. This compound is developed through chemical synthesis processes, derived from pyrimidine analogs, and is commonly used in medicinal chemistry and pharmacology research. It operates by inhibiting key enzymes involved in the folic acid pathway, crucial for bacterial growth and proliferation. By targeting this pathway, the compound prevents nucleic acid synthesis, ultimately leading to bacterial cell death.</p>Formula:C15H20N4O3Purezza:Min. 95%Peso molecolare:304.34 g/molBeclabuvir
CAS:Beclabuvir is an investigational antiviral agent, which is synthetically derived with the purpose of targeting the hepatitis C virus (HCV). It functions as a non-nucleoside inhibitor, specifically inhibiting the HCV NS5B RNA-dependent RNA polymerase, a crucial enzyme necessary for viral replication. By obstructing the polymerase activity, Beclabuvir effectively impedes the replication cycle of the virus, thereby reducing viral load in infected individuals.Formula:C36H45N5O5SPurezza:Min. 95%Peso molecolare:659.84 g/molFoscarnet sodium
CAS:<p>Foscarnet sodium is a pyrophosphate analog antiviral agent with action on viral DNA polymerase and is used for treating cytomegalovirus and herpes simplex virus infections.</p>Formula:CNa3O5PPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:191.95 g/molDL-chloramphenicol
CAS:<p>DL-chloramphenicol is a broad-spectrum antibiotic, which is a synthetic compound derived from natural chloramphenicol originally isolated from the bacterium Streptomyces venezuelae. This compound exerts its effects by inhibiting bacterial protein synthesis. It binds to the 50S subunit of the bacterial ribosome, preventing peptide bond formation and consequently halting the growth of susceptible bacteria. The optical isomer, DL-chloramphenicol, contains equal parts of both D- and L- isomers, with the L-form being responsible for its antibiotic activity.</p>Formula:C11H12Cl2N2O5Purezza:Min. 95%Peso molecolare:323.13 g/molUrdamycin B
CAS:<p>Urdamycin B is an anthracycline antibiotic, which is derived from the bacterium *Streptomyces fradiae*. This compound acts by intercalating into DNA, disrupting the replication and transcription processes, leading to cell death. Its mode of action involves inhibiting topoisomerase II, an enzyme critical for DNA replication and cell cycle progression. This mechanism impairs cellular proliferation, making it effective against rapidly dividing cells.</p>Formula:C37H44O13Purezza:Min. 95%Peso molecolare:696.70 g/molNeticonazole hydrochloride
CAS:<p>Neticonazole hydrochloride is an antifungal agent, which is a synthetic imidazole derivative with potent antifungal properties. It is synthesized through a multi-step chemical process in a laboratory setting, designed to enhance its efficacy and stability. Its mode of action involves the inhibition of ergosterol synthesis, a critical component of fungal cell membranes. By hindering this pathway, Neticonazole hydrochloride compromises the integrity and function of the fungal cell membrane, ultimately leading to cell death.</p>Formula:C17H23ClN2OSPurezza:Min. 95%Peso molecolare:338.9 g/molPenciclovir diacetate
CAS:<p>Penciclovir diacetate is an antiviral compound, which is synthesized as a prodrug derivative of penciclovir. This compound originates from chemical modification processes designed to improve the pharmacokinetic properties of its active metabolite. Once administered, penciclovir diacetate undergoes in vivo conversion to penciclovir, an active nucleoside analog. The mode of action involves selective inhibition of viral DNA polymerase after being phosphorylated to its triphosphate form, thereby impeding viral DNA synthesis and replication.</p>Formula:C14H19N5O5Purezza:Min. 95%Peso molecolare:337.33 g/molHBV-IN-4
CAS:<p>HBV-IN-4 is an antiviral compound that serves as a potent and selective inhibitor of hepatitis B virus (HBV). It is derived from chemical synthesis with a focus on targeting the viral replication machinery. The mode of action involves interrupting the HBV lifecycle by inhibiting the functioning of viral polymerase, thereby preventing the synthesis of viral DNA and subsequent viral propagation.</p>Formula:C24H19ClFN5O3Purezza:Min. 95%Peso molecolare:479.9 g/molMagnamycin B
CAS:<p>Magnamycin B is an antifungal antibiotic, which is derived from natural sources through microbial fermentation. Its mode of action involves the inhibition of cell wall synthesis in pathogenic fungi, thereby disrupting essential processes required for their growth and proliferation. Magnamycin B is particularly effective against a range of fungal pathogens that affect agricultural and clinical settings.</p>Formula:C42H67NO15Purezza:Min. 95%Peso molecolare:826.00 g/molTriadimenol-tert-butylhydroxy
CAS:<p>Triadimenol-tert-butylhydroxy is a systemic fungicide, originating from synthetic chemical processes, characterized by its ability to inhibit fungal sterol biosynthesis. This sterol biosynthesis disruption occurs through the demethylation of lanosterol or 24-methylene dihydrolanosterol, which impedes the production of ergosterol, a crucial component in fungal cell membranes. The inhibition results in disrupted cell membrane integrity and impaired fungal growth, leading to effective control over a range of plant-pathogenic fungi.</p>Formula:C14H18ClN3O3Purezza:Min. 95%Peso molecolare:311.76 g/molImazamox-o-desmethyl
CAS:<p>Imazamox-o-desmethyl is a herbicide metabolite, which is derived from the biotransformation of the imazamox compound, typically occurring during degradation processes. Its mode of action involves targeting the acetohydroxyacid synthase (AHAS) enzyme—a critical component in the biosynthesis of branched-chain amino acids in plants. This inhibition disrupts plant growth, leading to effective weed control.</p>Formula:C14H17N3O4Purezza:Min. 95%Peso molecolare:291.3 g/molHerbimycin
CAS:<p>Herbimycin is an antibiotic, which is a natural product derived from Streptomyces bacteria. It functions primarily as a tyrosine kinase inhibitor, disrupting cellular signaling pathways by binding to the ATP-binding site of kinases and inhibiting phosphorylation events. This mode of action makes it an effective tool for scientists studying signal transduction processes and oncogenic transformation.</p>Formula:C30H42N2O9Purezza:Min. 95%Peso molecolare:574.66 g/molSofosbuvir impurity I
CAS:<p>Sofosbuvir impurity I is an organic chemical impurity often associated with the active pharmaceutical ingredient (API) Sofosbuvir, which is used in the treatment of hepatitis C. This impurity arises during the manufacturing process of Sofosbuvir as a byproduct. It is crucial to monitor and identify such impurities to ensure the safety, efficacy, and quality of the final pharmaceutical product.</p>Formula:C21H27FN3O9PPurezza:Min. 95%Peso molecolare:515.4 g/molBentaluron
CAS:<p>Bentaluron is a synthetic fungicide, which is a chemical compound developed to combat fungal pathogens in agriculture. Its source originates from rigorous industrial chemical synthesis, ensuring efficacy and stability. The mode of action of Bentaluron involves disrupting essential biochemical pathways within fungal cells, specifically targeting and inhibiting enzymes critical for fungal growth and metabolism. This precise interference prevents the synthesis of vital cellular components, ultimately halting the proliferation of the fungus.</p>Formula:C11H13N3OSPurezza:Min. 95%Peso molecolare:235.31 g/molPirlimycin HCl
CAS:<p>Pirlimycin HCl is an antibacterial product, which is a semi-synthetic derivative of the natural antibiotic lincomycin produced by Streptomyces lincolnensis. Its mode of action involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, thereby preventing the elongation of peptide chains. This action is particularly effective against Gram-positive bacteria, including Staphylococcus and Streptococcus species.</p>Formula:C17H31ClN2O5S·HClPurezza:Min. 95%Colore e forma:White PowderPeso molecolare:447.42 g/molPenipurdin A
CAS:Please enquire for more information about Penipurdin A including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C18H16O6Purezza:Min. 95%Peso molecolare:328.3 g/molPseudomonic acid F
CAS:Pseudomonic acid F is a naturally occurring secondary metabolite, which is derived from the bacterium *Pseudomonas fluorescens*. Its mode of action involves the inhibition of bacterial protein synthesis by targeting the bacterial isoleucyl-tRNA synthetase enzyme. This inhibition disrupts the addition of isoleucine to the growing polypeptide chain, effectively impeding bacterial growth and proliferation.Formula:C24H40O9Purezza:Min. 95%Peso molecolare:472.60 g/molLexithromycin
CAS:<p>Please enquire for more information about Lexithromycin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C38H70N2O13Purezza:Min. 95%Peso molecolare:762.97 g/molMoxifloxacin
CAS:<p>Moxifloxacin is a synthetic broad-spectrum antibiotic, which is derived from the fluoroquinolones class. It functions by inhibiting bacterial topoisomerase II (DNA gyrase) and topoisomerase IV, enzymes critical for DNA replication, transcription, repair, and recombination. The inhibition of these enzymes results in DNA breakage, thereby leading to bacterial cell death.</p>Formula:C21H24FN3O4Purezza:Min. 95%Peso molecolare:401.4 g/molGeneticin Disulfate (G418), Antibiotic for Culture Media Use Only
CAS:Geneticin is very efficient against gram-negative bacteria, however it is not applied for treating infections due to high renal toxicity. Geneticin and its resistance genes found application in the selection of transgenic cell lines including yeasts such as P. pastoris and S. serevisiae, other eukaryotic cell lines such as CHO or HEK293, but also plant cells and bacterial cells.Formula:C20H44N4O18S2Purezza:Min. 97.0 Area-%Peso molecolare:692.71 g/molRef: 3D-G-2400
10gPrezzo su richiesta25gPrezzo su richiesta50gPrezzo su richiesta100gPrezzo su richiesta250gPrezzo su richiesta-Unit-ggPrezzo su richiestaML303
CAS:<p>Please enquire for more information about ML303 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C21H16F3N3O2Purezza:Min. 95%Peso molecolare:399.4 g/molBoromycin
CAS:Boromycin is a macrolide antibiotic, which is derived from the fermentation of certain strains of Streptomyces bacteria. It operates as an ionophore with the ability to transport ions across lipid membranes, effectively disrupting ionic gradients. This mechanism of action compromises essential cellular processes in target organisms, thereby exerting its antimicrobial effects.Formula:C45H74BNO15Purezza:Min. 95%Peso molecolare:879.88 g/molBRL 42715
CAS:BRL 42715 is an antibacterial agent, which is a synthetic compound with a unique mechanism of action. This compound is derived from rational drug design aimed at targeting specific bacterial enzymes critical for cell wall synthesis. By irreversibly inhibiting these enzymes, BRL 42715 disrupts the bacterial cell wall formation, leading to cell lysis and death.Formula:C10H7N4NaO3SPurezza:Min. 95%Peso molecolare:286.24 g/molAnhydro erythromycin A
CAS:<p>Anhydro erythromycin A is a semi-synthetic derivative of erythromycin A, which has been shown to be an effective inhibitor of bacterial growth, showing higher selectivity for this inhibition. It is a prodrug that is activated by acid catalysis and can be used as a substitute against methicillin-resistant staphylococcus. Anhydro erythromycin A was developed with the goal of increasing its stability and its potency against methicillin-resistant Staphylococcus aureus, which has been shown to be resistant to erythromycin.</p>Formula:C37H65NO12Purezza:Min. 95%Colore e forma:White PowderPeso molecolare:715.91 g/molOmaciclovir
CAS:<p>Please enquire for more information about Omaciclovir including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C10H15N5O3Purezza:Min. 95%Peso molecolare:253.26 g/molM4284
CAS:<p>M4284 is a potent biochemical inhibitor, derived from synthetic organic compounds, designed to target specific enzymes within cell signaling pathways. This product functions by competitively binding to the active site of a target enzyme, effectively blocking its catalytic activity. The competitive inhibition mechanism employed by M4284 enables it to modulate enzymatic activity with high specificity, allowing researchers to dissect complex biochemical processes with precision.</p>Formula:C23H28N2O8Purezza:Min. 95%Peso molecolare:460.5 g/mol(+)-Madindoline A
CAS:<p>(+)-Madindoline A is a chemical substance that inhibits the growth of cancer cells. It has been shown to inhibit colon cancer cell proliferation and induce apoptosis by inhibiting signal pathways and suppressing inflammatory responses. (+)-Madindoline A is an experimental model for the study of bowel disease and inflammatory diseases, as it can be used to treat both bowel disease and inflammatory diseases. It also has inhibitory effects on the production of proinflammatory cytokines in human protein cells and natural compounds in experimental models. (+)-Madindoline A is found in small amounts in food compositions such as apples, carrots, cauliflower, celery, cucumbers, garlic, leeks, lettuce, onions, peas, peppers, potatoes and tomatoes.</p>Formula:C22H27NO4Purezza:Min. 95%Peso molecolare:369.45 g/molNortadalafil-N-(2-hydroxy)propyl
CAS:<p>Nortadalafil-N-(2-hydroxy)propyl is a chemotherapeutic agent, which is synthesized through the chemical modification of tadalafil. It is characterized as a small-molecule inhibitor, derived from the structural alteration of the well-known phosphodiesterase type 5 (PDE5) inhibitor. The mechanism of action involves the attenuation of PDE5 activity, leading to increased levels of cyclic guanosine monophosphate (cGMP) within targeted cellular pathways. This elevation in cGMP concentration results in vasodilation and increased blood flow, primarily investigated within the context of vascular and erectile tissue.</p>Formula:C24H23N3O5Purezza:Min. 95%Peso molecolare:433.5 g/molAscomycin
CAS:<p>Ascomycin is an immunosuppressant macrolide lactone, which is derived from the soil bacterium *Streptomyces hygroscopicus*. It functions primarily by inhibiting the T-cell activation pathway. The mechanism involves binding to the immunophilin FKBP-12, forming a complex that inhibits the calcium-dependent phosphatase, calcineurin. This inhibition prevents the dephosphorylation and subsequent translocation of nuclear factor of activated T cells (NFAT), which is crucial for the transcription of interleukin-2 and other cytokines. Consequently, this suppresses the activation and proliferation of T-cells, which are essential components of the adaptive immune response.</p>Formula:C43H69NO12Purezza:Min. 95%Peso molecolare:792.01 g/mol1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-6-fluoro-7-[3-(methylamino)azetidin-1-yl]-4-oxoquinoline-3-carboxylic acid
CAS:<p>1-(6-Amino-3,5-difluoropyridin-2-yl)-8-bromo-6-fluoro-7-[3-(methylamino)azetidin-1-yl]-4-oxoquinoline-3-carboxylic acid is a synthetically derived quinoline derivative, which is produced through advanced organic chemistry methodologies involving halogenated pyridines and quinoline frameworks. The compound functions primarily as an antibacterial agent, targeting bacterial topoisomerase enzymes, thereby disrupting DNA replication and transcription processes.</p>Formula:C19H15BrF3N5O3Purezza:Min. 95%Peso molecolare:498.3 g/molDimidazon
CAS:Dimidazon is a synthetic herbicide, which is derived from chemical synthesis processes involving aromatic and heterocyclic compounds. It possesses a mode of action that primarily inhibits specific enzymatic pathways required for plant growth, targeting essential biosynthesis mechanisms within the plant's cellular structure. This disruption leads to the cessation of vital processes, eventually causing plant death.Formula:C12H12N2O3Purezza:Min. 95%Peso molecolare:232.23 g/molPolymyxin B nonapeptide hydrochloride
CAS:<p>Polymyxin B nonapeptide hydrochloride is a potent antibiotic compound derived from the bacterium *Bacillus polymyxa*. As a cationic polypeptide, it exhibits its antibacterial activity by interacting with the lipopolysaccharides and phospholipids in the bacterial cell membrane, leading to increased permeability and ultimately causing cell lysis. The compound is specifically effective against a broad range of Gram-negative bacteria, making it crucial in studying antibiotic resistance mechanisms.</p>Formula:C43H74N14O11•(HCl)xPurezza:Min. 95%Peso molecolare:963.14 g/molKanamycin C
CAS:<p>Inhibitor of protein synthesis; aminoglycoside</p>Formula:C18H36N4O11Purezza:Min. 95%Peso molecolare:484.5 g/molBixlozone
CAS:<p>Bixlozone is a pharmaceutical compound that serves as an antimicrobial agent, developed from synthetic origins. It operates by targeting specific microbial pathways, effectively disrupting the synthesis of essential cellular components within pathogenic organisms. The active mechanisms of Bixlozone involve inhibiting enzymatic functions that are crucial for the survival and replication of these pathogens.</p>Formula:C12H13Cl2NO2Purezza:Min. 95%Peso molecolare:274.14 g/molAT-527
CAS:<p>AT-527 is an investigational antiviral compound, which is a nucleoside analog prodrug with a specific mode of action inhibiting viral RNA polymerase. This product is derived from synthetic organic chemistry processes, uniquely designed to interfere with the replication machinery of certain RNA viruses. Upon administration, AT-527 undergoes intracellular conversion to its active triphosphate form, which then incorporates into the viral RNA. This incorporation results in premature chain termination or erroneous RNA synthesis, effectively disrupting the viral replication cycle.</p>Formula:C24H33FN7O7PPurezza:Min. 95%Peso molecolare:581.5 g/molTunicamycin V
CAS:<p>Tunicamycin V is an antibiotic and nucleoside analog, which is a secondary metabolite derived from various Streptomyces species. It functions predominantly by inhibiting the initial step of N-linked glycosylation, a critical post-translational modification process in eukaryotic cells. This inhibition occurs through the blockage of UDP-N-acetylglucosamine: dolichyl-phosphate N-acetylglucosamine-1-phosphate transferase, thereby preventing the synthesis of dolichol-linked oligosaccharides and ultimately affecting protein folding and quality control mechanisms within the endoplasmic reticulum.</p>Formula:C38H62N4O16Purezza:Min. 95%Peso molecolare:830.9 g/molFinafloxacin
CAS:Finafloxacin is a fluoroquinolone antibacterial agent, which is a synthetic compound derived from the quinolone family. It functions through the inhibition of bacterial DNA gyrase and topoisomerase IV, crucial enzymes in the replication, transcription, and repair of bacterial DNA. This mechanism leads to the prevention of bacterial cell division and ultimately results in cell death.Formula:C20H19FN4O4Purezza:Min. 95%Peso molecolare:398.39 g/molMalformin C
CAS:<p>Malformin C is a cyclic pentapeptide, which is a secondary metabolite derived from certain strains of the fungus Aspergillus. Its mode of action involves disrupting cellular processes by interfering with cell division. Specifically, it is thought to affect mitotic spindle formation, leading to abnormal cell cycle progression.</p>Formula:C23H39N5O5S2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:529.72 g/molAmikacin B Sulfate
CAS:<p>Inhibitor of protein synthesis; aminoglycoside</p>Formula:C22H44N6O12xH2so4Purezza:Min. 95%Peso molecolare:584.62 g/molHodgkinsine B
CAS:<p>Hodgkinsine B is an indole alkaloid, which is a complex organic compound derived from natural sources. It is isolated from the leaves of certain Rubiaceae family plants, including Psychotria colorata. Hodgkinsine B is characterized by its unique trimeric structure that contributes to its pharmacological properties.</p>Formula:C33H38N6Purezza:Min. 95%Peso molecolare:518.7 g/molTromantadine hydrochloride
CAS:Prodotto controllato<p>Tromantadine hydrochloride is a synthetic antiviral compound, which is a derivative of adamantane. It originates from chemical synthesis, tailored specifically to target viral processes. Tromantadine hydrochloride primarily exerts its effects by inhibiting the penetration of virus particles into host cells and impeding the subsequent stages of viral replication. This mode of action effectively reduces the viral load and hinders the progression of the infection.</p>Formula:C16H28N2O2•HClPurezza:Min. 95%Peso molecolare:316.87 g/molEntecavir-13C2,15N
CAS:Entecavir-13C2,15N is an isotopically labeled antiviral agent, which is a synthetic nucleoside analogue derived from natural sources. Its mode of action involves selectively inhibiting the reverse transcription activity of the hepatitis B virus (HBV) polymerase. By mimicking the natural substrates of the viral polymerase, Entecavir-13C2,15N becomes incorporated into viral DNA, ultimately leading to chain termination and suppression of viral replication.Formula:C12H15N5O3Purezza:Min. 95%Peso molecolare:280.26 g/molIvermectin
CAS:Naturally produced by the soil bacterium Streptomyces avermitili, it is clinically used in the treatment of parasitosis in both humans and animals. Ivermectin is commercially available as a mixture of 80% 22, 23-dihydroavermectin B1a and 20% 22, 23-dihydroavermectin B1b. In 2020, Ivermectin indicated that it was a good antiviral agent in the treatment of SARS-CoV-2 and a new mechanism of action has been suggested. Ivermectin would act on importin α/β heterodimer and affect nuclear transport and the translocation of viral proteins.Formula:C48H74O14Purezza:85%MinPeso molecolare:875.1 g/molInteriotherinA
CAS:<p>InteriotherinA is a bioactive compound, which is derived from specific strains of bacteria. It operates through a sophisticated mode of action that involves modulating the activity of nerve cells by binding to particular receptors on their membranes. This interaction can alter ion channel function, thereby influencing the electrochemical signaling within these cells.</p>Formula:C29H28O8Purezza:Min. 95%Peso molecolare:504.5 g/molDesethyl chloroquine (diphosphate)
CAS:<p>Desethyl chloroquine (diphosphate) is a pharmacological compound, which is a derivative and metabolite of chloroquine. Chloroquine itself is a synthetic drug originally derived from quinoline. The mode of action of Desethyl chloroquine involves the interference with heme polymerization in malaria parasites. This process disrupts the detoxification of heme, a byproduct of hemoglobin digestion, thereby exhibiting antimalarial effects.</p>Formula:C16H28ClN3O8P2Purezza:Min. 95%Peso molecolare:487.8 g/molHsv-tk substrate
CAS:HSV-tk substrate is a nucleotide analogue, which is a synthetic compound derived from the herpes simplex virus thymidine kinase (HSV-tk) gene. This substrate is specifically phosphorylated by the HSV-tk enzyme, a property that provides significant utility in molecular biology and genetic research. The mode of action involves the selective phosphorylation of the substrate by HSV-tk, which is typically absent in mammalian cells but can be introduced via genetic engineering. Once phosphorylated, the substrate becomes toxic to the host cell, allowing researchers to selectively target and eliminate cells expressing the HSV-tk gene.Formula:C11H15N5O4Purezza:Min. 95%Peso molecolare:281.27 g/molNorvancomycin trifluoroacetate
CAS:Norvancomycin trifluoroacetate is an antibiotic compound, which is a glycopeptide derived from the bacterium Amycolatopsis orientalis. Its mode of action involves inhibiting bacterial cell wall synthesis. Specifically, Norvancomycin disrupts the cross-linking of peptidoglycan layers in the bacterial cell wall by binding to the D-alanyl-D-alanine terminus of cell wall precursors. This disruption weakens the bacterial cell wall, ultimately leading to cell lysis and death, thereby exerting a bactericidal effect.Formula:C65H73Cl2N9O24•(C2HF3O2)xPurezza:Min. 95%Tigecycline, Antibiotic for Culture Media Use Only
CAS:Tigecycline is an antibiotic specifically tailored for use in culture media, which is derived from glycylcycline, a structural analogue of minocycline. Its mode of action involves binding to the 30S ribosomal subunit, thereby inhibiting protein synthesis in a broad spectrum of Gram-positive and Gram-negative bacteria. This action is distinct and not easily circumvented by common resistance mechanisms, such as efflux or ribosomal protection proteins, making tigecycline an effective agent in controlling bacterial contamination during microbiological studies.Formula:C29H39N5O8Purezza:Min. 95 Area-%Peso molecolare:585.65 g/molRef: 3D-Q-101396
1gPrezzo su richiesta5gPrezzo su richiesta10gPrezzo su richiesta25gPrezzo su richiesta2500mgPrezzo su richiestaTioconazole
CAS:<p>Tioconazole is an antifungal agent, which is a synthetic derivative of imidazole with broad-spectrum activity against fungi. This compound is chemically synthesized through complex organic reactions to enhance its antimycotic efficacy. Tioconazole functions by inhibiting the synthesis of ergosterol, an essential component of the fungal cell membrane. By disrupting the ergosterol biosynthesis pathway, tioconazole destabilizes the fungal cell membrane, leading to increased permeability and eventual cell death.</p>Formula:C16H13Cl3N2OSPurezza:Min. 95%Peso molecolare:387.71 g/molCladospirone bisepoxide
CAS:Cladospirone bisepoxide is a naturally occurring bioactive compound, classified specifically as a fungal metabolite, which is derived from species within the Cladosporium genus. The compound exhibits a complex bisepoxide structure, contributing to its unique chemical properties. Its mode of action involves disrupting microbial cellular processes, displaying potent antimicrobial activity by interfering with the synthesis and functioning of vital cellular components in targeted microorganisms.Formula:C20H14O7Purezza:Min. 95%Peso molecolare:366.3 g/molACX-362E
CAS:<p>ACX-362E is a novel antibacterial agent, which is a synthetic compound derived from small-molecule chemical libraries with selective action on bacterial pathogens. The mode of action of ACX-362E involves the inhibition of bacterial cell wall synthesis, specifically targeting essential enzymes involved in the peptidoglycan biosynthesis pathway. This interference disrupts cell wall integrity, leading to bacterial lysis and cell death.</p>Formula:C18H20Cl2N6O2Purezza:Min. 95%Peso molecolare:423.3 g/molTebufenozide-1-hydroxyethyl
CAS:<p>Tebufenozide-1-hydroxyethyl is an insect growth regulator, which is a synthetic chemical derived from a modified benzoic acid structure. Its mode of action involves mimicking the molting hormone ecdysone, which disrupts the normal development process of insects by inducing premature molting. This specific interference targets lepidopteran larvae, leading to incomplete development and eventual death, thereby controlling pest populations effectively without harming non-target organisms.</p>Formula:C22H28N2O3Purezza:Min. 95%Peso molecolare:368.5 g/molFamciclovir-d4
CAS:<p>Famciclovir-d4 is a deuterium-labeled antiviral nucleoside analog, which is a synthetic derivative of the guanine analog famciclovir. This compound is sourced through advanced chemical synthesis where deuterium atoms replace specific hydrogen atoms, providing an isotopic label that aids in the tracking and analysis of the pharmaceutical compound within biological systems.</p>Formula:C14H19N5O4Purezza:Min. 95%Peso molecolare:325.36 g/mol(R)-(+)-Pantoprazole
CAS:<p>(R)-(+)-Pantoprazole is a proton pump inhibitor (PPI), which is derived from benzimidazole compounds. Its mode of action involves the selective and irreversible inhibition of the H+/K+ ATPase enzyme system, commonly known as the proton pump, located on the gastric parietal cells. By binding covalently to this enzyme, (R)-(+)-Pantoprazole effectively reduces gastric acid secretion, leading to an increase in gastric pH.</p>Formula:C16H15F2N3O4SPurezza:Min. 95%Peso molecolare:383.4 g/molAqabamycin B
CAS:Aqabamycin B is a novel antibiotic compound, which is derived from marine microorganisms. This secondary metabolite is isolated from a marine sponge-associated bacterium, showcasing the rich potential of oceanic sources for discovering new antimicrobial agents. The mode of action of Aqabamycin B involves inhibition of bacterial cell wall synthesis, disrupting the structural integrity and leading to cell lysis. Its efficacy extends predominantly to combatting multi-drug resistant bacterial strains.Formula:C16H10N2O6Purezza:Min. 95%Peso molecolare:326.26 g/molAvermectin b1a aglycone
CAS:Avermectin B1a aglycone is a potent antiparasitic agent, which is a semi-synthetic derivative of avermectins. Avermectins are naturally sourced from the microorganism *Streptomyces avermitilis*, known for producing macrolide compounds. The mode of action of Avermectin B1a aglycone involves binding to glutamate-gated chloride channels in nerve and muscle cells of invertebrates, leading to increased permeability and disruption of neurotransmission. This action ultimately results in paralysis and death of the targeted parasites.Formula:C34H48O8Purezza:Min. 95%Peso molecolare:584.7 g/molCarbazomycin D
CAS:<p>Carbazomycin D is a bioactive product classified as an antibiotic, which is derived from the bacterium Streptomyces. These actinomycetes are well-known for their ability to produce a wide range of secondary metabolites with antimicrobial properties. The mode of action of Carbazomycin D involves the inhibition of bacterial cell wall synthesis, effectively disrupting the growth and replication of gram-positive bacteria.</p>Formula:C17H19NO3Purezza:Min. 95%Peso molecolare:285.34 g/molHexazinone metabolite B
CAS:<p>Hexazinone metabolite B is a chemical byproduct of the breakdown of Hexazinone, which is an herbicide. This metabolite emerges from an extensive metabolic pathway in plants, fungi, and soil microorganisms as they degrade the parent compound. Its mode of action involves interacting with plant processes, potentially affecting growth and development, as it may influence photosynthetic pathways or other vital physiological functions.</p>Formula:C11H18N4O2Purezza:Min. 95%Peso molecolare:238.29 g/molAphidicolin
CAS:<p>Aphidicolin is a tetracyclic diterpenoid that acts as a potent inhibitor of DNA polymerase. Derived from the fungus *Cephalosporium aphidicola*, it is primarily identified for its ability to impede DNA synthesis by targeting eukaryotic DNA polymerase α. This selective inhibition disrupts replication processes, making it a crucial tool for studying cell cycle dynamics.</p>Formula:C20H34O4Purezza:Min. 95%Peso molecolare:338.48 g/molPyraziflumid
CAS:Pyraziflumid is a fungicide, which is chemically synthesized with a specific mode of action as a succinate dehydrogenase inhibitor (SDHI). This compound is designed to target mitochondrial complex II, disrupting critical energy production within fungal cells. The inhibition of succinate dehydrogenase prevents the fungi from efficiently undergoing respiration, ultimately leading to cell death.Formula:C18H10F5N3OPurezza:Min. 95%Peso molecolare:379.3 g/molHexazinone metabolite E
CAS:Hexazinone metabolite E is a degradation product of the herbicide Hexazinone, which is derived from synthetic chemical processes. This metabolite emerges as a result of the biochemical breakdown of Hexazinone in soil and water environments. The mode of action involves the contamination and persistence in various environmental matrices, making it a key compound of interest for understanding the environmental impact of herbicide application. Hexazinone initially acts by inhibiting photosynthesis in plants, and its metabolites, including metabolite E, provide insights into the degradation pathways and long-term behavior of the herbicide in ecosystems.Formula:C10H15N3O4Purezza:Min. 95%Peso molecolare:241.24 g/mol9,11β-Dichloro-17,21-dihydroxy-16β-methyl-pregna-1,4-diene-3,20-dione dipropionate
CAS:9,11Beta-Dichloro-17,21-dihydroxy-16beta-methyl-pregna-1,4-diene-3,20-dione dipropionate is a synthetic corticosteroid, which is derived from chemical synthesis in laboratories. It functions by mimicking the actions of naturally occurring corticosteroids in the body, modulating immune responses and suppressing inflammatory mediators at the cellular level.Formula:C28H36Cl2O6Purezza:Min. 95%Peso molecolare:539.50 g/molSulfasymazine
CAS:<p>Sulfasymazine is a synthetic antibacterial agent, which is derived from sulfonamide compounds. These compounds originate from chemical synthesis processes involving the introduction of sulfonamide groups to aromatic amines, creating potent inhibitors of bacterial growth. Sulfasymazine functions by interfering with the synthesis of folic acid within bacterial cells. It inhibits the enzyme dihydropteroate synthase, which is crucial for the production of dihydrofolate, a precursor of folic acid. This disruption hampers nucleic acid synthesis, impeding bacterial proliferation.</p>Formula:C13H17N5O2SPurezza:Min. 95%Peso molecolare:307.37 g/molErythromycin propionate
CAS:<p>Erythromycin propionate is an antibiotic, which is derived from the bacterium *Saccharopolyspora erythraea*. This compound functions by inhibiting protein synthesis in susceptible bacteria, specifically targeting the 50S ribosomal subunit. Erythromycin propionate achieves this by binding to the ribosomal RNA, thereby preventing the translocation step of protein elongation.</p>Formula:C40H71NO14Purezza:Min. 95%Peso molecolare:790 g/molCefepime dihydrochloride monohydrate, Antibiotic for Culture Media Use Only
CAS:<p>Cefepime dihydrochloride monohydrate is a fourth-generation cephalosporin antibiotic utilized in scientific research, specifically formulated for culture media applications. It is derived from semi-synthetic processes, showcasing a broad spectrum of activity predominantly against Gram-positive and Gram-negative bacteria. The mode of action of cefepime involves the inhibition of bacterial cell wall synthesis by binding to penicillin-binding proteins, which interferes with peptidoglycan cross-linking, ultimately leading to cell lysis and death.</p>Formula:C19H28Cl2N6O6S2Purezza:Min. 98 Area-%Peso molecolare:571.5 g/molGentamicin B sulfate
CAS:<p>Gentamicin B sulfate is an aminoglycoside antibiotic, which is produced through the fermentation process involving the actinomycete Micromonospora purpurea. This antibiotic functions primarily by binding to the 30S ribosomal subunit of bacteria, thereby inhibiting protein synthesis. This action disrupts the initiation of protein chain formation, ultimately leading to bacterial cell death. Gentamicin B sulfate is particularly effective against a variety of Gram-negative bacteria and some Gram-positive strains.</p>Formula:C19H40N4O14SPurezza:Min. 95%Peso molecolare:580.60 g/molCeftarolin fosamil
CAS:<p>Ceftaroline fosamil is an advanced antibiotic, which is a cephalosporin derived from synthetic sources with a broad spectrum of activity. It is a prodrug that, once metabolized, becomes active in the body, binding to penicillin-binding proteins (PBPs) of bacteria. This binding inhibits the proteins responsible for cell wall synthesis, leading to bacterial cell lysis and death.</p>Formula:C22H21N8O8PS4Purezza:Min. 95%Peso molecolare:684.69 g/molLenacapavir
CAS:<p>Lenacapavir is a capsid inhibitor with a mode of action that interferes with the HIV capsid protein, disrupting multiple stages of the viral lifecycle. It is used for treating multidrug-resistant HIV infections.</p>Formula:C39H32ClF10N7O5S2Purezza:Min. 95%Colore e forma:PowderPeso molecolare:968.28 g/molAtramycin A
CAS:Atramycin A is an antibiotic, which is derived from the Streptomyces genus, a prolific source of bioactive compounds. Streptomyces species are renowned for their ability to produce a vast array of secondary metabolites with diverse pharmacological activities. Atramycin A operates primarily through the inhibition of bacterial protein synthesis. It achieves this by binding to bacterial ribosomal subunits, thus interfering with peptide chain elongation and effectively halting bacterial growth.Formula:C25H24O9Purezza:Min. 95%Peso molecolare:468.50 g/molDemethylbleomycin A2 sulfate
CAS:Demethylbleomycin A2 sulfate is an antineoplastic agent, which is derived from the bacterium Streptomyces verticillus. This compound functions by binding to DNA, inducing strand breaks and inhibiting DNA synthesis, ultimately leading to apoptosis or programmed cell death. Its mechanism of action involves the generation of free radicals, which cause oxidative damage to the DNA strands, impairing cellular replication and tumor growth.Formula:C55H84N17O21S3Purezza:Min. 95%Peso molecolare:1,415.6 g/molMetolachlor mercapturate
CAS:<p>Metolachlor mercapturate is a metabolite of the herbicide Metolachlor, which is derived from the degradation of the primary active ingredient found in various agricultural herbicide formulations. It is formed through biotransformation processes in plants, soil, and water, where the parent compound undergoes enzymatic reactions leading to its metabolic products. The primary mode of action involves the inhibition of elongase enzymes, which are crucial for the synthesis of fatty acids in plants, thus preventing cell division and impacting weed growth effectively.</p>Formula:C20H30N2O5SPurezza:Min. 95%Peso molecolare:410.5 g/molBalapiravir hydrochloride
CAS:<p>Balapiravir hydrochloride is an antiviral agent, which is synthesized through chemical processes. It operates as a prodrug, meaning it is metabolized in the body to produce the active compound that inhibits viral replication. The mode of action of Balapiravir involves targeting the viral RNA polymerase, an essential enzyme for the replication of viral genomes. By inhibiting this enzyme, the drug effectively reduces viral load within the host, impairing the spread and establishment of the virus.</p>Formula:C21H31ClN6O8Purezza:Min. 95%Peso molecolare:531 g/molSideroxylin
CAS:Sideroxylin is a C-methylated flavone with action as an antimicrobial agent against Staphylococcus aureus and is used for research on antimicrobial and anticancer properties.Formula:C18H16O5Purezza:Min. 95%Peso molecolare:312.3 g/molLeptomycin A
CAS:<p>Leptomycin A is a Streptomyces-produced inhibitor, which is derived from the bacterium Streptomyces spiroverticillatus. It functions by specifically binding to and inhibiting the CRM1 (exportin 1), a nuclear export receptor. This action blocks the nuclear export of proteins that contain a leucine-rich nuclear export signal (NES), thereby leading to their accumulation within the nucleus. The inhibition of CRM1 disrupts various cellular processes, including cell cycle regulation and signal transduction pathways.</p>Formula:C32H46O6Purezza:Min. 95%Peso molecolare:526.7 g/mol1-Chloro-2,2-bis(4'-chlorophenyl)ethane
CAS:<p>1-Chloro-2,2-bis(4'-chlorophenyl)ethane is an organochlorine pesticide known for its agricultural applications. It is a synthetic product derived from chlorinated hydrocarbons. It functions primarily through its mode of action as an insecticide by interfering with the nervous system of insects. It disrupts normal nerve function by causing prolonged opening of sodium channels in nerve cells, leading to hyperexcitation and eventual paralysis of the target pests.</p>Formula:C14H11Cl3Purezza:Min. 95%Peso molecolare:285.6 g/molBalapiravir
CAS:Balapiravir is an antiviral agent, which is a synthetic derivative based on natural compounds, specifically designed to inhibit the replication of various viral pathogens. The source of Balapiravir integrates bio-based elements with modifications to enhance its therapeutic efficacy.Formula:C21H30N6O8Purezza:Min. 95%Peso molecolare:494.5 g/molChlorsulfuron-5-hydroxy
CAS:<p>Chlorsulfuron-5-hydroxy is a herbicide derivative, specifically an active metabolite of chlorsulfuron, which is a sulfonylurea herbicide. This compound is derived from synthetic chemistry processes that focus on altering the molecular structure of chlorsulfuron to enhance its properties or study its breakdown. The mode of action of Chlorsulfuron-5-hydroxy involves the inhibition of the enzyme acetolactate synthase (ALS), which plays a crucial role in the biosynthesis of branched-chain amino acids in plants such as valine, leucine, and isoleucine. This inhibition disrupts protein synthesis, leading to halted cell division and plant growth.</p>Formula:C12H12ClN5O5SPurezza:Min. 95%Peso molecolare:373.77 g/molMtbHU-IN-1
CAS:<p>MtbHU-IN-1 is a small-molecule inhibitor designed specifically for targeting the HU protein in Mycobacterium tuberculosis. This compound is derived through rational drug design and computational modeling efforts, exploiting the vulnerabilities of the bacterial DNA-binding proteins. Its mode of action involves binding to the HU protein, inhibiting its function, which is crucial for DNA structuring and stability within the bacterial cell. By disrupting HU protein function, MtbHU-IN-1 impairs bacterial chromosomal architecture, leading to an inability to replicate and ultimately cell death.</p>Formula:C44H36N4O12S2Purezza:Min. 95%Peso molecolare:876.9 g/molPicloxidina
CAS:<p>Picloxidina is a chlorhexidine-based antiseptic, which is a synthetic compound with broad-spectrum antimicrobial activity. Its mode of action involves disrupting microbial cell membranes, leading to leakage of cellular contents and subsequent cell death. Picloxidina has been utilized extensively in ophthalmology due to its effectiveness in controlling ocular infections.</p>Formula:C20H24Cl2N10Purezza:Min. 95%Peso molecolare:475.4 g/molAvermectin a1a
CAS:<p>Avermectin A1a is a macrocyclic lactone used primarily as an anthelmintic and insecticide. It is derived from the fermentation of the soil bacterium *Streptomyces avermitilis*. The compound works through a neurotoxic mode of action, binding to glutamate-gated chloride channels in nerve and muscle cells of invertebrates, leading to paralysis and subsequent death of the parasites. This mechanism is highly specific, primarily affecting nematodes and arthropods.</p>Formula:C49H74O14Purezza:90%Peso molecolare:887.1 g/molKanzonol C
CAS:<p>Please enquire for more information about Kanzonol C including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formula:C25H28O4Purezza:Min. 95%Peso molecolare:392.5 g/molPK150
CAS:PK150 is a soil amendment product, which is derived from natural mineral sources with a specific focus on enhancing plant growth through optimized nutrient uptake efficiency. This product works by modifying the soil's physical and chemical properties, thereby improving the availability and mobility of essential nutrients like phosphorus (P) and potassium (K), which are crucial for the development and yield of plants.Formula:C15H8ClF5N2O3Purezza:Min. 95%Peso molecolare:394.68 g/molOxaquin
CAS:<p>Oxaquin is a synthetic antibiotic, which is a derivative of the fluoroquinolone class, developed through chemical synthesis. It disrupts bacterial DNA replication by inhibiting the DNA gyrase and topoisomerase IV enzymes, which are crucial for DNA synthesis and repair. This mode of action prevents bacterial cells from dividing and leading to cell death.</p>Formula:C31H33F2N4O11PPurezza:Min. 95%Peso molecolare:706.6 g/molOfloxacin d3 hydrochloride
CAS:<p>Ofloxacin d3 hydrochloride is a deuterated form of the quinolone antibiotic, which is a synthetic derivative designed for research purposes. It is sourced from the fluorinated carboxyquinolone class, where deuterium atoms replace certain hydrogen atoms to study metabolic pathways involving ofloxacin with minimal isotopic interference. Ofloxacin d3 inhibits bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication, transcription, and repair. By stabilizing the transient cleavable complex with DNA, it prevents the ligation of DNA strands, leading to bacterial cell death. This compound is utilized primarily in laboratory settings for studying the pharmacokinetics and biodistribution of quinolones, as well as for elucidating resistance mechanisms in bacterial strains. Its stable isotopic composition makes it ideal for advanced analytical techniques such as mass spectrometry. Through these investigations, insights into drug metabolism, efficacy, and resistance can be gleaned, contributing to the broader understanding of quinolone antibiotic activity.</p>Formula:C18H21ClFN3O4Purezza:Min. 95%Peso molecolare:400.8 g/molFomidacillin
CAS:Please enquire for more information about Fomidacillin including the price, delivery time and more detailed product information at the technical inquiry form on this pageFormula:C24H28N6O10SPurezza:Min. 95%Peso molecolare:592.60 g/molN-Nitroso-N-phenylbenzylamine
CAS:N-Nitroso-N-phenylbenzylamine is a nitroso compound, which is synthesized through a chemical reaction involving nitrosation. It arises typically from the interaction of secondary amines and nitrosating agents. This compound functions as a potential mutagen due to its ability to form reactive intermediates that can interact with DNA. These intermediates can lead to modifications in the DNA structure, potentially causing mutations.Formula:C13H12N2OPurezza:Min. 95%Peso molecolare:212.25 g/molKasugamycin
CAS:Kasugamycin is an aminoglycoside antibiotic, which is derived from the actinomycete Streptomyces kasugaensis. Its mode of action involves the inhibition of protein synthesis by interfering with the function of the 30S ribosomal subunit, ultimately preventing the growth and proliferation of sensitive organisms. In agricultural contexts, Kasugamycin is primarily utilized to control bacterial and fungal diseases in a variety of crops, including rice and fruit trees. It is particularly effective against Xanthomonas oryzae, which causes bacterial leaf blight in rice, and other pathogenic organisms detrimental to plant health. The application of Kasugamycin has been an important tool for integrated pest management programs focusing on sustainable agricultural practices. As a compound with a specific mode of activity, it helps to reduce the environmental impact typically associated with broader-spectrum antibiotics, while offering target-specific disease control. Its careful application supports the minimization of resistance development, ensuring continued efficacy in protecting crop yields.Formula:C14H25N3O9Purezza:Min. 95%Peso molecolare:379.36 g/mol
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