Antimicrobiens
Les antimicrobiens sont des agents qui détruisent ou inhibent la croissance des microorganismes, y compris les bactéries, les virus, les champignons et les parasites. Ces composés sont essentiels dans la prévention et le traitement des infections, jouant un rôle crucial en médecine, en agriculture et dans l'industrie alimentaire. Chez CymitQuimica, nous proposons une vaste gamme d'antimicrobiens de haute qualité et pureté, adaptés à diverses applications scientifiques et industrielles. Notre catalogue comprend des antibiotiques, des antifongiques, des antiviraux et des désinfectants, tous conçus pour répondre aux besoins de la recherche et du développement, ainsi qu'aux applications cliniques et de production. Avec nos produits, les professionnels peuvent garantir l'efficacité et la sécurité dans le contrôle des infections et la protection de la santé publique.
Sous-catégories appartenant à la catégorie "Antimicrobiens"
- Antibiotiques(4.111 produits)
- Antifongiques(835 produits)
- Antiparasitaires(704 produits)
- Antiviraux(762 produits)
2422 produits trouvés pour "Antimicrobiens"
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Aqabamycin B
CAS :<p>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.</p>Formule :C16H10N2O6Degré de pureté :Min. 95%Masse moléculaire :326.26 g/molAqabamycin C
CAS :<p>Aqabamycin C is an antibiotic compound, which is derived from marine bacteria, specifically, the actinomycete strain found in marine environments. Its mode of action involves the disruption of bacterial cell wall synthesis, making it particularly effective against certain gram-negative bacteria. This antibiotic selectively inhibits pathogens by interfering with their essential cellular processes.</p>Formule :C16H10N2O5Degré de pureté :Min. 95%Masse moléculaire :310.26 g/molClindamycin-2,4-diphosphate
CAS :<p>Clindamycin-2,4-diphosphate is a phosphorylated derivative of the antibiotic clindamycin, which is a semi-synthetic lincosamide antibiotic originally derived from Streptomyces lincolnensis. Its mode of action involves the inhibition of bacterial protein synthesis by binding to the 50S ribosomal subunit, thereby preventing peptide chain elongation during translation. This mechanism effectively disrupts protein production in susceptible bacteria, leading to their growth inhibition or death.</p>Formule :C18H35ClN2O11P2SDegré de pureté :Min. 95%Masse moléculaire :584.94 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>Formule :C16H15F2N3O4SDegré de pureté :Min. 95%Masse moléculaire :383.4 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>Formule :C10H6ClFN2O2Degré de pureté :Min. 95%Masse moléculaire :240.62 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>Formule :C13H22NO4PSDegré de pureté :Min. 95%Masse moléculaire :322.38 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>Formule :C14H19N5O4Degré de pureté :Min. 95%Masse moléculaire :325.36 g/molBPH-1358
CAS :<p>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.</p>Formule :C32H28N6O2Degré de pureté :Min. 95%Masse moléculaire :528.6 g/molThiabendazole NH d6
CAS :<p>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.</p>Formule :C10H7N3SDegré de pureté :Min. 95%Masse moléculaire :207.29 g/mol4'-Ethynyl-2'-deoxyadenosine
CAS :<p>4'-Ethynyl-2'-deoxyadenosine is a deoxynucleoside analogue, which is synthesized through chemical processes. This compound acts as an antiviral agent, primarily targeting the viral replication machinery. Its mode of action involves the incorporation into viral DNA by mimicking natural nucleosides, which subsequently inhibits the enzymatic activity of reverse transcriptase. This inhibition disrupts the synthesis of viral DNA, effectively curtailing viral replication.</p>Formule :C12H13N5O3Degré de pureté :Min. 95%Masse moléculaire :275.26 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>Formule :C22H28N2O3Degré de pureté :Min. 95%Masse moléculaire :368.5 g/molClarithromycin - EP
CAS :<p>A macrolide, broad-spectrum antibiotic that targets cytochrome P4503A4 (CYP3A4). Clarithromycin has been used to potentiate the pharmacological effects of some drugs that are metabolised by the cytochrome P450.</p>Formule :C38H69NO13Degré de pureté :Min. 95%Masse moléculaire :747.95 g/molCladospirone bisepoxide
CAS :<p>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.</p>Formule :C20H14O7Degré de pureté :Min. 95%Masse moléculaire :366.3 g/molTioconazole
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>Formule :C16H13Cl3N2OSDegré de pureté :Min. 95%Masse moléculaire :387.71 g/molTigecycline, Antibiotic for Culture Media Use Only
CAS :<p>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.</p>Formule :C29H39N5O8Degré de pureté :Min. 95 Area-%Masse moléculaire :585.65 g/molHsv-tk substrate
CAS :<p>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.</p>Formule :C11H15N5O4Degré de pureté :Min. 95%Masse moléculaire :281.27 g/molEntecavir-13C2,15N
CAS :<p>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.</p>Formule :C12H15N5O3Degré de pureté :Min. 95%Masse moléculaire :280.26 g/molSitafloxacin
CAS :<p>Sitafloxacin is an antibacterial agent belonging to the fluoroquinolone class of antibiotics, which is synthetically derived from chemical processes involving fluorinated quinolones. Its mode of action involves the inhibition of bacterial DNA gyrase and topoisomerase IV, enzymes crucial for bacterial DNA replication and transcription. By interfering with these enzymes, Sitafloxacin effectively hampers bacterial DNA synthesis, leading to the eventual demise of the bacterial cell.</p>Formule :C19H18ClF2N3O3Degré de pureté :Min. 95%Couleur et forme :SolidMasse moléculaire :409.81 g/molBensulide-oxon
CAS :<p>Bensulide-oxon is a metabolite derived from the organophosphate pesticide bensulide, which is predominantly used in agricultural settings. It forms as a result of environmental or biological processes that involve the oxidation of bensulide. As a potent acetylcholinesterase (AChE) inhibitor, bensulide-oxon disrupts normal neuronal signaling by preventing the breakdown of the neurotransmitter acetylcholine, leading to an accumulation that affects the nervous systems of target organisms.</p>Formule :C14H24NO5PS2Degré de pureté :Min. 95%Masse moléculaire :381.5 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>Formule :C17H14ClF3N2O6Degré de pureté :Min. 95%Masse moléculaire :434.7 g/molChloraniformethan
CAS :<p>Please enquire for more information about Chloraniformethan including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formule :C9H7Cl5N2ODegré de pureté :Min. 95%Masse moléculaire :336.4 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>Formule :C33H38N6Degré de pureté :Min. 95%Masse moléculaire :518.7 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>Formule :C10H13N3OSDegré de pureté :Min. 95%Masse moléculaire :223.3 g/molAmikacin B Sulfate
CAS :<p>Inhibitor of protein synthesis; aminoglycoside</p>Formule :C22H44N6O12xH2so4Degré de pureté :Min. 95%Masse moléculaire :584.62 g/molTebufloquin
CAS :<p>Tebufloquin is an insecticide, which is a synthetic compound designed to target specific pests. It is derived from chemical synthesis with a mode of action that interferes with critical biological pathways in insects, rendering them unable to survive or reproduce. Tebufloquin works primarily by targeting the nervous system of insects, leading to paralysis and eventual death.</p>Formule :C17H20FNO2Degré de pureté :Min. 95%Masse moléculaire :289.34 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>Formule :C23H39N5O5S2Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :529.72 g/mol25-Desacetyl rifapentin
CAS :<p>25-Desacetyl rifapentin is a derivative of rifapentin, an antibiotic belonging to the rifamycin class, sourced from the bacterial species *Amycolatopsis rifamycinica*. This compound functions by inhibiting bacterial DNA-dependent RNA polymerase, which is crucial for transcription in susceptible bacterial strains. By inhibiting this enzyme, 25-Desacetyl rifapentin effectively hampers RNA synthesis, ultimately leading to bacterial cell death.</p>Formule :C45H62N4O11Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :834.99 g/molBO3482
CAS :<p>Please enquire for more information about BO3482 including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>Formule :C14H20N2NaO5S2Degré de pureté :Min. 95%Masse moléculaire :383.4 g/molDimethenamid-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>Formule :C12H17NO4SDegré de pureté :Min. 95%Masse moléculaire :271.33 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>Formule :C38H62N4O16Degré de pureté :Min. 95%Masse moléculaire :830.9 g/mol2-(1-Hydroxyethyl)-6-ethylaniline
CAS :<p>2-(1-Hydroxyethyl)-6-ethylaniline is an organic chemical compound, which is often utilized as an intermediate in the synthesis of dyes, pigments, and other industrial chemicals. This compound is derived from aromatic amines and undergoes specific chemical reactions that enable its functionality in various synthetic processes.</p>Formule :C10H15NODegré de pureté :Min. 95%Masse moléculaire :165.23 g/molDihydropenicillin F potassium
CAS :<p>Dihydropenicillin F potassium is a novel antibiotic compound, which is semisynthetic in nature, derived from the penicillin family. It is sourced through the modification of natural penicillins, bringing about enhanced stability and efficacy against certain resistant bacterial strains. The mode of action involves the inhibition of bacterial cell wall synthesis, primarily targeting the penicillin-binding proteins (PBPs). This disruption consequently leads to cell lysis and the eventual bacterial death.</p>Formule :C14H22N2O4S•KDegré de pureté :Min. 95%Masse moléculaire :353.5 g/molNocardamine
CAS :<p>Nocardamine is a siderophore-based antioxidant, which is naturally derived from the soil-dwelling actinobacteria known as Streptomyces. Its primary mode of action involves the chelation of metal ions, effectively sequestering them and preventing metal-catalyzed oxidation reactions. By binding to iron and other transition metals, Nocardamine mitigates oxidative stress at a cellular level, which could otherwise contribute to cellular damage and dysfunction.</p>Formule :C27H48N6O9Degré de pureté :Min. 95%Masse moléculaire :600.71 g/molCurvularin
CAS :<p>Curvularin is a secondary metabolite, which is derived from the fungal genus *Curvularia*. This compound is produced through the natural biosynthetic pathways of filamentous fungi, specifically isolated from strains such as *Curvularia lunata*. Curvularin exerts its biological activity primarily through modulation of microtubule dynamics, making it a significant subject of study in cell biology. It disrupts the polymerization processes, impacting the assembly and stability of microtubules, which are critical components of the cytoskeleton involved in cell division, intracellular transport, and structural integrity.</p>Degré de pureté :Min. 95%Azithromycin Dihydrate
CAS :<p>Azithromycin Dihydrate is a macrolide antibiotic and is used for the treatment of various bacterial infections. It binds to the 23S rRNA of the 50S ribosomal subunit, inhibiting protein synthesis</p>Formule :C38H72N2O12·2H2ODegré de pureté :Min. 95 Area-%Couleur et forme :PowderMasse moléculaire :785.02 g/molPolymyxin B1-I
CAS :<p>Polymyxin B1-I is an antimicrobial peptide, which is sourced from the bacterium *Bacillus polymyxa*. It functions by interacting with and disrupting the bacterial cell membranes. The polypeptide inserts into the phospholipid bilayer, causing increased permeability and eventual cell lysis. This mechanism is particularly effective against Gram-negative bacteria due to the structural composition of their outer membranes.</p>Formule :C56H98N16O13Masse moléculaire :1,203.5 g/molNarasin sodium
CAS :<p>Narasin sodium is an ionophore antibiotic, which is a type of compound that facilitates ion transport across biological membranes. It is derived from the fermentation of the bacterium *Streptomyces aureofaciens*. The mode of action involves the disruption of ion gradients in target organisms, specifically inhibiting the growth of certain pathogenic bacteria and protozoa by altering their cellular ionic balance.</p>Formule :C43H71NaO11Degré de pureté :Min. 95%Masse moléculaire :787.02 g/molPefloxacin-d3
CAS :Produit contrôlé<p>Pefloxacin-d3 is a deuterated fluoroquinolone antibiotic, which is a synthetic derivative of pefloxacin utilized primarily for research purposes. This compound is chemically modified to include deuterium atoms, a stable isotope of hydrogen, thus offering unique properties essential for precise quantitative analysis in pharmacokinetic studies.</p>Formule :C17H17D3FN3O3Degré de pureté :Min. 95%Masse moléculaire :336.38 g/molFlucloxacillin
CAS :<p>Flucloxacillin is a beta-lactam antibiotic, which is derived from the penicillin family. It is synthetically produced through chemical modification to enhance its stability against beta-lactamase enzymes. The mode of action of flucloxacillin involves inhibiting bacterial cell wall synthesis. It binds to penicillin-binding proteins (PBPs) located inside the bacterial cell wall, which in turn inhibits the transpeptidation or cross-linking of peptidoglycan chains. This action leads to cell lysis and ultimately, bacterial death.</p>Formule :C19H17ClFN3O5SDegré de pureté :Min. 95%Masse moléculaire :453.87 g/molNikkomycin Z from streptomyces tendae
CAS :<p>Nikkomycin Z is an antifungal agent, which is a secondary metabolite isolated from the bacterium Streptomyces tendae. This compound functions as a competitive inhibitor of chitin synthase, an essential enzyme responsible for the synthesis of chitin, a vital component of the fungal cell wall. By inhibiting this enzyme, Nikkomycin Z disrupts the structural integrity of the fungal cell wall, leading to impaired growth and cell lysis in susceptible fungi.</p>Formule :C20H25N5O10Degré de pureté :Min. 95%Masse moléculaire :495.4 g/molLeptomycin B
CAS :<p>Leptomycin B is a bacterial secondary metabolite, which is derived from the bacterium Streptomyces sp. This compound is a potent nuclear export inhibitor with a mechanism of action that targets and inhibits the export receptor CRM1 (Chromosomal Maintenance 1), also known as Exportin 1. By binding irreversibly to CRM1, Leptomycin B prevents the nuclear export of proteins and RNA, disrupting the nuclear-cytoplasmic transport essential for cell function.</p>Formule :C33H48O6Degré de pureté :Min. 95%Masse moléculaire :540.73 g/molSpiramycin I
CAS :<p>Spiramycin I is a macrolide antibiotic with action on bacterial protein synthesis inhibition and is used for treating toxoplasmosis and bacterial infections.</p>Formule :C43H74N2O14Degré de pureté :Min. 95 Area-%Couleur et forme :White PowderMasse moléculaire :843.05 g/molPolymyxin B nonapeptide TFA
CAS :<p>Polymyxin B nonapeptide TFA is an antimicrobial peptide, which is derived from the bacterium *Bacillus polymyxa*. This peptide is a truncated form of polymyxin B, lacking the fatty acyl tail and N-terminal amino acid, resulting in a nonapeptide structure. Its mode of action involves binding to the lipid A portion of bacterial lipopolysaccharides, thereby disrupting the integrity of the bacterial cell membrane. This interaction increases membrane permeability and leads to cell lysis, particularly in Gram-negative bacteria.</p>Formule :C53H79F15N14O21Degré de pureté :Min. 95%Masse moléculaire :1,533.3 g/mol4-Demethyl daunomycinone
CAS :<p>4-Demethyl daunomycinone is an anthracycline derivative, which is a natural or semi-synthetic compound derived from the bacterium *Streptomyces*. It is primarily studied for its potential use in anticancer therapies, given its structural similarity to other well-known anthracyclines like daunorubicin and doxorubicin. These compounds are known to intercalate into DNA, thereby disrupting the function of DNA and RNA synthesis, leading to the inhibition of cell proliferation.</p>Formule :C20H16O8Degré de pureté :Min. 95%Masse moléculaire :384.34 g/molMicafungin FR-179642 impurity (acid)
CAS :<p>Micafungin is an antifungal drug that inhibits the synthesis of ergosterol, a vital component of fungal cell membranes. It is a cyclic peptide with a lipophilic fatty acid chain that has been modified to allow penetration into cells. Micafungin is active against Candida and Aspergillus species and has shown activity against some strains of Cryptococcus neoformans. The MIC (minimum inhibitory concentration) for this drug ranges from 0.06 to 1 microgram/mL, depending on the bacterial strain being tested. Micafungin FR-179642 impurity (acid) is an impurity in micafungin that can be present as trace amounts in the final product and may contribute to hemolytic activity. This impurity is formed by hydrolysis during the synthesis process.</p>Formule :C35H52N8O20SDegré de pureté :Min. 95 Area-%Couleur et forme :White PowderMasse moléculaire :936.9 g/molSisomicin sulfate
CAS :<p>Sisomicin sulfate is a sulfate salt form of sisomicin with similar action and applications as sisomicin.</p>Formule :C19H37N5O7·5H2SO4Degré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :1,385.45 g/molCecropin A
CAS :<p>Cecropin A is an antimicrobial peptide, which is derived from the immune systems of insects, specifically moths. It displays potent antimicrobial properties through its ability to disrupt bacterial cell membranes, leading to cell lysis and death. This peptide primarily targets Gram-negative bacteria but is also effective against some Gram-positive strains. Cecropin A has garnered significant scientific interest due to its potential applications in developing new antimicrobial agents, particularly in the face of increasing antibiotic resistance. By integrating Cecropin A into therapeutic strategies, researchers aim to broaden the spectrum of antimicrobial options available for use in both clinical and agricultural settings, offering a promising avenue for future drug development.</p>Formule :C184H313N53O46Degré de pureté :Min. 95%Masse moléculaire :4,003.78 g/molOteseconazole
CAS :<p>Oteseconazole is an antifungal medication, which is a synthetic triazole-derived agent. It functions by inhibiting the activity of the fungal enzyme lanosterol 14α-demethylase. This inhibition disrupts the synthesis of ergosterol, a vital component of fungal cell membranes, thereby interfering with cell membrane integrity and function, ultimately leading to fungal cell death.</p>Formule :C23H16F7N5O2Degré de pureté :Min. 95%Masse moléculaire :527.4 g/molCefmenoxime hydrochloride
CAS :<p>Cefmenoxime hydrochloride is a third-generation cephalosporin antibiotic with action on bacterial cell wall synthesis and is used for treating gynecological and obstetric infections.</p>Formule :C16H17N9O5S3HClDegré de pureté :Min. 95%Couleur et forme :White PowderMasse moléculaire :529.79 g/molCefepime Related Compound E
CAS :<p>Cefepime Related Compound E is a chemical impurity, which is typically encountered as a byproduct in the synthesis or degradation of the antibiotic cefepime. This impurity is derived from synthetic processes used in the pharmaceutical industry and can originate from a variety of pathways during the manufacturing or storage of cefepime.</p>Formule :C13H20ClN3O3SDegré de pureté :Min. 95%Masse moléculaire :333.83 g/mol
