Antifongiques
Les antifongiques sont des composés spécialement conçus pour arrêter, prévenir et éliminer la croissance des champignons. Dans cette catégorie, vous trouverez une large variété d'agents antifongiques essentiels pour la recherche et les applications thérapeutiques. Ces composés sont cruciaux pour traiter les infections fongiques et prévenir leur récurrence, ce qui en fait des outils vitaux tant dans les domaines médical qu'agricole. Les chercheurs et les professionnels de la santé peuvent explorer de nombreux antifongiques pour comprendre leurs mécanismes, optimiser leur efficacité et développer de nouveaux traitements pour combattre les souches de champignons résistantes. La vaste sélection d'antifongiques soutient les avancées continues dans la recherche sur les champignons et le développement de thérapies antifongiques efficaces.
835 produits trouvés pour "Antifongiques"
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Diamthazole
CAS :<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Formule :C15H23N3OSCouleur et forme :SolidMasse moléculaire :293.43Diethofencarb
CAS :<p>Diethofencarb: a fungicide effective against Botrytis cinerea and resistant Botryis strains.</p>Formule :C14H21NO4Couleur et forme :SolidMasse moléculaire :267.32BI-10
CAS :<p>BI-10, paired with fluconazole, hinders fungal growth, increases ROS, decreases MMP, and changes membrane permeability.</p>Formule :C23H17BrN2OCouleur et forme :SolidMasse moléculaire :417.3Antifungal agent 2
CAS :<p>Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.</p>Formule :C19H11Br2F3N4O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :544.12FBA-IN-1
CAS :<p>FBA-IN-1 (2a11) is the first covalent, allosteric CaFBA inhibitor, effective against Azole-resistant strains with a MIC 80 of 1 μg/mL.</p>Formule :C15H13NOSeDegré de pureté :98.79%Couleur et forme :SolidMasse moléculaire :302.23Lipoxamycin
CAS :<p>Lipoxamycin is an inhibitor of serine palmitoyl-transferase.</p>Formule :C19H36N2O5Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :372.541F5
CAS :<p>41F5: Anti-fungal with MIC50 0.4-0.8 μM and IC50 0.87 μM against Histoplasma; 62x more selective for yeast vs host cells.</p>Formule :C21H22N2OSCouleur et forme :SolidMasse moléculaire :350.48Flutolanil
CAS :<p>Flutolanil: a fungicide targeting R. solani in rice, toxic to zebrafish.</p>Formule :C17H16F3NO2Couleur et forme :SolidMasse moléculaire :323.31Debneyol
CAS :<p>Debneyol exhibits more potent fungicidal activity than validamycin.</p>Formule :C15H26O2Couleur et forme :SolidMasse moléculaire :238.371-(6-Amino-3,5-difluoro-2-pyridinyl)-7-[3-[3-[[1-(6-amino-3,5-difluoro-2-pyridinyl)-3-carboxy-8-chloro-6-fluoro-1,4-dihydro-4-oxo-7- quinolinyl]amino]-2-hydroxypropoxy]-1-azetidinyl]-8-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
CAS :<p>1-(6-Amino-3,5-difluoro-2-pyridinyl)-7-[3-[3-[[1-(6-amino-3,5-difluoro-2-pyridinyl)-3-carboxy-8-chloro-6-fluoro-1,4-dihydro-4-oxo-7-quinolinyl]amino]-2-hydroxypropoxy]-1-azetidinyl]-8-chloro-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid is a fluoroquinolone antibiotic, engineered through synthetic chemistry. It is derived from chemical sources involving complex organic synthesis, highlighting its intricate molecular architecture. Its mode of action is distinctive, as it inhibits bacterial DNA gyrase and topoisomerase IV, enzymes crucial for DNA replication and transcription. This interference with bacterial DNA processes results in bactericidal effects, effectively eliminating susceptible bacterial strains.</p>Formule :C36H24Cl2F6N8O8Degré de pureté :Min. 95%Masse moléculaire :881.52 g/molRilopirox
CAS :<p>Rilopirox is a synthetic fungicidal antimycotic with hydrophobic characteristics.</p>Formule :C19H16ClNO4Degré de pureté :99.17% - 99.72%Couleur et forme :SolidMasse moléculaire :357.79Pramiconazole
CAS :<p>Pramiconazole (R126638), an oral antifungal, treats dermatophyte and yeast infections in seborrheic dermatitis.</p>Formule :C35H39F2N7O4Degré de pureté :98.59% - 99.41%Couleur et forme :SolidMasse moléculaire :659.73Flutrimazole
CAS :<p>Flutrimazole: a dual-action imidazole with anti-inflammatory and antifungal effects; ideal for topical use due to limited skin penetration.</p>Formule :C22H16F2N2Degré de pureté :98.56%Couleur et forme :SolidMasse moléculaire :346.37ME1111
CAS :<p>ME1111, a succinate dehydrogenase inhibitor of Trichophyton species, serves as an antifungal agent effective against dermatophytes.</p>Formule :C12H14N2ODegré de pureté :99.45%Couleur et forme :SolidMasse moléculaire :202.25Micafungin 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/molPC945
CAS :<p>PC945 (Opelconazole) is an antifungal compound that inhibits CYP51A/CYP51B and can be used to study fungal infections of the lungs.</p>Formule :C38H37F3N6O3Degré de pureté :98.89% - 99.37%Couleur et forme :SolidMasse moléculaire :682.73Dihydropenicillin 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/molN,O-Diacetyltyramine
CAS :<p>N,O-Diacetyltyramine, isolated from the actinomycete Pseudonocardia endophytica VUK-10, exhibits both antibacterial activity against Gram-positive and Gram-negative bacteria, alongside fungi, and demonstrates cytotoxicity towards MDA-MB-231, HeLa, MCF-7, and OAW-42 cells [1].</p>Formule :C12H15NO3Couleur et forme :SolidMasse moléculaire :221.25Antifungal agent 24
CAS :<p>Antifungal agent 24 (Compound 6) is an antifungal agent that inhibits Candida albicans (MIC: 0.03 μg/ml).</p>Formule :C24H18F2N4OCouleur et forme :SolidMasse moléculaire :416.42FR194738 free base
CAS :<p>FR194738 free base inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM. </p>Formule :C27H37NO2SDegré de pureté :99.13%Couleur et forme :SolidMasse moléculaire :439.65
