Antifúngicos
Los antifúngicos son compuestos específicamente diseñados para detener, prevenir y eliminar el crecimiento de hongos. En esta categoría, encontrará una amplia variedad de agentes antifúngicos esenciales para aplicaciones de investigación y terapéuticas. Estos compuestos son cruciales en el tratamiento de infecciones fúngicas y en la prevención de su recurrencia, lo que los convierte en herramientas vitales tanto en entornos médicos como agrícolas. Investigadores y profesionales de la salud pueden explorar numerosos antifúngicos para comprender sus mecanismos, optimizar su eficacia y desarrollar nuevos tratamientos para combatir cepas de hongos resistentes. La extensa selección de antifúngicos respalda los avances continuos en la investigación fúngica y el desarrollo de terapias antifúngicas efectivas.
Se han encontrado 835 productos de "Antifúngicos"
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
Ditalimfos
CAS:<p>Ditalimfos is a fungicide.</p>Fórmula:C12H14NO4PSForma y color:SolidPeso molecular:299.28β-Nor-lapachone
CAS:<p>β-Nor-lapachone is an antibiofilm agent of Candida glabrata.</p>Fórmula:C14H12O3Forma y color:SolidPeso molecular:228.24Antifungal agent 46
CAS:<p>Compound 2f (Antifungal Agent 46) is a potent antifungal that inhibits Ras signaling by targeting protein farnesyltransferase [1].</p>Fórmula:C26H28BrF3N4O2Pureza:98%Forma y color:SolidPeso molecular:565.43Pterophyllin 2
CAS:<p>Pterophyllin 2 is an agent of natural antifungal. It also against postharvest fruit pathogenic fungi.</p>Fórmula:C15H12O3Pureza:98%Forma y color:SolidPeso molecular:240.25Antifungal agent 73
CAS:<p>Antifungal agent 73 (compound A32) effectively combats azole-resistant candidiasis by disrupting the fungal cell wall and membrane.</p>Fórmula:C21H16Cl2N2O3Forma y color:SolidPeso molecular:415.27Pyrisoxazole
CAS:<p>Pyrisoxazole is a novel fungicide inhibitor of Sterol 14α-demethylase.</p>Fórmula:C16H17ClN2OForma y color:SolidPeso molecular:288.77Fenpropimorph
CAS:<p>Fenpropimorph is used as a small molecule fungicide.</p>Fórmula:C20H33NOForma y color:SolidPeso molecular:303.48Stemphyperylenol
CAS:<p>Stemphyperylenol: antifungal, targets Alternaria solani, MIC at 1.57 μM.</p>Fórmula:C20H16O6Forma y color:SolidPeso molecular:352.3416,17-Dihydroheronamide C
CAS:<p>16,17-Dihydroheronamide C is a probe used for the analysis of the mode of action of heronamide C, which has antifungal properties.</p>Fórmula:C29H41NO3Forma y color:SolidPeso molecular:451.64NSC-670224
CAS:<p>NSC-670224 blocks HDAC6 and NF-κB, is toxic to yeast at low µM concentrations, similar to tamoxifen's action.</p>Fórmula:C21H34Cl3NOPureza:98%Forma y color:SolidPeso molecular:422.86Antifungal agent 36
CAS:<p>Antifungal agent 36 is a potent anti-fungal agent that shows anti-fungal activity for Basidiomycetes [1].</p>Fórmula:C14H21NO2Forma y color:SolidPeso molecular:235.32DHMB
CAS:<p>DHMB (2,3-Dihydroxy-4-Methoxybenzaldehyde) exerts protective effects on intestinal epithelial cells. DHMB exhibits anti-inflammatory and antifungal capacity.</p>Fórmula:C8H8O4Pureza:99.57%Forma y color:SolidPeso molecular:168.15Metyltetraprole
CAS:<p>Metyltetraprole: potent fungicide, effective against Zymoseptoria, low EC50 (0.002 ppm), inhibits respiratory chain.</p>Fórmula:C19H17ClN6O2Forma y color:SolidPeso molecular:396.83Succinate dehydrogenase-IN-1
CAS:<p>Succinate dehydrogenase-IN-1 (Compound 34) acts as an inhibitor of succinate dehydrogenase (SDH), exhibiting an IC50 value of 0.94 μM and a KD of 22.4 μM. This compound also demonstrates antifungal activity, with EC50 values against Rhizoctonia solani, Sclerotinia sclerotiorum, Monilinia fructicola, and Botrytis cinerea measured at 0.04 μM, 1.13 μM, 1.61 μM, and 1.21 μM, respectively.</p>Fórmula:C20H13F6N3OForma y color:SolidPeso molecular:425.33Antifungal agent 68
CAS:<p>Antifungal agent 68 (compound 10) effectively combats fungal infections caused by Candida and Cryptococcus gattii through the inhibition of ergosterol</p>Fórmula:C23H27ClN2O3Forma y color:SolidPeso molecular:414.93Tolindate
CAS:<p>Tolindate, a potent PXR agonist, demonstrates antifungal activity and possesses an EC50 value of 8.3 µM.</p>Fórmula:C18H19NOSForma y color:SolidPeso molecular:297.41Antifungal agent 32
CAS:<p>Antifungal 32 (1a) strongly inhibits Candida albicans growth, filamentation, biofilm, and adhesion.</p>Fórmula:C25H28N2OForma y color:SolidPeso molecular:372.5Tebuconazole-d9
CAS:<p>Tebuconazole-d9 is a GC/LC-MS standard for quantifying the triazole fungicide tebuconazole, affecting seed/foliar fungi and androgen receptors.</p>Fórmula:C16H13ClD9N3OForma y color:SolidPeso molecular:316.87Justicidin B
CAS:<p>Justicidin B: anticancer, proapoptotic, inhibits bone resorption & platelets, antiviral, fungicidal, antiprotozoal.</p>Fórmula:C21H16O6Forma y color:SolidPeso molecular:364.35(-)-Ketoconazole
CAS:<p>(-)-Ketoconazole is a potential mitochondrial CYP24A1 inhibitor and has antifungal activity against Aspergillus fumigatus.</p>Fórmula:C26H28Cl2N4O4Pureza:98%Forma y color:SolidPeso molecular:531.43Diamthazole
CAS:<p>Diamthazole (Dimazole) is an antifungal agent that can be used in the infection research[1].</p>Fórmula:C15H23N3OSForma y color:SolidPeso molecular:293.43Diethofencarb
CAS:<p>Diethofencarb: a fungicide effective against Botrytis cinerea and resistant Botryis strains.</p>Fórmula:C14H21NO4Forma y color:SolidPeso molecular:267.32BI-10
CAS:<p>BI-10, paired with fluconazole, hinders fungal growth, increases ROS, decreases MMP, and changes membrane permeability.</p>Fórmula:C23H17BrN2OForma y color:SolidPeso molecular:417.3Antifungal agent 2
CAS:<p>Antifungal agent 2 suppresses growth of Cryptococcus, Candida, Aspergillus at ≥0.5 μg/mL.</p>Fórmula:C19H11Br2F3N4O2Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C15H13NOSePureza:98.79%Forma y color:SolidPeso molecular:302.23Lipoxamycin
CAS:<p>Lipoxamycin is an inhibitor of serine palmitoyl-transferase.</p>Fórmula:C19H36N2O5Pureza:98%Forma y color:SolidPeso molecular: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>Fórmula:C21H22N2OSForma y color:SolidPeso molecular:350.48Flutolanil
CAS:<p>Flutolanil: a fungicide targeting R. solani in rice, toxic to zebrafish.</p>Fórmula:C17H16F3NO2Forma y color:SolidPeso molecular:323.31Debneyol
CAS:<p>Debneyol exhibits more potent fungicidal activity than validamycin.</p>Fórmula:C15H26O2Forma y color:SolidPeso molecular: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>Fórmula:C36H24Cl2F6N8O8Pureza:Min. 95%Peso molecular:881.52 g/molRilopirox
CAS:<p>Rilopirox is a synthetic fungicidal antimycotic with hydrophobic characteristics.</p>Fórmula:C19H16ClNO4Pureza:99.17% - 99.72%Forma y color:SolidPeso molecular:357.79Pramiconazole
CAS:<p>Pramiconazole (R126638), an oral antifungal, treats dermatophyte and yeast infections in seborrheic dermatitis.</p>Fórmula:C35H39F2N7O4Pureza:98.59% - 99.41%Forma y color:SolidPeso molecular: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>Fórmula:C22H16F2N2Pureza:98.56%Forma y color:SolidPeso molecular:346.37ME1111
CAS:<p>ME1111, a succinate dehydrogenase inhibitor of Trichophyton species, serves as an antifungal agent effective against dermatophytes.</p>Fórmula:C12H14N2OPureza:99.45%Forma y color:SolidPeso molecular: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>Fórmula:C35H52N8O20SPureza:Min. 95 Area-%Forma y color:White PowderPeso molecular: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>Fórmula:C38H37F3N6O3Pureza:98.89% - 99.37%Forma y color:SolidPeso molecular: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>Fórmula:C14H22N2O4S•KPureza:Min. 95%Peso molecular: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>Fórmula:C12H15NO3Forma y color:SolidPeso molecular: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>Fórmula:C24H18F2N4OForma y color:SolidPeso molecular: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>Fórmula:C27H37NO2SPureza:99.13%Forma y color:SolidPeso molecular:439.65Laxifloran
CAS:<p>Laxifloran possesses antibacterial and antifungal properties.</p>Fórmula:C17H18O5Forma y color:SolidPeso molecular:302.32Azaconazole
CAS:<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Fórmula:C12H11Cl2N3O2Forma y color:SolidPeso molecular:300.14Antifungal agent 50
CAS:<p>Antifungal agent 50 exhibits minimum inhibitory concentrations (MICs) ranging from less than 0.063 to 1 μg/mL [1].</p>Fórmula:C25H20ClN5O2SForma y color:SolidPeso molecular:489.98Alteconazole
CAS:<p>Alteconazole is an antifungal drug.</p>Fórmula:C17H12Cl3N3OPureza:98%Forma y color:SolidPeso molecular:380.66FT895
CAS:<p>FT895 is a selective and potent HDAC11 inhibitor with antifungal and antitumor activity that inhibits HDAC11 expression and limits EV71 replication in vitro.</p>Fórmula:C16H15F3N4O2Pureza:98.95% - >99.99%Forma y color:SolidPeso molecular:352.31Inz-1
CAS:<p>Inz-1 is an effective and fungal-selective inhibitor of mitochondrial cytochrome bc1 with IC50s of 8.092 and 45.320 μM for yeast and human.</p>Fórmula:C16H14N2O2Pureza:99.55% - 99.88%Forma y color:SolidPeso molecular:266.29PF-184563
CAS:<p>PF-184563 is an effective and selective non-peptide antagonist of the V1a receptor with oral activity, suitable for studying Raynaud's disease dysmenorrhoea.</p>Fórmula:C21H23ClN6Pureza:99.67%Forma y color:SolidPeso molecular:394.9Methyl 3,4-dimethoxycinnamate
CAS:<p>Methyl 3,4-dimethoxycinnamate impedes uredospore germination and concurrently inhibits global DNA methylation in Hep3B cells [1] [2].</p>Fórmula:C12H14O4Forma y color:SolidPeso molecular:222.246-Chloro-7-deazapurine-β-D-riboside
CAS:<p>6-Chloro-7-deazapurine-β-D-riboside shows antifungal activity.</p>Fórmula:C11H12ClN3O4Pureza:98.26%Forma y color:SolidPeso molecular:285.68Icofungipen
CAS:<p>Icofungipen is an oral antifungals with active against Candida species.</p>Fórmula:C7H11NO2Pureza:98%Forma y color:SolidPeso molecular:141.17
