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"
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(R)-(-)-2-Oxothiazolidine-4-carboxylic Acid
CAS:Producto controladoFórmula:C4H5NO3SForma y color:NeatPeso molecular:147.15Gibberellin A7 Methyl Ester
CAS:Producto controladoFórmula:C20H24O5Forma y color:NeatPeso molecular:344.42-(1-(Allyloxy)-2-(1H-imidazol-1-yl)ethyl)-3,5-dichlorophenol
Producto controladoFórmula:C14H14Cl2N2O2Forma y color:NeatPeso molecular:313.1795-Fluoro-2-mercaptobenzothiazole
CAS:Producto controlado<p>Applications 5-Fluoro-2-mercaptobenzothiazole is used as a reagent in the synthesis of [[(benzothiazolyl)thio]methyl]phenyl]furanone derivatives with agrochemical fungicidal activities.<br>References Zhao, P., et al.: Youji Huaxue, 30, 1567 (2010);<br></p>Fórmula:C7H4FNS2Forma y color:NeatPeso molecular:185.24TH-302
CAS:Producto controlado<p>Applications TH-302 is a 2-nitroimidazole triggered hypoxia-activated prodrug (HAP) of bromo-isophosphoramide mustard. Studies have shown that TH-302 treatment exhibited hypoxia-selective cytotoxicity and DNA damage in human cancer cell<br>References Meng, F. et al.: Mol. Cancer Ther., 11, 740 (2012); Liu, Q. et al.: Cancer Chemother. Pharmacol., 69, 1487 (2012); Sun, J.D. et al.: Clin. Cancer Res., 18, 758 (2012);<br></p>Fórmula:C9H16Br2N5O4PForma y color:NeatPeso molecular:449.04α-Butylpiperonyl Alcohol
CAS:Producto controlado<p>Applications Intermediate in the preparation of insecticides, fungicides, and other pesticides.<br>References Wilkinson, C., et al.: J. Agric. Food Chem., 14, 73 (1966), Zhong, W., et al.: J. Chem. Res., 6, 370 (2009),<br></p>Fórmula:C12H16O3Forma y color:NeatPeso molecular:208.25cis-2-(2,4-Dichlorophenyl)-2-(4H-1,2,4-triazol-4-ylmethyl)-1,3-dioxolane-4-methanol
CAS:Producto controlado<p>Applications cis-2-(2,4-Dichlorophenyl)-2-(4H-1,2,4-triazol-4-ylmethyl)-1,3-dioxolane-4-methanol is an impurity in the synthesis of Itraconazole (I937500); an orally active antimycotic structurally related to Ketoconazol.<br>References Espinel-Ingroff, A., et al.: Antimicrob. Agents Chemother., 26, 5 (1984); Heykants, J., et al.: Mycoses, 32, Suppl 1, 67 (1989); Sugar, A.M.,et al.: Curr. Clin. Top. Infect. Dis., 13, 74 (1993)<br></p>Fórmula:C13H13Cl2N3O3Forma y color:NeatPeso molecular:330.171-(4-Chlorophenyl)-3-[(2-nitrophenyl)methoxy]pyrazole
CAS:Producto controlado<p>Applications 1-(4-Chlorophenyl)-3-[(2-nitrophenyl)methoxy]pyrazole is an intermediate for the synthesis of Pyraclostrobin-d6 (P840402). Isotope labelled Pyraclostrobin is a fungicide for use in seed grass and food crops.<br>References Gyldenkaerne, S., et al.: Pestic Sci., 55, 1210 (1999), Pennington, D., et al.: Environ. Sci. Technol., 39, 1119 (2005), Wang, S., et al.: Food Control., 18, 731 (2007),<br></p>Fórmula:C16H12ClN3O3Forma y color:NeatPeso molecular:329.74Nitrefazole
CAS:Producto controlado<p>Applications Nitrefazole is a nitroimidazole derivative with the ability to inhibit aldehyde dehydrogenase, and enzyme crucial to the metabolism of alcohol. This compound is suitable for aldehyde dehydrogenase (ALDH) related research.<br>References Klink, R. et al.: Arzneimittelforschung., 35, 1220 (1985); Koda L. et al.: Life Sci., 35, 1659 (1984);<br></p>Fórmula:C10H8N4O4Forma y color:Light Yellow To YellowPeso molecular:248.195-Mercapto-1H-1,2,3-triazole Sodium Salt
CAS:Producto controlado<p>Applications 5-Mercapto-1H-1,2,3-triazole Sodium Salt is used as a reactant in the preparation of cephem derivatives as anti-Helicobacter pylori agents in relation to lability towards β-lactamase and potential for causing diarrhea.<br>References Yoshida, Y., et al.: Bioorg. Med. Chem., 8, 2317 (2000);<br></p>Fórmula:C2H2N3NaSForma y color:NeatPeso molecular:123.111-Methyl-4-nitroimidazole
CAS:Producto controlado<p>Applications 1-Methyl-4-nitroimidazole is a moiety of Azathioprine (A803350) and is predicted to have mutagenic potential.<br>References Rosenkranz, H. S., et al.: Mutat. Res-Fund. Mol. M., 251, 157 (1991); Kelly, G. E., et al.: Photochem. Photobiol., 49, 59 (1989)<br></p>Fórmula:C4H5N3O2Forma y color:White To Light YellowPeso molecular:127.12-Methylbenzothiazole-6-carboxylic Acid (~90%)
CAS:Producto controlado<p>Applications 2-Methylbenzothiazole-6-carboxylic Acid (~90%) is a useful research chemical, a reagent for the synthetic studies on fungicidal agents.<br>References Saikachi, H., et al.: Yakugaku Zasshi, 78, 376 (1958); Bosco, M., et al.: Annali di Chimica, 58, 1148 (1968)<br></p>Fórmula:C9H7NO2SPureza:~90%Forma y color:NeatPeso molecular:193.22(AlphaE)-2-[(6-Chloro-4-pyrimidinyl)oxy]-α-(methoxymethylene)benzeneacetic Acid Methyl Ester
CAS:Producto controlado<p>Applications (αE)-2-[(6-chloro-4-pyrimidinyl)oxy]-α-(methoxymethylene)benzeneacetic Acid Methyl Ester is an intermediate in the synthesis of Azoxystrobin (A965150), an strobilurin fungicide.<br></p>Fórmula:C15H13ClN2O4Forma y color:NeatPeso molecular:320.73[1,1'-Biphenyl]-4-yl(phenyl)(1-trityl-1H-imidazol-5-yl)methanol
Producto controlado<p>Applications [1,1'-Biphenyl]-4-yl(phenyl)(1-trityl-1H-imidazol-5-yl)methanol is an intermediate in synthesizing 2-Biphenylyl Sulfate-d5 Potassium Salt (B397897), which is the isotope labelled analog of 2-Biphenylyl Sulfate Potassium Salt. 2-Biphenylyl Sulfate Potassium Salt is a derivative of 2-Phenylphenol (P335870). 2-Phenylphenol is a agriculture fungicide and is no longer used as a food additive.<br>References Scheuhly, W., et al.: Chem. Biol., 18, 1053 (2011); Singh, H.P., et al.: Food. Chem. Toxicol., 48, 1040 (2010); Gouin, T., et al.: Envro. Pollu., 165, 208 (2012);<br></p>Fórmula:C41H32N2OForma y color:NeatPeso molecular:568.706Levofloxacin
CAS:<p>Levofloxacin is a fluoroquinolone antibiotic with a mode of action that inhibits bacterial DNA gyrase and topoisomerase IV. It is used for treating bacterial infections like pneumonia and urinary tract infections.</p>Fórmula:C18H20FN3O4Pureza:Min. 95%Forma y color:PowderPeso molecular:361.37 g/molBeauvericin
CAS:<p>Beauvericin is a cyclic peptide that is isolated from the fungus Fusarium. It has been shown to have antimicrobial activity against bacteria, as well as a variety of other biological properties. Beauvericin has been shown to inhibit mitochondrial membrane potential and induce toxicity in some animal models. Beauvericin also inhibits protein synthesis and causes cell death by inhibiting DNA polymerase activity. This compound is active against cancer cells, including HL-60 cells, which are derived from human lymphocytes and are used as a model for leukemia. Beauvericin can be extracted from an ETOA extract of the fungus Fusarium oxysporum; this extract has shown anti-cancer effects in vitro assays.</p>Fórmula:C45H57N3O9Pureza:Min. 95%Peso molecular:783.95 g/mol2-Methyl-4-isothiazolin-3-one
CAS:Producto controlado<p>2-Methyl-4-isothiazolin-3-one or MIT is a powerful antimicrobial and antifungal agent which is widely used in personal care products. It is also used in industrial applications as a preservative and antifouling agent.</p>Fórmula:C4H5NOSPureza:Min. 96%Forma y color:Yellow PowderPeso molecular:115.15 g/molAureothin
CAS:<p>Aureothin is a bioactive compound, classified as a polyketide antibiotic, which is derived from the culture of the bacterium Streptomyces thioluteus. This compound operates primarily through the inhibition of protein synthesis by interfering with the aminoacylation of tRNA with specific amino acids. Its mode of action disrupts cellular protein synthesis, which is essential for cell growth and function, leading to its potent antibacterial and antifungal activities.</p>Fórmula:C22H23NO6Pureza:Min. 95%Forma y color:PowderPeso molecular:397.42 g/molCaerulomycin A
CAS:<p>Caerulomycin A is a bioactive compound classified as a natural broad-spectrum antibiotic, which is derived from various Streptomyces species found in soil. Its mode of action involves inhibiting fungal and bacterial growth by interfering with essential cellular processes, effectively curbing the proliferation of pathogenic microorganisms. This potent molecule achieves its effects by binding to specific cellular targets, thereby disrupting cell wall synthesis and other critical metabolic pathways.</p>Fórmula:C12H11N3O2Pureza:Min. 95%Peso molecular:229.23 g/molSordarin sodium salt
CAS:<p>Sordarin sodium salt is an antifungal agent, characterized as a semisynthetic derivative produced from the fermentation products of filamentous fungi, specifically belonging to the phylum Ascomycota. This compound exerts its effects by selectively inhibiting fungal protein synthesis. It achieves this by obstructing the function of elongation factor 2 (EF-2), an essential component of fungal ribosomal activity, thereby disrupting the translational elongation step of protein synthesis.</p>Fórmula:C27H39NaO8Pureza:Min. 95%Peso molecular:514.58 g/molFilipin III
CAS:<p>Filipin III is a polyene macrolide antibiotic, which is extracted from Streptomyces filipinensis. Known for its unique mode of action, Filipin III interferes with cholesterol-rich membranes by binding to ergosterol and cholesterol. This interaction disrupts the membrane structure, altering membrane permeability and ultimately affecting cell viability.</p>Pureza:Min. 95%Naftifine N-Oxide
CAS:<p>Naftifine N-Oxide is an antifungal agent, which is derived from synthetic chemical processes. Its structure is based on the modification of the known antifungal, naftifine, by introducing an N-oxide functional group, which may enhance certain pharmacokinetic properties. As a synthetic derivative, Naftifine N-Oxide is specifically designed to interfere with the biosynthesis of ergosterol, an essential component of fungal cell membranes. By inhibiting squalene epoxidase, an enzyme crucial to the ergosterol pathway, Naftifine N-Oxide effectively disrupts the development and maintenance of the fungal cell membrane, compromising cell integrity and leading to antifungal activity.</p>Fórmula:C21H21NOPureza:Min. 95%Peso molecular:303.4 g/molNeoaureothin
CAS:<p>Neoaureothin is a natural antibiotic product, which is derived from marine actinomycetes with a complex polyketide structure. Its mode of action involves the inhibition of bacterial protein synthesis by binding selectively to the ribosomal subunits, thereby obstructing the translation process in susceptible microbial strains. The specificity of its action allows it to target a broad spectrum of Gram-positive bacteria while presenting a lower risk of resistance development compared to traditional antibiotics.</p>Fórmula:C28H31NO6Pureza:Min. 95%Peso molecular:477.5 g/mol21-Norrapamycin
CAS:<p>21-Norrapamycin is a macrocyclic lactone antibiotic, which is derived from the bacterium Streptomyces hygroscopicus. Its chemical structure is closely related to that of rapamycin, a well-known immunosuppressant. The mode of action of 21-Norrapamycin involves the inhibition of the mechanistic target of rapamycin (mTOR) signaling pathway. By binding to the FK506-binding protein 12 (FKBP12), it forms a complex that then inhibits mTOR, a crucial regulator of cell growth, proliferation, and survival.</p>Fórmula:C50H77NO13Pureza:Min. 95%Peso molecular:900.1 g/molZelkovamycin
CAS:<p>Zelkovamycin is a novel antibacterial compound isolated from endophytic microorganisms, specifically Streptomyces sp. Endophytes are bacteria or fungi that reside within plant tissues, forming symbiotic relationships and often producing bioactive metabolites. The mode of action of Zelkovamycin involves the inhibition of bacterial cell wall synthesis, interfering with the biosynthesis pathways essential for maintaining the structural integrity and function of bacterial cell walls, particularly in Gram-positive strains.</p>Fórmula:C36H45N9O9SPureza:Min. 95%Forma y color:PowderPeso molecular:779.86 g/molPropiconazole
CAS:<p>Propiconazole is a triazole fungicide with action on fungal cell membranes by inhibiting ergosterol biosynthesis and is used for controlling fungal diseases in crops and turf.</p>Fórmula:C15H17Cl2N3O2Pureza:Min. 95%Forma y color:Clear LiquidPeso molecular:342.22 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>Fórmula:C23H39N5O5S2Pureza:Min. 95%Forma y color:PowderPeso molecular:529.72 g/molMiconazole
CAS:<p>Anti-fungal; sterol 14α-demethylase inhibitor</p>Fórmula:C18H14Cl4N2OPureza:Min. 95 Area-%Forma y color:White Off-White PowderPeso molecular:416.13 g/mol41-Oxo-rapamycin
CAS:<p>41-Oxo-rapamycin is a synthetic derivative of rapamycin, which is a macrocyclic lactone. It is derived from Streptomyces hygroscopicus, a gram-positive bacterium known for producing various bioactive compounds. The mode of action of 41-Oxo-rapamycin involves binding to the FK506-binding protein (FKBP12), forming a complex that subsequently inhibits the mammalian target of rapamycin (mTOR) pathway. This inhibition results in the suppression of T-cell proliferation and modulation of immune responses.</p>Fórmula:C51H77NO13Pureza:Min. 95%Peso molecular:912.2 g/molHexamide
CAS:<p>Hexamide is a protein inhibitor.</p>Fórmula:C13H17NOForma y color:SolidPeso molecular:203.28SSF-109
CAS:<p>SSF-109 is a broad-spectrum fungicide, has protective activity against plant disease.</p>Fórmula:C15H18ClN3OPureza:98%Forma y color:SolidPeso molecular:291.78Kayahope
CAS:<p>Kayahope is a novel antifungals.</p>Fórmula:C15H14ClNO3SPureza:98%Forma y color:SolidPeso molecular:323.79Fenhexamid
CAS:<p>Fenhexamid (Elevate), a sterol biosynthesis inhibitor, shows antifungal activity against the plant pathogenic fungus.</p>Fórmula:C14H17Cl2NO2Pureza:99.56%Forma y color:SolidPeso molecular:302.20Fosravuconazole
CAS:<p>Fosravuconazole is a ravuconazole prodrug. It has antifungal activity.</p>Fórmula:C23H20F2N5O5PSPureza:98%Forma y color:SolidPeso molecular:547.47Prochloraz
CAS:<p>Prochloraz: broad-spectrum imidazole fungicide; blocks placental aromatase (IC50=40nM), estrogen/androgen receptors; activates aryl hydrocarbon receptors.</p>Fórmula:C15H16Cl3N3O2Pureza:99.75% - 99.79%Forma y color:Colorless SolidPeso molecular:376.67Antifungal agent 67
CAS:<p>Compound 9 (Antifungal agent 67), an imidazole class antifungal, exhibits efficacy against Candida and possesses a CC50 value of 33.6 μM in neonatal rat</p>Fórmula:C23H25ClN2O3Forma y color:SolidPeso molecular:412.91Fuberidazole
CAS:<p>Fuberidazole is an antifungal agent.</p>Fórmula:C11H8N2OPureza:98.95%Peso molecular:184.19Silthiofam
CAS:<p>Silthiofam effectively combats Ggt, a wheat take-all fungus, now widely used for control in China.</p>Fórmula:C13H21NOSSiPureza:98%Forma y color:SolidPeso molecular:267.46Fungicide4
CAS:<p>Fungicide4 exhibits the high activity against the P. infestans strain.</p>Fórmula:C14H11N3OForma y color:SolidPeso molecular:237.26Chitin synthase inhibitor 10
CAS:<p>Chitin Synthase Inhibitor 10: potent antifungal with 0.11 mM IC50, effective against resistant C. albicans and C. neoformans. Used in IFI research.</p>Fórmula:C24H23Br2N3O6Forma y color:SolidPeso molecular:609.26Isobellidifolin
CAS:<p>Isobellidifolin, a xanthone compound, serves as a free radical scavenger and antioxidant. It exhibits a potent antifungal effect.</p>Fórmula:C14H10O6Forma y color:SolidPeso molecular:274.23Cercosporamide
CAS:<p>Cercosporamide is a ATP-competitive Pkc1 kinase inhibitor (IC50 <50 nM; Ki <7 nM). It also is a unique Mnk inhibitor.</p>Fórmula:C16H13NO7Pureza:98%Forma y color:SolidPeso molecular:331.289-OxoOTrE
CAS:<p>9-OxoOTrE, made by oxidizing 9-HpOTrE, has antimicrobial effects on plant pathogens like bacteria and fungi.</p>Fórmula:C18H28O3Forma y color:SolidPeso molecular:292.41BHBM
CAS:<p>BHBM, an acylhydrazone antifungal, halts C. neoformans growth (MIC80 = 1 μg/ml) by blocking glucosylceramide synthesis.</p>Fórmula:C15H13BrN2O2Forma y color:SolidPeso molecular:333.18Ametoctradin
CAS:<p>Ametoctradin is a Qo-site inhibitor of mitochondrial respiratory complex III and is used in the study of oomycete diseases.</p>Fórmula:C15H25N5Pureza:99.65%Forma y color:SolidPeso molecular:275.39NB-598 hydrochloride
CAS:<p>NB-598 hydrochloride is a competitive squalene epoxidase (SE) inhibitor.</p>Fórmula:C27H32ClNOS2Pureza:98%Forma y color:SolidPeso molecular:486.13Antifungal agent 33
CAS:<p>Antifungal 33 (4e) strongly inhibits Candida albicans. MIC: 16 μg/ml; IC50: 0.19 μg/ml.</p>Fórmula:C21H14ClN5O3Forma y color:SolidPeso molecular:419.82Antifungal agent 22
CAS:<p>Orally active antifungal D16 (IC50: 0.5 μg/mL) passes blood-brain barrier, stable, low toxicity, targets C. neoformansH99 cells.</p>Fórmula:C21H26Cl3NOSForma y color:SolidPeso molecular:446.86P163-0892
CAS:<p>P163-0892: potent, specific antifungal for Cryptococcus; moderate blood-brain barrier penetration.</p>Fórmula:C19H20N2O3SForma y color:SolidPeso molecular:356.44Antifungal agent 35
CAS:<p>Antifungal agent 35 is an effective antifungal agent that potentiates the antifungal activity of fluconazole against C. albicans.</p>Fórmula:C26H27BrN4O4Forma y color:SolidPeso molecular:539.42Apogossypolone (ApoG2)
CAS:<p>Apogossypolone (ApoG2) is a semi-synthesized derivative of gossypol which is a nonpeptidic small molecule inhibitor targeting Bcl-2 family proteins with K i</p>Fórmula:C28H26O8Forma y color:SolidPeso molecular:490.5Chitin synthase inhibitor 13
CAS:<p>Chitin Synthase Inhibitor 13 (compound 12g), a non-competitive antagonist of chitin synthase, demonstrates broad-spectrum antifungal activity and has an</p>Fórmula:C21H19N5O5SForma y color:SolidPeso molecular:453.47Posaconazole hydrate
CAS:<p>Posaconazole: broad-spectrum antifungal, second-gen triazole, strong C14α demethylase inhibitor (IC50: 0.25 nM).</p>Fórmula:C37H44F2N8O5Pureza:98%Forma y color:SolidPeso molecular:718.79S-F24
CAS:<p>S-F24 is a broad-spectrum antifungal agent that demonstrates potent inhibition of CYP3A4, with an IC50 of 0.4 μM.</p>Fórmula:C25H27BrF2N6OForma y color:SolidPeso molecular:545.42Exalamide
CAS:<p>Exalamide (2-(Hexyloxy)benzamide) is an aromatic amide with antifungal activity used in the study of dermatophytes.</p>Fórmula:C13H19NO2Pureza:99.61%Forma y color:White PowderPeso molecular:221.3Antifungal agent 65
CAS:<p>Compound 5d (Antifungal Agent 65) exhibits potent fungicidal activity against Fusarium oxysporum f.sp.</p>Fórmula:C29H29N3O2S2Forma y color:SolidPeso molecular:515.69Chlorothalonil
CAS:<p>Chlorothalonil (DAC 2787): Broad-spectrum, efficient, low-toxicity fungicide for fruits, vegetables, rice, wheat, cotton.</p>Fórmula:C8Cl4N2Pureza:98.01% - 98.71%Forma y color:Colorless Crystals SolidPeso molecular:265.91Buclosamide
CAS:<p>Buclosamide is a topical antimycotic agent that can be used in dermatomycoses [1].</p>Fórmula:C11H14ClNO2Forma y color:SolidPeso molecular:227.69Antifungal agent 70
CAS:<p>Antifungal Agent 70 (Compound 13), a dihydroeugenol-imidazole, exhibits efficacy against multi-resistant Candida auris with a minimum inhibitory concentration (</p>Fórmula:C23H25ClN2O4Forma y color:SolidPeso molecular:428.91Tropesin
CAS:<p>Tropesin is a non-steroidal anti-inflammatory agent (NSAIA) that has inhibitory effects on the growth of Xylaria green.</p>Fórmula:C28H24ClNO6Forma y color:SolidPeso molecular:505.95Rustmicin
CAS:<p>Rustmicin is a 14-membered macrolide identified as an inhibitor of plant pathogenic fungi.</p>Fórmula:C21H32O6Forma y color:SolidPeso molecular:380.48CID-4785700
CAS:<p>CID-4785700 is a potent pan-GTPase inhibitor that inhibits Rab7 and inhibits the fungal histone acetyltransferase Rtt109 that binds to Asf1 and Vps75</p>Fórmula:C22H23ClFN3O3Pureza:98.16%Forma y color:SolidPeso molecular:431.89Antifungal agent 69
CAS:<p>Antifungal agent 69 (compound 13), a eugenol-imidazole derivative, demonstrates targeted activity against Candida albicans with a minimum inhibitory</p>Fórmula:C23H23ClN2O4Forma y color:SolidPeso molecular:426.89SDH-IN-5
CAS:<p>SDH-IN-5 (compound 7d), a potent inhibitor of succinate dehydrogenase (SDH) with an IC50 of 3.293 μM, additionally demonstrates antifungal efficacy, exhibiting</p>Fórmula:C16H19F2N3O2Forma y color:SolidPeso molecular:323.34Furalaxyl
CAS:<p>Furalaxyl is an fungicide of acyl amino chiral.</p>Fórmula:C17H19NO4Forma y color:SolidPeso molecular:301.34Haloprogin
CAS:<p>Haloprogin is an antifungal agent used as a topical cream for the treatment of beriberi and other fungal infections.</p>Fórmula:C9H4Cl3IOForma y color:SolidPeso molecular:361.39(Z)-Fluoxastrobin
CAS:<p>(Z)-Fluoxastrobin is a fungicide that exhibits effective control of important seed and soil-borne pathogens.</p>Fórmula:C21H16ClFN4O5Forma y color:SolidPeso molecular:458.83Antifungal agent 31
CAS:<p>Orally active triazole, antifungal 31 with pyrrolizinone structure, combats Candida, reduces mortality and renal infection in mice.</p>Fórmula:C25H22F2N6O3Forma y color:SolidPeso molecular:492.48Antifungal agent 74
CAS:<p>Antifungal agent 74 (compound 3c), is a potent substance that exhibits excellent fungicidal activity against C.</p>Fórmula:C4HCl3N4SForma y color:SolidPeso molecular:243.5Vibunazole
CAS:<p>Vibunazole is an antifungal agent.</p>Fórmula:C15H20ClN3O2Forma y color:SolidPeso molecular:309.79SC-58272
CAS:<p>SC-58272 is an inhibitor of N-myristoyltransferase (Nmt), a target for anti-fungal and anti-viral therapy.</p>Fórmula:C33H52N6O4Pureza:98%Forma y color:SolidPeso molecular:596.8Etisazole
CAS:<p>Etisazole is an animal antifungal agent with skin sensitizing properties to humans.</p>Fórmula:C9H10N2SForma y color:SolidPeso molecular:178.25Iodiconazole
CAS:<p>Iodiconazole, an azole antifungal, is used potentially for the treatment of fungal infection.</p>Fórmula:C19H19F2IN4OPureza:98%Forma y color:SolidPeso molecular:484.28Tolciclate
CAS:<p>Tolciclate is an agent of antifungal medication.</p>Fórmula:C20H21NOSPureza:98%Forma y color:SolidPeso molecular:323.45Nifuroxime
CAS:<p>Nifuroxime, an anti-infective agent, is utilized in researching fungal infections.</p>Fórmula:C5H4N2O4Forma y color:SolidPeso molecular:156.1Ofurace
CAS:<p>Ofurace is a fungicide.</p>Fórmula:C14H16ClNO3Pureza:98%Forma y color:SolidPeso molecular:281.73Sortin2
CAS:<p>Sortin2 is a sorting inhibitor that acts upstream from the morphological marker of lateral root primordium formation, the mitotic activity.</p>Fórmula:C16H12ClNO5S3Pureza:98%Forma y color:SolidPeso molecular:429.92Mollugogenol A
CAS:<p>Mollugogenol A: a Gammacerane saponin from Mollugo pentaphylla with antifungal and spermatocidal properties; damages sperm membrane.</p>Fórmula:C30H52O4Forma y color:SolidPeso molecular:476.73Iprovalicarb
CAS:<p>Iprovalicarb is a fungicide aimed at oomycetes.</p>Fórmula:C18H28N2O3Pureza:98%Forma y color:SolidPeso molecular:320.43Chitin synthase inhibitor 3
CAS:<p>Compound 2d is a potent chitin synthase inhibitor (IC50: 0.16 mM, MIC: 1 μg/mL vs. Candida albicans) with antifungal properties.</p>Fórmula:C20H19N3O4Forma y color:SolidPeso molecular:365.38Antifungal agent 30
CAS:<p>Potent antifungal, works against Candida albicans (MIC: 0.03 μg/mL) & Aspergillus fumigatus (MIC: 0.5 μg/mL) via CYP51 interactions.</p>Fórmula:C18H14Cl2F2N2SeForma y color:SolidPeso molecular:446.18PD 113270
CAS:<p>PD 113,270 is an analog of the fermentation products fostriecin with antitumor activity in vitro and in vivo.</p>Fórmula:C19H27O8PForma y color:SolidPeso molecular:414.39Antibacterial agent 67
CAS:<p>Antibacterial agent 67 blocks succinate dehydrogenase more effectively than haloperidol, with IC50 of 0.03 μM vs 4.40 μM.</p>Fórmula:C24H15F6N5OForma y color:SolidPeso molecular:503.4Amorolfine
CAS:<p>Amorolfine is available in the nail lacquer and can be used to treat fungal nail infections.</p>Fórmula:C21H35NOForma y color:White To Off-White Crystalline PowderPeso molecular:317.517Benthiavalicarb isopropyl
CAS:<p>Benthiavalicarb isopropyl is a fungicide, specifically targeting downy mildew and blight.</p>Fórmula:C18H24FN3O3SPureza:98%Forma y color:SolidPeso molecular:381.465-Dehydroepisterol
CAS:<p>5-Dehydroepisterol, an anti-fungal episterol form, made by C-5 sterol desaturase, turns into 24-methylenecholesterol.</p>Fórmula:C28H44OPureza:98%Forma y color:SolidPeso molecular:396.65Saperconazole
CAS:<p>Saperconazole is a broad-spectrum antifungal triazole (MIC90: 0.19 mg/L).</p>Fórmula:C35H38F2N8O4Pureza:98%Forma y color:SolidPeso molecular:672.72Bivittoside A
CAS:<p>Bivittoside A is a non-sulfated hexoside analog obtained from Bovine sea cucumber with antifungal activity and potential antitumor activity.</p>Fórmula:C41H66O12Pureza:98%Forma y color:SolidPeso molecular:750.96Penflufen
CAS:<p>Penflufen, a broad-spectrum succinate dehydrogenase inhibitor (SDHI), serves effectively as a fungicide.</p>Fórmula:C18H24FN3OForma y color:SolidPeso molecular:317.4Chlordantoin
CAS:<p>Chlordantoin is an antifungal agent with the potential for vaginal candidiasis treatment.</p>Fórmula:C11H17Cl3N2O2SPureza:98%Forma y color:SolidPeso molecular:347.69Inz-4
CAS:<p>Inz-4 is a fungal-selective inhibitor of mitochondrial cytochrome bc1.</p>Fórmula:C18H14F4N2O2Forma y color:SolidPeso molecular:366.31Diamthazole hydrochloride
CAS:<p>Diamthazole (Dimazole) hydrochloride, an antifungal agent, is utilized in infection research.</p>Fórmula:C15H24ClN3OSForma y color:SolidPeso molecular:329.89Aliconazole
CAS:<p>Aliconazole is an imidazole derivative with antifungal activity for the study of skin infections.</p>Fórmula:C18H13Cl3N2Pureza:99.21% - 99.79%Forma y color:SolidPeso molecular:363.67Pyribencarb
CAS:<p>Pyribencarb, a benzylcarbamate-type fungicide, exhibits broad-spectrum activity against various plant pathogenic fungi.</p>Fórmula:C18H20ClN3O3Pureza:99.75%Forma y color:SolidPeso molecular:361.82Antifungal agent 59
CAS:<p>Antifungal agent 59 exhibits potent activity, reflected by MIC values ranging from 0.01 to 1 μg/mL, and inhibits the formation of fungal biofilms, while</p>Fórmula:C18H15BrF2N2SeForma y color:SolidPeso molecular:456.19Zarilamide
CAS:<p>Zarilamide disrupts microtubules, inhibiting mitosis in Phytophthora capsici zoospore cysts.</p>Fórmula:C11H11ClN2O2Forma y color:SolidPeso molecular:238.67Globosuxanthone A
CAS:<p>Globosuxanthone A: a dihydroxanthenone with anticancer and antifungal properties (MIC: F. graminearum 4, F. solani 8, B. cinerea 16 μg/mL).</p>Fórmula:C15H12O7Forma y color:SolidPeso molecular:304.25CYP51/HDAC-IN-1
CAS:<p>Orally active CYP51/HDAC-IN-1 dual inhibitor targets virulence factors and resistance genes; effective against Candidiasis and Cryptococcal meningitis.</p>Fórmula:C30H40F2N6O4Forma y color:SolidPeso molecular:586.67Oosponol
CAS:<p>Oosponol is a dopamine beta-hydroxylase inhibitor exhibiting hypotensive effects.</p>Fórmula:C11H8O5Pureza:98%Forma y color:SolidPeso molecular:220.18Ditalimfos
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:141.17APX001
CAS:<p>APX001 is a prodrug of APX-001A. APX001 is the first-in-class inhibitor of the fungal protein Gwt1.</p>Fórmula:C22H21N4O6PPureza:98%Forma y color:SolidPeso molecular:468.4VT-1598
CAS:<p>VT-1598 is a novel, selective, orally active fungal CYP51 inhibitor. VT-1598 exhibits antifungal effects against Candida albicans.</p>Fórmula:C31H20F4N6O2Forma y color:SolidPeso molecular:584.52Antifungal agent 26
CAS:<p>Pradimicin A derivative 26 exhibits antifungal, antiviral, and antiparasitic properties by attaching to d-mannose (Man)-rich glycans in pathogenic organisms [1</p>Fórmula:C40H45N3O18Forma y color:SolidPeso molecular:855.79Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Fórmula:C13H9Cl2FN2SPureza:98.08% - 98.15%Forma y color:SolidPeso molecular:315.19TMV-IN-5
CAS:<p>TMV-IN-5 (compound 1a) serves as an antiviral/antifungal agent, specifically targeting and inhibiting the assembly of the tobacco mosaic virus (TMV) by binding</p>Fórmula:C22H23N3SForma y color:SolidPeso molecular:361.5Antifungal agent 66
CAS:<p>Antifungal agent 66 (compound 10) exhibits broad-spectrum antifungal activity against seven phytopathogenic fungal mycelia and significant inhibitory effects on</p>Fórmula:C19H25ClO6Forma y color:SolidPeso molecular:384.85Antifungal agent 48
CAS:<p>Antifungal agent 48 (Example 308), active against Cryptococcus neoformans, exhibits a minimum inhibitory concentration (MIC) value of 11 μM [1].</p>Fórmula:C13H10O4SForma y color:SolidPeso molecular:262.28Eucalyptacid A
CAS:<p>Eucalyptacid A, a metabolite with antifungal properties, demonstrates efficacy against Alternaria solani, displaying minimum inhibitory concentrations (MIC)</p>Fórmula:C17H32O5Forma y color:SolidPeso molecular:316.43Prochloraz manganese
CAS:<p>Prochloraz manganese, an antifungal agent utilized in the agricultural sectors [1], serves to protect crops by inhibiting fungal growth.</p>Fórmula:C60H64Cl14MnN12O8Forma y color:SolidPeso molecular:1632.51MoTPS1-IN-1
CAS:<p>MoTPS1-IN-1 is a potent MoTPS1 inhibitor with antifungal anti-inflammatory activity that acts through interaction with Glu396 study ulcerative colitis.</p>Fórmula:C23H27F3N2O4Pureza:99.28%Forma y color:SoildPeso molecular:452.47Verazine
CAS:<p>(-)-Verazine is an antifungal agent isolated from the dried roots and rhizome of Veratrum maackii Regel, which induces DNA damage in the cerebellum and cerebral</p>Fórmula:C27H43NOForma y color:SolidPeso molecular:397.642-Dodecanol
CAS:<p>2-Dodecanol suppresses both hyphal development and SIR2 gene expression in Candida albicans [1].</p>Fórmula:C12H26OForma y color:SolidPeso molecular:186.33Antifungal agent 49
CAS:<p>Antifungal agent 49 (Example 112) exhibits activity against Cryptococcus neoformans, demonstrating a minimum inhibitory concentration (MIC) of 49 μM [1].</p>Fórmula:C15H12O4Forma y color:SolidPeso molecular:256.25APX2039
CAS:<p>APX2039 is an orally active fungal Gwt1 enzyme inhibitor and a prodrug of the novel Gwt2096 inhibitor APX1.APX2039 exhibits potent anti-Kryptococcal activity</p>Fórmula:C20H15FN4O2Pureza:98.72% - 99.07%Forma y color:SolidPeso molecular:362.36Fenpropidin
CAS:<p>Fenpropidin (Ro-12-3049), a fungicide, is a specific inhibitor of sterol 14-reductase and biosynthesis.</p>Fórmula:C19H31NPureza:98.58% - 99.54%Forma y color:SolidPeso molecular:273.46Y18501
CAS:<p>Y18501, an oxysterol-binding protein (OSBPI) inhibitor structurally akin to Oxathiapiprolin, demonstrates potent inhibition against Phytophthora spp.</p>Fórmula:C27H26F2N6O2SForma y color:SolidPeso molecular:536.6Dihydroaltenuene B
CAS:<p>Dihydroaltenuene B inhibits mushroom tyrosinase (IC50: 38.33µM) and binds His244, Met280, Gly281 via hydrogen bonds.</p>Fórmula:C15H18O6Forma y color:SolidPeso molecular:294.3HDAC/HSP90-IN-3
CAS:<p>HDAC/HSP90-IN-3, a dual inhibitor targeting fungal Hsp90 (IC50: 0.83 μM) & HDAC (IC50: 0.91 μM), counters azole-resistant C. albicans.</p>Fórmula:C26H33N5O6Forma y color:SolidPeso molecular:511.57Antiproliferative agent-18
CAS:<p>Compound 5k (Antiproliferative Agent-18) is an antiproliferative agent that exhibits moderate antibacterial and antifungal activities [1].</p>Fórmula:C26H27FN2OSForma y color:SolidPeso molecular:434.57Antifungal agent 77
CAS:<p>Antifungal agent 77 (Compound 13h) exhibits not only antifungal properties, but also effective insecticidal activity against Mythimna separata, Helicoverpa</p>Fórmula:C21H18FN5O2Forma y color:SolidPeso molecular:391.4Chitin synthase inhibitor 14
CAS:<p>Chitin Synthase Inhibitor 14 (compound 4n), a potent chitin synthase (CHS) inhibitor, exhibits antifungal activity and is effective against drug-resistant</p>Fórmula:C25H26ClN5O5Forma y color:SolidPeso molecular:511.96Orysastrobin
CAS:<p>Orysastrobin, a "quinone outside inhibitor" (QoI) fungicide, demonstrates outstanding efficacy in controlling rice leaf and panicle blast as well as sheath</p>Fórmula:C18H25N5O5Forma y color:SolidPeso molecular:391.42Zoxamide
CAS:<p>Zoxamide (RH-7281) is an oomycete-specific fungicide that impedes nuclear division in Phytophthora capsici germlings and disrupts the microtubule cytoskeleton [</p>Fórmula:C14H16Cl3NO2Forma y color:SolidPeso molecular:336.64Inz-5
CAS:<p>Inz-5 is a fungal-selective inhibitor of mitochondrial cytochrome bc1. Inz-5 impairs fungal virulence. It also prevents the evolution of drug resistance.</p>Fórmula:C18H14F4N6Forma y color:SolidPeso molecular:390.34Econazole
CAS:<p>Econazole is an imidazole antifungal agent with action on fungal cell membrane disruption and is used for treating fungal skin infections like athlete's foot and ringworm.</p>Fórmula:C18H15Cl3N2OPureza:Min. 98 Area-%Forma y color:White PowderPeso molecular:381.68 g/molFengycin
CAS:<p>Fengycin is a cyclic lipopeptide from Bacillus subtilis acts as a biosurfactant and antifungal. As a fungicide, it has a mode of action that involves the formation of ion channels in the fungal lipid membrane, leading to membrane leakage This activity is negatively correlated to cholesterol levels, and may explain why mammalian cells, with higher cholesterol present, are not sensitive to fengycin.</p>Fórmula:C72H110N12O20Pureza:Min. 90 Area-%Forma y color:PowderPeso molecular:1,463.71 g/mol2,4′-Dichloroacetanilide
CAS:<p>2,4′-Dichloroacetanilide (2-chloro-N-(4-chlorophenyl)acetamide) has antifungal activity and inhibits T. asteroides with a MIC value of 6.25 μg/mL.</p>Fórmula:C8H7Cl2NOPureza:99.36%Forma y color:SolidPeso molecular:204.05Fosmanogepix
CAS:<p>Fosmanogepix (APX001) is a broad-spectrum oral antifungal that targets Gwt1 enzyme, transforming into active APX001A in the body.</p>Fórmula:C22H21N4O6PPureza:98%Forma y color:SolidPeso molecular:468.40Antifungal agent 43
<p>Antifungal agent 43 inhibits biofilms with low toxicity to human cancer cells.</p>Fórmula:C24H26N4Se2Forma y color:SolidPeso molecular:528.41CDA-IN-4
CAS:<p>CDA-IN-4 (compound VS-24) is an inhibitor of chitin deacetylase (CDA). At a concentration of 100 μg/mL, CDA-IN-4 provides a protective effect of 61.2% against rice blast disease.</p>Fórmula:C10H9BrN4O2SForma y color:SolidPeso molecular:329.17HDAC-IN-87
CAS:<p>HDAC-IN-87 (Compound XII6) is a non-selective HDAC inhibitor with pIC50 values of 6.9 for HDAC4 and 5.8 for HDAC6. It exhibits fungicidal activity against P. sorghi and P. pachyrhizi. The acute oral LD50 in both male and female rats is greater than 500 mg/kg.</p>Fórmula:C13H7F5N4O2SForma y color:SolidPeso molecular:378.277Chitin synthase inhibitor 9
<p>CHS inhibitor 9: a broad-spectrum antifungal for studying fungal infections.</p>Fórmula:C24H25N3O6Forma y color:SolidPeso molecular:451.47Antifungal agent 28
<p>Antifungal 28 disrupts Candida, hits fluconazole-resistant strains, and inhibits biofilms.</p>Fórmula:C22H29N5OSForma y color:SolidPeso molecular:411.56AnCDA-IN-1
CAS:<p>AnCDA-IN-1 (Compound J075-4187) is an inhibitor of chitin deacetylase (CDA) exhibiting antifungal properties. It possesses an IC50 of 4.24 μM against A. nidulans AnCDA. The compound demonstrates a minimum inhibitory concentration (MIC) of 260 μg/mL and a minimum fungicidal concentration (MFC) of 520 μg/mL for food spoilage fungi and plant pathogenic fungi. AnCDA-IN-1 is applicable for research in the antifungal domain.</p>Fórmula:C16H13ClN4O2Forma y color:SolidPeso molecular:328.753Antifungal agent 17
<p>Antifungal agent 17 showed good antifungal activity against B. cinerea (EC50: 2.86 μg/mL).</p>Fórmula:C18H16Br2O2Forma y color:SolidPeso molecular:424.13Antifungal agent 100
CAS:<p>Antifungal agent 100 (compound 3i) demonstrates notable antifungal activity, exhibiting an EC 50 of 0.33 mg/L against S. sclerotiorum. It also possesses an IC 50 value of 0.63 mg/mL targeting the Succinate dehydrogenase (SDH) of the same organism [1].</p>Fórmula:C23H21N3O4SForma y color:SolidPeso molecular:435.5Antibacterial agent 188
CAS:<p>Compound 2d (Antibacterial agent 188) serves as an antibacterial agent that suppresses the activity of dermatophytes [1].</p>Fórmula:C12H10N4SForma y color:SolidPeso molecular:242.3HSP90-IN-9
<p>HSP90-IN-9: potent HSP90 inhibitor, dose-dependent fungicide, impedes biofilm/morphology with FLC, reverses FLC resistance.</p>Forma y color:SolidIsopyrazam
CAS:<p>Isopyrazam, a plant protection product, exhibits potent antifungal activity. When applied to crops, it effectively inhibits the growth of various plant pathogenic fungi, significantly enhancing both the yield and quality of the crops. This compound demonstrates exceptional disease resistance capabilities in agricultural applications.</p>Fórmula:C20H23F2N3OForma y color:SolidPeso molecular:359.41Antifungal agent 127
CAS:<p>Antifungalagent 127 (Compound 6c) is an antifungal agent with potent inhibitory activity against Botrytis cinerea and Rhizoctonia solani.</p>Fórmula:C13H12ClN3OForma y color:SolidPeso molecular:261.707Antifungal agent 125
CAS:<p>Antifungalagent 125 (compound 4H) is a potent succinate dehydrogenase (SDH) inhibitor with an IC50 of 3.59 μg/mL and exhibits fungicidal activity against Alternaria alternata.</p>Fórmula:C13H10BrNO4SForma y color:SolidPeso molecular:356.192Hyalodendrin
CAS:<p>Hyalodendrin ((+)-Hyalodendrin) acts as a fungal growth inhibitor, specifically targeting wood decay fungi. It exhibits low phytotoxicity and possesses an acute toxicity (LD50) level of 75 mg/kg in mice.</p>Fórmula:C14H16N2O3S2Forma y color:SolidPeso molecular:324.42WQ3810 TFA
<p>WQ3810 TFA is an orally available fluoroquinolone with antimicrobial activity against Mycobacterium tuberculosis and inhibits the DNA rotamase activity of</p>Fórmula:C24H23F6N5O5Pureza:99.52%Forma y color:SoildPeso molecular:575.46CDA-IN-3
CAS:<p>CDA-IN-3 (NCDI) is a chitin deacetylase (CDA) inhibitor with antiparasitic properties. It disrupts chitin metabolism in nematodes, increasing ROS levels within these organisms and causing cellular damage. CDA-IN-3 significantly inhibits all developmental stages of Caenorhabditis elegans and can be utilized in research focused on anti-infective applications.</p>Fórmula:C16H27N3O3S2Forma y color:SolidPeso molecular:373.534CDA-IN-2
CAS:<p>CDA-IN-2 (Compound VS#2-3) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal properties. At a concentration of 100 μM, it inhibits P. xanthii's CDAPxCDA1 by 83.7% and PxCDA2 by 74.5%. CDA-IN-2 is applicable in research on agricultural fungal diseases, including resistance to powdery mildew and gray mold.</p>Fórmula:C17H16N2O7Forma y color:SolidPeso molecular:360.318CDA-IN-1
CAS:<p>CDA-IN-1 (Compound vs#2-1) is an inhibitor of chitin deacetylase (CDA) that exhibits antifungal activity. By inhibiting fungal CDA activity, it activates plant immune responses and leads to the accumulation of reactive oxygen species (ROS), hindering fungal growth. At a concentration of 100 μM, CDA-IN-1 achieves inhibition rates of 86.9% on P. xanthii's PxCDA1 and 74.5% on PxCDA2. CDA-IN-1 is applicable in research on fungal plant diseases, such as cucumber powdery mildew and tomato gray mold.</p>Fórmula:C15H14N2O6Forma y color:SolidPeso molecular:318.281Chitin synthase inhibitor 8
<p>Chitin synthase inhibitor 8 is a chitin synthase (CHS) inhibitor with broad-spectrum antifungal effects that can be used in studies related to fungal infections</p>Fórmula:C23H23N3O5Forma y color:SolidPeso molecular:421.45Furametpyr
CAS:<p>Furametpyr is a kind of low toxicity pesticides used to control plant diseases caused by various pathogenic microorganisms.</p>Fórmula:C17H20ClN3O2Pureza:98%Forma y color:SolidPeso molecular:333.81Antifungal agent 12
<p>Antifungal agent 12 is a new fluconazole-like compound that exhibits good antifungal effects.</p>Fórmula:C20H16F3N7O2S2Forma y color:SolidPeso molecular:507.51Antifungal agent 11
<p>Antifungal agent 11 has a good antifungal effect.</p>Fórmula:C21H19F2N7O3S2Forma y color:SolidPeso molecular:519.55
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