Antifúngicos
Os antifúngicos são compostos especificamente projetados para interromper, prevenir e eliminar o crescimento de fungos. Nesta categoria, você encontrará uma ampla variedade de agentes antifúngicos essenciais para pesquisa e aplicações terapêuticas. Esses compostos são cruciais no tratamento de infecções fúngicas e na prevenção de sua recorrência, tornando-os ferramentas vitais tanto em ambientes médicos quanto agrícolas. Pesquisadores e profissionais de saúde podem explorar inúmeros antifúngicos para entender seus mecanismos, otimizar sua eficácia e desenvolver novos tratamentos para combater cepas fúngicas resistentes. A extensa seleção de antifúngicos apoia os avanços contínuos na pesquisa sobre fungos e no desenvolvimento de terapias antifúngicas eficazes.
Foram encontrados 835 produtos de "Antifúngicos"
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Laxifloran
CAS:<p>Laxifloran possesses antibacterial and antifungal properties.</p>Fórmula:C17H18O5Cor e Forma:SolidPeso molecular:302.32Azaconazole
CAS:<p>Azaconazole, an agricultural fungicide, is used for controlling powdery mildew on crops and bean rust.</p>Fórmula:C12H11Cl2N3O2Cor e Forma: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:C25H20ClN5O2SCor e Forma:SolidPeso molecular:489.98Alteconazole
CAS:<p>Alteconazole is an antifungal drug.</p>Fórmula:C17H12Cl3N3OPureza:98%Cor e Forma: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%Cor e Forma: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%Cor e Forma: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%Cor e Forma: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:C12H14O4Cor e Forma: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%Cor e Forma:SolidPeso molecular:285.68Icofungipen
CAS:<p>Icofungipen is an oral antifungals with active against Candida species.</p>Fórmula:C7H11NO2Pureza:98%Cor e Forma: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%Cor e Forma: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:C31H20F4N6O2Cor e Forma: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:C40H45N3O18Cor e Forma:SolidPeso molecular:855.79Loflucarban
CAS:<p>Loflucarban (Fluonilid) is an antimycotic compoud.</p>Fórmula:C13H9Cl2FN2SPureza:98.08% - 98.15%Cor e Forma: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:C22H23N3SCor e Forma: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:C19H25ClO6Cor e Forma: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:C13H10O4SCor e Forma: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:C17H32O5Cor e Forma: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:C60H64Cl14MnN12O8Cor e Forma: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%Cor e Forma:SoildPeso molecular:452.47
