Pan Assay Interference Compounds (PAINS) and other promiscuous compounds in antifungal research: Miniperspective

M Pouliot, S Jeanmart - Journal of medicinal chemistry, 2016 - ACS Publications
Every week, articles disclosing new antifungal leads reported as promising starting points for
optimization projects are published. In many cases, the mechanism that accounts for their …

Insights into the chemistry and therapeutic potential of furanones: A versatile pharmacophore

A Husain, SA Khan, F Iram, MA Iqbal, M Asif - European Journal of …, 2019 - Elsevier
Furanone, a five-membered heteroaromatic ring containing oxygen atom, is of immense
pharmaceutical importance. Presence of this nucleus in biologically active compounds of …

Synthesis of α-ketols by functionalization of captodative alkenes and divergent preparation of heterocycles and natural products

D Zarate-Zarate, R Aguilar, RI Hernández-Benitez… - Tetrahedron, 2015 - Elsevier
Captodative alkene 1-acetylvinyl p-nitrobenzenecarboxylate 1a was evaluated for its
reactivity in Lewis acid-catalyzed Michael additions with functionalized benzene rings and …

Palladium-Catalyzed α-Arylation of Zinc Enolates of Esters: Reaction Conditions and Substrate Scope

T Hama, S Ge, JF Hartwig - The Journal of organic chemistry, 2013 - ACS Publications
The intermolecular α-arylation of esters by palladium-catalyzed coupling of aryl bromides
with zinc enolates of esters is reported. Reactions of three different types of zinc enolates …

Synthesis and structure–antifungal activity relationships of 3-aryl-5-alkyl-2, 5-dihydrofuran-2-ones and their carbanalogues: Further refinement of tentative …

M Pour, M Špulák, V Balšánek, J Kuneš… - Bioorganic & medicinal …, 2003 - Elsevier
Two series of 3-(substituted phenyl)-5-alkyl-2, 5-dihydrofuran-2-ones related to a natural
product,(−) incrustoporine, were synthesized and their in vitro antifungal activity evaluated …

3-Phenyl-5-acyloxymethyl-2H,5H-furan-2-ones:  Synthesis and Biological Activity of a Novel Group of Potential Antifungal Drugs

M Pour, M Špulák, V Buchta, P Kubanová… - Journal of medicinal …, 2001 - ACS Publications
3-(Substituted phenyl)-5-acyloxymethyl-2 H, 5 H-furan-2-ones related to the natural product
(−) incrustoporine were synthesized and their in vitro antifungal activity evaluated. The …

[HTML][HTML] Effect of selected silyl groups on the anticancer activity of 3, 4-dibromo-5-hydroxy-furan-2 (5H)-one derivatives

R Kitel, A Byczek-Wyrostek, K Hopko, A Kasprzycka… - Pharmaceuticals, 2021 - mdpi.com
The pharmacological effects of carbon to silicon bioisosteric replacements have been widely
explored in drug design and medicinal chemistry. Here, we present a systematic …

Simple 2 (5H)-furanone derivatives with selective cytotoxicity towards non-small cell lung cancer cell line A549–Synthesis, structure-activity relationship and biological …

A Byczek-Wyrostek, R Kitel, K Rumak… - European journal of …, 2018 - Elsevier
A series of 5-alkoxy derivatives of 3, 4-dichloro-5-hydroxyfuran-2-(5H)-one (mucochloric
acid, MCA) were obtained and subsequently subjected to modification in the C-4 position of …

Synthesis and biological evaluation of potent antifungal agents

A Geronikaki, M Fesatidou, V Kartsev… - Current topics in …, 2013 - ingentaconnect.com
The last two decades are characterized by major increases in the incidence of systemic
fungal infections caused by the yeast Candida albicans, particularly in immunocompromised …

[HTML][HTML] Synthesis and antimicrobial activity of methoxy-substituted γ-oxa-ε-lactones derived from flavanones

W Gładkowski, M Siepka, T Janeczko… - Molecules, 2019 - mdpi.com
Six γ-oxa-ε-lactones, 4-phenyl-3, 4-dihydro-2 H-1, 5-benzodioxepin-2-one (5a) and its five
derivatives with methoxy groups in different positions of A and B rings (5b–f), were …