Results 1 to 10 of about 3,541 (213)

The Bucherer–Bergs Multicomponent Synthesis of Hydantoins—Excellence in Simplicity [PDF]

open access: yesMolecules, 2021
Hydantoins and their hybrids with other molecules represent a very important group of heterocycles because they exhibit diverse biological and pharmacological activities in medicinal and agrochemical applications. They also serve as key precursors in the
Martin Kalník   +2 more
exaly   +4 more sources

N-Alkylhydantoins as New Organogelators and Their Ability to Create Thixotropic Mixed Molecular Organogels. [PDF]

open access: yesGels, 2022
The author reported molecular organogels using N-alkylhydantoins as new low-molecular-weight gelators for the first time, and thixotropic mixed molecular organogels using a set of N-alkylhydantoin gelators with different alkyl chain lengths.
Ohsedo Y.
europepmc   +2 more sources

Recent Applications of Hydantoins in Drug Discovery: Updates (2019~Present) [PDF]

open access: yesMolecules
Hydantoins, exemplified by the imidazolidine-2,4-dione core, are privileged scaffolds in medicinal chemistry due to their compact structure, versatile hydrogen-bonding capacity, ability to fine-tune physicochemical properties for drug-like molecules, and
Jyoti Dnyaneshwar Palkhede   +3 more
europepmc   +2 more sources

Synthesis, Absolute Configuration, Biological Profile and Antiproliferative Activity of New 3,5-Disubstituted Hydantoins. [PDF]

open access: yesPharmaceuticals (Basel)
Hydantoins, a class of five-membered heterocyclic compounds, exhibit diverse biological activities. The aim of this study was to synthesize and characterize a series of novel 3,5-disubstituted hydantoins and to investigate their antiproliferative ...
Jurin M   +8 more
europepmc   +2 more sources

Sequential two-step, one-pot microwave-assisted Urech synthesis of 5-monosubstituted hydantoins from L-amino acids in water. [PDF]

open access: yesBeilstein J Org Chem
The hydantoin scaffold is renowned for its wide-ranging biological activities, including antibacterial, antiviral, anticancer, anti-inflammatory, and anticonvulsant effects.
Chang WJ, Liew SY, Kurz T, Tan SP.
europepmc   +2 more sources

Synthesis and Evaluation of 5-(Heteroarylmethylene)hydantoins as Glycogen Synthase Kinase-3β Inhibitors. [PDF]

open access: yesPharmaceuticals (Basel)
Glycogen synthase kinase-3 (GSK-3) is a serine/threonine kinase which plays a center role in the phosphorylation of a wide variety of proteins, generally leading to their inactivation. As such, GSK-3 is viewed as a therapeutic target.
Schneider NO   +4 more
europepmc   +2 more sources

Solvent effects on the structure-property relationship of anticonvulsant hydantoin derivatives: A solvatochromic analysis [PDF]

open access: yesChemistry Central Journal, 2011
Considering the pharmaceutical importance of hydantoins, a set of 25 derivatives of phenytoin, nirvanol and 5-methyl-5-phenylhydantoin, the lipophilicities of which were gradually increased by the introduction of different alkyl, cycloalkyl and alkenyl ...
Gordana Ušćumlić   +2 more
core   +3 more sources

Anti-Inflammatory Activity of Cyclic Imide Derivatives. [PDF]

open access: yesPharmaceuticals (Basel)
Imide derivatives constitute an interesting group of compounds exhibiting broad biological activity. Structures containing the imide moiety [–CO–N(R)–CO–] occur in both natural and synthetic compounds.
Redzicka A, Tylińska B, Wójcicka A.
europepmc   +2 more sources

Synthesis, carbonic anhydrase inhibition studies and modelling investigations of phthalimide-hydantoin hybrids. [PDF]

open access: yesJ Enzyme Inhib Med Chem
A novel series of hydantoins incorporating phthalimides has been synthesised by condensation of activated phthalimides with 1-aminohydantoin and investigated for their inhibitory activity against a panel of human (h) carbonic anhydrase (CA, EC 4.2.1.1 ...
Abdoli M   +4 more
europepmc   +2 more sources

Facile synthesis of hydantoin/1,2,4-oxadiazoline spiro-compounds via 1,3-dipolar cycloaddition of nitrile oxides to 5-iminohydantoins. [PDF]

open access: yesBeilstein J Org Chem
The cycloaddition of 1,3-dipoles at C=N bonds is a relatively rare process, in contrast to the widespread cycloaddition reactions at C=C, C≡C, and C=S bonds.
Petrova JV   +6 more
europepmc   +2 more sources

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