Privileged scaffolds or promiscuous binders: a comparative study on rhodanines and related heterocycles in medicinal chemistry
T Mendgen, C Steuer, CD Klein - Journal of medicinal chemistry, 2012 - ACS Publications
Rhodanines and related five-membered heterocycles with multiple heteroatoms have
recently gained a reputation of being unselective compounds that appear as “frequent …
recently gained a reputation of being unselective compounds that appear as “frequent …
Recent developments with rhodanine as a scaffold for drug discovery
D Kaminskyy, A Kryshchyshyn… - Expert Opinion on Drug …, 2017 - Taylor & Francis
Introduction: Rhodanines, as one of the 4-thiazolidinones subtypes, are recognized as
privileged heterocycles in medicinal chemistry. The main achievements include the …
privileged heterocycles in medicinal chemistry. The main achievements include the …
Rhodanine as a scaffold in drug discovery: a critical review of its biological activities and mechanisms of target modulation
T Tomašić, L Peterlin Mašič - Expert opinion on drug discovery, 2012 - Taylor & Francis
Introduction: Rhodanine-based compounds have been associated with numerous biological
activities. After many years of research in drug discovery, they have gained a reputation as …
activities. After many years of research in drug discovery, they have gained a reputation as …
Rhodanine as a privileged scaffold in drug discovery
Rhodanines, thiazolidine-2, 4-diones and pseudothiohydantoins have become a very
interesting class of heterocyclic compounds since the introduction of various glitazones and …
interesting class of heterocyclic compounds since the introduction of various glitazones and …
Heterocycles in drugs and drug discovery
A Gomtsyan - Chemistry of heterocyclic compounds, 2012 - Springer
Heterocycles are common fragments of the vast majority of marketed drugs. This is a
reflection of the central role that heterocycles play in modern drug design. They can serve as …
reflection of the central role that heterocycles play in modern drug design. They can serve as …
Four-membered ring-containing spirocycles: synthetic strategies and opportunities
EM Carreira, TC Fessard - Chemical reviews, 2014 - ACS Publications
Four-membered rings are witnessing significant prominence in medicinal chemistry
discovery programs. For example, a search of the chemical databases shows exponential …
discovery programs. For example, a search of the chemical databases shows exponential …
[HTML][HTML] Review of anticancer potentials and structure-activity relationships (SAR) of rhodanine derivatives
LJ Yin, AKD bin Ahmad Kamar, GT Fung… - Biomedicine & …, 2022 - Elsevier
Rhodanine has been recognized as a privileged scaffold in medicinal chemistry due to its
well-known ability to demonstrate a broad range of biological activities. The possibility of …
well-known ability to demonstrate a broad range of biological activities. The possibility of …
The pyridazine heterocycle in molecular recognition and drug discovery
NA Meanwell - Medicinal Chemistry Research, 2023 - Springer
The pyridazine ring is endowed with unique physicochemical properties, characterized by
weak basicity, a high dipole moment that subtends π-π stacking interactions and robust …
weak basicity, a high dipole moment that subtends π-π stacking interactions and robust …
Modern advances in heterocyclic chemistry in drug discovery
AP Taylor, RP Robinson, YM Fobian… - Organic & …, 2016 - pubs.rsc.org
New advances in synthetic methodologies that allow rapid access to a wide variety of
functionalized heterocyclic compounds are of critical importance to the medicinal chemist as …
functionalized heterocyclic compounds are of critical importance to the medicinal chemist as …
Heterocycles in medicinal chemistry
J Jampilek - Molecules, 2019 - mdpi.com
Heteroatoms constitute a very common fragment of a number of active pharmaceutical
ingredients as well as excipients; from the point of view of significance, it is all the same if …
ingredients as well as excipients; from the point of view of significance, it is all the same if …