Imidazole: synthesis, functionalization and physicochemical properties of a privileged structure in medicinal chemistry

HV Tolomeu, CAM Fraga - Molecules, 2023 - mdpi.com
Imidazole was first synthesized by Heinrich Debus in 1858 and was obtained by the reaction
of glyoxal and formaldehyde in ammonia, initially called glyoxaline. The current literature …

Chemistry and biology of multicomponent reactions

A Domling, W Wang, K Wang - Chemical reviews, 2012 - ACS Publications
Multicomponent reactions (MCRs) are one-pot reactions employing more than two starting
materials, for example, 3, 4,..., 7, where most of the atoms of the starting materials are …

Fluorine in pharmaceuticals: looking beyond intuition

K Müller, C Faeh, F Diederich - science, 2007 - science.org
Fluorine substituents have become a widespread and important drug component, their
introduction facilitated by the development of safe and selective fluorinating agents …

Mitogen-activated protein (MAP) kinase pathways: regulation and physiological functions

G Pearson, F Robinson, T Beers Gibson, B Xu… - Endocrine …, 2001 - academic.oup.com
Mitogen-activated protein (MAP) kinases comprise a family of ubiquitous proline-directed,
protein-serine/threonine kinases, which participate in signal transduction pathways that …

[HTML][HTML] The conformational plasticity of protein kinases

M Huse, J Kuriyan - Cell, 2002 - cell.com
Protein kinases operate in a large number of distinct signaling pathways, where the tight
regulation of their catalytic activity is crucial to the development and maintenance of …

Structural mechanism for STI-571 inhibition of abelson tyrosine kinase

T Schindler, W Bornmann, P Pellicena, WT Miller… - Science, 2000 - science.org
The inadvertent activation of the Abelson tyrosine kinase (Abl) causes chronic myelogenous
leukemia (CML). A small-molecule inhibitor of Abl (STI-571) is effective in the treatment of …

Rational design of inhibitors that bind to inactive kinase conformations

Y Liu, NS Gray - Nature chemical biology, 2006 - nature.com
The majority of kinase inhibitors that have been developed so far—known as type I inhibitors—
target the ATP binding site of the kinase in its active conformation, in which the activation …

p38 MAP kinases: key signalling molecules as therapeutic targets for inflammatory diseases

S Kumar, J Boehm, JC Lee - Nature reviews Drug discovery, 2003 - nature.com
The p38 MAP kinases are a family of serine/threonine protein kinases that play important
roles in cellular responses to external stress signals. Since their identification about 10 years …

Potential mean force from umbrella sampling simulations: what can we learn and what is missed?

W You, Z Tang, CEA Chang - Journal of chemical theory and …, 2019 - ACS Publications
Changes in free energy provide valuable information for molecular recognition, including
both ligand–receptor binding thermodynamics and kinetics. Umbrella sampling (US), a …

MAP kinases

Z Chen, TB Gibson, F Robinson, L Silvestro… - Chemical …, 2001 - ACS Publications
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