The chalcone synthase superfamily of type III polyketide synthases

MB Austin, JP Noel - Natural product reports, 2003 - pubs.rsc.org
Covering 1970–2001This review covers the functionally diverse type III polyketide synthase
(PKS) superfamily of plant and bacterial biosynthetic enzymes, from the discovery of …

Review on polyphenols in Theobroma cacao: changes in composition during the manufacture of chocolate and methodology for identification and quantification

J Wollgast, E Anklam - Food Research International, 2000 - Elsevier
Polyphenols have become an intense focus of research interest because of their perceived
health-beneficial effects, such as anti-carcinogenic, anti-atherogenic, anti-inflammatory, anti …

[HTML][HTML] Design of allele-specific inhibitors to probe protein kinase signaling

AC Bishop, K Shah, Y Liu, L Witucki, C Kung… - Current Biology, 1998 - cell.com
Background: Deconvoluting protein kinase signaling pathways using conventional genetic
and biochemical approaches has been difficult because of the overwhelming number of …

Binding mode of the 4-anilinoquinazoline class of protein kinase inhibitor: X-ray crystallographic studies of 4-anilinoquinazolines bound to cyclin-dependent kinase 2 …

L Shewchuk, A Hassell, B Wisely… - Journal of medicinal …, 2000 - ACS Publications
4-Anilinoquinazolines represent an important class of protein kinase inhibitor. Modes of
binding for two members of this inhibitor class were determined by X-ray crystallographic …

Protein tyrosine kinase inhibitors as novel therapeutic agents

A Levitzki - Pharmacology & therapeutics, 1999 - Elsevier
Protein tyrosine kinases (PTKs) play a key role in normal cell and tissue development.
Enhanced PTK activity is intimately correlated with proliferative diseases, such as cancers …

Signal‐transduction therapy: a novel approach to disease management

A Levitzki - European journal of biochemistry, 1994 - Wiley Online Library
In the past decade it has become apparent that many diseases result from aberrations in
signaling pathways. These include proliferative diseases such as cancers, atherosclerosis …

Mappability of drug-like space: towards a polypharmacologically competent map of drug-relevant compounds

P Sidorov, H Gaspar, G Marcou, A Varnek… - Journal of computer …, 2015 - Springer
Intuitive, visual rendering—mapping—of high-dimensional chemical spaces (CS), is an
important topic in chemoinformatics. Such maps were so far dedicated to specific compound …

IκB kinases α and β show a random sequential kinetic mechanism and are inhibited by staurosporine and quercetin

GW Peet, J Li - Journal of Biological Chemistry, 1999 - ASBMB
Activation of transcription factor NF-κB is regulated by phosphorylation and subsequent
degradation of its inhibitory subunit IκB. The signal-induced phosphorylation of IκB involves …

Structural classification of protein kinases using 3D molecular interaction field analysis of their ligand binding sites: target family landscapes

T Naumann, H Matter - Journal of medicinal chemistry, 2002 - ACS Publications
Protein kinases are critical components of signaling pathways and trigger various biological
events. Several members of this superfamily are interesting targets for novel therapeutic …

A versatile route to 2-alkyl-/aryl-amino-3-formyl-and hetero-annelated-chromones, through a facile nucleophilic substitution at C2 in 2-(N-methylanilino)-3 …

G Singh, R Singh, NK Girdhar, MPS Ishar - Tetrahedron, 2002 - Elsevier
The N-methylanilino group in 2-(N-methylanilino)-3-formylchromones, obtained in high yield
by rearrangement of C (4-oxo-4H [1]-benzopyran-3-yl)-N-phenylnitrones to 2-anilino-3 …