Chemistry of biologically important synthetic organoselenium compounds

G Mugesh, WW du Mont, H Sies - Chemical reviews, 2001 - ACS Publications
The element selenium was discovered in 1818 by the Swedish chemist Berzelius and was
named after the Greek goddess of the moon, Selene. 1 In biology, selenium was long …

Chemical inhibitors of protein kinases

AJ Bridges - Chemical reviews, 2001 - ACS Publications
Many excellent and up to date reviews on kinase inhibitors exist, and this area certainly
does not meet the normal criteria for a Chemical Reviews article. However, most of these …

Tyrosine kinase inhibitors. 8. An unusually steep structure− activity relationship for analogues of 4-(3-bromoanilino)-6, 7-dimethoxyquinazoline (PD 153035), a potent …

AJ Bridges, H Zhou, DR Cody… - Journal of medicinal …, 1996 - ACS Publications
4-(3-Bromoanilino)-6, 7-dimethoxyquinazoline (32, PD 153035) is a very potent inhibitor
(IC50 0.025 nM) of the tyrosine kinase activity of the epidermal growth factor receptor …

Tyrosine kinase receptors as attractive targets of cancer therapy

A Bennasroune, A Gardin, D Aunis, G Crémel… - Critical reviews in …, 2004 - Elsevier
Receptor tyrosine kinases (RTKs) are the main mediators of the signaling network that
transmit extracellular signals into the cell, and control cellular differentiation and …

Efficient synthesis of disulfides by air oxidation of thiols under sonication

JLG Ruano, A Parra, J Alemán - Green Chemistry, 2008 - pubs.rsc.org
Alkyl, aryl and heteroaryl symmetrical disulfides can be easily obtained by heating the
corresponding thiols for several hours at 80° C with Et3N in DMF under atmospheric oxygen …

Kinomics—structural biology and chemogenomics of kinase inhibitors and targets

M Vieth, RE Higgs, DH Robertson, M Shapiro… - … et Biophysica Acta (BBA …, 2004 - Elsevier
Classifying kinases based entirely on small molecule selectivity data is a new approach to
drug discovery that allows scientists to understand relationships between targets. This …

Protein kinase inhibitors: the tyrosine-specific protein kinases

DS Lawrence, J Niu - Pharmacology & therapeutics, 1998 - Elsevier
Inhibitors for tyrosine-specific protein kinases ultimately may constitute a novel family of
medicinally active agents. Unfortunately, the challenges associated with the acquisition of …

Synthesis of organochalcogen compounds using non‐conventional reaction media

G Perin, D Alves, RG Jacob, AM Barcellos… - …, 2016 - Wiley Online Library
Organochalcogen compounds (containing S, Se and Te) are interesting either for use as an
intermediate in the synthesis of complex molecules or for the exploitation of their biological …

Tyrosine kinase inhibitors. 7. 7-Amino-4-(phenylamino)-and 7-amino-4-[(phenylmethyl) amino] pyrido [4, 3-d] pyrimidines: a new class of inhibitors of the tyrosine …

AM Thompson, AJ Bridges, DW Fry… - Journal of Medicinal …, 1995 - ACS Publications
The synthesis of 7-aminopyrido [4, 3-d] pyrimidines bearing aromatic side chains at the 4-
position is reported. These compounds are shown to be a new class of inhibitors of the …

Tyrosine Kinase Inhibitors. 10. Isomeric 4-[(3-Bromophenyl)amino]pyrido[d]- pyrimidines Are Potent ATP Binding Site Inhibitors of the Tyrosine Kinase Function of the …

GW Rewcastle, BD Palmer, AM Thompson… - Journal of Medicinal …, 1996 - ACS Publications
Following the discovery of the very high inhibitory ability of the 4-[(3-bromophenyl) amino]
quinazolines against the tyrosine kinase activity of the epidermal growth factor receptor …