A new series of PDGF receptor tyrosine kinase inhibitors: 3-substituted quinoline derivatives

MP Maguire, KR Sheets, K McVety… - … medicinal chemistry, 1994 - ACS Publications
… This leads to tyrosine phosphorylation of numerous proteins, … An inhibitor of the PDGF
receptor tyrosine kinase activity … as epidermal growth factor receptor tyrosine kinase (EGF-RTK) …

How the structural properties of the indole derivatives are important in kinase targeted drug design?: A case study on tyrosine kinase inhibitors

D Mondal, SA Amin, M Moinul, K Das, T Jha… - … & Medicinal Chemistry, 2022 - Elsevier
… indoles in the design of different tyrosine kinases inhibitors. … of inhibitors against different
tyrosine kinases such as epidermal … based tyrosine kinase inhibitors with improved potency. …

Synthesis of quinazolines as tyrosine kinase inhibitors

SK Srivastava, V Kumar, SK Agarwal… - … Medicinal Chemistry …, 2009 - ingentaconnect.com
… in quinazoline are appropriate sites for designing new tyrosine kinase inhibitors. This review
should help the medicinal chemist in designing more effective tyrosine kinase inhibitors. …

Protein tyrosine kinases and cancer

EM Dobrusin, DW Fry - Annual reports in medicinal chemistry, 1992 - Elsevier
… abl Tyrosine Kinase - c-abl encodes for a 145 Kd non-receptor tyrosine kinase. Its natural …
which encodes a fusion protein with activated abl tyrosine kinase activity (16). This molecule …

… and biological evaluations of 3-substituted indolin-2-ones: a novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases

L Sun, N Tran, F Tang, H App, P Hirth… - … medicinal chemistry, 1998 - ACS Publications
… This report describes the identification, characterization, and SAR analysis of a novel chemical
series of tyrosine kinase inhibitors, 3-substituted indolin-2-ones, which exhibit selectivity …

Btk inhibitors: a medicinal chemistry and drug delivery perspective

C Brullo, C Villa, B Tasso, E Russo… - International journal of …, 2021 - mdpi.com
… , Bruton’s tyrosine Kinase (Btk) has emerged as new target in medicinal chemistry. Since …
, covering advances in the field of medicinal chemistry. Furthermore, the nanoformulations …

… of 4-[(3-Bromophenyl)amino]-6-(methylamino)- pyrido[3,4-d]pyrimidine (PD 158780), a Potent and Specific Inhibitor of the Tyrosine Kinase Activity of Receptors for …

GW Rewcastle, DK Murray, WL Elliott… - … medicinal chemistry, 1998 - ACS Publications
The 4-[(3-bromophenyl)amino]pyrido[3,4-d]pyrimidine PD 158780 is a very potent in vitro
inhibitor of the tyrosine kinase activity of the epidermal growth factor receptor (EGFR) (IC 50 …

Synthesis and biochemical evaluation of a series of aminoflavones as potential inhibitors of protein-tyrosine kinases p56lck, EGFr, and p60v-src

M Cushman, H Zhu, RL Geahlen… - … of medicinal chemistry, 1994 - ACS Publications
… proteinserine/threonine kinases.13,14 However, we … -tyrosine kinase p56Zc* over
protein-serine/threonine kinases.16 … much less active against protein kinase C and protein kinase

[图书][B] An introduction to medicinal chemistry

GL Patrick - 2023 - books.google.com
… In so doing, it highlights the importance of medicinal chemistry in all our lives and the
fascination of working in a field which overlaps the disciplines of chemistry, biochemistry, …

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… - … Medicinal Chemistry, 1995 - ACS Publications
tyrosine kinase signal transduction enzymes,10 containing neighboring binding domains for
both the tyrosine-… of this enzyme are considered to bind to the tyrosine site,7,8,11,12 we and …