The following articles (labelled with PubMed ID or TBD) are for your review
PMID | Data | Article Title | Organization |
12238930 |
94 |
Potent and selective inhibitors of PDGF receptor phosphorylation. 2. Synthesis, structure activity relationship, improvement of aqueous solubility, and biological effects of 4-[4-(N-substituted (thio)carbamoyl)-1-piperazinyl]-6,7-dimethoxyquinazoline derivatives. |
Kyowa Hakko Kogyo |
12166950 |
208 |
Identification of orally active, potent, and selective 4-piperazinylquinazolines as antagonists of the platelet-derived growth factor receptor tyrosine kinase family. |
Millennium Pharmaceuticals |
1652014 |
44 |
Sulfonylbenzoyl-nitrostyrenes: potential bisubstrate type inhibitors of the EGF-receptor tyrosine protein kinase. |
Ciba-Geigy |
12951113 |
11 |
Synthesis of pyrimidinopyridine-triazene conjugates targeted to abl tyrosine kinase. |
Mcgill University/Royal Victoria Hospital |
11277536 |
130 |
7-Pyrrolidinyl- and 7-piperidinyl-5-aryl-pyrrolo[2,3-d]pyrimidines--potent inhibitors of the tyrosine kinase c-Src. |
Novartis Pharma Research |
11277535 |
80 |
7-Alkyl- and 7-cycloalkyl-5-aryl-pyrrolo[2,3-d]pyrimidines--potent inhibitors of the tyrosine kinase c-Src. |
Novartis Pharma Research |
10999468 |
30 |
1-Phenyl-5-pyrazolyl ureas: potent and selective p38 kinase inhibitors. |
Bayer Research Center |
10853665 |
104 |
Substituted 5,7-diphenyl-pyrrolo[2,3d]pyrimidines: potent inhibitors of the tyrosine kinase c-Src. |
Novartis Pharma |
10090785 |
63 |
Use of a pharmacophore model for the design of EGFR tyrosine kinase inhibitors: isoflavones and 3-phenyl-4(1H)-quinolones. |
Novartis |
8691423 |
89 |
4-(Phenylamino)pyrrolopyrimidines: potent and selective, ATP site directed inhibitors of the EGF-receptor protein tyrosine kinase. |
Ciba Pharmaceuticals |
8151612 |
88 |
Dianilinophthalimides: potent and selective, ATP-competitive inhibitors of the EGF-receptor protein tyrosine kinase. |
Ciba-Geigy |
15027848 |
28 |
7-Alkoxy-4-phenylamino-3-quinolinecar-bonitriles as dual inhibitors of Src and Abl kinases. |
Wyeth Research |