-
2
-
-
0031957879
-
Current progress towards the development of tyrosine kinase inhibitors as anticancer agents
-
(1998)
Emerging Drugs
, vol.3
, pp. 279-292
-
-
Bridges, A.1
-
11
-
-
0033614838
-
Restenosis following angioplasty in the swine coronary artery is inhibited by an orally active PDGF-receptor tyrosine kinase inhibitor, RPR101511A
-
(1999)
Circulation
, vol.99
, pp. 3292-3299
-
-
Bilder, G.1
Wentz, T.2
Leadley, R.3
-
12
-
-
0028023104
-
5,7-Dimethoxy-3-(4-pyridinyl)quinoline is a potent and selective inhibitor of human vascular β-type platelet-derived growth factor receptor tyrosine kinase
-
(1994)
J. Med. Chem.
, vol.37
, Issue.17
, pp. 2627-2629
-
-
Dolle, R.E.1
Dunn, J.A.2
Bobko, M.3
-
15
-
-
0030039555
-
Tyrosine kinase inhibitors. 8 An unusually steep structure activity relationship for analogs of 4-(3-bromoanilino)-6,7-dimethoxy quinazoline (PD 153035), a potent inhibitor of the epidermal growth factor receptor
-
(1996)
J. Med. Chem.
, vol.39
, pp. 267-276
-
-
Bridges, A.J.1
Zhou, H.2
Cody, D.R.3
-
17
-
-
0034710707
-
4-Anilino-6,7-dialkoxyquinoline-3-carbonitrile inhibitors of epidermal growth factor receptor kinase and their bioisosteric relationship to the 4-anilimo-6,7-dialkoxyquinazoline inhibitors
-
(2000)
J. Med. Chem.
, vol.43
, pp. 3244-3256
-
-
Wissner, A.1
Berger, D.M.2
Boschelli, D.H.3
-
18
-
-
0005961717
-
-
Inhibition of src kinase activity by a series of 4-anilino-3-cyanoquinolines. Book of Abstracts, 220th ACS National Meeting. Washington, USA MEDI-52.
-
(2000)
-
-
Ye, F.1
Boschelli, D.H.2
Wang, D.3
-
19
-
-
0032893263
-
SU5416 is a potent and selective inhibitor of the vascular endothelial growth factor receptor (flk-1/KDR) that inhibits tyrosine kinase catalysis, tumor vascularization and growth of multiple tumor types
-
(1999)
Cancer Res.
, vol.59
, pp. 99-106
-
-
Fong, T.A.T.1
Shawyer, L.K.2
Sun, L.3
-
20
-
-
0032474915
-
Synthesis and biological evaluations of 3-substituted indolin-2-ones: A novel class of tyrosine kinase inhibitors that exhibit selectivity toward particular receptor tyrosine kinases
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2588-2603
-
-
Sun, L.1
Tran, N.2
Tang, F.3
-
21
-
-
0034644272
-
Identification of substituted 3-[(4,5,6,7,-tetrahydro-1H-indol-2-yl)methyl ene]-1,3,-dihydroindol-2-ones as growth factor receptor inhibitors for VEGF-R2 (flk-1/KDR), FGF-R1 and PDGF-Rβ tyrosine kinases
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2655-2663
-
-
Sun, L.1
Tran, N.2
Liang, C.3
-
22
-
-
0005993042
-
3-Substituted indolin-2-ones are potent and selective inhibitors of cyclin-dependent kinases and exhibit effects on cell cycle and tumor growth
-
Proceedings of the 91st Meeting of the American Association for Cancer Research. San Francisco, USA Abstract
-
(2000)
, pp. 1592
-
-
Rice, A.G.1
-
23
-
-
0005925139
-
-
Identification of inhibitors of cyclin-dependent kinases. Book of Abstracts, 218th ACS National Meeting. New Orleans, USA MEDI-314.
-
(1999)
-
-
Veal, J.M.1
Bramson, N.2
Dickerson, S.3
-
24
-
-
4243974458
-
Novel cyclin dependent kinase inhibitors prevent chemotherapy-induced alopecia
-
Proceedings of the 91st Meeting of the American Association for Cancer Research. San Francisco, USA Abstract
-
(2000)
, pp. 200
-
-
Davis, S.T.1
Bramson, N.2
Dickerson, S.3
-
29
-
-
19244370071
-
Design, synthesis and evaluations of substituted 3-[(3-or4-carboxy-ethylpyrrol-2-y1) methylideny1]indolin-2-ones as inhibitors of VEGF, FGF and PDGF receptor tyrosine kinases
-
(1999)
J. Med. Chem.
, vol.42
, pp. 5120-5130
-
-
Sun, L.1
Tran, N.2
Liang, C.3
-
33
-
-
4244102259
-
Pharmacological characterization of p38 kinase inhibitors from the urea class
-
Book of Abstracts, 220th ACS National Meeting. Washington, USA MEDI-149.
-
(2000)
-
-
Ranges, G.E.1
Bhargava, A.2
Bortolon, E.3
-
34
-
-
0002046857
-
Discovery of a new class of potent raf kinase inhibitors: Structure activity relationships
-
Book of Abstracts, 11th NCI-EORTC-AACR Symposium on New Drugs in Cancer Therapy. Amsterdam, Netherlands Abstract
-
(2000)
, pp. 335
-
-
Lowinger, T.B.1
Riedl, B.2
Wood, J.3
-
35
-
-
0005991706
-
Potent and selective MEK inhibitors: Synthesis and SAR of 2-(4-iodo-phenylamino)benzoic acids and hydroxamic acid derivatives thereof
-
Proceedings of the 90th Meeting of the American Association for Cancer Research. Philadelphia. USA Abstract
-
(1999)
, pp. 806
-
-
Tecle, H.1
Barrett, S.2
Bridges, A.3
-
36
-
-
0005923997
-
N-alkoxy-2-(4-iodo-phenylamino)-benzamides: O-alkyl benhydroxamate esters as a novel class of potent MEK inhibitors
-
Book of Abstracts, 218th ACS National Meeting. New Orleans, USA MEDI-203.
-
(1999)
-
-
Barrett, S.D.1
Bridges, A.J.2
Leopold, W.R.3
-
38
-
-
0033947625
-
New anilinophthalazines as potent and orally well absorbed inhibitors of the VEGF receptor tyrosine kinases useful as antagonists of tumor-driven angiogenesis
-
(2000)
J. Med. Chem.
, vol.43
, pp. 2310-2323
-
-
Bold, G.1
Altmann, K.H.2
Frei, J.3
-
39
-
-
0034655182
-
PTK787/ZK 222584, a novel and potent inhibitor of vascular endothelial growth factor receptor tyrosine kinases, impairs vascular endothelial growth factor-induced responses and tumor growth after oral administration
-
(2000)
Cancer Res.
, vol.60
, Issue.8
, pp. 2178-2189
-
-
Wood, J.M.1
Bold, G.2
Buchdunger, E.3
-
40
-
-
4244102258
-
Alkyl-substituted indenopyrazoles as inhibitors of cyclin-dependent kinases
-
Book of Abstracts, 219th ACS National Meeting. San Francisco, USA MEDI-39.
-
(2000)
-
-
Higley, C.A.1
Yue, E.W.2
Benfield, P.A.3
-
45
-
-
0033614949
-
Paullones, a series of cyclin-dependent kinase inhibitors: Synthesis, evaluation of CDK1/cyclin B inhibition and in vitro antitumor activity
-
(1999)
J. Med. Chem.
, vol.42
, pp. 2909-2919
-
-
Schultz, C.1
Link, A.2
Leost, M.3
-
47
-
-
0005965706
-
5-Acylpyrazolo[3,4-b]pyrimidines
-
Potent inhibitors of cyclin-dependent kinases. Proceedings of the 91st Meeting of the American Association for Cancer Research. San Francisco, USA Abstract
-
(2000)
, pp. 3002
-
-
Misra, R.N.1
Rawlins, D.B.2
Batorski, R.3
-
52
-
-
0342314481
-
Inhibition of Rho-associated kinase results in suppression of neointimal formation of balloon-injured arteries
-
(2000)
Circulation
, vol.101
, Issue.17
, pp. 2030-2033
-
-
Sawada, N.1
Itoh, H.2
Ueyama, K.3
-
53
-
-
0000863502
-
Structure-based inhibitor design for CDK2, a cell cycle controlling protein kinase
-
(1998)
Pure Appl. Chem.
, vol.70
, Issue.3
, pp. 555-565
-
-
Kim, S.H.1
-
55
-
-
0029020282
-
The eucaryotic protein kinase superfamily: Kinase (catalytic) domain structure and classification
-
(1995)
FASEB J.
, vol.9
, pp. 576-596
-
-
Hanks, S.K.1
Hunter, T.2
-
57
-
-
0032802397
-
Structure-activity relationship homology (SARAH): A conceptual framework for drug discovery in the genomic era
-
(1999)
Chem. Biol.
, vol.6
, Issue.1
-
-
Frye, S.V.1
|