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Inhibitors of Src tyrosine kinase: The preparation and structure-activity relationship of 4-anilino-3-cyanoquinolines and 4-anilinoquinazolines
被引:68
作者:

Wang, YD
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Miller, K
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Boschelli, DH
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Ye, F
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Wu, BQ
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Floyd, MB
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Powell, DW
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Wissner, A
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Weber, JM
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA

Boschelli, F
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Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA
机构:
[1] Wyeth Ayerst Res, Chem Sci & Oncol, Pearl River, NY 10965 USA
关键词:
D O I:
10.1016/S0960-894X(00)00493-5
中图分类号:
R914 [药物化学];
学科分类号:
100701 ;
摘要:
Src is a nonreceptor tyrosine kinase involved in signaling pathways that control proliferation, migration, and angiogenesis. Increased Src expression and activity are associated with an increase in tumor malignancy and poor prognosis. Several quinolines and quinazolines were identified as potent and selective inhibitors of Src kinase activity. (C) 2000 Elsevier Science Ltd. All rights reserved.
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页码:2477 / 2480
页数:4
相关论文
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机构: Novartis Pharma AG, Therapeut Areas Arthrit & Bone Metab, CH-4002 Basel, Switzerland

Meyer, T
论文数: 0 引用数: 0
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机构: Novartis Pharma AG, Therapeut Areas Arthrit & Bone Metab, CH-4002 Basel, Switzerland

Green, J
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机构: Novartis Pharma AG, Therapeut Areas Arthrit & Bone Metab, CH-4002 Basel, Switzerland
[10]
A novel inhibitor of the tyrosine kinase Src suppresses phosphorylation of its major cellular substrates and reduces bone resorption in vitro and in rodent models in vivo
[J].
Missbach, M
;
Jeschke, M
;
Feyen, J
;
Müller, K
;
Glatt, M
;
Green, J
;
Susa, M
.
BONE,
1999, 24 (05)
:437-449

Missbach, M
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机构:
Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland

Jeschke, M
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Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland

Feyen, J
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Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland

Müller, K
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Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland

Glatt, M
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Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland

Green, J
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Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland

Susa, M
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Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland Novartis Pharma AG, Res Bone Metab, CH-4002 Basel, Switzerland