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US 2003/0158199 A1Published application
Novel compounds for inhibition of Tie-2
AssigneeKylix B.V.
InventorsFrank Stieber, Klaus Hellmuth, Herbert Waldmann, Ralph Mazitschek, Athanassios Giannis
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Abstract
The present invention provides a method of inhibiting or moderating the kinase activity of tyrosine kinases comprising the administration of a compound represented by formula (1) said kinase in sufficient concentration to inhibit or moderate the enzyme activity of said kinase.
Claims17
A compound of formula I
- 39
- wherein V is H or
- 40
- R1 can be independently H, alkyl, alkenyl, cycloalkyl, heteroalkyl, aryl, heteroaryl, arylalkyl, alkylaryl, N—R6R7, N—(CO)R6R7, N—R6(CO)R7 or N—(CO)—O—R6R7,
- R8 can be independently H, alkyl, alkenyl, cycloalkyl, heteroalkyl, aryl, heteroaryl, arylalkyl, alkylaryl, N—R3R4, N—(CO)R3R4, N—R3(CO)R4, N—(CO)—O—R3R4, O—R3, CO—R3, CO—OR3 or O—CO—R3,
- R2, R5, can be independently H, alkyl, alkenyl, cycloalkyl, heteroalkyl, aryl, heteroaryl, arylalkyl, alkylaryl, Br, Cl, F, CF3,
- R3, R4, R6, R7 can be independently H, alkyl, alkenyl, cycloalkyl, heteroalkyl, aryl, heteroaryl, arylalkyl, alkylaryl, COOR5 and CO—R5, and may for a ring structure,
- X, Y, Z can be independently CH or N, and
- U can be independently S or NH,
- W can be independently NH, O or S, and
- racemic-diastereomeric mixtures, optical isomers, and pharmaceutically acceptable salts thereof.
8 more elements
Compound 1-37.
Dependencies are inferred from the claim text.