摘要:
The present invention encompasses compounds of general formula (1), wherein the groups R 1 to R 4 , X 1 , X 2 , X 3 , X 4 , X 5 , Q, L 1 and L 2 are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, as well as pharmaceutical preparations and formulations of these compounds.
摘要:
Compounds of formula (I), wherein X, a, b, R 1, R 2 , R 3 , R 4 and R 5 are as defined in the specification, processes for their production, their uses and pharmaceutical compositions containing them.
摘要:
The present invention encompasses compounds of general formula (1) wherein the groups R 0 to R 3 and L are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, pharmaceutical preparations which contain such compounds and their use as medicaments.
摘要:
The present invention encompasses compounds of general formula (1) wherein the groups R 2 to R 4 , L, Q and n are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, and their use for preparing a pharmaceutical composition with the above-mentioned properties.
摘要:
The present invention relates to biphenylyl derivatives, processes for their production, their uses and pharmaceutical compositions containing them.
摘要:
An amine, which is substituted y phenyl-substituted pyrimidin; and phenyl; and a third substituent and its use as an immvmoglofulin E (Ige ) inhibitor.
摘要:
The present invention relates to new compounds of general formula (I), wherein the groups R1 to R3, X1, X2, X3 and L1 are defined as in claim 1, which are suitable for the treatment of diseases characterised by excessive or abnormal cell proliferation, and the use thereof in such a treatment.
摘要:
Die vorliegende Erfindung umfasst Verbindungen der allgemeinen Formel (I), wobei die Reste R 2 bis R 4 , L, Q und n wie in Anspruch 1 definiert sind, welche zur Behandlung von Krankheiten, die durch exzessive oder anomale Zellproliferation charakterisiert sind, geeignet sind, sowie deren Verwendung zur Herstellung eines Arzneimittels mit den vorstehend genannten Eigenschaften.
摘要:
The present invention relates to a method (assay) for determining the activity of an enzyme selected from the group consisting of a sphingosine kinase and a phosphatase involved in the sphingolipid pathway by use of a labeled sphingosine.