193902-80-6Relevant articles and documents
PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES AND THEIR USE IN THE TREATMENT OF CANCER
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Page/Page column 91, (2021/04/23)
The invention provides compounds of the formula (1): or a salt or tautomer thereof wherein A, R1, R2, R3, R4, R5 and R6 are as defined herein. The compounds are inhibitors of Wee1 and/or PLK1 kinase and are envisaged to be useful in the treatment of cancers.
BICYCLIC INHIBITORS OF ALK
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Page/Page column 84, (2012/08/07)
The present invention relates to compounds of formula (1) or pharmaceutical acceptable salts, wherein R1, X, Y, Z, A, B, G1, and n are defined in the description. The present invention relates also to compositions containing said compounds which are useful for inhibiting kinases such as ALK and methods of treating diseases such as cancer.
The identification of a series of novel, soluble non-peptidic neuropeptide y Y2 receptor antagonists
Lunniss, Gillian E.,Barnes, Ashley A.,Barton, Nick,Biagetti, Matteo,Bianchi, Federica,Blowers, Stephen M.,Caberlotto, Laura L.,Emmons, Amanda,Holmes, Ian P.,Montanari, Dino,Norris, Roz,Puckey, Gemma V.,Walters, Dewi J.,Watson, Steve P.,Willis, John
scheme or table, p. 7341 - 7344 (2011/01/12)
The identification and subsequent optimisation of a selective non-peptidic NPY Y2 antagonist series is described. This led to the development of amine 2, a selective, soluble NPY Y2 receptor antagonist with enhanced CNS exposure.