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filingDate 2016-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2018-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d145997365df1082d26845874bab6ec
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8fcd4cc4147f29f4d3cf85a676607260
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f2688121570642d4c5d51bf9d038bf1
publicationDate 2018-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-10112955-B2
titleOfInvention Isoindoline, azaisoindoline, dihydroindenone and dihydroazaindenone inhibitors of Mnk1 and Mnk2
abstract The present invention provides synthesis, pharmaceutically acceptable formulations and uses of compounds in accordance with Formula I, or a stereoisomer, tautomer or pharmaceutically acceptable salt thereof. n nFor Formula I compounds A 1 , A 2 , A 3 , A 4 , A 5 , W 1 , Y, R 1 , R 2 , R 3 , R 4 , R 5 , R 6a , R 6b , R 7 , R 8 , R 8a , R 8b , R 9 , R 9a , R 9b , and R 10 and subscript ā€œnā€ are as defined in the specification. The inventive Formula I compounds are inhibitors of Mnk and find utility in any number of therapeutic applications, including but not limited to treatment of inflammation and various cancers.
priorityDate 2015-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 2921.