24630-85-1Relevant academic research and scientific papers
Aminopyridinecarboxamide-based inhaled IKK-2 inhibitors for asthma and COPD: Structure-activity relationship
Xie, Jin,Poda, Gennadiy I.,Hu, Yiding,Chen, Natalie X.,Heier, Richard F.,Wolfson, Serge G.,Reding, Matthew T.,Lennon, Patrick J.,Kurumbail, Ravi G.,Selness, Shaun R.,Li, Xiong,Kishore, Nandini N.,Sommers, Cynthia D.,Christine, Lori,Bonar, Sheri L.,Venkatraman, Neetu,Mathialagan, Sumathy,Brustkern, Sarah J.,Huang, Horng-Chih
experimental part, p. 1242 - 1255 (2011/04/12)
Installation of sites for metabolism in the lead compound PHA-767408 was the key focus of the IKK-2 inhaled program. This paper reports our efforts to identify a novel series of aminopyridinecarboxamide-based IKK-2 inhibitors, which display low nanomolar potency against IKK-2 with long duration of action (DOA), and metabolically labile to phase I and/or phase II metabolizing enzymes with potential capability for multiple routes of clearance. Several compounds have demonstrated their potential usefulness in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
Synthesis of COX-2 and FAAH inhibitors
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, (2008/06/13)
Methods for preparing indoles that are useful COX-2 inhibitors and intermediates useful in such methods are described.
Pyridazino quinoline compounds
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, (2008/06/13)
The invention relates to pyridazinoquinoline compounds of the formulas B and B′ wherein Ring A is selected from an ortho fused aromatic or heteroaromatic five- or six-membered ring and R1, R3and R4are substituents selected from halo, OH, OCF3, NO2, CN, NR′R″, SO2NR′R″, SOmR′alkyl, and a variety of alkyl, aryl, heterocyclic and heteroaryl groups, to pharmaceutical compositions containing them and to methods utilizing them for the treatment of neurological disorders.
Pyridazion quinoline compounds
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, (2008/06/13)
The present invention relates to compounds, pharmaceutical compositions and methods of using compounds of formula (I) in the treatment and/or prevention of certain diseases or conditions. In formula (I), A is chosen from ortho substituted aryl or heteroaryl species, X is chosen from --OH, --SH, NHR and R 1 or R 2 is chosen from --(CH 2) n L wherein L may be selected from a variety of substituents including aryl, heteroaryl and heterocyclic groups. The compounds are useful in treating and/or preventing neurological disorders associated with excitatory amino acids. STR1
