Aminopyridinecarboxamide-based inhaled IKK-2 inhibitors for asthma and COPD: Structure–activity relationship

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 ac...

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Veröffentlicht in:Bioorganic & medicinal chemistry 2011-02, Vol.19 (3), p.1242-1255
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung: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 with potential capability for multiple routes of clearance. Several lead compounds have demonstrated their potential usefulness in the treatment of asthma and chronic obstructive pulmonary disease (COPD). 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).
ISSN:0968-0896
1464-3391
DOI:10.1016/j.bmc.2010.12.027