1609545-83-6Relevant academic research and scientific papers
Optimization of Nicotinamides as Potent and Selective IRAK4 Inhibitors with Efficacy in a Murine Model of Psoriasis
Nair, Satheesh,Kumar, Sreekantha Ratna,Paidi, Venkatram Reddy,Sistla, Ramesh,Kantheti, Durgarao,Polimera, Subba Rao,Thangavel, Soodamani,Mukherjee, Amrita Jha,Das, Mitalee,Bhide, Rajeev S.,Pitts, William J.,Murugesan, Natesan,Dudhgoankar, Shailesh,Nagar, Jignesh,Subramani, Siva,Mazumder, Debarati,Carman, Julie A.,Holloway, Deborah A.,Li, Xin,Fereshteh, Mark P.,Ruepp, Stefan,Palanisamy, Kamalavenkatesh,Mariappan, T. Thanga,Maddi, Srinivas,Saxena, Ajay,Elzinga, Paul,Chimalakonda, Anjaneya,Ruan, Qian,Ghosh, Kaushik,Bose, Sucharita,Sack, John,Yan, Chunhong,Kiefer, Susan E.,Xie, Dianlin,Newitt, John A.,Saravanakumar, S. Pon,Rampulla, Richard A.,Barrish, Joel C.,Carter, Percy H.,Hynes, John
supporting information, p. 1402 - 1409 (2020/07/02)
IRAK4 is an attractive therapeutic target for the treatment of inflammatory conditions. Structure guided optimization of a nicotinamide series of inhibitors has been expanded to explore the IRAK4 front pocket. This has resulted in the identification of co
HETEROARYL SUBSTITUTED AMINOPYRIDINE COMPOUNDS
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Page/Page column 117; 118, (2017/01/09)
Disclosed are compounds of Formula (I) Formula(I) or salts thereof, wherein HET is a heteroaryl selected from oxazolyl, pyrazolyl, imidazo[l,2-b]pyridazin-3-yl, and pyrazolo[l,5-a]pyrimidin-3-yl, wherein said heteroaryl is attached to the pyridinyl group in the compound of Formula (I) by a carbon ring atom in the heteroaryl and wherein said heteroaryl is substituted with zero to 2 Rb; and R1, R3, and Rb are define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases, or in the treatment of cancer.
HETEROARYL SUBSTITUTED NICOTINAMIDE COMPOUNDS
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Paragraph 0395, (2015/07/15)
Disclosed are compounds of Formula (I) or salts thereof, wherein: HET is a heteroaryl selected from pyrazolyl, indolyl, pyrrolo[2,3-b]pyridinyl, pyrrolo[2,3-d]pyrimidinyl, pyrazolo[3,4-b]pyridinyl, pyrazolo[3,4-d]pyrimidinyl, 2,3-dihydro-1H-pyrrolo[2,3-b]pyridinyl, imidazo[4,5-b]pyridinyl, and purinyl, wherein said heteroaryl is substituted with Ra and Rb; and R1 and R2 are define herein. Also disclosed are methods of using such compounds as modulators of IRAK4, and pharmaceutical compositions comprising such compounds. These compounds are useful in treating, preventing, or slowing inflammatory and autoimmune diseases.
HETEROARYL SUBSTITUTED PYRIDYL COMPOUNDS USEFUL AS KINASE MODULATORS
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Paragraph 00234, (2019/03/15)
Compounds having the following formula (I) or a stereoisomer or a pharmaceutically-acceptable salt thereof, wherein R2 is a monocyclic heteroaryl group, and R1, R3, R4, R5 and R6 are as defined herein, are useful as kinase modulators, including IRAK-4 inhibition.
