Optimization of a Novel Mandelamide-Derived Pyrrolopyrimidine Series of PERK Inhibitors

The protein kinase R (PKR)-like endoplasmic reticulum kinase (PERK) is one of three endoplasmic reticulum (ER) transmembrane sensors of the unfolded protein response (UPR) responsible for regulating protein synthesis and alleviating ER stress. PERK has been implicated in tumorigenesis, cancer cell s...

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Váldodahkkit: Michael E. Stokes (Dahkki), Matthew D. Surman (Dahkki), Veronica Calvo (Dahkki), David Surguladze (Dahkki), An-Hu Li (Dahkki), Jennifer Gasparek (Dahkki), Matthew Betzenhauser (Dahkki), Guangyu Zhu (Dahkki), Hongwen Du (Dahkki), Alan C. Rigby (Dahkki), Mark J. Mulvihill (Dahkki)
Materiálatiipa: Girji
Almmustuhtton: MDPI AG, 2022-10-01T00:00:00Z.
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LEADER 00000 am a22000003u 4500
001 doaj_bfdce10972624d15be3669c45666742f
042 |a dc 
100 1 0 |a Michael E. Stokes  |e author 
700 1 0 |a Matthew D. Surman  |e author 
700 1 0 |a Veronica Calvo  |e author 
700 1 0 |a David Surguladze  |e author 
700 1 0 |a An-Hu Li  |e author 
700 1 0 |a Jennifer Gasparek  |e author 
700 1 0 |a Matthew Betzenhauser  |e author 
700 1 0 |a Guangyu Zhu  |e author 
700 1 0 |a Hongwen Du  |e author 
700 1 0 |a Alan C. Rigby  |e author 
700 1 0 |a Mark J. Mulvihill  |e author 
245 0 0 |a Optimization of a Novel Mandelamide-Derived Pyrrolopyrimidine Series of PERK Inhibitors 
260 |b MDPI AG,   |c 2022-10-01T00:00:00Z. 
500 |a 10.3390/pharmaceutics14102233 
500 |a 1999-4923 
520 |a The protein kinase R (PKR)-like endoplasmic reticulum kinase (PERK) is one of three endoplasmic reticulum (ER) transmembrane sensors of the unfolded protein response (UPR) responsible for regulating protein synthesis and alleviating ER stress. PERK has been implicated in tumorigenesis, cancer cell survival as well metabolic diseases such as diabetes. The structure-based design and optimization of a novel mandelamide-derived pyrrolopyrimidine series of PERK inhibitors as described herein, resulted in the identification of compound <b>26</b>, a potent, selective, and orally bioavailable compound suitable for interrogating PERK pathway biology in vitro and in vivo, with pharmacokinetics suitable for once-a-day oral dosing in mice. 
546 |a EN 
690 |a ER stress 
690 |a PERK 
690 |a UPR 
690 |a kinase 
690 |a inhibitor 
690 |a cancer 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 14, Iss 10, p 2233 (2022) 
787 0 |n https://www.mdpi.com/1999-4923/14/10/2233 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/bfdce10972624d15be3669c45666742f  |z Connect to this object online.