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Synthesis and structural optimization of multiple H-bonding region of diarylalkyl (thio)amides as novel TRPV1 antagonists

Authors
Li, Fu-NanKim, Nam-JungChang, Dong-JoJang, JaebongJang, HannahJung, Jong-WhaMin, Kyung-HoonJeong, Yeon-SuKim, Sun-YoungPark, Young-HoKim, Hee-DooPark, Hyeung-GeunSuh, Young-Ger
Issue Date
Dec-2009
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Citation
BIOORGANIC & MEDICINAL CHEMISTRY, v.17, no.24, pp 8149 - 8160
Pages
12
Journal Title
BIOORGANIC & MEDICINAL CHEMISTRY
Volume
17
Number
24
Start Page
8149
End Page
8160
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22846
DOI
10.1016/j.bmc.2009.10.043
ISSN
0968-0896
1464-3391
Abstract
Structural optimization of multiple H-bonding region and structure-activity relationship of diarylalkyl amides/thioamides as novel TRPV1 antagonists are described. In particular, we identified amide 34o and thioamides 35o and 35r, of which antagonistic activities were highly enhanced by an incorporation of cyano or vinyl-substituent to the multiple H-bonding region. They exhibited potent Ca-45(2+) uptake inhibitions in rat DRG neuron with IC(50)s of 25, 32 and 28 nM, respectively. (C) 2009 Elsevier Ltd. All rights reserved.
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대학원 (글로벌혁신신약학과)
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