Structure-activity relationship study of a series of novel oxazolidinone derivatives as IL-6 signaling blockers

  • Singh, Sarbjit; 
  • Gajulapati, Veeraswamy; 
  • Gajulapati, Kondaji; 
  • Goo, Ja-Il; 
  • Park, Yeon-Hwa; 
  • ... Choi, Yongseok; 
  • 외 6명
Citations

WEB OF SCIENCE

18
Citations

SCOPUS

20

초록

A series of oxazolidinone and indole derivatives were synthesized and evaluated as IL-6 signaling blockers by measuring the effects of these compounds on IL-6-induced luciferase expression in human hepatocarcinoma HepG2 cells transfected with p-STAT3-Luc. Among different compounds screened, compound 4d was emerged as the most potent IL-6 signaling blockers with IC50 value of 5.9 mu M which was much better than (+)-Madindoline A (IC50 = 21 mu M), a known inhibitor of IL-6. (C) 2016 Elsevier Ltd. All rights reserved.

키워드

Rheumatoid arthritis; IL-6 antagonists; IL-6 signaling inhibitor; STAT3; gp130; Oxazolidinone; ACUTE-PANCREATITIS; GLYCOPROTEIN 130; MADINDOLINE-A; INTERLEUKIN-6; INHIBITION; ANTAGONIST; GP130
제목
Structure-activity relationship study of a series of novel oxazolidinone derivatives as IL-6 signaling blockers
저자
Singh, Sarbjit; Gajulapati, Veeraswamy; Gajulapati, Kondaji; Goo, Ja-Il; Park, Yeon-Hwa; Jung, Hwa Young; Lee, Sung Yoon; Choi, Jung Ho; Kim, Young Kook; Lee, Kyeong; Heo, Tae-Hwe; Choi, Yongseok
DOI
10.1016/j.bmcl.2016.01.016
발행일
2016-02-15
유형
Article
저널명
Bioorganic & Medicinal Chemistry Letters
권
26
호
4
페이지
1282 ~ 1286