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Volumn 24, Issue 11, 2014, Pages 2539-2545

Synthesis and structure-activity relationship of dihydrobenzofuran derivatives as novel human GPR119 agonists

Author keywords

Agonist; GPR119; Type 2 diabetes

Indexed keywords

DIHYDROBENZOFURAN DERIVATIVE; G PROTEIN COUPLED RECEPTOR; G PROTEIN COUPLED RECEPTOR 119 AGONIST; NITROGEN; PIPERAZINE; PIPERIDINE; PYRIMIDINE; UNCLASSIFIED DRUG; BENZOFURAN DERIVATIVE; GPR119 PROTEIN, HUMAN;

EID: 84899936775     PISSN: 0960894X     EISSN: 14643405     Source Type: Journal    
DOI: 10.1016/j.bmcl.2014.03.096     Document Type: Article
Times cited : (21)

References (32)
  • 14
    • 84899970745 scopus 로고    scopus 로고
    • Minnesota, MN, June 6-9, oral session 2
    • PSN821 structure has not been disclosed. Its close lead PSN408 was disclosed, see The 32nd Annual National Medicinal Chemistry Symposium, Minnesota, MN, June 6-9, 2010, oral session 2.
    • (2010) The 32nd Annual National Medicinal Chemistry Symposium
  • 31
    • 84899991051 scopus 로고    scopus 로고
    • Unpublished results. Our efforts in this area were terminated upon publication of the patent application WO2 009/038974A1
    • Unpublished results. Our efforts in this area were terminated upon publication of the patent application WO2 009/038974A1.
  • 32
    • 77049220618 scopus 로고
    • 50 when a compound is repeated are 0.20. The intrinsic activity was expressed as the percent effect compared to that of the control, 20 μM of propan-2-yl 4-({6-[(2-fluoro-4- methanesulfonylphenyl)amino]pyrimidin-4-yl}oxy)piperidine-1-carboxylate, defined as 100% as per the following reference: E.J. Ariens Arch. Int. Pharmacodyn. Ther. 99 1954 32
    • (1954) Arch. Int. Pharmacodyn. Ther. , vol.99 , pp. 32
    • Ariens, E.J.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.