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Volumn 18, Issue 15, 2008, Pages 4393-4396

Discovery of imidazole carboxamides as potent and selective CCK1R agonists

Author keywords

1,2 Diaryl imidazole; CCK1R agonist; Cholecystokinin; Food intake reduction; Obesity

Indexed keywords

CHOLECYSTOKININ RECEPTOR STIMULATING AGENT; IMIDAZOLECARBOXAMIDE;

EID: 47749126115     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2008.06.057     Document Type: Article
Times cited : (22)

References (21)
  • 7
    • 0038660488 scopus 로고    scopus 로고
    • For lead CCK1R medicinal chemistry reviews see
    • For lead CCK1R medicinal chemistry reviews see. Szewczyk J.R., and Laudeman C. Curr. Top. Med. Chem. 3 (2003) 837
    • (2003) Curr. Top. Med. Chem. , vol.3 , pp. 837
    • Szewczyk, J.R.1    Laudeman, C.2
  • 11
    • 47749127374 scopus 로고    scopus 로고
    • note
    • 50 values are human IP3 (NFAT) agonist data except in Table 6 which are mouse CCK1R IP3 data. Both CCK1 and CCK2 % activation are expressed as the % of activation relative to CCK-8. Additional assay protocols are given in Supporting Information.
  • 18
    • 47749096399 scopus 로고    scopus 로고
    • note
    • CCK2R % activation and CCK2R % inhibition at 10,000 nM data for compounds 38-50 are given in Supporting Information.
  • 19
    • 47749128171 scopus 로고    scopus 로고
    • note
    • No distinguishable behavioral features were noted between treatment and vehicle control groups of the ONFI mice at both administered doses (0.3 and 3 mg/kg). Subsequent manuscripts describing the in vivo characteristics (tolerability and efficacy) are in preparation.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.