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Volumn 13, Issue 6, 2003, Pages 1141-1145

Synthesis and Biological activity of kappa opioid receptor agonists. Part 2: Preparation of 3-aryl-2-pyridone analogues generated by solution- and solid-phase parallel synthesis methods

Author keywords

[No Author keywords available]

Indexed keywords

KAPPA OPIATE RECEPTOR AGONIST; OPIATE RECEPTOR; PYRIDONE DERIVATIVE;

EID: 0037463770     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(03)00033-7     Document Type: Article
Times cited : (47)

References (17)
  • 7
    • 85031201156 scopus 로고    scopus 로고
    • note
    • 125I]-Deltorphin (δ).
  • 8
    • 85031198906 scopus 로고    scopus 로고
    • note
    • 35S]-GTPγS assay, again using membranes of HEK-293 cells overexpressing the human kappa opioid receptor.
  • 15
    • 0029743317 scopus 로고    scopus 로고
    • 3 and R-BINAP, were placed in each well of a dry Robbins block. Dry dioxan was added and the block sealed and agitated under argon for 18 h at 90°C. The reaction mixtures were filtered thorough silica plugs (eluting with 0.2% ammonia in EtOAc), and then purified by ion exchange on pre-packed SCX columns.
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 7215
    • Wolfe, J.P.1    Wagaw, S.2    Buchwald, S.L.3
  • 16
    • 85031202484 scopus 로고    scopus 로고
    • note
    • 16 and its des-hydroxy analogue showed that the former is around 10-fold more potent in both binding and function at the KOR. In addition it is the S-isomer at the hydroxyl position which is most active.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.