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Volumn 7, Issue 3, 1997, Pages 291-296

Trans N-Methyl-N-[2-(1-pyrrolidinyl)cyclohexyl] cycloprop-2-ene-1-carboxamides: Novel lipophilic kappa opioid agonists

Author keywords

[No Author keywords available]

Indexed keywords

3,4 DICHLORO N METHYL N [2 (1 PYRROLIDINYL)CYCLOHEXYL]BENZENEACETAMIDE; ENADOLINE; KAPPA OPIATE RECEPTOR; MU OPIATE RECEPTOR; OPIATE AGONIST;

EID: 0031552091     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(96)00615-4     Document Type: Article
Times cited : (10)

References (19)
  • 7
    • 0019793415 scopus 로고
    • 7. Compounds were evaluated for their ability to inhibit the contractions af electrically stimualted rabbit vas deferens. The procedure was based on that of Oka, T.; Negishi, K.; Suda, M.; Matsumiya, T.; Inazu, T.; Ueki, M. Eur. J. Pharmacol., 1980, 73, 235.
    • (1980) Eur. J. Pharmacol. , vol.73 , pp. 235
    • Oka, T.1    Negishi, K.2    Suda, M.3    Matsumiya, T.4    Inazu, T.5    Ueki, M.6
  • 9
    • 0011386304 scopus 로고    scopus 로고
    • All new compounds gave satisfactory spectroscopic and analytical data
    • 9. All new compounds gave satisfactory spectroscopic and analytical data.
  • 11
    • 0011432011 scopus 로고
    • 11. Prepared according to the procedure of Hermann, W. A. Chem. Ber., 1979, 1731.
    • (1979) Chem. Ber. , pp. 1731
    • Hermann, W.A.1
  • 12
    • 33947481476 scopus 로고
    • 12. Diphenylacetylene was commercially available. 2(3 and 4-chlorophenyl)phenylacetylene were prepared following the procedure of Stevens, D.; Castro, C. E. J. Org. Chem., 1963, 28, 3313. 2(3-acetoxyphenyl)phenylacetylene was prepared following the procedure of Sonogashira, K.; Tohda, Y.; Hagihara, N. Tetrahedron Lett., 1975, 4467.
    • (1963) J. Org. Chem. , vol.28 , pp. 3313
    • Stevens, D.1    Castro, C.E.2
  • 13
    • 9644285669 scopus 로고
    • 12. Diphenylacetylene was commercially available. 2(3 and 4-chlorophenyl)phenylacetylene were prepared following the procedure of Stevens, D.; Castro, C. E. J. Org. Chem., 1963, 28, 3313. 2(3-acetoxyphenyl)phenylacetylene was prepared following the procedure of Sonogashira, K.; Tohda, Y.; Hagihara, N. Tetrahedron Lett., 1975, 4467.
    • (1975) Tetrahedron Lett. , pp. 4467
    • Sonogashira, K.1    Tohda, Y.2    Hagihara, N.3
  • 14
    • 0011433127 scopus 로고
    • US Patent 4,438,130, March 20
    • 13. Kaplan, L. J. US Patent 4,438,130, March 20, 1984; Chem Abstr., 1984, 101, 54912w.
    • (1984)
    • Kaplan, L.J.1
  • 15
    • 84910760230 scopus 로고
    • 13. Kaplan, L. J. US Patent 4,438,130, March 20, 1984; Chem Abstr., 1984, 101, 54912w.
    • (1984) Chem Abstr. , vol.101
  • 16
    • 0011386927 scopus 로고    scopus 로고
    • The Log P and interpolated Log D values were determined at Sirius Analytical Instruments, East Sussex, UK
    • 14. The Log P and interpolated Log D values were determined at Sirius Analytical Instruments, East Sussex, UK.
  • 17
    • 0011480949 scopus 로고    scopus 로고
    • 3H]-U-69593 in cloned rat kappa opioid receptor, expressed in CHO cell line
    • 3H]-U-69593 in cloned rat kappa opioid receptor, expressed in CHO cell line.
  • 18
    • 0011441945 scopus 로고    scopus 로고
    • 3H]-DAGO in rat brain mu opioid receptor
    • 3H]-DAGO in rat brain mu opioid receptor.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.