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Volumn 5, Issue 3, 1999, Pages 155-158

Benzotriazonine as a new core structure for the design of CCK-receptor antagonists

Author keywords

Benzotriazonine; CCK; CCK receptor antagonists; Gastrin; Peptide hormone

Indexed keywords

BENZOTRIAZONINE DERIVATIVE; CHOLECYSTOKININ A RECEPTOR; CHOLECYSTOKININ A RECEPTOR ANTAGONIST; CHOLECYSTOKININ B RECEPTOR; UNCLASSIFIED DRUG;

EID: 0032950157     PISSN: 10752617     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-1387(199903)5:3<155::AID-PSC195>3.0.CO;2-E     Document Type: Article
Times cited : (4)

References (11)
  • 2
    • 0024361890 scopus 로고
    • Cholecystokinin and gastrin antagonists
    • R.M. Freidinger (1989). Cholecystokinin and gastrin antagonists. Med. Res. Rev. 9, 271-290.
    • (1989) Med. Res. Rev. , vol.9 , pp. 271-290
    • Freidinger, R.M.1
  • 3
    • 0028850559 scopus 로고
    • 1,5-Benzodiazepines as CCK-B antagonists. Effect of halogen substitution at the benzo-fused ring on potency and selectivity
    • G. Curoto, D. Donati, G. Pentassuglia and A. Ursini (1995). 1,5-Benzodiazepines as CCK-B antagonists. Effect of halogen substitution at the benzo-fused ring on potency and selectivity. Bioorg. Med. Chem. Lett. 5, 3011-3016.
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 3011-3016
    • Curoto, G.1    Donati, D.2    Pentassuglia, G.3    Ursini, A.4
  • 4
    • 0001603410 scopus 로고
    • Biochemical and pharmacological characterization of an extremely potent and selective non-peptide cholecystokinin antagonist
    • R.S.L. Chang and V.J. Lotti (1986). Biochemical and pharmacological characterization of an extremely potent and selective non-peptide cholecystokinin antagonist. Proc. Natl. Acad. Sci. USA 83, 4923-4926.
    • (1986) Proc. Natl. Acad. Sci. USA , vol.83 , pp. 4923-4926
    • Chang, R.S.L.1    Lotti, V.J.2
  • 5
    • 0024520619 scopus 로고
    • A new potent and selective non-peptide gastrin antagonist and brain cholecystokinin receptor (CCK-B) ligand: L-365260
    • V.J. Lotti and R.S.L. Chang (1989). A new potent and selective non-peptide gastrin antagonist and brain cholecystokinin receptor (CCK-B) ligand: L-365260. Eur. J. Pharmacol. 162, 273-280.
    • (1989) Eur. J. Pharmacol. , vol.162 , pp. 273-280
    • Lotti, V.J.1    Chang, R.S.L.2
  • 7
    • 0031579945 scopus 로고    scopus 로고
    • Incorporation of conformationally constrained phenylalanine derivatives Tic, Sic, Hic and Nic into a cholecystokinin-B/gastrin receptor antagonist
    • S.E. Gibson, N. Guillo, S.B. Kalindjian and M.J. Tozer (1997). Incorporation of conformationally constrained phenylalanine derivatives Tic, Sic, Hic and Nic into a cholecystokinin-B/gastrin receptor antagonist. Bioorg. Med. Chem. Lett. 7, 1289-1292.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1289-1292
    • Gibson, S.E.1    Guillo, N.2    Kalindjian, S.B.3    Tozer, M.J.4
  • 8
    • 0026671170 scopus 로고
    • Synthesis of new derivatives of 2,3,4,5,6,7-hexahydro-1H-1,4,7-benzotriazonine with expected biological activity
    • E. Miklciuk-Olasik (1992). Synthesis of new derivatives of 2,3,4,5,6,7-hexahydro-1H-1,4,7-benzotriazonine with expected biological activity. Pharmazie 47, 711-712.
    • (1992) Pharmazie , vol.47 , pp. 711-712
    • Miklciuk-Olasik, E.1
  • 10
    • 0025004247 scopus 로고
    • Synthesis of new derivatives of 2,3,4,5,6,7-hexahydro-1H-1,4,7-benzotriazonine
    • E. Mikiciuk-Olasik (1990). Synthesis of new derivatives of 2,3,4,5,6,7-hexahydro-1H-1,4,7-benzotriazonine. Pharmazie 45, 436-437.
    • (1990) Pharmazie , vol.45 , pp. 436-437
    • Mikiciuk-Olasik, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.