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Volumn 40, Issue 26, 1997, Pages 4290-4301

Structure-activity relationship of 3-substituted N-(pyridinylacetyl)-4- (8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)- piperidine inhibitors of farnesyl-protein transferase: Design and synthesis of in vivo active antitumor compounds

Author keywords

[No Author keywords available]

Indexed keywords

2 HYDROXYPROPYL BETA CYCLODEXTRIN; 4 (3 BROMO 5,6 DIHYDRO 11H BENZO[5,6]CYCLOHEPTA[1,2B]PYRIDIN 11 YLIDENE) 1 (4 PYRIDINYLACETYL)PIPERIDINE; 4 (3 BROMO 8 CHLORO 5,6 DIHYDRO 11H BENZO[5,6]CYCLOHEPTA[1,2B]PYRIDIN 11 YLIDENE) 1 (4 PYRIDINYLACETYL)PIPERIDINE N1 OXIDE; 4 (3,8 DICHLORO 5,6 DIHYDRO 11H BENZO[5,6]CYCLOHEPTA[1,2B]PYRIDIN 11 YLIDENE) 1 (4 PYRIDINYLACETYL)PIPERIDINE; 4 (8 CHLORO 3 IODO 5,6 DIHYDRO 11H BENZO[5,6]CYCLOHEPTA[1,2B]PYRIDIN 11 YLIDENE) 1 (4 PYRIDINYLACETYL)PIPERIDINE; 4 (8 CHLORO 5,6 DIHYDRO 3 METHYL 11H BENZO[5,6]CYCLOHEPTA[1,2 B]PYRIDIN 11 YLIDENE) 1 (4 PYRIDYLACETYL)PIPERIDINE; AGAR; DRUG VEHICLE; GERANYLTRANSFERASE; PIPERIDINE DERIVATIVE; PROTEIN FARNESYLTRANSFERASE INHIBITOR; RAS PROTEIN; UNCLASSIFIED DRUG;

EID: 6844259851     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm970464g     Document Type: Article
Times cited : (54)

References (27)
  • 1
    • 0003111499 scopus 로고
    • Cholecystokinin: Isolation, Structure and Functions
    • Glass, G. B. J., Ed.; Raven Press: New York
    • Mutt, V. Cholecystokinin: Isolation, Structure and Functions. In Gastrointestinal Hormones; Glass, G. B. J., Ed.; Raven Press: New York, 1980; pp 169-221.
    • (1980) Gastrointestinal Hormones , pp. 169-221
    • Mutt, V.1
  • 3
    • 0028300692 scopus 로고
    • Biological Actions of Cholecystokinin
    • Crawley, J. N.; Corwin, R. L. Biological Actions of Cholecystokinin. Peptides 1994, 15, 731-755.
    • (1994) Peptides , vol.15 , pp. 731-755
    • Crawley, J.N.1    Corwin, R.L.2
  • 4
    • 0001669859 scopus 로고
    • Classification and Function of CCK Receptors
    • Dourish, C., T.; Hill, D. R. Classification and Function of CCK Receptors. Trends Pharmacol. Sci. 1987, 8, 207-208.
    • (1987) Trends Pharmacol. Sci. , vol.8 , pp. 207-208
    • Dourish, C.T.1    Hill, D.R.2
  • 5
    • 0028340876 scopus 로고
    • Satiating Effect of Cholecystokinin
    • Smith, G. P.; Gibbs, J. Satiating Effect of Cholecystokinin. Ann. N.Y. Acad. Sci. 1994, 713, 236-241.
    • (1994) Ann. N.Y. Acad. Sci. , vol.713 , pp. 236-241
    • Smith, G.P.1    Gibbs, J.2
  • 6
    • 0028338447 scopus 로고
    • Integration of Postprandial Function in the Proximal Gastrointestinal Tract. Role of CCK and Sensory Pathways
    • Raybould, H. E.; Lloyd, K. C. Integration of Postprandial Function in the Proximal Gastrointestinal Tract. Role of CCK and Sensory Pathways. Ann. N.Y. Acad. Sci. 1994, 713, 143-156.
    • (1994) Ann. N.Y. Acad. Sci. , vol.713 , pp. 143-156
    • Raybould, H.E.1    Lloyd, K.C.2
  • 8
    • 0022912465 scopus 로고
    • Role of Cholecystokinin and Opioid Peptides in Control of Food Intake
    • Baile, C. A.; McLaughlin, C. L.; Della-Fera, M. A. Role of Cholecystokinin and Opioid Peptides in Control of Food Intake. Physiol. Rev. 1986, 66, 172-230.
    • (1986) Physiol. Rev. , vol.66 , pp. 172-230
    • Baile, C.A.1    McLaughlin, C.L.2    Della-Fera, M.A.3
  • 9
    • 0019381381 scopus 로고
    • C-terminal Octapeptide of Cholecystokinin Decrease Food Intake in Man
    • Kissileff, H. R.; Pi-Sunyer, X.; Thornton, J.; Smith, G. P. C-terminal Octapeptide of Cholecystokinin Decrease Food Intake In Man. Am. J. Clin. Nutr. 1981, 34, 154-160.
    • (1981) Am. J. Clin. Nutr. , vol.34 , pp. 154-160
    • Kissileff, H.R.1    Pi-Sunyer, X.2    Thornton, J.3    Smith, G.P.4
  • 10
    • 0028198272 scopus 로고
    • FPL 14294: A Novel CCK-8 Agonist with Potent Intranasal Anorectic Activity in the Rat
    • Simmons, R. D.; Blossser, J. C.; Rosamond, J. D. FPL 14294: A Novel CCK-8 Agonist with Potent Intranasal Anorectic Activity in the Rat. Pharmacol. Biochem. Behav. 1994, 47, 701-708.
    • (1994) Pharmacol. Biochem. Behav. , vol.47 , pp. 701-708
    • Simmons, R.D.1    Blossser, J.C.2    Rosamond, J.D.3
  • 11
    • 0000114007 scopus 로고
    • Comparative Potencies of CCK Antagonist for the Reversal of the Satiating Effect of Cholecystokinin
    • Wang, R. Y., Schoenfeld, R., Eds.; A. R. Liss: New York
    • Schneider, L. H.; Murphy, R. B.; Gibbs, J.; Smith, G. P. Comparative Potencies of CCK Antagonist for the Reversal of the Satiating Effect of Cholecystokinin. In Cholecystokinin Antagonist; Wang, R. Y., Schoenfeld, R., Eds.; A. R. Liss: New York, 1988; pp 263-284.
    • (1988) Cholecystokinin Antagonist , pp. 263-284
    • Schneider, L.H.1    Murphy, R.B.2    Gibbs, J.3    Smith, G.P.4
  • 12
    • 77956808092 scopus 로고
    • Cholecystokinin Agonists and Antagonists
    • Bristol, J. A., Ed.; Academic: San Diego, CA
    • Nadzan, A. M.; Kerwin, J. F., Jr. Cholecystokinin Agonists and Antagonists. In Annual Reports in Medicinal Chemistry; Bristol, J. A., Ed.; Academic: San Diego, CA, 1991; pp 191-200.
    • (1991) Annual Reports in Medicinal Chemistry , pp. 191-200
    • Nadzan, A.M.1    Kerwin Jr., J.F.2
  • 14
    • 0026699197 scopus 로고
    • Synthesis and Biological Activities of CCK Heptapeptide Analogues. Effects on Conformational Constraints and Standard Modifications on Receptor Subtype Selectivity and Functional Activity in Vitro and Appetite Suppression in Vivo
    • Holladay, M. W.; Bennett, M.; Tufano, M.; Lin, C.; Asin, K.; Witte, D.; Miller, T.; Bianchi, B.; Bednarz, L.; Nadzan, A. Synthesis and Biological Activities of CCK Heptapeptide Analogues. Effects on Conformational Constraints and Standard Modifications on Receptor Subtype Selectivity and Functional Activity in Vitro and Appetite Suppression In Vivo. J. Med. Chem. 1992, 35, 2919-2928.
    • (1992) J. Med. Chem. , vol.35 , pp. 2919-2928
    • Holladay, M.W.1    Bennett, M.2    Tufano, M.3    Lin, C.4    Asin, K.5    Witte, D.6    Miller, T.7    Bianchi, B.8    Bednarz, L.9    Nadzan, A.10
  • 16
    • 6844240267 scopus 로고
    • Structural Requirements for Satiety Effect of CCK-8
    • Deber, C. M., Hruby, V. J., Kopple, K. D., Eds.; Pierce: Rockford, IL
    • Rosamond, J. D.; Comstock, J.; Blosser, J. C.; Augello-Vaisey, S. J. Structural Requirements for Satiety Effect of CCK-8. In Peptides: Structure and Function; Deber, C. M., Hruby, V. J., Kopple, K. D., Eds.; Pierce: Rockford, IL, 1985; pp 241-244.
    • (1985) Peptides: Structure and Function , pp. 241-244
    • Rosamond, J.D.1    Comstock, J.2    Blosser, J.C.3    Augello-Vaisey, S.J.4
  • 19
    • 0025103048 scopus 로고
    • A Cleavage Method Which Minimizes Side Reactions Following Fmoc Solid-Phase Peptide Synthesis
    • King, D. S.; Fields, C. G.; Fields, G. B. A Cleavage Method Which Minimizes Side Reactions Following Fmoc Solid-Phase Peptide Synthesis. Int. J. Pept. Protein Res. 1990, 36, 255-266.
    • (1990) Int. J. Pept. Protein Res. , vol.36 , pp. 255-266
    • King, D.S.1    Fields, C.G.2    Fields, G.B.3
  • 20
    • 0022557566 scopus 로고
    • 3H-(±)-L-364,718: A New Potent, Nonpeptide Cholecystokinin Antagonist Radioligand Selective for Peripheral Receptors
    • 3H-(±)-L-364,718: A New Potent, Nonpeptide Cholecystokinin Antagonist Radioligand Selective for Peripheral Receptors. Mol. Pharmacol. 1986, 30, 212-217.
    • (1986) Mol. Pharmacol. , vol.30 , pp. 212-217
    • Chang, R.S.L.1    Lotti, V.J.2    Chen, T.B.3    Kunkel, K.A.4
  • 21
    • 0001603410 scopus 로고
    • Biochemical and Pharmacological Characterization of an Extremely Potent and Selective Nonpeptide Cholecystokinin Antagonist
    • Chang, R. S. L.; Lotti, V. J. Biochemical and Pharmacological Characterization of an Extremely Potent and Selective Nonpeptide Cholecystokinin Antagonist. Proc. Natl. Acad. Sci. U.S.A. 1986, 83, 4923-4926.
    • (1986) Proc. Natl. Acad. Sci. U.S.A. , vol.83 , pp. 4923-4926
    • Chang, R.S.L.1    Lotti, V.J.2
  • 22
    • 0015318507 scopus 로고
    • Comparison of Anorexigenic and Behavioral Potency of Phenylethylamines
    • Cox, R. H.; Maickel, R. P. Comparison of Anorexigenic and Behavioral Potency of Phenylethylamines. J. Pharmacol. Exp. Ther. 1972, 181, 1-9.
    • (1972) J. Pharmacol. Exp. Ther. , vol.181 , pp. 1-9
    • Cox, R.H.1    Maickel, R.P.2
  • 24
    • 17744402639 scopus 로고
    • Are Peptides Truly Satiety Agents? A Method of Testing for Neurohumoral Satiety Effects
    • Billington, C. J.; Levine, A. S.; Morley, J. E. Are Peptides Truly Satiety Agents? A Method of Testing for Neurohumoral Satiety Effects. Am. J. Physiol. 1983, 245, R920-R926.
    • (1983) Am. J. Physiol. , vol.245
    • Billington, C.J.1    Levine, A.S.2    Morley, J.E.3
  • 26
    • 84908742429 scopus 로고
    • Peptide nomenclature follows the guidelines of the IUPAC-IUB Joint Commission on Biochemical Nomenclature
    • Peptide nomenclature follows the guidelines of the IUPAC-IUB Joint Commission on Biochemical Nomenclature. Eur. J. Biochem. 1984, 138, 9-37.
    • (1984) Eur. J. Biochem. , vol.138 , pp. 9-37
  • 27
    • 0022478580 scopus 로고
    • New Antiarrhythmic Agents. 2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamides and 2,2,5,5-Tetramethylpyrrolidine-3-carboxamides
    • Hankovszky, O. H.; Hideg, K.; Bódi, I.; Frank, L. New Antiarrhythmic Agents. 2,2,5,5-Tetramethyl-3-pyrroline-3-carboxamides and 2,2,5,5-Tetramethylpyrrolidine-3-carboxamides. J. Med. Chem. 1986, 29, 1138-1152.
    • (1986) J. Med. Chem. , vol.29 , pp. 1138-1152
    • Hankovszky, O.H.1    Hideg, K.2    Bódi, I.3    Frank, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.