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Volumn 39, Issue 15, 1996, Pages 2907-2914

N-heteroaryl-2-phenyl-3-(benzyloxy)piperidines: A novel class of potent orally active human NK1 antagonists

Author keywords

[No Author keywords available]

Indexed keywords

5 [[3 [3,5 BIS(TRIFLUOROMETHYL)BENZYLOXY] 2 PHENYL 1 PIPERIDINYL]METHYL] 1,2 DIHYDRO 3H 1,2,4 TRIAZOL 3 ONE; CALCIUM CHANNEL; ETHER DERIVATIVE; NEUROKININ 1 RECEPTOR ANTAGONIST; PIPERIDINE DERIVATIVE; SUBSTANCE P ANTAGONIST; UNCLASSIFIED DRUG;

EID: 8944260413     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm9506534     Document Type: Article
Times cited : (76)

References (34)
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    • Salter, M. W.; Henry, J. L. Responses of Functionally Identified Neurons in the Dorsal Horn of the Cat Spinal Cord to Substance P, Neurokinin A and Physalaemin. Neuroscience 1991, 43, 601-610.
    • (1991) Neuroscience , vol.43 , pp. 601-610
    • Salter, M.W.1    Henry, J.L.2
  • 2
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    • Effect of RP 67580, a Non Peptide Neurokinin Receptor Antagonist on Facilitation of a Nociceptive Spinal Flexion Reflex in the Rat
    • Laird, J. M. A.; Hargreaves, R. J.; Hill, R. G. Effect of RP 67580, A Non Peptide Neurokinin Receptor Antagonist on Facilitation of a Nociceptive Spinal Flexion Reflex in the Rat. Br. J. Pharmacol. 1993, 109, 713-718.
    • (1993) Br. J. Pharmacol. , vol.109 , pp. 713-718
    • Laird, J.M.A.1    Hargreaves, R.J.2    Hill, R.G.3
  • 4
    • 0026683693 scopus 로고
    • Neurogenic versus Vascular Mechanisms of Sumatriptan and Ergot Alkaloids in Migraine
    • (a) Mosokowitz, M. A. Neurogenic versus Vascular Mechanisms of Sumatriptan and Ergot Alkaloids in Migraine. Trends Pharmacol. Sci. 1992, 307-311.
    • (1992) Trends Pharmacol. Sci. , pp. 307-311
    • Mosokowitz, M.A.1
  • 10
    • 0026632489 scopus 로고
    • Studies on Neurokinin Antagonists. 1. The Design of Novel Tripeptides Possessing the Glutaminyl-D-Tryptophylphenylalanine Sequence as Substance P Antagonist
    • (a) Hagiwara, D.; Miyaka, H.; Morimoto, H.; Murai, M.; Fujii, T.; Matsuo, M. Studies on Neurokinin Antagonists. 1. The Design of Novel Tripeptides Possessing the Glutaminyl-D-Tryptophylphenylalanine Sequence as Substance P Antagonist. J. Med. Chem. 1992, 35, 2015-2025.
    • (1992) J. Med. Chem. , vol.35 , pp. 2015-2025
    • Hagiwara, D.1    Miyaka, H.2    Morimoto, H.3    Murai, M.4    Fujii, T.5    Matsuo, M.6
  • 27
    • 0021287857 scopus 로고
    • 2 Receptor Antagonists. 1. Synthesis of N-Cyano and N-Carbamoyl Amidine Derivatives and their Biological Activities
    • 2 Receptor Antagonists. 1. Synthesis of N-Cyano and N-Carbamoyl Amidine Derivatives and their Biological Activities. J. Med. Chem. 1984, 27, 849-857.
    • (1984) J. Med. Chem. , vol.27 , pp. 849-857
    • Yanagisawa, I.1    Hirata, Y.2    Ishii, Y.3
  • 32
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    • note
    • 1 receptor. The even greater potency of the triazole 11 (a 7-fold increase over CP-99,994) in this assay, however, is intriguing.
  • 34
    • 85082654470 scopus 로고
    • Rapid and Selective Formylation with Pentafluorophenylformate
    • Kisfauldy, L.; Ötvös, L., Jr. Rapid and Selective Formylation with Pentafluorophenylformate. Synthesis 1987, 510.
    • (1987) Synthesis , pp. 510
    • Kisfauldy, L.1    Ötvös Jr., L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.