메뉴 건너뛰기




Volumn 47, Issue 12, 2004, Pages 2973-2976

A novel series of piperidin-4-yl-1,3-dihydroindol-2-ones as agonist and antagonist ligands at the nociceptin receptor

Author keywords

[No Author keywords available]

Indexed keywords

1 (1 CYCLOOCTYLMETHYL 3 HYDROXYMETHYL 4 PIPERIDYL) 3 ETHYL 1,3 DIHYDRO 2H BENZIMIDAZOL 2 ONE; 7 [4 (2,6 DICHLOROPHENYL) 1 PIPERIDINYLMETHYL] 6,7,8,9 TETRAHYDRO 1 METHYL 5H BENZOCYCLOHEPTEN 5 OL; 8 (2,3,3A,4,5,6 HEXAHYDRO 1H PHENALEN 1 YL) 1 PHENYL 1,3,8 TRIAZASPIRO[4.5]DECAN 4 ONE; INDOLE DERIVATIVE; N (4 AMINO 2 METHYL 6 QUINOLINYL) 2 (4 ETHYLPHENOXYMETHYL)BENZAMIDE; NOCICEPTIN RECEPTOR; PIPERIDIN 4 YL 1,3 DIHYDROINDOL 2 ONE; PIPERIDIN 4 YL 1,3 DIHYDROINDOL 2 ONE AGONIST; PIPERIDIN 4 YL 1,3 DIHYDROINDOL 2 ONE ANTAGONIST; PYRROLE DERIVATIVE; RO 64 65198; SPIRODECANONE; UNCLASSIFIED DRUG;

EID: 2542609191     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm034249d     Document Type: Article
Times cited : (74)

References (28)
  • 4
    • 0034101011 scopus 로고    scopus 로고
    • Pharmacology of nociceptin and its receptor: A novel therapeutic target
    • Calo, G.; Guerrini, R.; Rizzi, A.; Salvadori, S.; Regoli, D. Pharmacology of nociceptin and its receptor: A novel therapeutic target. Br. J. Pharmacol. 2000, 129, 1261-1283.
    • (2000) Br. J. Pharmacol. , vol.129 , pp. 1261-1283
    • Calo, G.1    Guerrini, R.2    Rizzi, A.3    Salvadori, S.4    Regoli, D.5
  • 6
    • 0033620924 scopus 로고    scopus 로고
    • Orphanin FQ a novel neuropeptide with anti-stress-like activity
    • (b) Griebel, G.; Perrault, G.; Sanger, D. J. Orphanin FQ, a novel neuropeptide with anti-stress-like activity. Brain Res. 1999, 836, 221-224.
    • (1999) Brain Res. , vol.836 , pp. 221-224
    • Griebel, G.1    Perrault, G.2    Sanger, D.J.3
  • 7
    • 0032849969 scopus 로고    scopus 로고
    • Inhibitory effect of nociceptin on [3H]-5-HT release from rat cerebral cortex slices
    • (a) Siniscalchi, A.; Rodi, D.; Beani, L.; Bianchi, C. Inhibitory effect of nociceptin on [3H]-5-HT release from rat cerebral cortex slices. Br. J. Pharmacol. 1999, 128, 119-123.
    • (1999) Br. J. Pharmacol. , vol.128 , pp. 119-123
    • Siniscalchi, A.1    Rodi, D.2    Beani, L.3    Bianchi, C.4
  • 8
    • 0029854933 scopus 로고    scopus 로고
    • Intracerebroventricular orphanin FQ/nociceptin suppresses dopamine release in the nucleus accumbens of anaesthetized rats
    • (b) Murphy, N. P.; Ly, H. T.; Maidment, N. T. Intracerebroventricular orphanin FQ/nociceptin suppresses dopamine release in the nucleus accumbens of anaesthetized rats. Neuroscience 1996, 75, 1-4.
    • (1996) Neuroscience , vol.75 , pp. 1-4
    • Murphy, N.P.1    Ly, H.T.2    Maidment, N.T.3
  • 9
    • 0033821477 scopus 로고    scopus 로고
    • Nociceptin/orphanin FQ and neurotransmitter release in the central nervous system
    • (c) Schlicker, E.; Morari, M. Nociceptin/orphanin FQ and neurotransmitter release in the central nervous system. Peptides 2000, 21, 1023-1029.
    • (2000) Peptides , vol.21 , pp. 1023-1029
    • Schlicker, E.1    Morari, M.2
  • 10
    • 0033583931 scopus 로고    scopus 로고
    • Orphanin FQ/nociceptin blocks acquisition of morphine place preference
    • Murphy, N. P.; Lee, Y.; Maidment, N. T. Orphanin FQ/nociceptin blocks acquisition of morphine place preference. Brain Res. 1999, 832, 168-170.
    • (1999) Brain Res. , vol.832 , pp. 168-170
    • Murphy, N.P.1    Lee, Y.2    Maidment, N.T.3
  • 12
    • 0031912743 scopus 로고    scopus 로고
    • Enhancement of spatial attention in nociceptin/orphanin FQ receptor knock-out mice
    • (b) Mamiya, T.; Noda, Y.; Nishi, M.; Takeshima, H.; Nabeshima, T. Enhancement of spatial attention in nociceptin/ orphanin FQ receptor knock-out mice. Brain Res. 1998, 783, 236-240.
    • (1998) Brain Res. , vol.783 , pp. 236-240
    • Mamiya, T.1    Noda, Y.2    Nishi, M.3    Takeshima, H.4    Nabeshima, T.5
  • 15
    • 0034667560 scopus 로고    scopus 로고
    • Enhanced spinal nociceptin receptor expression develops morphine tolerance and dependence
    • (b) Ueda, H.; Inoue, M.; Takeshima, H.; Iwasawa, Y. Enhanced spinal nociceptin receptor expression develops morphine tolerance and dependence. J. Neurosci. 2000, 20, 7640-7647.
    • (2000) J. Neurosci. , vol.20 , pp. 7640-7647
    • Ueda, H.1    Inoue, M.2    Takeshima, H.3    Iwasawa, Y.4
  • 16
    • 0037498440 scopus 로고    scopus 로고
    • Peptide and nonpeptide ligands for the nociceptin/orphanin FQ receptor ORL1: Research tools and potential therapeutic agents
    • Zaveri, N. Peptide and nonpeptide ligands for the nociceptin/ orphanin FQ receptor ORL1: Research tools and potential therapeutic agents. Life Sci. 2003, 73, 663-678.
    • (2003) Life Sci. , vol.73 , pp. 663-678
    • Zaveri, N.1
  • 19
    • 0033576679 scopus 로고    scopus 로고
    • Discovery of the first potent and selective small molecule opioid receptor-like (ORL1) antagonist: 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1, 3-dihydro-2H-benzimidazol-2-one (J-113397)
    • Kawamoto, H.; Ozaki, S.; Itoh, Y.; Miyaji, M.; Arai, S.; Nakashima, H.; Kato, T.; Ohta, H.; Iwasawa, Y. Discovery of the first potent and selective small molecule opioid receptor-like (ORL1) antagonist: 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidyl]-3-ethyl-1, 3-dihydro-2H-benzimidazol-2-one (J-113397). J. Med. Chem. 1999, 42, 5061-5063.
    • (1999) J. Med. Chem. , vol.42 , pp. 5061-5063
    • Kawamoto, H.1    Ozaki, S.2    Itoh, Y.3    Miyaji, M.4    Arai, S.5    Nakashima, H.6    Kato, T.7    Ohta, H.8    Iwasawa, Y.9
  • 20
    • 0034736150 scopus 로고    scopus 로고
    • 4-Aminoquinolines: Novel nociceptin antagonists with analgesic activity
    • Shinkai, H.; Ito, T.; Iida, T.; Kitao, Y.; Yamada, H.; Uchida, I. 4-Aminoquinolines: novel nociceptin antagonists with analgesic activity. J. Med. Chem. 2000, 43, 4667-4677.
    • (2000) J. Med. Chem. , vol.43 , pp. 4667-4677
    • Shinkai, H.1    Ito, T.2    Iida, T.3    Kitao, Y.4    Yamada, H.5    Uchida, I.6
  • 21
    • 2542524146 scopus 로고    scopus 로고
    • 1-(1-Hydrocarbyl-4-piperidyl)-2-indolinone. U.S. Patent 3,325,499, 1967
    • Poos, G. I.; Ambler, P. 1-(1-Hydrocarbyl-4-piperidyl)-2-indolinone. U.S. Patent 3,325,499, 1967.
    • Poos, G.I.1    Ambler, P.2
  • 22
    • 0035944209 scopus 로고    scopus 로고
    • A short and efficient synthesis of N-substituted indol-2-ones (oxindoles)
    • Forbes, I. T. A short and efficient synthesis of N-substituted indol-2-ones (oxindoles). Tetrahedron Lett. 2001, 2, 6943-6945.
    • (2001) Tetrahedron Lett. , vol.2 , pp. 6943-6945
    • Forbes, I.T.1
  • 23
    • 4043071644 scopus 로고
    • The cyanohydridoborate anion as a selective reducing agent
    • Borch, R. F.; Bernstein, M. D.; Durst, H. D. The cyanohydridoborate anion as a selective reducing agent. J. Am. Chem. Soc. 1971, 93, 2897-2904.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 2897-2904
    • Borch, R.F.1    Bernstein, M.D.2    Durst, H.D.3
  • 25
    • 0030734901 scopus 로고    scopus 로고
    • Relationship between binding affinity and functional activity of nociceptin/orphanin FQ
    • Adapa, D. I.; Toll, L. Relationship between binding affinity and functional activity of nociceptin/orphanin FQ. Neuropeptides 1997, 31, 403-408.
    • (1997) Neuropeptides , vol.31 , pp. 403-408
    • Adapa, D.I.1    Toll, L.2
  • 28
    • 2542586548 scopus 로고    scopus 로고
    • See Supporting Information
    • See Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.