메뉴 건너뛰기




Volumn 53, Issue 6, 2010, Pages 2646-2650

Dopamine receptor ligands. Part 18: Modification of the structural skeleton of indolobenzazecine-type dopamine receptor antagonists

Author keywords

[No Author keywords available]

Indexed keywords

2,6,7,9,10,14B HEXAHYDROINDOLO[3',4':3,4,5]AZEPINO[2,1 A]ISOQUINOLINE; 2,8,9,13B TETRAHYDRO 6H ISOQUINO[2,1 B]PYRROLO[4,3,2 DE]ISOQUINOLINE; 5 METHYL 4,5,6,7 TETRAHYDROINDOLO[4,3A,3 EF][3]BENZAZECINE; 5,6,8,9,10,14C HEXAHYDROINDOLO[3',2':3,4,]PYRIDO[2,1 A]ISOQUINOLINE; 6 METHYL 5,6,7,8,13,15 HEXAHYDRO 4H INDOLO[4,3A,3 FG][3]BENZAZACYCLOUNDECENE; 7 METHYL 6,7,8,9,10,15 HEXAHYDROINDOLO[2,3 F ][3]BENZAZECINE; 7 METHYL 6,7,8,9,14,15 HEXAHYDRO 5H INDOLO[3,2 F][3]BENZAZECINE; DOPAMINE RECEPTOR BLOCKING AGENT; LE 300; UNCLASSIFIED DRUG;

EID: 77949788997     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm901291r     Document Type: Article
Times cited : (24)

References (17)
  • 2
    • 2942536851 scopus 로고    scopus 로고
    • Dopamine/ Serotonin receptor ligands. Part VIII: The dopamine receptor antagonist le
    • Decker, M.; Schleifer, K. J.; Nieger, M.; Lehmann, J. Dopamine/ Serotonin receptor ligands. Part VIII: the dopamine receptor antagonist LE. Eur. J. Med. Chem. 2004, 39, 481-489.
    • (2004) Eur. J. Med. Chem. , vol.39 , pp. 481-489
    • Decker, M.1    Schleifer, K.J.2    Nieger, M.3    Lehmann, J.4
  • 4
    • 0034076585 scopus 로고    scopus 로고
    • 7-Methyl-6,7,8,9,14,15-hexahydro-5H-benz[d]indolo[2,3-g]azecine: A new heterocyclic system and a new lead compound for dopamine receptor antagonists
    • Witt, T.; Hock, F. J.; Lehmann, J. 7-Methyl-6,7,8,9,14,15-hexahydro-5H- benz[d]indolo[2,3-g]azecine: a new heterocyclic system and a new lead compound for dopamine receptor antagonists. J. Med. Chem. 2000, 43, 2079-2081.
    • (2000) J. Med. Chem. , vol.43 , pp. 2079-2081
    • Witt, T.1    Hock, F.J.2    Lehmann, J.3
  • 5
    • 0025978775 scopus 로고
    • TransHexahydroindolo[4,3-ab]phenanthridines ("benzergolines"), the first structural class of potent and selective dopamine D1 receptor agonists lacking a catechol group
    • Seiler, M. P.; Hagenbach, A.; Wuthrich, H. J.; Markstein, R. transHexahydroindolo[4,3-ab]phenanthridines ("benzergolines"), the first structural class of potent and selective dopamine D1 receptor agonists lacking a catechol group. J. Med. Chem. 1991, 34, 303-307.
    • (1991) J. Med. Chem. , vol.34 , pp. 303-307
    • Seiler, M.P.1    Hagenbach, A.2    Wuthrich, H.J.3    Markstein, R.4
  • 6
    • 0027153976 scopus 로고
    • 1 agonist CY 208-243 and its implication for an "extended rotamerbased dopamine receptor model
    • 1 agonist CY 208-243 and its implication for an "extended rotamerbased dopamine receptor model. J. Med. Chem. 1993,36,977-984.
    • (1993) J. Med. Chem. , vol.36 , pp. 977-984
    • Seiler, M.P.1    Floersheim, P.2    Markstein, R.3    Widmer, A.4
  • 7
    • 0034604541 scopus 로고    scopus 로고
    • 5 receptor agonist high affinity and constitutive activity profile conferred by carboxyl-terminal tail sequence
    • 5 receptor agonist high affinity and constitutive activity profile conferred by carboxyl-terminal tail sequence. J. Biol. Chem. 2000, 275, 23446-23455.
    • (2000) J. Biol. Chem. , vol.275 , pp. 23446-23455
    • Demchyshyn, L.L.1    McConkey, F.2    Niznik, H.B.3
  • 8
    • 0024413734 scopus 로고
    • Antiparkinsonian activity of CY 208-243, a partial D-1 dopamine receptor agonist, in MPTP-treated marmosets and patients with Parkinson's disease
    • Temlett, J. A.; Quinn, N. P.; Jenner, P. G.; Marsden, C. D.; Pourcher, E.; Bonnet, A. M.; Agid, Y.; Markstein, R.; Lataste, X. Antiparkinsonian activity of CY 208-243, a partial D-1 dopamine receptor agonist, in MPTP-treated marmosets and patients with Parkinson's disease. Mov. Disord. 1989, 4, 261-265.
    • (1989) Mov. Disord. , vol.4 , pp. 261-265
    • Temlett, J.A.1    Quinn, N.P.2    Jenner, P.G.3    Marsden, C.D.4    Pourcher, E.5    Bonnet, A.M.6    Agid, Y.7    Markstein, R.8    Lataste, X.9
  • 9
    • 33645404572 scopus 로고    scopus 로고
    • Dopamine/ serotonin receptor ligands. 12(1): SAR studies on hexahydrodibenz[d,g]azecines lead to 4-chloro-7-methyl-5,6,7,8,9,14- hexahydrodibenz[d,g]azecin-3-ol, the first picomolar D5-selective dopamine-receptor antagonist
    • Mohr, P.; Decker, M.; Enzensperger, C.; Lehmann, J. Dopamine/ serotonin receptor ligands. 12(1): SAR studies on hexahydrodibenz[d,g]azecines lead to 4-chloro-7-methyl-5,6,7,8,9,14-hexahydrodibenz[d,g]azecin-3-ol, the first picomolar D5-selective dopamine-receptor antagonist. J. Med. Chem. 2006, 49, 2110-2116.
    • (2006) J. Med. Chem. , vol.49 , pp. 2110-2116
    • Mohr, P.1    Decker, M.2    Enzensperger, C.3    Lehmann, J.4
  • 12
    • 84970582978 scopus 로고
    • Synthesis of Benzo[d]thieno[2,3-g]azecine and benzo[d][1]benzothieno[2,3- g]azecine derivatives
    • Browne, E. J. Synthesis of Benzo[d]thieno[2,3-g]azecine and benzo[d][1]benzothieno[2,3-g]azecine derivatives. Aust. J. Chem. 1986, 39, 783-790.
    • (1986) Aust. J. Chem. , vol.39 , pp. 783-790
    • Browne, E.J.1
  • 13
    • 30144441512 scopus 로고    scopus 로고
    • A chemogenomic analysis of the transmembrane binding cavity of human G-protein-coupled receptors
    • Surgand, J. S.; Rodrigo, J.; Kellenberger, E.; Rognan, D. A chemogenomic analysis of the transmembrane binding cavity of human G-protein-coupled receptors. Proteins 2006, 62, 509-538.
    • (2006) Proteins , vol.62 , pp. 509-538
    • Surgand, J.S.1    Rodrigo, J.2    Kellenberger, E.3    Rognan, D.4
  • 14
    • 0006351546 scopus 로고
    • 3,4-Bridgedindoles: Part 2. Synthesis of 6-keto-1,5-dihydro-4, 5diazepino[6,5,4-cd]indoles and 3,4-disubstituted indoles as 5-HT antagonists
    • Ananthanarayanan, C. V.; Rastogi, S. N.; Patnaik, G. K.; Anand, N. 3,4-Bridgedindoles: Part 2. Synthesis of 6-keto-1,5-dihydro-4,5diazepino[6,5,4- cd]indoles and 3,4-disubstituted indoles as 5-HT antagonists. Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. 1977, 15,710-714.
    • (1977) Indian J. Chem., Sect. B: Org. Chem. Incl. Med. Chem. , vol.15 , pp. 710-714
    • Ananthanarayanan, C.V.1    Rastogi, S.N.2    Patnaik, G.K.3    Anand, N.4
  • 15
    • 29044450393 scopus 로고    scopus 로고
    • Highly efficient catalysts for epoxidation mediated by iminium salts
    • Page, P. C. B.; Buckley, B. R.; Appleby, L. F.; Alsters, P. A. Highly efficient catalysts for epoxidation mediated by iminium salts. Synthesis 2005, 3405-3411.
    • (2005) Synthesis , pp. 3405-3411
    • Page, P.C.B.1    Buckley, B.R.2    Appleby, L.F.3    Alsters, P.A.4
  • 16
    • 84982336060 scopus 로고
    • Synthetic indole compounds. V. Syntheses of indoles with (2-aminoethyl)-, (2-aminopropyl)-, or alkanolamine side chains on the six-membered ring
    • Troxler, F.; Harnisch, A.; Bormann, G.; Seemann, F.; Szabo, L. Synthetic indole compounds. V. Syntheses of indoles with (2-aminoethyl)-, (2-aminopropyl)-, or alkanolamine side chains on the six-membered ring. Helv. Chim. Acta 1968, 51,1616-1628.
    • (1968) Helv. Chim. Acta , vol.51 , pp. 1616-1628
    • Troxler, F.1    Harnisch, A.2    Bormann, G.3    Seemann, F.4    Szabo, L.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.