메뉴 건너뛰기




Volumn 48, Issue 8, 2005, Pages 3076-3079

Synthesis and structure-activity relationship of fluoro analogues of 8-{2-[4-(4-methoxyphenyl)piperazin-1yl]ethyl}-8-azaspiro[4.5]decane-7,9-dione as selective α1d-adrenergic receptor antagonists

Author keywords

[No Author keywords available]

Indexed keywords

8 [2 [4 (2,4,5 TRIFLUOROPHENYL)PIPERAZIN 1 YL] 1 METHYLETHYL] 8 AZASPIRO[4.5]DECANE 7,9 DIONE; 8 [2 [4 (2,4,5 TRIFLUOROPHENYL)PIPERAZIN 1 YL]ETHYL] 8 AZASPIRO[4.5]DECANE 7,9 DIONE; 8 [2 [4 (4 METHOXYPHENYL)PIPERAZIN 1 YL]ETHYL] 8 AZASPIRO[4.5]DECANE 7,9 DIONE; ALPHA 1 ADRENERGIC RECEPTOR BLOCKING AGENT; G PROTEIN COUPLED RECEPTOR; UNCLASSIFIED DRUG;

EID: 17444425758     PISSN: 00222623     EISSN: None     Source Type: Journal    
DOI: 10.1021/jm0491391     Document Type: Article
Times cited : (16)

References (19)
  • 2
    • 0029134812 scopus 로고
    • α and β-adrenoceptors: From the gene to the clinic. 1. Molecular biology and adrenoceptor subclassification
    • and references therein
    • (b) Hieble, J. P.; Bondinell, W. E.; Ruffolo, R. R., Jr. α and β-Adrenoceptors: From the Gene to the Clinic. 1. Molecular Biology and Adrenoceptor Subclassification. J. Med. Chem. 1995, 38, 3415-3444 and references therein,
    • (1995) J. Med. Chem. , vol.38 , pp. 3415-3444
    • Hieble, J.P.1    Bondinell, W.E.2    Ruffolo Jr., R.R.3
  • 3
    • 0029113808 scopus 로고
    • α and β-adrenoceptors: From the gene to the Clinic. 2. Structure-activity relationships and therapeutic applications
    • and references therein
    • (c) Ruffolo, R. R., Jr.; Bondinell, W. E.; Hieble, J. P. α and β-Adrenoceptors: From the Gene to the Clinic. 2. Structure-Activity Relationships and Therapeutic Applications. J. Med. Chem. 1995, 38, 3681-3716 and references therein.
    • (1995) J. Med. Chem. , vol.38 , pp. 3681-3716
    • Ruffolo Jr., R.R.1    Bondinell, W.E.2    Hieble, J.P.3
  • 6
    • 17444364317 scopus 로고    scopus 로고
    • Azaspirodecanediones and Azaspiroundecanediones. U.S. Patent 3,398,151, 1968
    • (a) Wu, Y. H. Azaspirodecanediones and Azaspiroundecanediones. U.S. Patent 3,398,151, 1968.
    • Wu, Y.H.1
  • 7
    • 0014573535 scopus 로고
    • Psychosedative agents. N-(4-phenyl-1-piperazinylalky)-substituted cyclic imides
    • (b) Wu, Y. H.; Smith, K. R.; Rayburn, J. W. Psychosedative Agents. N-(4-Phenyl-1-piperazinylalky)-Substituted Cyclic Imides. J. Med. Chem. 1969, 12, 876-881.
    • (1969) J. Med. Chem. , vol.12 , pp. 876-881
    • Wu, Y.H.1    Smith, K.R.2    Rayburn, J.W.3
  • 9
    • 12644299616 scopus 로고    scopus 로고
    • Structure activity relationships of a series of buspirone analogs at alpha-1 adrenoceptors: Further evidence that rat aorta alpha-1 adrenoceptors are of the alpha-1D-subtype
    • (b) Saussy, D. L., Jr.; Goetz, A. S.; Queen, K. L.; King, H. K.; Lutz, M. W.; Rimele, T. J. Structure Activity Relationships of a Series of Buspirone Analogs at Alpha-1 Adrenoceptors: Further Evidence That Rat Aorta Alpha-1 Adrenoceptors Are of the Alpha-1D-Subtype. J. Pharmacol. Exp. Ther. 1996, 278, 136-144.
    • (1996) J. Pharmacol. Exp. Ther. , vol.278 , pp. 136-144
    • Saussy Jr., D.L.1    Goetz, A.S.2    Queen, K.L.3    King, H.K.4    Lutz, M.W.5    Rimele, T.J.6
  • 14
    • 0035043183 scopus 로고    scopus 로고
    • Ligand design for alpha(1) adrenoceptors
    • Two compounds described in this paper have been cited in reviews: (a) Bremner, J. B.; Griffith, R.; Coban, B. Ligand Design for Alpha(1) Adrenoceptors. Curr. Med. Chem. 2001, 8, 607-620.
    • (2001) Curr. Med. Chem. , vol.8 , pp. 607-620
    • Bremner, J.B.1    Griffith, R.2    Coban, B.3
  • 19
    • 17444432090 scopus 로고    scopus 로고
    • note
    • i = 124 nM) could be accounted for by the 1% of 12 in the sample.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.