메뉴 건너뛰기




Volumn 43, Issue 3, 2008, Pages 513-539

Synthesis and cannabinoid activity of 1-substituted-indole-3-oxadiazole derivatives: Novel agonists for the CB1 receptor

Author keywords

Aminoalkylindoles; Cannabinoid CB1 receptors; CB1 agonists; Design; Pain control; Synthesis

Indexed keywords

(1H INDOL 3 YL)(3 PHENYL 1,2,4 OXADIAZOL 5 YL)METHANONE; (3 BENZYL 1,2,4 OXADIAZOL 5 YL)[1 (2 MORPHOLINOETHYL) 1H INDOL 3 YL)METHANONE; (3 BENZYL [1,2,4]OXADIAZOL 5 YL)(1H INDOL 3 YL)METHANONE; (3 NAPHTHALEN 2 YLMETHYL) 5 [1 [2 (PYRROLIDINE 1 YL) ETHYL] 1H INDOL 3 YL] 1,2,4 OXADIAZOLE; 1 MORPHOLINO 2 (3 PHENYL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 1 YL ETHANONE; 2 [3 (3 BENZYL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 1 YL] 1 MORPHOLINOETHANONE; 3 (2 CHLOROBENZYL) 5 (1H INDOL 3 YL) 1,2,4 OXADIAZOLE; 3 (4 BROMOBENZYL) 5 (1H INDOL 3 YL) 1,2,4 OXADIAZOLE; 3 (BIPHENYL 4 YL) 5 (1H INDOL 3 YL) 1,2,4 OXADIAZOLE; 3 BENZYL 5 (1 PENTYL 1H INDOL 3 YL) 1,2,4 OXADIAZOLE; 3 BENZYL 5 (1H INDOL 3 YL) 1,2,4 OXADIAZOLE; 3 BENZYL 5 [1 (2 PYRROLIDIN 1 YL)ETHYL 1H INDOL 3 YL] 1,2,4 OXADIAZOLE; 4 [2 [3 (3 BENZYL [1,2,4]OXADIAZOL 5 YL) 1H INDOL 1 YL]ETHYL]MORPHOLINE; 4 [2 [3 (3 BIPHENYL 4 YL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 1 YL]ETHYL]MORPHOLINE; 4 [2 [3 (3 PHENYL 1,2,4 OXADIAZOL 5 YL) 1H INDOL 1 YL]ETHYL]MORPHOLINE; 4 [2 [3 [3 (NAPHTHALENE 2 YLMETHYL) 1,2,4 OXADIAZOL 5 YL] 1H INDOL 1 YL]ETHYL]MORPHOLINE; 5 (1H IMIDAZOL 4 YL) 3 (THIOPHEN 2 YLMETHYL) 1,2,4 OXADIAZOLE; 5 (1H INDOL 3 YL) 3 (4 METHOXYBENZYL) 1,2,4 OXADIAZOLE; 5 (1H INDOL 3 YL) 3 (NAPHTHALENE 2 YLMETHYL) 1,2,4 OXADIAZOLE; 5 (1H INDOL 3 YL) 3 (THIOPHEN 2 YLMETHYL) 1,2,4 OXADIAZOLE; 5 (1H INDOL 3 YL) 3 PHENETHYL 1,2,4 OXADIAZOLE; 5 (1H INDOL 3 YL) 3 PHENYL 1,2,4 OXADIAZOLE; 5 [3 [3 (NAPHTHALENE 2 YLMETHYL) 1,2,4 OXADIAZOL 5 YL] 1H INDOL 1 YL]PENTANOIC ACID; ANANDAMIDE; CANNABINOID 1 RECEPTOR AGONIST; DEXANABINOL; ETHYL 5 [3 [3 (NAPHTHALEN 2 YLMETHYL) 1,2,4 OXADIAZOL 5 YL] 1H INDOL 1 YL]PENTANOATE; OXADIAZOLE DERIVATIVE; RIMONABANT; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 40149100335     PISSN: 02235234     EISSN: 17683254     Source Type: Journal    
DOI: 10.1016/j.ejmech.2007.04.007     Document Type: Article
Times cited : (16)

References (50)
  • 18
    • 85120124803 scopus 로고    scopus 로고
    • M. Gallant, Y. Gareau, D. Guay, M. Labelle, P. Prasit, U.S., Patent No. US 5532237, Type. A, 1996, 16 pp.
  • 19
    • 85120120324 scopus 로고    scopus 로고
    • K.J. Fahey, G.J. Cullinan, PCT UsS5 08455, 1995.
  • 37
    • 85120135660 scopus 로고    scopus 로고
    • M. Rinaldi, F. Barth, P. Casellas, C. Congy, D. Oustric, M.R. Bell, T.E. D'Ambra, R.E. Philion, Fr. Demande, Patent No. FR 2735774, Type. A1, 1996, 54 pp.
  • 40
    • 85120146588 scopus 로고    scopus 로고
    • Sybyl 6.1 molecular modeling package. Tripos Associates, St Louis MO 63144, U.S.A, 1992.
  • 43
    • 85120100557 scopus 로고    scopus 로고
    • G.P. Moloney, A.D. Robertson, PCT Int. Appl. Patent No. WO 2002036590, Type. A1, 2002, 47 pp.
  • 46
    • 85120139997 scopus 로고    scopus 로고
    • A. Tasker, M.C. Rutledge, L. Liu, N. Han, C. Comingues, E. Grenazer-Laber, Z. Chen, O.A. Moreno, PCT Int. Appl. Patent No. WO 2001023357, Type. A2, 2001, 262 pp.
  • 48
    • 85120108421 scopus 로고    scopus 로고
    • T. Kimura, T. Murakami, J. Ohmori, T. Morita, S-i. Tsukamoto, PCT Int. Appl. Patent No. WO 9800420, Kind. A1, 1998, pp. 90.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.