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Volumn 56, Issue 1-2, 2001, Pages 91-94

Metabotropic glutamate receptors: structure and new subtype-selective ligands

Author keywords

Amino terminal domain; Metabotropic glutamate receptors; mGluR1 antagonists; Neuroprotection

Indexed keywords

ADENYLATE CYCLASE; GLUTAMATE RECEPTOR; GLUTAMATE RECEPTOR ANTAGONIST; LIGAND; METABOTROPIC RECEPTOR; RECEPTOR SUBTYPE;

EID: 0035273095     PISSN: 0014827X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0014-827X(01)01006-0     Document Type: Conference Paper
Times cited : (9)

References (18)
  • 1
    • 0004997314 scopus 로고    scopus 로고
    • For recent reviews see: (a) H. Brauner-Osborne, J. Egebjerg, E.O. Nielsen, U. Madsen, P. Krogsgaard-Larsen, Ligands for glutamate receptors: design and therapeutic prospects, J. Med. Chem. 43 (2000) 2609-2645. (b) R. Pellicciari, G. Costantino, Metabotropic G-protein-coupled glutamate receptors as therapeutic targets, Curr. Opin. Chem. Biol. 4 (1999) 433-440. (c) J.P. Pin, C. De Colle, A.S. Bessis, F. Acher, New perspectives for the development of selective metabotropic glutamate receptor ligands, Eur. J. Pharmacol. 375 (1999) 277-294.
  • 3
    • 0005061934 scopus 로고    scopus 로고
    • M.M. Behrens, V. Heidenger, P. Manzerra, T. Ichinose, S.-P. Yu, D.W. Choi, Neuronal mGluR1 activation enhances NMDA receptor function via src-family kinase-mediated phosphorylation, Soc. Neurosci. Abstr. (2001) in press.
  • 4
    • 0033118334 scopus 로고    scopus 로고
    • Molecular tinkering of G protein-coupled receptors: an evolutionary success
    • (1999) EMBOJ. , vol.18 , pp. 1723-1729
    • Bockaert, J.1    Pin, J.P.2
  • 18
    • 0005036624 scopus 로고    scopus 로고
    • G. Costantino, K. Maltoni, M. Marinozzi, E. Camaioni, L. Prezeau, J.P. Pin, R. Pellicciari, Synthesis and biological evaluation of 2-(3′-(1H-tetrazol-5-yl)bicyclo[1.1.1]pent-1-yl)glycine (S-TBPG), a novel mGlu1 receptor antagonist, Bioorg. Med. Chem. (2001) in press.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.