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Volumn 7, Issue 5, 1999, Pages 869-880

1,3-Dimethyl-7-substituted-1,2,3,4-tetrahydroisoquinolines as probes for the binding orientation of tetrahydroisoquinoline at the active site of phenylethanolamine N-methyltransferase

Author keywords

Antihypertension; Enzyme inhibitors; Neurologically active cmpds; Stereospecificity

Indexed keywords

1,2,3,4 TETRAHYDRO 7 ISOQUINOLINESULFONAMIDE; 7,8 DICHLORO 1,2,3,4 TETRAHYDROISOQUINOLINE; ALPHA 2 ADRENERGIC RECEPTOR; PHENYLETHANOLAMINE N METHYLTRANSFERASE; TETRAHYDROISOQUINOLINE; TETRAHYDROISOQUINOLINE DERIVATIVE;

EID: 0033135059     PISSN: 09680896     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0896(99)00031-0     Document Type: Article
Times cited : (13)

References (49)
  • 1
    • 0013493889 scopus 로고    scopus 로고
    • note
    • This paper is dedicated to the memory of Sir D. H. R. Barton for the fundamental contributions he made in conformation and its importance in chemistry. It was Barton, at a cocktail party following a research seminar at the University of Wisconsin in the 1950s, who discussed with Edward E. Smissman the thoughts Barton had of the importance of conformation to organic chemistry that sparked Smissman's realization of the relevance of conformation to the interaction of drugs with receptors. Smissman embarked on his highly successful research in the 1950s and 1960s to exploit this with the design and synthesis of conformationally-restricted (rigid) analogues of drugs and neurotransmitters. Today the concept of rigid analogues in drug design is taken for granted, and it was Smissman, later reinforced by conversations this author had with Barton, that sparked my own interest in applications of the concept of rigid analogues to an understanding of the molecular mechanism of action of amphetamine, and further to the subject of this paper. Both men were giants in their field, and it is noteworthy that there was a synergism in the recognition of the work of one by the other in ways that neither would have seen alone.
  • 2
    • 0013533971 scopus 로고    scopus 로고
    • Taken in large part from the Ph.D. dissertation of T.M.C., University of Kansas
    • Taken in large part from the Ph.D. dissertation of T.M.C., University of Kansas, 1998.
    • (1998)
  • 29
    • 0013545977 scopus 로고
    • Ph.D. dissertation, University of Kansas, Lawrence, KS
    • Dahanukar, Vilas H., Ph.D. dissertation, University of Kansas, Lawrence, KS, 1994.
    • (1994)
    • Dahanukar1    Vilas, H.2
  • 32
    • 0013525985 scopus 로고    scopus 로고
    • 20 =+20° (c 0.79, EtOH)
    • 20 =+20° (c 0.79, EtOH).
  • 43
    • 0013501107 scopus 로고    scopus 로고
    • o)=e.s.d. based on counting statistics and p=p- factor
    • o)=e.s.d. based on counting statistics and p=p- factor.
  • 44
    • 0013526289 scopus 로고    scopus 로고
    • v=number of variables
    • v=number of variables.
  • 47
    • 0000029575 scopus 로고
    • Ed., Wilson, A. J. C.; Kluwer Academic Publishers; Boston Table 4.2.6.8
    • Creagh, D. C.; McAuley, W. J. 'International Tables for Crystallography'; Ed., Wilson, A. J. C.; Kluwer Academic Publishers; Boston, 1992, Vol. C, pp 219-222, Table 4.2.6.8.
    • (1992) International Tables for Crystallography , vol.C , pp. 219-222
    • Creagh, D.C.1    McAuley, W.J.2
  • 48
    • 0000191360 scopus 로고
    • Ed., Wilson, A. J. C.; Kluwer Academic Publishers; Boston Table 4.2.4.3
    • Creagh, D. C.; Hubbell, J. H. 'International Tables for Crystallography'; Ed., Wilson, A. J. C.; Kluwer Academic Publishers; Boston, 1992, Vol. C, pp 200-206, Table 4.2.4.3.
    • (1992) International Tables for Crystallography , vol.C , pp. 200-206
    • Creagh, D.C.1    Hubbell, J.H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.