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Volumn 33, Issue 2, 1990, Pages 781-789

Some Benzyl-Substituted Imidazoles, Triazoles, Tetrazoles, Pyridinethiones, and Structural Relatives as Multisubstrate Inhibitors of Dopamine β-Hydroxylase. 4.1Structure-Activity Relationships at the Copper Binding Site

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3,4 TETRAZOLE 5 THIOL DERIVATIVE; 1,2,4 TRIAZOLE 3 THIONE DERIVATIVE; 2 BENZIMIDAZOLETHIOL DERIVATIVE; 2 PYRIDINETHIOL DERIVATIVE; 2 PYRIMIDINETHIONE DERIVATIVE; DOPAMINE BETA MONOOXYGENASE; IMIDAZOLINETHIONE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0025058617     PISSN: 00222623     EISSN: 15204804     Source Type: Journal    
DOI: 10.1021/jm00164a051     Document Type: Article
Times cited : (54)

References (17)
  • 11
    • 85023412154 scopus 로고    scopus 로고
    • An alternative explanation would have enzyme binding that fraction of inhibitor which is present in solution in the deprotonated, anionic form
    • -15M. An inhibitor of this potency would exhibit essentially irreversible inhibition or at minimum, tight binding behavior. Neither has been observed (see ref 3)
    • -15M. An inhibitor of this potency would exhibit essentially irreversible inhibition or at minimum, tight binding behavior. Neither has been observed (see ref 3).
    • aca. 12.5)


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.