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Volumn 17, Issue 5, 2003, Pages 318-324

Estimation of the lipophilicity of antiarrhythmic and antihypertensive active 1-substituted pyrrolidin-2-one and pyrrolidine derivatives

Author keywords

Partition coefficient; Quantitative structure activity relationship; Reversed phase chromatography

Indexed keywords

THIN LAYER CHROMATOGRAPHY;

EID: 0041562585     PISSN: 02693879     EISSN: None     Source Type: Journal    
DOI: 10.1002/bmc.246     Document Type: Article
Times cited : (14)

References (14)
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    • Andersson, J.T.1    Schräder, W.2
  • 2
    • 84958593100 scopus 로고    scopus 로고
    • Assessment of distribution - pH profiles
    • Pliška V, Testa B, van de Waterbeemd H (eds). VCH: Weinheim
    • Avdeef A. Assessment of distribution - pH profiles. In Lipophilicity in Drug Action and Toxicology, Pliška V, Testa B, van de Waterbeemd H (eds). VCH: Weinheim, 1996; 109.
    • (1996) Lipophilicity in Drug Action and Toxicology , pp. 109
    • Avdeef, A.1
  • 4
    • 0001477154 scopus 로고
    • A simple assessment of partition data for correlating structure and biological activity using thin-layer chromatography
    • Boyce CBC and Milborrow BV. A simple assessment of partition data for correlating structure and biological activity using thin-layer chromatography. Nature 1965; 208: 537.
    • (1965) Nature , vol.208 , pp. 537
    • Boyce, C.B.C.1    Milborrow, B.V.2
  • 9
    • 0037708259 scopus 로고
    • Physicochemical properties and drug design
    • King FD (ed.). The Royal Society of Chemistry: London
    • Gensmantel NP. Physicochemical properties and drug design. In Medicinal Chemistry Principles and Practice, King FD (ed.). The Royal Society of Chemistry: London, 1994; 98.
    • (1994) Medicinal Chemistry Principles and Practice , pp. 98
    • Gensmantel, N.P.1
  • 10
    • 0000130397 scopus 로고
    • The quantitative analysis of structure-activity relationships
    • Wolff M (ed.). John Wiley: New York
    • Kubinyi H. The quantitative analysis of structure-activity relationships. In Burger's Medicinal Chemistry and Drug Discovery, Wolff M (ed.). John Wiley: New York, 1995; 497.
    • (1995) Burger's Medicinal Chemistry and Drug Discovery , pp. 497
    • Kubinyi, H.1
  • 11
    • 0007915780 scopus 로고    scopus 로고
    • Determination of ionization constants of some N-1-arylpiperazine-propylpyrrolidin-2-one derivatives
    • Malawska B and Kulig K. Determination of ionization constants of some N-1-arylpiperazine-propylpyrrolidin-2-one derivatives. Acta Poloniae Pharmacentica-Drug Research. 1999; 56 (Suppl.): 91.
    • (1999) Acta Poloniae Pharmacentica-Drug Research , vol.56 , Issue.SUPPL. , pp. 91
    • Malawska, B.1    Kulig, K.2
  • 13
    • 84958605534 scopus 로고    scopus 로고
    • The role of lipophilicity in biological response to drug and endogenous ligands
    • Pliška V, Testa B, van de Waterbeemd H (eds). VCH: Weinheim
    • Pliška V. The role of lipophilicity in biological response to drug and endogenous ligands. In Lipophilicity in Drug Action and Toxicology, Pliška V, Testa B, van de Waterbeemd H (eds). VCH: Weinheim 1996; 263.
    • (1996) Lipophilicity in Drug Action and Toxicology , pp. 263
    • Pliška, V.1
  • 14
    • 84958623621 scopus 로고    scopus 로고
    • Lipophilicity measurement by reversed-phase high performance liquid chromatography (RP-HPLC)
    • Pliška V, Testa B, van de Waterbeemd H (eds). VCH: Weinheim
    • Van de Waterbeemd H, Kansy M, Wagner B and Fischer H. Lipophilicity measurement by reversed-phase high performance liquid chromatography (RP-HPLC). In Lipophilicity in Drug Action and Toxicology, Pliška V, Testa B, van de Waterbeemd H (eds). VCH: Weinheim 1996;
    • (1996) Lipophilicity in Drug Action and Toxicology , pp. 73
    • Van de Waterbeemd, H.1    Kansy, M.2    Wagner, B.3    Fischer, H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.