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Volumn 22, Issue 4, 2008, Pages 428-432

Determination of lipophilicity of α-(4-phenylpiperazine) derivatives of N-benzylamides using chromatographic and computational methods

Author keywords

Calculated partition coefficient; Derivatives of 4 phenylpiperazine; Lipophilicity; N benzylamides; Retention parameters RM0 capacity factors; RP TLC and HPLC

Indexed keywords

C (PROGRAMMING LANGUAGE); HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; THIN LAYER CHROMATOGRAPHY;

EID: 42549131866     PISSN: 02693879     EISSN: 10990801     Source Type: Journal    
DOI: 10.1002/bmc.951     Document Type: Article
Times cited : (12)

References (20)
  • 1
    • 0033957297 scopus 로고    scopus 로고
    • Lipophilicity characterization by reversed-phase liquid chromatography of some furan derivatives
    • Cimpan G, Hadaruga M and Miclaus V. Lipophilicity characterization by reversed-phase liquid chromatography of some furan derivatives. Journal of Chromatography A 2000; 869: 49-55.
    • (2000) Journal of Chromatography A , vol.869 , pp. 49-55
    • Cimpan, G.1    Hadaruga, M.2    Miclaus, V.3
  • 4
    • 0038393305 scopus 로고    scopus 로고
    • Relative hydrophobicity and lipophilicity of drugs measured by aqueous two-phase partitioning, octanol-buffer partitioning and HPLC. A simple model for predicting blood-brain distribution
    • Gulyaeva N, Zaslavsky A, Lechner P, Chlenov M, McConnell O, Chait A, Kipnis V and Zaslavsky B. Relative hydrophobicity and lipophilicity of drugs measured by aqueous two-phase partitioning, octanol-buffer partitioning and HPLC. A simple model for predicting blood-brain distribution. European Journal of Medicinal Chemistry 2003; 38: 391-396.
    • (2003) European Journal of Medicinal Chemistry , vol.38 , pp. 391-396
    • Gulyaeva, N.1    Zaslavsky, A.2    Lechner, P.3    Chlenov, M.4    McConnell, O.5    Chait, A.6    Kipnis, V.7    Zaslavsky, B.8
  • 5
    • 13244282955 scopus 로고    scopus 로고
    • Lipophilicity - beyond octanol/water: A short comparison of modern technologies
    • Hartmann T and Schmitt J. Lipophilicity - beyond octanol/water: a short comparison of modern technologies. Drug Discovery Today: Technologies 2004; 1: 431-439.
    • (2004) Drug Discovery Today: Technologies , vol.1 , pp. 431-439
    • Hartmann, T.1    Schmitt, J.2
  • 7
    • 4644263283 scopus 로고    scopus 로고
    • Reversed-phase high performance liquid chromatographic determination of lipophilicity of potential antituberculosis compounds
    • Kresta J, Kastner P, Klimeš J and Klimešová V. Reversed-phase high performance liquid chromatographic determination of lipophilicity of potential antituberculosis compounds. Journal Liquid Chromatography and Related Technologies 2004; 27: 2539-2545.
    • (2004) Journal Liquid Chromatography and Related Technologies , vol.27 , pp. 2539-2545
    • Kresta, J.1    Kastner, P.2    Klimeš, J.3    Klimešová, V.4
  • 8
    • 0000130397 scopus 로고
    • The quantitative analysis of structure-activity relationship
    • Wolff M ed, Wiley: New York
    • Kubinyi H. The quantitative analysis of structure-activity relationship. In Burger's Medicinal Chemistry and Drug Discovery, Wolff M (ed.). Wiley: New York, 1995; 497.
    • (1995) Burger's Medicinal Chemistry and Drug Discovery , pp. 497
    • Kubinyi, H.1
  • 9
    • 24544469216 scopus 로고
    • oct from structures
    • oct from structures. Chemical Reviews 1993; 93: 1281-1305.
    • (1993) Chemical Reviews , vol.93 , pp. 1281-1305
    • Leo, A.J.1
  • 10
    • 0344308307 scopus 로고    scopus 로고
    • Comparison of chromatographically determined values of the lipophilicity of anticonvulsant active N-substituted amides of α-arylalkylamine-γ-hydroxybutyric acid with values estimated by computational methods
    • Malawska B, Kulig K and Bendieck E. Comparison of chromatographically determined values of the lipophilicity of anticonvulsant active N-substituted amides of α-arylalkylamine-γ-hydroxybutyric acid with values estimated by computational methods. Journal Planar Chromatography 2003; 16: 390-395.
    • (2003) Journal Planar Chromatography , vol.16 , pp. 390-395
    • Malawska, B.1    Kulig, K.2    Bendieck, E.3
  • 11
    • 0347761409 scopus 로고    scopus 로고
    • Investigation into new anticonvulsant derivatives of α-substituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5. Search for new anticonvulsant compounds
    • Malawska B, Kulig K, Śpiewak A and Stables JP. Investigation into new anticonvulsant derivatives of α-substituted N-benzylamides of γ-hydroxy- and γ-acetoxybutyric acid. Part 5. Search for new anticonvulsant compounds. Bioorganic and Medicinal Chemistry 2004; 12: 625-632.
    • (2004) Bioorganic and Medicinal Chemistry , vol.12 , pp. 625-632
    • Malawska, B.1    Kulig, K.2    Śpiewak, A.3    Stables, J.P.4
  • 13
    • 20544432279 scopus 로고    scopus 로고
    • Synthesis of novel N-alkyl carbamates of α-substituted amides of γ-hydroxybutyric acid as potential acetylcholinesterase inhibitors
    • Musiał A and Malawska B. Synthesis of novel N-alkyl carbamates of α-substituted amides of γ-hydroxybutyric acid as potential acetylcholinesterase inhibitors. Acta Poloniae Pharmaceutica - Drug Research 2004; 61(suppl.): 94-97.
    • (2004) Acta Poloniae Pharmaceutica - Drug Research , vol.61 , Issue.SUPPL. , pp. 94-97
    • Musiał, A.1    Malawska, B.2
  • 14
    • 0000855358 scopus 로고    scopus 로고
    • Rapid Gradient RP-HPLC method for lipophilicity determination: A solvation equation based comparison with isocratic methods
    • My Du C, Valko K, Bevan C, Reynolds D and Abraham MH. Rapid Gradient RP-HPLC method for lipophilicity determination: a solvation equation based comparison with isocratic methods. Analytical Chemistry 1998; 70: 4228-4234.
    • (1998) Analytical Chemistry , vol.70 , pp. 4228-4234
    • My Du, C.1    Valko, K.2    Bevan, C.3    Reynolds, D.4    Abraham, M.H.5
  • 15
    • 13944268698 scopus 로고    scopus 로고
    • Greater than the sum of its parts: Combining models for useful ADMET prediction
    • O'Brien SE and de Groot MJ. Greater than the sum of its parts: Combining models for useful ADMET prediction. Journal of Medicinal Chemistry 2005; 48: 1287-1291.
    • (2005) Journal of Medicinal Chemistry , vol.48 , pp. 1287-1291
    • O'Brien, S.E.1    de Groot, M.J.2
  • 16
    • 0034887195 scopus 로고    scopus 로고
    • Study of the lipophilicity of arylpropionic non-steroidal anti-inflammatory drugs. A comparison between LC retention data on a polymer-based column and octanol-water partition coefficients
    • Péhourcq F, Matoga M, Jarry C and Bannwarth B. Study of the lipophilicity of arylpropionic non-steroidal anti-inflammatory drugs. A comparison between LC retention data on a polymer-based column and octanol-water partition coefficients. Journal of Liquid Chromatography and Related Technologies 2001; 24: 2177-2186.
    • (2001) Journal of Liquid Chromatography and Related Technologies , vol.24 , pp. 2177-2186
    • Péhourcq, F.1    Matoga, M.2    Jarry, C.3    Bannwarth, B.4
  • 17
  • 18
    • 7444258512 scopus 로고    scopus 로고
    • Application of ALOGPS 2.1 to predict logD distribution coefficient for Pfizer proprietary compounds
    • Tetko IV and Poda GI. Application of ALOGPS 2.1 to predict logD distribution coefficient for Pfizer proprietary compounds. Journal of Medicinal Chemistry 2004; 47: 5601-5604.
    • (2004) Journal of Medicinal Chemistry , vol.47 , pp. 5601-5604
    • Tetko, I.V.1    Poda, G.I.2
  • 19
    • 0036757804 scopus 로고    scopus 로고
    • Application of associative neural networks for prediction of lipophilicity in ALOGPS 2.1 program
    • Tetko IV and Tanchuk VY. Application of associative neural networks for prediction of lipophilicity in ALOGPS 2.1 program. Journal of Chemistry Informatics and Computing Sciences 2002; 42: 1136-1145.
    • (2002) Journal of Chemistry Informatics and Computing Sciences , vol.42 , pp. 1136-1145
    • Tetko, I.V.1    Tanchuk, V.Y.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.