Comparison of measured and calculated lipophilicity of substituted aurones and related compounds

被引:29
作者
Hallgas, B
Patonay, T
Kiss-Szikszai, A
Dobos, Z
Hollósy, F
Eros, D
Orfi, L
Kéri, G
Idei, M
机构
[1] Semmelweis Univ, Hungarian Acad Sci, Dept Med Chem, Peptidbiochem Res Grp, H-1088 Budapest, Hungary
[2] Univ Debrecen, Dept Organ Chem, H-4032 Debrecen, Hungary
[3] Semmelweis Univ, Inst Pharmaceut Chem, H-1088 Budapest, Hungary
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2004年 / 801卷 / 02期
关键词
lipophilicity; aurones;
D O I
10.1016/j.jchromb.2003.11.021
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A molecule library containing 55 aurone- and thioaurone-type structures has been designed and synthesised. Reversed phase high performance liquid chromatographic (RP-HPLC) method has been developed to separate these compounds and to characterise their lipophilicity by experimental method (k'). The experimental lipophilicity data have been compared with the computer calculated lipophilicity parameters (CLOGPs) of the same molecules. In general, good correlations between the measured and calculated lipophilicities have been found with the exception of structure isomers and compounds capable for hydrogen bonding. The chromatographic method was suitable to separate the structure (ortho and para) isomers of aurone and thioaurones and was sensitive enough to differentiate their lipophilicities. Our findings suggest the usefulness of the chromatographic method in fast characterisation of the lipophilicity of structurally closely related molecules. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 235
页数:7
相关论文
共 34 条
[1]   DIOXIRANE OXIDATION OF (Z)-1-THIOAURONES, (E)-3-ARYLIDENE-1-THIOCHROMAN-4-ONES AND (E)-3-ARYLIDENE-1-THIOFLAVAN-4-ONES [J].
ADAM, W ;
GOLSCH, D ;
HADJIARAPOGLOU, L ;
LEVAI, A ;
NEMES, C ;
PATONAY, T .
TETRAHEDRON, 1994, 50 (46) :13113-13120
[2]   RELATIONSHIP BETWEEN VARIABLE SELECTION AND DATA AUGMENTATION AND A METHOD FOR PREDICTION [J].
ALLEN, DM .
TECHNOMETRICS, 1974, 16 (01) :125-127
[3]  
BAKER SR, 1980, Patent No. 2936730
[4]   QUANTITATIVE STRUCTURE-ACTIVITY-RELATIONSHIPS FOR HERBICIDES - REVERSED-PHASE LIQUID-CHROMATOGRAPHIC RETENTION PARAMETER, LOG KW, VERSUS LIQUID-LIQUID PARTITION-COEFFICIENT AS A MODEL OF THE HYDROPHOBICITY OF PHENYLUREAS, S-TRIAZINES AND PHENOXYCARBONIC ACID-DERIVATIVES [J].
BRAUMANN, T ;
WEBER, G ;
GRIMME, LH .
JOURNAL OF CHROMATOGRAPHY, 1983, 261 (03) :329-343
[5]  
CASTEL J, 1976, Travaux de la Societe de Pharmacie de Montpellier, V36, P239
[6]  
CASTEL J, 1977, CHEM ABSTR 50498, V86
[7]   Role of stationary phase and eluent composition on the determination of log P values of N-hydroxyethylamide of aryloxyalkylen- and pyridine carboxylic acids by reversed-phase high-performance liquid chromatography [J].
Cimpan, G ;
Irimie, F ;
Gocan, S ;
Claessens, HA .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 1998, 714 (02) :247-261
[8]   Method for measuring the logarithm of the octanol-water partition coefficient by using short octadecyl-poly(vinyl alcohol) high-performance liquid chromatography columns [J].
Donovan, SF ;
Pescatore, MC .
JOURNAL OF CHROMATOGRAPHY A, 2002, 952 (1-2) :47-61
[9]  
FARMITALIA C, 1979, Patent No. 873826
[10]  
FLANDRE O, 1977, CHEM ABSTR 96015, V87