Comparative molecular field analysis (CoMFA) and comparative molecular similarity index analysis (CoMSIA) study of mutagen X

被引:0
|
作者
Bang, SJ [1 ]
Cho, SJ [1 ]
机构
[1] Korea Inst Sci & Technol, Div Life Sci, Seoul 130650, South Korea
来源
关键词
mutagen X; mutagenicity; CoMFA; CoMSIA; QSAR;
D O I
暂无
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mutagen X (MX) exists in our drinking water as the bi-products of chlorine disinfection. Being one of the most potent mutagen, it attracted much attention from many researchers. MX and its analogs are synthesized and modeled by quantitative structure activity relationship (QSAR) methods. As a result, factors affecting this class of compounds have been found to be steric and electrostatic effects. We tried to collect all the data available from the literature. With both CoMFA and CoMSIA various combinations of physiochemical parameters were systematically studied to produce reasonable 3-dimensional models. The best model for CoMFA gave q(2) = 0.90 and r(2) = 0.97, while for CoMSIA q(2) = 0.85 and r(2) = 0.94. So the models seem to be reasonable. Unlike previous result of CoMFA, in our case steric parameter alone gave the best statistics. Although the steric contribution was found to be the most important in both CoMFA and CoMSIA, steric parameter along with electrostatic parameter produced slightly better model in CoMSIA. Overall, steric contribution is clearly the most important single factor. However, when we compare chlorine and bromine substitution, chlorine substitution can be more mutagenic. This indicates that other factors such as electrostatic effect also influence the mutagenicity. From the contour maps, steric contribution seems to be focused on rather small area near C6 substituent of the furanone ring, rather than C3 substituent. Therefore the locality of steric contribution can play a significant role in mutagenicity.
引用
收藏
页码:1525 / 1530
页数:6
相关论文
共 50 条
  • [41] Selectivity fields: Comparative molecular field analysis (CoMFA) of the glycine/NMDA and AMPA receptors
    Baskin, II
    Tikhonova, IG
    Palyulin, VA
    Zefirov, NS
    JOURNAL OF MEDICINAL CHEMISTRY, 2003, 46 (19) : 4063 - 4069
  • [42] Synthesis and comparative molecular field analysis (CoMFA) of antitumor 3-arylisoquinoline derivatives
    Cho, WJ
    Kim, EK
    Park, MJ
    Choi, SU
    Lee, CO
    Cheon, SH
    Choi, BG
    Chung, BH
    BIOORGANIC & MEDICINAL CHEMISTRY, 1998, 6 (12) : 2449 - 2458
  • [43] Structure-activity relationships of artemisinin analogs by comparative molecular similarity indices analysis-CoMSIA.
    Alvim-Gaston, M
    Sabnis, YA
    Avery, MA
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2001, 221 : U425 - U425
  • [44] APPLICATION OF COMPARATIVE MOLECULAR-FIELD ANALYSIS (COMFA) TO INHIBITORS OF PHOTOSYSTEM-II
    PATTERSON, D
    CRAMER, R
    HECHT, P
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 208 : 29 - AGRO
  • [45] Comparative Molecular Field Analysis(CoMFA) of Curcumin-related Compounds for Anticancer Activity
    周代营
    杜志云
    汤志恺
    郑希
    丁宁
    郑俊霞
    王辉
    张焜
    结构化学, 2014, 33 (02) : 179 - 188
  • [46] Comparative Molecular Field Analysis (CoMFA) of Curcumin-related Compounds for Anticancer Activity
    Zhou Dai-Ying
    Du Zhi-Yun
    Tang Zhi-Kai
    Zheng Xi
    Ding Ning
    Zheng Jun-Xia
    Wang Hui
    Zhang Kun
    CHINESE JOURNAL OF STRUCTURAL CHEMISTRY, 2014, 33 (02) : 179 - 188
  • [47] Evaluation of hydrophobic/hydrophilic balance of bile acids by comparative molecular field analysis (CoMFA)
    Costantino, G
    Wolf, C
    Natalini, B
    Pellicciari, R
    STEROIDS, 2000, 65 (09) : 483 - 489
  • [48] A comparative molecular field analysis (CoMFA) study of nucleoside analog inhibitors of es adenosine transport.
    Buolamwini, JK
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1996, 211 : 93 - MEDI
  • [49] Comparative molecular field analysis and comparative molecular similarity index analysis studies on 1H NMR chemical shift of NH group of diaryl triazene derivatives
    Rofouie, M. K.
    Salahinejad, M.
    Ghasemi, J. B.
    Aghaei, A.
    MAGNETIC RESONANCE IN CHEMISTRY, 2013, 51 (05) : 269 - 274
  • [50] STRUCTURE-BASED COMPARATIVE MOLECULAR-FIELD ANALYSIS (COMFA) OF ACETYLCHOLINESTERASE INHIBITORS
    SERRANO, ML
    CHO, SJ
    BIER, J
    TROPSHA, A
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 1994, 208 : 187 - COMP