Medicinal Chemistry Strategies to Minimize Phospholipidosis

被引:26
作者
Ratcliffe, Andrew J. [1 ]
机构
[1] Cellzome Ltd, Dept Med Chem, Cambridge CB10 1XL, England
关键词
Drug-induced phospholipidosis; in silico models; toxicology; physicochemical; medicinal chemistry; strategies; prediction; cationic amphiphilic drugs; DRUG-INDUCED PHOSPHOLIPIDOSIS; ANTAGONISTS; INHIBITORS; POTENT;
D O I
10.2174/092986709788803213
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Drug-induced phospholipidosis is characterised by an excessive accumulation of polar phospholipids in cells or tissues. However, from a toxicological perspective the functional consequences of phospholipidosis remain uncertain and a regulatory position unclear. As a consequence, to minimize compound development risk pharmaceutical companies are beginning to proactively address phospholipidosis within drug discovery programs, and implement strategies to identify compounds predicted to show no phospholipidosis. Examples of optimization of compounds to minimize phospholipidosis, and the status of current in silico prediction models, are presented and discussed.
引用
收藏
页码:2816 / 2823
页数:8
相关论文
共 21 条
  • [1] Neutral 5-substituted 4-anilinoquinazolines as potent, orally active inhibitors of erbB2 receptor tyrosine kinase
    Ballard, Peter
    Barlaam, Bernard C.
    Bradbury, Robert H.
    Dishington, Allan
    Hennequin, Laurent F. A.
    Hickinson, D. Mark
    Hollingsworth, Ian M.
    Kettle, Jason G.
    Klinowska, Teresa
    Ogilvie, Donald J.
    Pearson, Stuart E.
    Scott, James S.
    Suleman, Abid
    Whittaker, Robin
    Williams, Emma J.
    Wood, Robin
    Wright, Lindsay
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2007, 17 (22) : 6326 - 6329
  • [2] Novel heterocyclic-substituted benzofuran histamine H3 receptor antagonists:: In vitro properties, drug-likeness, and behavioral activity
    Cowart, Marion
    Gfesser, Gregory A.
    Browman, Kaitlin E.
    Faghih, Ramin
    Miller, Thomas R.
    Milicic, Ivan
    Baranowski, John L.
    Krueger, Kathleen M.
    Witte, David G.
    Molesky, Angela L.
    Komater, Victoria A.
    Buckley, Michael J.
    Diaz, Gilbert J.
    Gagne, Gerard D.
    Zhou, Deliang
    Deng, Xiaoqing
    Pan, Liping
    Roberts, Ellen M.
    Diehl, Marilyn S.
    Wetter, Jill M.
    Marsh, Kennan C.
    Fox, Gerard B.
    Brioni, Jorge D.
    Esbenshade, Timothy A.
    Hancock, Arthur A.
    [J]. BIOCHEMICAL PHARMACOLOGY, 2007, 73 (08) : 1243 - 1255
  • [3] BIOTRANSFORMATION OF MIANSERIN IN LABORATORY-ANIMALS AND MAN
    DELBRESSINE, LPC
    MOONEN, MEG
    KASPERSEN, FM
    JACOBS, PL
    WAGENAARS, GL
    [J]. XENOBIOTICA, 1992, 22 (02) : 227 - 236
  • [4] Fischer H, 2000, CHIMIA, V54, P640
  • [5] FISCHER H, 2001, P 13 EUR S QUANT STR
  • [6] Analysis of two matrix metalloproteinase inhibitors and their metabolites for induction of phospholipidosis in rat and human hepatocytes
    Gum, RJ
    Hickman, D
    Fagerland, JA
    Heindel, MA
    Gagne, GD
    Schmidt, JM
    Michaelides, MR
    Davidsen, SK
    Ulrich, RG
    [J]. BIOCHEMICAL PHARMACOLOGY, 2001, 62 (12) : 1661 - 1673
  • [7] Weka Machine Learning for Predicting the Phospholipidosis Inducing Potential
    Ivanciuc, Ovidiu
    [J]. CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2008, 8 (18) : 1691 - 1709
  • [8] JACOBSON MM, 1972, J PHARMACOL EXP THER, V182, P312
  • [9] Medicinal chemistry of hERG optimizations: Highlights and hang-ups
    Jamieson, Craig
    Moir, Elizabeth M.
    Rankovic, Zoran
    Wishart, Grant
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (17) : 5029 - 5046
  • [10] Development of a phospholipidosis database and predictive quantitative structure-activity relationship (QSAR) models
    Kruhlak, Naomi L.
    Choi, Sydney S.
    Contrera, Joseph F.
    Weaver, James L.
    Willard, James M.
    Hastings, Kenneth L.
    Sancilio, Lawrence F.
    [J]. TOXICOLOGY MECHANISMS AND METHODS, 2008, 18 (2-3) : 217 - 227