Identification of 2-mercaptohexanoic acids as dual inhibitors of 5-lipoxygenase and microsomal prostaglandin E2 synthase-1

被引:16
作者
Greiner, Christine [2 ]
Zettl, Heiko [3 ]
Koeberle, Andreas [2 ]
Pergola, Carlo [1 ]
Northoff, Hinnak [4 ]
Schubert-Zsilavecz, Manfred [3 ]
Werz, Oliver [1 ]
机构
[1] Univ Jena, Inst Pharm, Chair Pharmaceut Med Chem, D-07743 Jena, Germany
[2] Eberhard Karls Univ Tuebingen, Inst Pharmaceut, Dept Pharmaceut Analyt, D-72076 Tubingen, Germany
[3] Goethe Univ Frankfurt, Inst Pharmaceut Chem, ZAFES OSF, D-60438 Frankfurt, Germany
[4] Univ Med Ctr, Inst Clin & Expt Transfus Med, D-72076 Tubingen, Germany
关键词
5-Lipoxygenase; Leukotriene; Neutrophils; Inflammation; Prostaglandin; ANTIINFLAMMATORY DRUGS; PIRINIXIC ACID; IN-VIVO; THERAPEUTIC TARGET; POTENT INHIBITORS; MPGES-1; BIOSYNTHESIS; DERIVATIVES; MYRTUCOMMULONE; ENZYME;
D O I
10.1016/j.bmc.2011.04.034
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
5-Lipoxygenase (5-LO) and microsomal prostaglandin E-2 synthase (mPGES)-1 are key enzymes in the biosynthesis of leukotrienes and prostaglandin (PG)E-2, respectively, and are considered as valuable targets for the treatment of inflammatory diseases. Here, we present the identification of 2-mercaptohexanoic acid derivatives as dual inhibitors of 5-LO and mPGES-1. The lead compound 2(4-(3-biphenyloxypropoxy) phenylthio) hexanoic acid (21) inhibits human 5-LO and mPGES-1 in cell-free assays with an IC50 = 3.5 and 2.2 mu M, respectively, and suppresses 5-LO in intact cells with even a higher potency (IC50 = 0.9 mu M). Compound 21 (10 mu M) neither significantly inhibited the related 12- or 15-LOs nor cyclooxygenase-1 and -2 or cytosolic phospholipase A(2). Based on the selective and potent inhibition of 5-LO and mPGES-1, further assessment of these 2-mercaptohexanoic acids in preclinical models of inflammation are warranted. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3394 / 3401
页数:8
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