Literature DB >> 19684251

E6201 [(3S,4R,5Z,8S,9S,11E)-14-(ethylamino)-8, 9,16-trihydroxy-3,4-dimethyl-3,4,9,19-tetrahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione], a novel kinase inhibitor of mitogen-activated protein kinase/extracellular signal-regulated kinase kinase (MEK)-1 and MEK kinase-1: in vitro characterization of its anti-inflammatory and antihyperproliferative activities.

Masaki Goto1, Jesse Chow, Kenzo Muramoto, Ken-ichi Chiba, Satoshi Yamamoto, Masanori Fujita, Hiroshi Obaishi, Kenji Tai, Yoshiharu Mizui, Isao Tanaka, Donna Young, Hua Yang, Yuan J Wang, Hiroshi Shirota, Fabian Gusovsky.   

Abstract

The goal of this study is to identify a novel inhibitor with anti-inflammatory and antiproliferative properties for the treatment of psoriasis. Compound f152A1 [(3S,5Z,8S,11E)-8,9,16-trihydroxy-14-methoxy-3-methyl-3,4,9,10-tetrahydro-1H-benzo[c][1]oxacyclotetradecine1,7(8H)-dione] was identified as the main active metabolite with strong inhibitory activity against tumor necrosis factor-alpha (TNFalpha) transcription in a fraction originated from the fermentation broth of the fungus Curvularia verruculosa. Although active in cell-based assays, f152A1 was unstable in plasma and liver microsome preparations, thus limiting its pharmaceutical utilization. To improve the metabolic properties of f152A1, a medicinal chemistry program was undertaken, resulting in the generation of over 400 analogs of f152A1. Eventually, E6201 [(3S,4R,5Z,8S,9S,11E)-14-(ethylamino)-8,9,16-trihydroxy-3,4-dimethyl-3,4,9,19-tetrahydro-1H-2-benzoxacyclotetradecine-1,7(8H)-dione] was identified as a promising analog in this series. In the present study, we characterized the in vitro activities of E6201 and discovered that the compound inhibits lipopolysaccharide-activated TNFalpha reporter activity in THP-1-33 cells with an IC(50) value of 50 nM and selectively inhibits mitogen-activated protein kinase/extracellular signal-regulated kinase kinase (MEK)-1 and MEK kinase-1 in cell-free biochemical assays. In addition, E6201 showed inhibitory activity in several other cell-based systems: 1) phosphorylation of c-jun N-terminal kinase and p38 MAPKs; 2) nuclear factor-kappaB and activated protein-1 activation in various cell types; 3) interleukin (IL)-2 production from human lymphocytes; 4) hyperproliferation of human keratinocytes; 5) IL-8 production from human keratinocytes; and 6) proinflammatory cytokine production from human peripheral blood mononuclear cells. Based on the data presented here, E6201 may be beneficial for treatment of inflammatory and hyperproliferative diseases such as psoriasis through its anti-inflammatory activities on immune cells and antihyperproliferative activities on keratinocytes.

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Year:  2009        PMID: 19684251     DOI: 10.1124/jpet.109.156554

Source DB:  PubMed          Journal:  J Pharmacol Exp Ther        ISSN: 0022-3565            Impact factor:   4.030


  14 in total

Review 1.  Developing irreversible inhibitors of the protein kinase cysteinome.

Authors:  Qingsong Liu; Yogesh Sabnis; Zheng Zhao; Tinghu Zhang; Sara J Buhrlage; Lyn H Jones; Nathanael S Gray
Journal:  Chem Biol       Date:  2013-02-21

2.  Kinase inhibition by deoxy analogues of the resorcylic lactone L-783277.

Authors:  Marc Liniger; Christian Neuhaus; Tatjana Hofmann; Luca Fransioli-Ignazio; Michel Jordi; Peter Drueckes; Jörg Trappe; Doriano Fabbro; Karl-Heinz Altmann
Journal:  ACS Med Chem Lett       Date:  2010-10-20       Impact factor: 4.345

3.  Brain Distribution of a Novel MEK Inhibitor E6201: Implications in the Treatment of Melanoma Brain Metastases.

Authors:  Gautham Gampa; Minjee Kim; Nicholas Cook-Rostie; Janice K Laramy; Jann N Sarkaria; Linda Paradiso; Louis DePalatis; William F Elmquist
Journal:  Drug Metab Dispos       Date:  2018-02-02       Impact factor: 3.922

Review 4.  Signaling pathways as therapeutic targets in biliary tract cancer.

Authors:  Jennifer Yang; Matthew R Farren; Daniel Ahn; Tanios Bekaii-Saab; Gregory B Lesinski
Journal:  Expert Opin Ther Targets       Date:  2017-03-17       Impact factor: 6.902

Review 5.  MEK1/2 Inhibitors: Molecular Activity and Resistance Mechanisms.

Authors:  Pui-Kei Wu; Jong-In Park
Journal:  Semin Oncol       Date:  2015-09-24       Impact factor: 4.929

6.  Allele-Specific Mechanisms of Activation of MEK1 Mutants Determine Their Properties.

Authors:  Yijun Gao; Matthew T Chang; Daniel McKay; Na Na; Bing Zhou; Rona Yaeger; Neilawattie M Torres; Keven Muniz; Matthias Drosten; Mariano Barbacid; Giordano Caponigro; Darrin Stuart; Henrik Moebitz; David B Solit; Omar Abdel-Wahab; Barry S Taylor; Zhan Yao; Neal Rosen
Journal:  Cancer Discov       Date:  2018-02-26       Impact factor: 39.397

7.  Allenamide as a bioisostere of acrylamide in the design and synthesis of targeted covalent inhibitors.

Authors:  Deheng Chen; Dexiang Guo; Ziqin Yan; Yujun Zhao
Journal:  Medchemcomm       Date:  2017-12-11       Impact factor: 3.597

8.  The Dual MEK/FLT3 Inhibitor E6201 Exerts Cytotoxic Activity against Acute Myeloid Leukemia Cells Harboring Resistance-Conferring FLT3 Mutations.

Authors:  Weiguo Zhang; Gautam Borthakur; Chen Gao; Ye Chen; Hong Mu; Vivian R Ruvolo; Kenichi Nomoto; Nanding Zhao; Marina Konopleva; Michael Andreeff
Journal:  Cancer Res       Date:  2016-01-28       Impact factor: 12.701

9.  Effects of (5Z)-7-oxozeaenol on MDA-MB-231 breast cancer cells.

Authors:  Ulyana Muñoz Acuña; Jennifer Wittwer; Sloan Ayers; Cedric J Pearce; Nicholas H Oberlies; Esperanza J Carcache DE Blanco
Journal:  Anticancer Res       Date:  2012-07       Impact factor: 2.435

10.  Sensitivity to the MEK inhibitor E6201 in melanoma cells is associated with mutant BRAF and wildtype PTEN status.

Authors:  Sara A Byron; David C Loch; Candice L Wellens; Andreas Wortmann; Jiayi Wu; John Wang; Kenichi Nomoto; Pamela M Pollock
Journal:  Mol Cancer       Date:  2012-10-05       Impact factor: 27.401

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