Literature DB >> 20639685

Identification of 4-[4-(4-fluoro-phenyl)-thiazol-2-ylamino]-2,6-dimethyl-phenol (KR-33749) as an inhibitor of 5-lipoxygenase with potent antiinflammatory activity.

Young Sik Cho1, Chi Hyun Kim, Ji Hee Surh, Nam Sook Kang, Sung-Eun Yoo, Hyae Gyeong Cheon.   

Abstract

BACKGROUND/AIM: To discover new 5-lipoxygenase (5-LO) inhibitors applicable to inflammation-related skin disease, we identified and examined antiinflammatory properties of a novel 5-LO inhibitor, KR-33749, in vitro and in vivo.
METHODS: 5-LO enzyme activity was assayed using insect cell lysates overexpressing rat 5-LO. The leukotriene B(4) (LTB(4)) level was assayed in rat basophilic leukemia (RBL-1) cell line. Mouse ear edema was induced by topical application of arachidonic acid. Atopic dermatitis-like skin lesion was induced by topical application of 1-chloro-2,4-dinitrobenzene (DNCB) to NC/Nga mice.
RESULTS: KR-33749 inhibited 5-LO activity with an IC(50) value of 70.5 +/- 6.0 nmol/l in parallel with LTB(4) inhibition in RBL-1 cells. The compound exhibited a >1,000-fold selectivity against 12-LO and 15-LO. KR-33749 showed in vivo protective effects against arachidonic acid-induced ear edema and DNCB-induced atopic dermatitis-like symptoms in NC/Nga mice.
CONCLUSION: Our results show that KR-33749, a new 5-LO inhibitor exhibits potent antiinflammatory activities in vitro as well as in vivo. Copyright 2010 S. Karger AG, Basel.

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Year:  2010        PMID: 20639685     DOI: 10.1159/000315488

Source DB:  PubMed          Journal:  Pharmacology        ISSN: 0031-7012            Impact factor:   2.547


  2 in total

1.  A (S)-(+)-decursin derivative, (S)-(+)-3-(3,4-dihydroxy-phenyl)-acrylic acid 2,2-dimethyl-8-oxo-3,4-dihydro-2H,8H-pyrano[3,2-g]-chromen-3-yl-ester, attenuates the development of atopic dermatitis-like lesions in NC/Nga mice.

Authors:  In Sik Kim; Dong-Hee Kim; Chi-Young Yun; Ji-Sook Lee
Journal:  Mol Biol Rep       Date:  2013-01-05       Impact factor: 2.316

2.  Inhibition of microsomal prostaglandin E synthase-1 by aminothiazoles decreases prostaglandin E2 synthesis in vitro and ameliorates experimental periodontitis in vivo.

Authors:  Anna Kats; Tove Båge; Pierre Georgsson; Jörgen Jönsson; Hernán Concha Quezada; Anders Gustafsson; Leif Jansson; Claes Lindberg; Karin Näsström; Tülay Yucel-Lindberg
Journal:  FASEB J       Date:  2013-02-27       Impact factor: 5.191

  2 in total

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