Molecular pharmacological profile of the nonredox-type 5-lipoxygenase inhibitor CJ-13,610.
Br J Pharmacol. 2004.
PMID: 15197110
Free PMC article.
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Molecular pharmacological profile of the nonredox-type 5-lipoxygenase inhibitor CJ-13,610.
Fischer L, Steinhilber D, Werz O.
Fischer L, et al.
Br J Pharmacol. 2004 Jul;142(5):861-8. doi: 10.1038/sj.bjp.0705860. Epub 2004 Jun 14.
Br J Pharmacol. 2004.
PMID: 15197110
Free PMC article.
In this study, we present the molecular pharmacological profile of the novel nonredox-type 5-LO inhibitor CJ-13,610 that was evaluated in various in vitro assays. ...In analogy to ZM230487 and L-739.010, two closely related …
In this study, we present the molecular pharmacological profile of the novel nonredox-type 5-LO inhibitor …
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Comparative protection against liver inflammation and fibrosis by a selective cyclooxygenase-2 inhibitor and a nonredox-type 5-lipoxygenase inhibitor.
Horrillo R, Planagumà A, González-Périz A, Ferré N, Titos E, Miquel R, López-Parra M, Masferrer JL, Arroyo V, Clària J.
Horrillo R, et al.
J Pharmacol Exp Ther. 2007 Dec;323(3):778-86. doi: 10.1124/jpet.107.128264. Epub 2007 Aug 31.
J Pharmacol Exp Ther. 2007.
PMID: 17766677
Additional pharmacological profiling of SC-236 and CJ-13,610 was performed in macrophages, the primary hepatic inflammatory cell type. In these cells, SC-236 inhibited prostaglandin (PG) E2 formation in a concentration-dependent manner, w …
Additional pharmacological profiling of SC-236 and CJ-13,610 was performed in macrophages, the primary he …
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