Development of a novel nitric oxide (NO) production inhibitor with potential therapeutic effect on chronic inflammation

• Published in: European journal of medicinal chemistry Vol. 193; p. 112216
• Main Authors: Yang, Youzhe, Wei, Zhe, Teichmann, Alexander Tobias, Wieland, Frank Heinrich, Wang, Amu, Lei, Xiangui, Zhu, Yue, Yin, Jinxiang, Fan, Tiantian, Zhou, Li, Wang, Chao, Chen, Lijuan
• Format: Journal Article
• Language: English
• Published: France Elsevier Masson SAS 01-05-2020
• Subjects: Inducible nitric oxide synthase (iNOS); Inflammation; Kava chalcones; Nitric oxide (NO); Structure-activity relationship (SAR); Inducible nitric oxide synthase (iNOS); NO; PGE2; UV; SAR; Inflammation; TLC; IL-1β; DPT cells; PVDF; LPS; RA; HRMS; Structure-activity relationship (SAR); TNF-α; Kava chalcones; iNOS; AIA; CIA; Nitric oxide (NO)
• ISSN: 0223-5234; 1768-3254
• DOI: 10.1016/j.ejmech.2020.112216

Inflammation is a complex biological response to stimuli. Activated macrophages induced excessively release of pro-inflammatory cytokines and mediators such as endogenous radical nitric oxide (NO) play a significant role in the progression of multiple inflammatory diseases. Both natural and synthetic chalcones possess a wide range of bioactivities. In this work, thirty-nine chalcones and three related compounds, including several novel ones, based on bioactive kava chalcones were designed, synthesized and their inhibitory effects on NO production in RAW 264.7 cells were evaluated. The novel compound (E)-1-(2′-hydroxy-4′,6′-dimethoxyphenyl)-3-(3-methoxy-4-(3-morpholinopropoxy)phenyl)prop-2-en-1-one (53) exhibited a better inhibitory activity (84.0%) on NO production at 10 μM (IC50 = 6.4 μM) with the lowest cytotoxicity (IC50 > 80 μM) among the tested compounds. Besides, western blot analysis indicated that compound 53 was a potent down-regulator of inducible nitric oxide synthase (iNOS) protein. Docking study revealed that compound 53 also can dock into the active site of iNOS. Furthermore, at the dose of 10 mg/kg/day, compound 53 could both significantly suppress the progression of inflammation on collagen-induced arthritis (CIA) and adjuvant-induced arthritis (AIA) models. In addition, the structure-activity relationship (SAR) of the kava chalcones based analogs was also depicted.
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•The novel compound 53 effectively inhibited the production of NO with much lower cytotoxicity than any other compound.•Compound 53 could down-regulate the expression of iNOS and dock into the active site of iNOS.•Compound 53 could suppress the progression of inflammation on two arthritis models.•Compound 53 has a potential therapeutic effect on chronic inflammation.