نتایج جستجو برای: pyridinyl

تعداد نتایج: 490  

Journal: :Acta poloniae pharmaceutica 2008
Krzysztof Kamiński Jolanta Obniska

The synthesis and anticonvulsant properties of new 1-(2-pyridinyl)- succinimides [I-XXII] differently substituted at the position-3 of imide ring have been described. The profile of pharmacological activity of these compounds was examined by a maximal electroshock (MES) and pentylenetetrazole (scPTZ) tests, whereas their neurotoxicity was determined using a rotarod screen. The results obtained ...

2016
Wenbo Zhou Wenshu Tang Zhenliang Sun Yunqi Li Yanmin Dong Haixiang Pei Yangrui Peng Jinhua Wang Ting Shao Zhenran Jiang Zhengfang Yi Yihua Chen

Inhibition of angiogenesis is considered as one of the desirable pathways for the treatment of tumor growth and metastasis. Herein we demonstrated that a series of pyridinyl-thiazolyl carboxamide derivatives were designed, synthesized and examined against angiogenesis through a colony formation and migration assays of human umbilical vein endothelial cells (HUVECs) in vitro. A structure-activit...

Journal: :Dalton transactions 2011
Yung-Hung Chang Zu-Yin Liu Yi-Hung Liu Shei-Ming Peng Jwu-Ting Chen Shiuh-Tzung Liu

Palladium complexes containing 2,7-bis(mesitylimidazolylidenyl)naphthyridine (NHC-NP) have been synthesized and characterized. Reaction of [{Ag(3)(NHC-NP)(2)}(PF(6))(3)] with [Pd(PhCN)(2)Cl(2)] provided an unusual dipalladium complex bridged by two NHC-NP units, forming a 20-membered dinuclear metallacycle [{Pd(2)(NHC-NP)(2)Cl(2)}(PF(6))] (2) in high yield. Treatment of 2 with KI in acetone yie...

2017
Trudy McGarry Monika Biniecka Wei Gao Deborah Cluxton Mary Canavan Siobhan Wade Sarah Wade Lorna Gallagher Carl Orr Douglas J. Veale Ursula Fearon

During inflammation, immune cells activated by toll-like receptors (TLRs) have the ability to undergo a bioenergetic switch towards glycolysis in a manner similar to that observed in tumour cells. While TLRs have been implicated in the pathogenesis of rheumatoid arthritis (RA), their role in regulating cellular metabolism in synovial cells, however, is still unknown. In this study, we investiga...

Journal: :European journal of medicinal chemistry 2021

KRAS is the most commonly altered oncogene of RAS family, especially G12C mutant (KRASG12C), which has been a promising drug target for many cancers. On basis bicyclic pyridopyrimidinone framework first-in-class clinical KRASG12C inhibitor AMG510, scaffold hopping strategy was conducted including F–OH cyclization approach and pyridinyl N-atom working leading to new tetracyclic analogues. Compou...

Journal: :The Journal of organic chemistry 2003
P Acharya O Plashkevych C Morita S Yamada J Chattopadhyaya

Direct intramolecular cation-pi interaction between phenyl and pyridinium moieties in 1a(+) has been experimentally evidenced through pH-dependent (1)H NMR titration. The basicity of the pyridinyl group (pK(a) 2.9) in 1a can be measured both from the pH-dependent chemical shifts of the pyridinyl protons as well as from the protons of the neighboring phenyl and methyl groups as a result of elect...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید