نتایج جستجو برای: protein tyrosine phosphatase non

تعداد نتایج: 2476159  

Journal: :Journal of neuroscience research 2002
Jeffrey D Sorbel Diane M Brooks Diana I Lurie

The central nervous system response to injury includes astrocyte proliferation and hypertrophy as well as microglial activation and proliferation. However, not all glial cells enter the cell cycle following damage, and the mechanism that determines which glial cells will proliferate and which will remain quiescent has yet to be elucidated. Protein tyrosine phosphorylation has been shown to play...

2012
Ahmet Bakan Neysa Nevins Ami S. Lakdawala Ivet Bahar

Druggability assessment of a target protein has emerged in recent years as an important concept in hit-to-lead optimization. A reliable and physically relevant measure of druggability would allow informed decisions on the risk of investing in a particular target. Here, we define "druggability" as a quantitative estimate of binding sites and affinities for a potential drug acting on a specific p...

2017
Caroline Chandra Tjin Kate D. Otley Tyler D. Baguley Pradeep Kurup Jian Xu Angus C. Nairn Paul J. Lombroso Jonathan A. Ellman

Dysregulation of protein tyrosine phosphorylation has been implicated in a number of human diseases, including cancer, diabetes, and neurodegenerative diseases. As a result of their essential role in regulating protein tyrosine phosphorylation levels, protein tyrosine phosphatases (PTPs) have emerged as important yet challenging therapeutic targets. Here we report on the development and applica...

Journal: :The Journal of biological chemistry 2002
Tong R Wu Y Kate Hong Xu-Dong Wang Mike Y Ling Ana M Dragoi Alicia S Chung Andrew G Campbell Zhi-Yong Han Gen-Sheng Feng Y Eugene Chin

Signal transducer and activator of transcription (STAT) proteins are both tyrosine- and serine-phosphorylated, mediating signal transduction and gene regulation. Following gene regulation, STAT activity in the nucleus is then terminated by a nuclear protein phosphatase(s), which remains unidentified. Using novel antibody arrays to screen the Stat1-specific protein phosphatase(s), we identified ...

Journal: :Molecules 2013
Wen-Long Wang Dong-Lin Yang Li-Xin Gao Chun-Lan Tang Wei-Ping Ma Hui-Hua Ye Si-Qi Zhang Ya-Nan Zhao Hao-Jie Xu Zhao Hu Xia Chen Wen-Hua Fan Hai-Jun Chen Jing-Ya Li Fa-Jun Nan Jia Li Bainian Feng

A series of 1H-2,3-dihydroperimidine derivatives was designed, synthesized, and evaluated as a new class of inhibitors of protein tyrosine phosphatase 1B (PTP1B) with IC50 values in the micromolar range. Compounds 46 and 49 showed submicromolar inhibitory activity against PTP1B, and good selectivity (3.48-fold and 2.10-fold respectively) over T-cell protein tyrosine phosphatases (TCPTP). These ...

Journal: :Biochemistry and cell biology = Biochimie et biologie cellulaire 2002
Sanchita Hati Sudeep Bhattacharyya James V Price Alan S Tracey

The components and functions of the insulin receptor kinase signaling pathway have been conserved in a broad range of Metazoa ranging from mammals to insects and nematodes. There is a high degree of sequence homology and functional similarity between the human insulin receptor kinase (IRK) and the drosophila (Drosophila melanogaster) form (DIRK) of this enzyme. Similarly, a high degree of homol...

Journal: :The Journal of organic chemistry 2015
Kasi Viswanatharaju Ruddraraju Zachary D Parsons Elizabeth M Llufrio Natasha L Frost Kent S Gates

Protein tyrosine phosphatase 1B (PTP1B) is a validated therapeutic target for the treatment of type 2 diabetes; however, the enzyme has been classified by some as an "undruggable target". Here we describe studies directed toward the development of agents that covalently capture the sulfenyl amide "oxoform" of PTP1B generated during insulin signaling events. The sulfenyl amide residue found in o...

2015
Kasi Viswanatharaju Ruddraraju Roman Hillebrand Charles L. Barnes Kent S. Gates

The title compound, C24H32N4O8S, (I), crystallizes as a zwitterion. The terminal amine N atom of the [(2-{2-[2-(2-ammonio-eth-oxy)eth-oxy]eth-oxy}eth-yl)carbamo-yl] side chain is protonated, while the 1,2,5-thia-diazo-lidin-3-one 1,1-dioxide N atom is deprotonated. The side chain is turned over on itself with an intra-molecular N-H⋯O hydrogen bond. The 1,2,5-thia-diazo-lidin-3-one 1,1-dioxide r...

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