نتایج جستجو برای: p38 map kinase inhibitors

تعداد نتایج: 577103  

Journal: :Current opinion in investigational drugs 2006
Changhai Ding

Vertex Pharmaceuticals Inc, in collaboration with Kissei Pharmaceutical Co Ltd, is developing VX-702, one of a series of second-generation, orally active p38 MAP kinase inhibitors, for the potential treatment of inflammation, rheumatoid arthritis and cardiovascular diseases. In June 2005, a phase II clinical trial of VX-702 was initiated in rheumatoid arthritis. In July 2006, Vertex was plannin...

Journal: :Circulation 2011
Mustafa Zakkar Le Anh Luong Hera Chaudhury Oeyvind Ruud Prakash P Punjabi Jon R Anderson John W Mullholand Anne T Clements Rob Krams Nicholas Foin Thanos Athanasiou Edward L S Leen Justin C Mason Dorian O Haskard Paul C Evans

BACKGROUND Vein grafting in coronary artery surgery is complicated by a high restenosis rate resulting from the development of vascular inflammation, intimal hyperplasia, and accelerated atherosclerosis. In contrast, arterial grafts are relatively resistant to these processes. Vascular inflammation is regulated by signaling intermediaries, including p38 mitogen-activated protein (MAP) kinase, t...

2016
Martin A. Bewley Kylie B. R. Belchamber Kirandeep K. Chana Richard C. Budd Gavin Donaldson Jadwiga A. Wedzicha Christopher E. Brightling Iain Kilty Louise E. Donnelly Peter J. Barnes Dave Singh Moira K. B. Whyte David H. Dockrell

Pulmonary inflammation and bacterial colonization are central to the pathogenesis of chronic obstructive pulmonary disease (COPD). Defects in macrophage phagocytosis of both bacteria and apoptotic cells contribute to the COPD phenotype. Small molecule inhibitors with anti-inflammatory activity against p38 mitogen activated protein kinases (MAPKs), phosphatidyl-inositol-3 kinase (PI3K) and Rho k...

Journal: :international journal of molecular and cellular medicine 0
saurabh kumar jha molecular neuroscience and functional genomics laboratory, department of biotechnology, delhi technological university (formerly dce), delhi, india. niraj kumar jha molecular neuroscience and functional genomics laboratory, department of biotechnology, delhi technological university (formerly dce), delhi, india. rohan kar molecular neuroscience and functional genomics laboratory, department of biotechnology, delhi technological university (formerly dce), delhi, india. rashmi kumar ambasta molecular neuroscience and functional genomics laboratory, department of biotechnology, delhi technological university (formerly dce), delhi, india. pravir kumar molecular neuroscience and functional genomics laboratory, department of biotechnology, delhi technological university (formerly dce), delhi, india.سازمان های دیگر: department of neurology, tufts university school of medicine, boston, ma (usa).

parkinson's disease (pd) is a chronic neurodegenerative condition which has the second largest incidence rate among all other neurodegenerative disorders barring alzheimer's disease (ad). currently there is no cure and researchers continue to probe the therapeutic prospect in cell cultures and animal models of pd. out of several factors contributing to pd prognosis, the role of p38 mapks (mitog...

Journal: :The Journal of pharmacology and experimental therapeutics 2010
Tuija Turpeinen Riina Nieminen Eeva Moilanen Riku Korhonen

Mitogen-activated protein kinase phosphatase (MKP)-1 is a protein phosphatase that regulates the activity of p38 mitogen-activated protein (MAP) kinase and c-Jun NH2-terminal kinase (JNK) and, to lesser extent, p42/44 extracellular signal-regulated kinase. Studies with MKP-1(-/-) mice show that MKP-1 is a regulating factor suppressing excessive cytokine production and inflammatory response. The...

Journal: :The EMBO journal 1997
R Janknecht T Hunter

The serum response element (SRE), which is pivotal for transcriptional up-regulation of the c-fos protooncogene, is constitutively occupied by a protein complex comprising the serum response factor and a ternary complex factor (TCF). Phosphorylation of the TCFs Elk-1 and Sap-1a by the ERK and JNK subclasses of MAP kinases triggers c-fos transcription. We demonstrate here that Elk-1 is barely ac...

Journal: :Biological & pharmaceutical bulletin 2011
Kenji Sakamoto Tsutomu Nakahara Kunio Ishii

It has been shown that p38 mitogen-activated protein (MAP) kinase is absolutely necessary for the cardioprotection of early ischemic preconditioning in the heart. Reorganization of actin cytoskeleton after translocation of HSP27, which is mediated by p38 MAP kinase, was reported to be necessary for the cardioprotective effect of early ischemic preconditioning. Although Rho and Rho kinase are re...

Journal: :American journal of physiology. Heart and circulatory physiology 2007
Guo-Xing Zhang Yukiko Nagai Toshitaka Nakagawa Hiroshi Miyanaka Yoshihide Fujisawa Akira Nishiyama Kunihiko Izuishi Koji Ohmori Shoji Kimura

Angiotensin II (ANG II) is a powerful activator of mitogen-activated protein (MAP) kinase cascades in cardiovascular tissues through a redox-sensitive mechanism. Nitric oxide (NO) is considered to antagonize the vasoconstrictive and proarteriosclerotic actions of ANG II. However, the role of endogenous NO in ANG II-induced redox-sensitive signal transduction is not yet clear. In this study usin...

Journal: :The Journal of pharmacology and experimental therapeutics 2006
Thomas R Hundley Basil Rigas

Nitric oxide-donating aspirin (NO-aspirin), representing a new concept in the development of more efficacious nonsteroidal anti-inflammatory drugs, consists of traditional aspirin bearing -ONO(2), which releases NO. Conventional aspirin prevents human colon cancer, but its toxicity precludes its application as a chemopreventive agent. NO-aspirin seems safer and in cultured cancer cells it is >1...

Journal: :Science 1998
M Camps A Nichols C Gillieron B Antonsson M Muda C Chabert U Boschert S Arkinstall

MAP kinase phosphatase-3 (MKP-3) dephosphorylates phosphotyrosine and phosphothreonine and inactivates selectively ERK family mitogen-activated protein (MAP) kinases. MKP-3 was activated by direct binding to purified ERK2. Activation was independent of protein kinase activity and required binding of ERK2 to the noncatalytic amino-terminus of MKP-3. Neither the gain-of-function Sevenmaker ERK2 m...

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