نتایج جستجو برای: gleevec

تعداد نتایج: 513  

2003
William J. Netzer Fei Dou Dongming Cai Darren Veach Stephanie Jean Yueming Li William G. Bornmann Bayard Clarkson Huaxi Xu Paul Greengard

Amyloid(A ) peptides, consisting mainly of 40 and 42 aa (A 40 and A 42, respectively), are metabolites of the amyloid precursor protein and are believed to be major pathological determinants of Alzheimer’s disease. The proteolytic cleavages that form the A N and C termini are catalyzed by -secretase and -secretase, respectively. Here we demonstrate that -secretase generation of A in an N2a cell...

Journal: :Journal of medicinal chemistry 2005
Zoltán Szakács Szabolcs Béni Zoltán Varga László Orfi György Kéri Béla Noszál

The site-specific basicities of imatinib (Gleevec, a new signal transduction inhibitor drug of chronic myeloid leukemia) and two of its fragment compounds were quantitated in terms of protonation macroconstants, microconstants, and group constants by NMR-pH and pH-potentiometric titrations. Sequential protonation of imatinib follows the N(34), N(11), N(31), N(13) order, in which N(11) and N(31)...

Journal: :Bio Systems 2014
F. S. Borges K. C. Iarosz Hai-Peng Ren Antonio M. Batista Murilo S. Baptista Ricardo L. Viana S. R. Lopes Celso Grebogi

In this work we investigate a mathematical model describing tumour growth under a treatment by chemotherapy that incorporates time-delay related to the conversion from resting to hunting cells. We study the model using values for the parameters according to experimental results and vary some parameters relevant to the treatment of cancer. We find that our model exhibits a dynamical behaviour as...

Journal: :Structure 2005
Sandra W Cowan-Jacob Gabriele Fendrich Paul W Manley Wolfgang Jahnke Doriano Fabbro Janis Liebetanz Thomas Meyer

The regulation of the activity of Abl and Src family tyrosine kinases is mediated by intramolecular interactions between the SH3, SH2, and kinase (SH1) domains. We have determined the crystal structure of an unphosphorylated form of c-Src in which the SH2 domain is not bound to the C-terminal tail. This results in an open structure where the kinase domain adopts an active conformation and the C...

Journal: :Journal of biochemistry and molecular biology 2005
Jungeun Park Sangmi Kim Jong K Oh Jin Y Kim Sung Soo Yoon Dongsoon Lee Youngsoo Kim

Resistance to imatinib mesylate (also known as Gleevec, Glivec, and STI571) often becomes a barrier to the treatment of chronic myelogenous leukemia (CML). In order to identify markers of the action of imatinib mesylate, we used a mass spectrometry approach to compare protein expression profiles in human leukemia cells (K562) and in imatinib mesylate-resistant human leukemia cells (K562-R) in t...

2016
John Q Le Puneet S Braich Vikram S Brar

We report a case of a 59-year-old man with a history of atypical chronic myelogenous leukemia who presented with a several-week history of decreased vision in both eyes. His clinical examination revealed bilateral foveal infiltration, which was also demonstrated on optical coherence tomography. After a failed induction with imatinib (Gleevec(®)), he was treated with omacetaxine (Synribo(®)) wit...

Journal: :Singapore medical journal 2008
T J K Thia H H Tan T H C Chuah W C Chow H F Lui

Imatinib mesylate (Gleevec) is widely-used in the treatment of chronic myeloid leukaemia (CML) and gastrointestinal stromal tumour. Up to four percent of patients treated with imatinib may develop hepatotoxicity, which usually resolves with discontinuation of the drug. We report a 45-year-old Chinese man with CML and chronic hepatitis B virus infection, on imatinib treatment, presenting with he...

2015
Ali Kadivar Behnam Kamalidehghan Hamid Akbari Javar Ehsan Taghizadeh Davoudi Nurul Dhania Zaharuddin Bahareh Sabeti Lip Yong Chung Mohamed Ibrahim Noordin Shian-Ying Sung

INTRODUCTION Imatinib mesylate is an antineoplastic agent which has high absorption in the upper part of the gastrointestinal tract (GIT). Conventional imatinib mesylate (Gleevec) tablets produce rapid and relatively high peak blood levels and requires frequent administration to keep the plasma drug level at an effective range. This might cause side effects, reduced effectiveness and poor thera...

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