نتایج جستجو برای: metalated flavopiridol

تعداد نتایج: 668  

Journal: :Journal of the American Society of Nephrology : JASN 2001
P J Nelson I H Gelman P E Klotman

The glomerular lesions of HIV-associated nephropathy (HIVAN) are associated with the expression of HIV-1 in podocytes. Infected podocytes proliferate and lose several differentiation markers in vivo and in vitro, which suggests that HIV-1 gene expression induces these changes. Flavopiridol and roscovitine, newly identified inhibitors of cyclin-dependent kinase-9, markedly decrease HIV-1 promote...

Journal: :Sarcoma 2006
Don G. Morris Vivien H. C. Bramwell Robert Turcotte Alvaro T. Figueredo Martin E. Blackstein Shail Verma Sarah Matthews Elizabeth A. Eisenhauer

Purpose. Flavopiridol is a potent cyclin-dependent kinase (CDK) inhibitor that has preclinical activity in many tumours. This synthetic flavonoid was tested in a phase II nonrandomized, nonblinded multicentre clinical trial to determine its activity and toxicity in patients with previously untreated metastatic or locally advanced soft tissue sarcoma. Methods. A total of 18 patients with histolo...

Journal: :Physical chemistry chemical physics : PCCP 2015
Petru Apostol Juliana Eccher Marta Elisa Rosso Dotto Cassiano Batesttin Costa Thiago Cazati Elizabeth A Hillard Harald Bock Ivan H Bechtold

The optical and electrical properties of mesogenic metal-free and metalated phthalocyanines (PCs) with a moderately sized and regioregular alkyl periphery were investigated. In solution, the individualized molecules show fluorescence lifetimes of 4-6 ns in THF. When deposited as solid thin films the materials exhibit significantly shorter fluorescence lifetimes with bi-exponential decay (1.4-1....

2017
Lennart T Scharf Viktoria H Gessner

The development and design of new ligand systems with special donor properties has been essential for crucial advances made in main-group-element and transition-metal chemistry over the years. This Forum Article focuses on metalated ylides as novel ligand systems. These anionic congeners of bisylides possess likewise two lone pairs of electrons at the central carbon atom and can thus function a...

Journal: :Fitoterapia 2010
Patel Mohanakumara Nambiar Sreejayan Vaidayanathan Priti Bheemanahally Thimmappa Ramesha Gudasalamani Ravikanth Kotiganahalli Narayanagowda Ganeshaiah Ramesh Vasudeva John Mohan Thankayyan Retnabai Santhoshkumar Prabhu Dutt Mishra Viswakarma Ram Ramanan Uma Shaanker

Rohitukine, a chromane alkaloid, is a precursor of flavopiridol, a promising anti-cancer compound. Currently in Phase III clinical trials, flavopiridol is a potent inhibitor of several cyclin-dependent kinases (CDKs). Rohitukine was first reported from Amoora rohituka (0.083% dry weight) followed by that in Dysoxylum binectariferum (0.9% dry weight), both belonging to the family Meliaceae. Here...

Journal: :Cancer research 2002
Rita Nahta J Dirk Iglehart Bettina Kempkes Emmett V Schmidt

Cyclin D1 is downstream of erbB2 and is required for erbB2 transformation. Here we report thatcyclin D1 functions are essential, rate limiting for erbB2 transformation, and reciprocally increase erbB2 levels. This interaction depends on three cyclin D1 activities: cyclin-dependent kinase 4-dependent kinase activity, titration of p27, and an intrinsic transcriptional activity of cyclin D1. Drugs...

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