Results 21 to 30 of about 219,778 (281)

Magic power of phosphoinositide 3-kinase inhibitors

open access: yesMolecular and Cellular Therapies, 2017
Phosphoinositide 3-kinases (PI3K) play critical roles in the maintenance of cell biological functions and are suggested as a therapeutic target for drug discovery and development.
Xiangdong Wang
semanticscholar   +2 more sources

Effects of novel isoform-selective phosphoinositide 3-kinase inhibitors on natural killer cell function. [PDF]

open access: yesPLoS ONE, 2014
Phosphoinositide 3-kinases (PI3Ks) are promising targets for therapeutic development in cancer. The class I PI3K isoform p110α has received considerable attention in oncology because the gene encoding p110α (PIK3CA) is frequently mutated in human cancer.
Sung Su Yea   +6 more
doaj   +2 more sources

Antithrombotic phosphoinositide 3‐kinase β inhibitors in humans: a ‘shear’ delight! [PDF]

open access: yesJournal of Thrombosis and Haemostasis, 2012
Jackson SP, Schoenwaelder SM. Antithrombotic phosphoinositide 3-kinase β inhibitors in humans: a ‘shear’ delight!J Thromb Haemost 2012; 10: 2123–6.See also Nylander S, Kull B, Bjorkman JA, Ulvinge J-C, Oakes N, Emanuelsson BM, Andersson M, Skarby T, Inghardt T, Fjellstrom O, Gustafsson D.
Shaun P. Jackson, S. Schoenwaelder
semanticscholar   +3 more sources

Evidence for Apical Endocytosis in Polarized Hepatic Cells: Phosphoinositide 3-Kinase Inhibitors Lead to the Lysosomal Accumulation of Resident Apical Plasma Membrane Proteins

open access: yesJournal of Cell Biology, 1999
The architectural complexity of the hepatocyte canalicular surface has prevented examination of apical membrane dynamics with methods used for other epithelial cells.
A L Hubbard, Hubbard Ann L
exaly   +2 more sources

Identification of novel piperazinylquinoxaline derivatives as potent phosphoinositide 3-kinase (PI3K) inhibitors. [PDF]

open access: yesPLoS ONE, 2012
Development of small-molecule inhibitors targeting phosphoinositide 3-kinase (PI3K) has been an appealing strategy for the treatment of various types of cancers.Our approach was to perform structural modification and optimization based on previously ...
Peng Wu   +7 more
doaj   +4 more sources

Targeting Melanoma with Dual Phosphoinositide 3-Kinase/Mammalian Target of Rapamycin Inhibitors [PDF]

open access: yesMolecular Cancer Research, 2009
Phosphoinositide 3-kinase (PI3K)/protein kinase B/Akt and Ras/mitogen-activated protein kinase pathways are often constitutively activated in melanoma and have thus been considered as promising drug targets.
Romina Marone   +10 more
semanticscholar   +4 more sources

Serum and glucocorticoid-regulated kinase 1: Structure, biological functions, and its inhibitors

open access: yesFrontiers in Pharmacology, 2022
Serum and glucocorticoid-regulated kinase 1 (SGK1) is a serine/threonine kinase belonging to the protein kinase A, G, and C (AGC) family. Upon initiation of the phosphoinositide 3-kinase (PI3K) signaling pathway, mammalian target of rapamycin complex 2 ...
Hyunsoo Jang   +3 more
doaj   +1 more source

Resveratrol is a class IA phosphoinositide 3-kinase inhibitor [PDF]

open access: yesBiochemical Journal, 2007
Resveratrol, a polyphenol found in fruits, possesses chemopreventive and chemotherapeutic properties and has been shown to increase lifespan in yeast and metazoans, including mice. Genetic evidence and in vitro enzymatic measurements indicate that the deacetylase Sir2/SIRT1, an enzyme promoting stress resistance and aging, is the target of resveratrol.
Fröjdö, Sara   +3 more
openaire   +4 more sources

Leveraging molecular structure and bioactivity with chemical language models for de novo drug design

open access: yesNature Communications, 2023
Generative Deep Learning holds promise for mining the unexplored “chemical universe” for new drugs. Here, the authors demonstrate the de novo design of phosphoinositide 3-kinase gamma (PI3Kγ) inhibitors for the PI3K/Akt pathway in human tumor cells.
Michael Moret   +8 more
doaj   +1 more source

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