LY 294002是磷脂酰肌醇3-激酶的选择性细胞渗透性强效和特异性抑制剂（IC 50 = 1.4 μ M;纯化PI 3-激酶）。在50 μ M的浓度下，它不显著抑制PKC PKA MAP激酶S6激酶EGFrK c-src激酶PI 4-激酶DAG激酶或兔肾ATP酶。诱导细胞凋亡。在用fMet-Leu-Phe刺激的完整中性粒细胞中，LY 294002在50 μ M时完全消除PI 3-激酶活性，而无细胞毒性。出版物Powered by Bioz See more details on Bioz 1. Coronas-Serna JM Fernánán-Acero T Molina M Cid VJ.人源化酵母为基础的工具包监测磷脂酰肌醇3-激酶活性在单细胞和群体水平。微生物细胞2018;5（12）：545-54.2。张P步行者MC威廉姆斯RS。癫痫发作诱导的PIP 3水平降低有助于抑制活性，并被丙戊酸挽救。Neurobiol Dis. 2014;62：296-306.3. Ferná necessar-Acero T Rodríguez-Escudero I Vicente F Monteiro MCn Tormo JR Cantizani J et al. A Yeast-Based In Vivo Bioassay to Screen for Class I Phosphatidylinositol 3-Kinase Specific Inhibitors.生物分子筛选杂志。2012;17（8）：1018-29.
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LY294002 is a selective cell permeable potent and specific inhibitor of phosphatidylinositol 3-kinase (IC50 = 1.4 μM; purified PI 3-kinase). It does not significantly inhibit PKC PKA MAP kinase S6 kinase EGFrK c-src kinase PI 4-kinase DAG kinase or rabbit kidney ATPase at concentrations of 50 μM. Induces apoptosis. In intact neutrophils stimulated with fMet-Leu-Phe LY294002 completely abolished PI 3-kinase activity at 50 μM without cell toxicity.Publications Powered by Bioz See more details on Bioz1. Coronas-Serna JM Fernández-Acero T Molina M Cid VJ. A humanized yeast-based toolkit for monitoring phosphatidylinositol 3-kinase activity at both single cell and population levels. Microbial Cell. 2018;5(12):545-54.2. Chang P Walker MC Williams RS. Seizure-induced reduction in PIP3 levels contributes to seizure-activity and is rescued by valproic acid. Neurobiol Dis. 2014;62:296-306.3. Fernández-Acero T RodrÃguez-Escudero I Vicente F Monteiro MCn Tormo JR Cantizani J et al. A Yeast-Based In Vivo Bioassay to Screen for Class I Phosphatidylinositol 3-Kinase Specific Inhibitors. Journal of Biomolecular Screening. 2012;17(8):1018-29.
