Antitumor Efficacy of PKI-587, a Highly Potent Dual PI3K/mTOR Kinase Inhibitor-Reference-Cited by-同舟云学术

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Antitumor Efficacy of PKI-587, a Highly Potent Dual PI3K/mTOR Kinase Inhibitor

Published:2011-02-15 Issue:10 Volume:17 Page:3193-3203
ISSN:1078-0432
Container-title:Clinical Cancer Research
language:en
Short-container-title:Clin Cancer Res

Author:

Mallon Robert,Feldberg Larry R.,Lucas Judy,Chaudhary Inder,Dehnhardt Christoph,Santos Efren Delos,Chen Zecheng,dos Santos Osvaldo,Ayral-Kaloustian Semiramis,Venkatesan Aranapakam,Hollander Irwin

Publisher

American Association for Cancer Research (AACR)

Subject

Cancer Research,Oncology

Cited by 144 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Targeting PI3K family with small-molecule inhibitors in cancer therapy: current clinical status and future directions;Molecular Cancer;2024-08-10

2. Assessments of prostate cancer cell functions highlight differences between a pan‐PI3K/mTOR inhibitor, gedatolisib, and single‐node inhibitors of the PI3K/AKT/mTOR pathway;Molecular Oncology;2024-08-02

3. 1,3,5-triazine derivatives as potential anticancer agents against lung and breast cancer cell lines: Synthesis, biological evaluation, and structure-based drug design studies;Journal of Molecular Structure;2024-07

4. Gedatolisib shows superior potency and efficacy versus single-node PI3K/AKT/mTOR inhibitors in breast cancer models;npj Breast Cancer;2024-06-05

5. Method development and validation for the estimation of gedatolisib in mouse plasma by tandem mass spectrometry and its application to pharmacokinetics studies;Biomedical Chromatography;2024-04-10

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