Antitumour potential of BPT: a dual inhibitor of cdk4 and tubulin polymerization
Published 2015 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Antitumour potential of BPT: a dual inhibitor of cdk4 and tubulin polymerization
Authors
Keywords
-
Journal
Cell Death & Disease
Volume 6, Issue 5, Pages e1743-e1743
Publisher
Springer Nature
Online
2015-05-07
DOI
10.1038/cddis.2015.96
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Mutant p53 stimulates chemoresistance of pancreatic adenocarcinoma cells to gemcitabine
- (2015) Claudia Fiorini et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
- Preclinical characterization of the CDK4/6 inhibitor LY2835219: in-vivo cell cycle-dependent/independent anti-tumor activities alone/in combination with gemcitabine
- (2014) Lawrence M. Gelbert et al. INVESTIGATIONAL NEW DRUGS
- Biphenyl-4-carboxylic Acid [2-(1H-Indol-3-yl)-ethyl]-methylamide (CA224), a Nonplanar Analogue of Fascaplysin, Inhibits Cdk4 and Tubulin Polymerization: Evaluation of in Vitro and in Vivo Anticancer Activity
- (2014) Sachin Mahale et al. JOURNAL OF MEDICINAL CHEMISTRY
- Cyclin-Dependent Kinase 4/6–Specific Activities as a Biomarker for Prognosis and Chemosensitivity in Endometrial Cancer
- (2014) Yujio Ikeda et al. OBSTETRICS AND GYNECOLOGY
- The Cell-Cycle Regulator CDK4: An Emerging Therapeutic Target in Melanoma
- (2013) K. E. Sheppard et al. CLINICAL CANCER RESEARCH
- Phase II Trial of the CDK4 Inhibitor PD0332991 in Patients With Advanced CDK4-Amplified Well-Differentiated or Dedifferentiated Liposarcoma
- (2013) Mark A. Dickson et al. JOURNAL OF CLINICAL ONCOLOGY
- Abstract 3054: P1446A-05: a new oral cyclin-dependent kinase inhibitor with potent preclinical antitumor activity
- (2012) Kalpana S. Joshi et al. CANCER RESEARCH
- FASCAPLYSIN as a Specific Inhibitor for CDK4: Insights from Molecular Modelling
- (2012) Muhammad Imtiaz Shafiq et al. PLoS One
- Fragment-Based Discovery of 7-Azabenzimidazoles as Potent, Highly Selective, and Orally Active CDK4/6 Inhibitors
- (2012) Young Shin Cho et al. ACS Medicinal Chemistry Letters
- Recent Research in Selective Cyclin-Dependent Kinase 4 Inhibitors for Anti-Cancer Treatment
- (2009) Ning Liu et al. CURRENT MEDICINAL CHEMISTRY
- Discovery of 4-(Benzylaminomethylene)isoquinoline-1,3-(2H,4H)-diones and 4-[(Pyridylmethyl)aminomethylene]isoquinoline-1,3-(2H,4H)-diones as Potent and Selective Inhibitors of the Cyclin-Dependent Kinase 4
- (2009) Hwei-Ru Tsou et al. JOURNAL OF MEDICINAL CHEMISTRY
- Crystal structure of human CDK4 in complex with a D-type cyclin
- (2009) P. J. Day et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Combined Ligand and Structure Based Approaches for Narrowing on the Essential Physicochemical Characteristics for CDK4 Inhibition
- (2008) Nahren Manuel Mascarenhas et al. Journal of Chemical Information and Modeling
- 4-(Phenylaminomethylene)isoquinoline-1,3(2H,4H)-diones as Potent and Selective Inhibitors of the Cyclin-Dependent Kinase 4 (CDK4)
- (2008) Hwei-Ru Tsou et al. JOURNAL OF MEDICINAL CHEMISTRY
Publish scientific posters with Peeref
Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.
Learn MoreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started