New Potent and Selective Inhibitor of Pim-1/3 Protein Kinases Sensitizes Human Colon Carcinoma Cells to Doxorubicin (original) (raw)

Structure-Based Development of Anticancer Drugs

Mario Bianchet

Structure, 2001

View PDFchevron_right

Structure-Based Design and Synthesis of Lipophilic 2,4-Diamino-6-Substituted Quinazolines and Their Evaluation as Inhibitors of Dihydrofolate Reductases and Potential Antitumor Agents

Sherry Queener

Journal of Medicinal Chemistry, 1998

View PDFchevron_right

Structure based drug design of Pim-1 kinase followed by pharmacophore guided synthesis of quinolone-based inhibitors

Yusuf Al-hiari

Bioorganic & Medicinal Chemistry, 2017

View PDFchevron_right

Structural prediction of novel pyrazolo-pyrimidine derivatives against PIM-1 kinase: In-silico drug design studies

Vivek Asati

Journal of Molecular Structure, 2020

View PDFchevron_right

Structure-based design of thienobenzoxepin inhibitors of PI3-kinase

Vickie Tsui

Bioorganic & Medicinal Chemistry Letters, 2011

View PDFchevron_right

Discovery of novel anticancer candidates based on a combination strategy of synthesis, characterization, biological activity evaluation, consensus docking and molecular modeling

hend hekal

Journal of the Iranian Chemical Society

View PDFchevron_right

Identification of 4, 5-Dihydro-1 H-pyrazolo [4, 3-h] quinazoline Derivatives as a New Class of Orally and Selective Polo-Like Kinase 1 Inhibitors

Paolo Cappella

Journal of medicinal …, 2010

View PDFchevron_right

Structure-based drug design and AutoDock study of potential protein tyrosine kinase inhibitors

hamed ali

Bioinformation, 2011

View PDFchevron_right

Synthesis, biological evaluation, and in silico studies of new CDK2 inhibitors based on pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e] [1,2,4]triazolo[1,5-c]pyrimidine scaffold with apoptotic activity

Ibrahim F . Nassar

View PDFchevron_right

Antitumor Activity of Pyridocarbazole and Benzopyridoindole Derivatives that Inhibit Protein Kinase CK2

Freja Schmidt

2010

View PDFchevron_right

Interfacing chemical biology and drug discovery: report from the 50th International Conference on Medicinal Chemistry of the SCT (French Medicinal Chemistry Society), July 2-4, 2014, Rouen, France

Luc Van Hijfte

ACS chemical biology, 2014

View PDFchevron_right

Anti-Cancer Agents in Medicinal Chemistry

Chinweike Eze

Bentham sciences, 2022

View PDFchevron_right

Synthesis, molecular modeling and anti-cancer evaluation of a series of quinazoline derivatives

Ahmed Khodair

Carbohydrate Research, 2019

View PDFchevron_right

Synthesis, anticancer activity, toxicity evaluation and molecular docking studies of novel phenylaminopyrimidine-(thio)urea hybrids as potential kinase inhibitors

İlkay Küçükgüzel

View PDFchevron_right

Computational analysis of benzofuran-2-carboxlic acids as potent Pim-1 kinase inhibitors

Abdul Wadood

Pharmaceutical Biology, 2014

View PDFchevron_right

Bioorganic Chemistry 79 (2018) 46–59 -5.pdf

Rajeshwar Reddy

View PDFchevron_right

Discovery of pyrazolo[3,4-d]pyrimidine and pyrazolo[4,3-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives as novel CDK2 inhibitors: synthesis, biological and molecular modeling investigations†

Ibrahim F . Nassar

2022

View PDFchevron_right

QSAR and Anticancer Drug Design on Benzothienopyrimidinones as Promising Pim Kinase Inhibitors Utilizing Structural Descriptors

sarfaraz ahmed

International Journal of Quantitative Structure-Property Relationships, 2019

View PDFchevron_right

Molecular Modeling, Synthesis and Biological Evaluation of N-Phenyl-4-Hydroxy-6-Methyl-2-Quinolone-3-CarboxAmides as Anticancer Agents

Dima Sabbah

Molecules

View PDFchevron_right

Design, One Pot Synthesis and Molecular Docking Studies of Substituted-1H-Pyrido[2,1-b] Quinazolines as Apoptosis-Inducing Anticancer Agents

Raju Bathula

Asian Pacific Journal of Cancer Prevention, 2020

View PDFchevron_right

Structure−Activity Relationships of the p38α MAP Kinase Inhibitor 1-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-3-[4-(2-morpholin-4-yl-ethoxy)naph- thalen-1-yl]urea (BIRB 796)

Jeffrey Madwed

Journal of Medicinal Chemistry, 2003

View PDFchevron_right

Design, synthesis and structure–activity relationship study of novel pyrazole-based heterocycles as potential antitumor agents

Korany Ali

European Journal of Medicinal Chemistry, 2010

View PDFchevron_right

Tyrosine kinase inhibition effects of novel Pyrazolo[1,5-a]pyrimidines and Pyrido[2,3-d]pyrimidines ligand: Synthesis, biological screening and molecular modeling studies

Ghada Hassan

View PDFchevron_right

Exploring the novel heterocyclic derivatives as lead molecules for design and development of potent anticancer agents

Iqbal Azad

Journal of Molecular Graphics & Modelling, 2018

View PDFchevron_right

Structure-Based Drug Design and Synthesis of PI3Kα-Selective Inhibitor (PF-06843195)

Zhenxiong Wang

Journal of Medicinal Chemistry, 2020

View PDFchevron_right

Discovery of 8-Cyclopentyl-2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-7-oxo-7,8-dihydro-pyrido[2,3- d ]pyrimidine-6-carbonitrile ( 7x ) as a Potent Inhibitor of Cyclin-Dependent Kinase 4 (CDK4) and AMPK-Related Kinase 5 (ARK5)

Venkat Pallela

Journal of Medicinal Chemistry, 2014

View PDFchevron_right

Synthesis and biological evaluation of novel substituted pyrrolo[1,2-a]quinoxaline derivatives as inhibitors of the human protein kinase CK2

Adali Pecci

European Journal of Medicinal Chemistry, 2013

View PDFchevron_right

3D-QSAR and Docking Studies of a Series of β-Carboline Derivatives as Antitumor Agents of PLK1

Jahan B Ghasemi

Journal of Chemistry, 2014

View PDFchevron_right

Structure-based design of low-nanomolar PIM kinase inhibitors

Istvan Enyedy

Bioorganic & Medicinal Chemistry Letters, 2015

View PDFchevron_right

Non-ATP-Mimetic Organometallic Protein Kinase Inhibitor

Katja Kräling, Kathrin Wähler

ChemistryOpen, 2013

View PDFchevron_right

Discovery and Optimization of Macrocyclic Quinoxaline-pyrrolo-dihydropiperidinones as Potent Pim-1/2 Kinase Inhibitors

Ryan Wurz

ACS Medicinal Chemistry Letters, 2016

View PDFchevron_right

Synthesis, characterization, molecular docking and in vitro anticancer activity of 3-(4-methoxyphenyl)-5-substituted phenyl-2-pyrazoline-1- carbothioamide

Avik Maji

International Journal of Research in Pharmaceutical Sciences, 2021

View PDFchevron_right