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Author Details
Full Name
Edward J Hennessy
Affiliation
Oncology R&D
ORCID
Career Start Year
2002
Papers
22
H Index
14
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37343272
Discovery and Optimization of the First ATP Competitive Type-III c-MET Inhibitor.
J Med Chem
2023
34478292
Optimization of an Imidazo[1,2-<i>a</i>]pyridine Series to Afford Highly Selective Type I1/2 Dual Mer/Axl Kinase Inhibitors with <i>In Vivo</i> Efficacy.
J Med Chem
2021
33683117
Generating Selective Leads for Mer Kinase Inhibitors-Example of a Comprehensive Lead-Generation Strategy.
J Med Chem
2021
33495510
Design and optimisation of dendrimer-conjugated Bcl-2/x<sub>L</sub> inhibitor, AZD0466, with improved therapeutic index for cancer therapy.
Commun Biol
2021
32988967
AZD4320, A Dual Inhibitor of Bcl-2 and Bcl-x<sub>L</sub>, Induces Tumor Regression in Hematologic Cancer Models without Dose-limiting Thrombocytopenia.
Clin Cancer Res
2020
31531204
Structural and Molecular Insight into Resistance Mechanisms of First Generation cMET Inhibitors.
ACS Med Chem Lett
2019
26988306
Selective inhibitors of Bcl-2 and Bcl-xL: Balancing antitumor activity with on-target toxicity.
Bioorg Med Chem Lett
2016
27994749
Optimization of Highly Kinase Selective Bis-anilino Pyrimidine PAK1 Inhibitors.
ACS Med Chem Lett
2016
27190603
Utilization of Structure-Based Design to Identify Novel, Irreversible Inhibitors of EGFR Harboring the T790M Mutation.
ACS Med Chem Lett
2016
25980951
Small molecule inhibitor of apoptosis proteins antagonists: a patent review.
Expert Opin Ther Pat
2015
26291341
Identification and Optimization of Benzimidazole Sulfonamides as Orally Bioavailable Sphingosine 1-Phosphate Receptor 1 Antagonists with in Vivo Activity.
J Med Chem
2015
25890801
Discovery of heterocyclic sulfonamides as sphingosine 1-phosphate receptor 1 (S1P1) antagonists.
Bioorg Med Chem Lett
2015
24631189
Structure-based design and synthesis of tricyclic IAP (Inhibitors of Apoptosis Proteins) inhibitors.
Bioorg Med Chem Lett
2014
25458601
Discovery of potent KIFC1 inhibitors using a method of integrated high-throughput synthesis and screening.
J Med Chem
2014
23398453
Discovery and optimization of a novel series of potent mutant B-Raf(V600E) selective kinase inhibitors.
J Med Chem
2013
24320998
Discovery of a novel class of dimeric Smac mimetics as potent IAP antagonists resulting in a clinical candidate for the treatment of cancer (AZD5582).
J Med Chem
2013
22264476
Discovery of aminopiperidine-based Smac mimetics as IAP antagonists.
Bioorg Med Chem Lett
2012
18480256
Direct and selective elimination of specific prions and amyloids by 4,5-dianilinophthalimide and analogs.
Proc Natl Acad Sci U S A
2008
16122261
Synthesis of 4,5-dianilinophthalimide and related analogues for potential treatment of Alzheimer's disease via palladium-catalyzed amination.
J Org Chem
2005
14518981
Synthesis of substituted oxindoles from alpha-chloroacetanilides via palladium-catalyzed C[bond]H functionalization.
J Am Chem Soc
2003
14510571
trans-Cyclopropyl beta-amino acid derivatives via asymmetric cyclopropanation using a (Salen)Ru(II) catalyst.
J Org Chem
2003
11796067
A general and mild copper-catalyzed arylation of diethyl malonate.
Org Lett
2002
1 - 22 of 22
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