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Author Details
Full Name
Eric Feyfant
Affiliation
Schrodinger Inc.
ORCID
Career Start Year
1997
Papers
22
H Index
14
Expertise
CM4AI Collaborator
Andrej Sali (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37439511
Discovery of Sulanemadlin (ALRN-6924), the First Cell-Permeating, Stabilized α-Helical Peptide in Clinical Development.
J Med Chem
2023
30380198
The Role of Bridging Water and Hydrogen Bonding as Key Determinants of Noncovalent Protein-Carbohydrate Recognition.
ChemMedChem
2018
27964946
Predicting the Effect of Amino Acid Single-Point Mutations on Protein Stability-Large-Scale Validation of MD-Based Relative Free Energy Calculations.
J Mol Biol
2017
29138295
Generation of specific inhibitors of SUMO-1- and SUMO-2/3-mediated protein-protein interactions using Affimer (Adhiron) technology.
Sci Signal
2017
27217590
Peripheral Administration of a Long-Acting Peptide Oxytocin Receptor Agonist Inhibits Fear-Induced Freezing.
J Pharmacol Exp Ther
2016
24443552
A general approach to site-specific antibody drug conjugates.
Proc Natl Acad Sci U S A
2014
23946421
Stapled α-helical peptide drug development: a potent dual inhibitor of MDM2 and MDMX for p53-dependent cancer therapy.
Proc Natl Acad Sci U S A
2013
24099460
Development of an informatics platform for therapeutic protein and peptide analytics.
J Chem Inf Model
2013
20981527
Fragment-based drug design.
Methods Mol Biol
2011
19948242
A structural informatics approach to mine kinase knowledge bases.
Drug Discov Today
2010
20629978
A protein relational database and protein family knowledge bases to facilitate structure-based design analyses.
Chem Biol Drug Des
2010
19329309
Synthesis and biological evaluation of ((4-keto)-phenoxy)methyl biphenyl-4-sulfonamides: a class of potent aggrecanase-1 inhibitors.
Bioorg Med Chem Lett
2009
18612831
CONFIRM: connecting fragments found in receptor molecules.
J Comput Aided Mol Des
2008
17766392
Modeling mutations in protein structures.
Protein Sci
2007
17531482
Design and synthesis of 3,3-piperidine hydroxamate analogs as selective TACE inhibitors.
Bioorg Med Chem Lett
2007
17554852
Lead optimization via high-throughput molecular docking.
Curr Opin Drug Discov Devel
2007
16723578
Functional, biophysical, and structural bases for antibacterial activity of tigecycline.
Antimicrob Agents Chemother
2006
11839154
Pharmacophore determination of a gp120 C terminal-derived anti-HIV peptide construct interfering with membrane fusion suggesting that processing of the gp120 C terminus is a prelude to fusion.
AIDS Res Hum Retroviruses
2002
10617625
Formation of enzymatically active, homotypic, and heterotypic tetramers of mouse mast cell tryptases. Dependence on a conserved Trp-rich domain on the surface.
J Biol Chem
2000
10521469
Identification of a new member of the tryptase family of mouse and human mast cell proteases which possesses a novel COOH-terminal hydrophobic extension.
J Biol Chem
1999
9395089
Influence of a NH2-terminal extension on the activity of KTX2, a K+ channel blocker purified from Androctonus australis scorpion venom.
FEBS Lett
1997
9360993
Mouse mast cell protease 9, a novel member of the chromosome 14 family of serine proteases that is selectively expressed in uterine mast cells.
J Biol Chem
1997
1 - 22 of 22
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G Morales
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William W Wong
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