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Author Details
Full Name
Priyadarshini Jaishankar
Affiliation
Department of Pharmaceutical Chemistry, University of California san francisco
ORCID
Career Start Year
2005
Papers
29
H Index
15
Expertise
CM4AI Collaborator
Nevan J Krogan (CM4AI)
PMID
Paper Title
Journal Title
Published Year
37104712
Engaging a Non-catalytic Cysteine Residue Drives Potent and Selective Inhibition of Caspase-6.
J Am Chem Soc
2023
37676236
Structure-Based Optimization of Covalent, Small-Molecule Stabilizers of the 14-3-3Ͽ/ERα Protein-Protein Interaction from Nonselective Fragments.
J Am Chem Soc
2023
37455289
From Tethered to Freestanding Stabilizers of 14-3-3 Protein-Protein Interactions through Fragment Linking.
Angew Chem Int Ed Engl
2023
35364007
Inhibiting a dynamic viral protease by targeting a non-catalytic cysteine.
Cell Chem Biol
2022
32302100
Cyanopyrrolidine Inhibitors of Ubiquitin Specific Protease 7 Mediate Desulfhydration of the Active-Site Cysteine.
ACS Chem Biol
2020
30942078
Active-Site Druggability of Carbapenemases and Broad-Spectrum Inhibitor Discovery.
ACS Infect Dis
2019
31667472
Zebrafish studies identify serotonin receptors mediating antiepileptic activity in Dravet syndrome.
Brain Commun
2019
31353319
Activation of Caspase-6 Is Promoted by a Mutant Huntingtin Fragment and Blocked by an Allosteric Inhibitor Compound.
Cell Chem Biol
2019
31483651
Heteroaryl Phosphonates as Noncovalent Inhibitors of Both Serine- and Metallocarbapenemases.
J Med Chem
2019
29599213
Structure of the nucleotide exchange factor eIF2B reveals mechanism of memory-enhancing molecule.
Science
2018
29844038
Antibacterial Spectrum of a Tetrazole-Based Reversible Inhibitor of Serine β-Lactamases.
Antimicrob Agents Chemother
2018
30340023
Cilia-Associated Oxysterols Activate Smoothened.
Mol Cell
2018
28759216
Allosteric Inhibitors, Crystallography, and Comparative Analysis Reveal Network of Coordinated Movement across Human Herpesvirus Proteases.
J Am Chem Soc
2017
29045385
USP7 small-molecule inhibitors interfere with ubiquitin binding.
Nature
2017
26789650
Structure-Activity Studies of Bis-O-Arylglycolamides: Inhibitors of the Integrated Stress Response.
ChemMedChem
2016
27435960
Ceapins are a new class of unfolded protein response inhibitors, selectively targeting the ATF6α branch.
Elife
2016
25875391
Pharmacological dimerization and activation of the exchange factor eIF2B antagonizes the integrated stress response.
Elife
2015
26057252
Ligand-Induced Proton Transfer and Low-Barrier Hydrogen Bond Revealed by X-ray Crystallography.
J Am Chem Soc
2015
24259468
Tailoring small molecules for an allosteric site on procaspase-6.
ChemMedChem
2014
25489201
Congenital epulis in a newborn: a case report, immunoprofiling and review of literature.
Ethiop J Health Sci
2014
24977643
Broad-spectrum allosteric inhibition of herpesvirus proteases.
Biochemistry
2014
22296601
Structure-based design of potent and ligand-efficient inhibitors of CTX-M class A β-lactamase.
J Med Chem
2012
23227217
Mechanistic and structural understanding of uncompetitive inhibitors of caspase-6.
PLoS One
2012
19773167
Novel non-peptidic vinylsulfones targeting the S2 and S3 subsites of parasite cysteine proteases.
Bioorg Med Chem Lett
2009
18055204
Potency and selectivity of P2/P3-modified inhibitors of cysteine proteases from trypanosomes.
Bioorg Med Chem Lett
2008
17681758
A distal methyl substituent attenuates mitochondrial protein synthesis inhibition in oxazolidinone antibacterials.
Bioorg Med Chem Lett
2007
16387498
Conformational constraint in oxazolidinone antibacterials. Part 2: Synthesis and structure-activity studies of oxa-, aza-, and thiabicyclo[3.1.0]hexylphenyl oxazolidinones.
Bioorg Med Chem Lett
2006
15957907
Synthesis of aza-, oxa-, and thiabicyclo[3.1.0]hexane heterocycles from a common synthetic intermediate.
Org Lett
2005
16033280
Conformational constraint in oxazolidinone antibacterials. Synthesis and structure-activity studies of (azabicyclo[3.1.0]hexylphenyl)oxazolidinones.
J Med Chem
2005
1 - 29 of 29
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