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Jocelyn Staunton
Observed names:
J. Staunton,
Staunton, Jocelyn
Institution:
Frontier Medicines (United States)
Observed institutions:
Amgen (United States),
Intel (United States),
Frontier Medicines (United States),
eFFECTOR Therapeutics (United States),
University of California, Berkeley
OpenAlex ID:
A5051502319
Structure-based Design of Pyridone–Aminal eFT508 Targeting Dysregulated Translation by Selective Mitogen-activated Protein Kinase Interacting Kinases 1 and 2 (MNK1/2) Inhibition
2018
·
Siegfried H. Reich
, Paul A. Sprengeler
, et al.
·
Journal of Medicinal Chemistry
·
188
Design of Development Candidate eFT226, a First in Class Inhibitor of Eukaryotic Initiation Factor 4A RNA Helicase
2020
·
Justin T. Ernst
, Peggy A. Thompson
, et al.
·
Journal of Medicinal Chemistry
·
147
INT131: A Selective Modulator of PPARγ
2009
·
Alykhan Motani
, Zhulun Wang
, et al.
·
Journal of Molecular Biology
·
125
The Scaling of Carbon Dioxide Release and Respiratory Water Loss in Flying Fruit Flies (Drosophila Spp.)
2000
·
Fritz-Olaf Lehmann
, Michael H. Dickinson
, et al.
·
Journal of Experimental Biology
·
68
Targeting Oncogene mRNA Translation in B-Cell Malignancies with eFT226, a Potent and Selective Inhibitor of eIF4A
2020
·
Peggy A. Thompson
, Boreth Eam
, et al.
·
Molecular Cancer Therapeutics
·
50
Zotatifin, an eIF4A-Selective Inhibitor, Blocks Tumor Growth in Receptor Tyrosine Kinase Driven Tumors
2021
·
Adina Gerson-Gurwitz
, Nathan P. Young
, et al.
·
Frontiers in Oncology
·
48
Hit-to-Lead Optimization and Discovery of 5-((5-([1,1′-Biphenyl]-4-yl)-6-chloro-1 H -benzo[ d ]imidazol-2-yl)oxy)-2-methylbenzoic Acid (MK-3903): A Novel Class of Benzimidazole-Based Activators of AMP-Activated Protein Kinase
2017
·
Ping Lan
, F. Anthony Romero
, et al.
·
Journal of Medicinal Chemistry
·
28
eFT508, a Potent and Selective Mitogen-Activated Protein Kinase Interacting Kinase (MNK) 1 and 2 Inhibitor, Is Efficacious in Preclinical Models of Diffuse Large B-Cell Lymphoma (DLBCL)
2015
·
Kevin R. Webster
, Vikas K Goel
, et al.
·
Blood
·
27
Abstract B148: INK128 is a potent and selective TORC1/2 inhibitor with broad oral antitumor activity
2009
·
Katayoun Jessen
, Shunyou Wang
, et al.
·
Molecular Cancer Therapeutics
·
25
Abstract 1142: Discovery of FMC-376 a novel orally bioavailable inhibitor of activated KRASG12C
2023
·
Snahel Patel
, Barun Bhhatarai
, et al.
·
Cancer Research
·
21
Abstract A171: A potent and selective PI3K inhibitor, INK1117, targets human cancers harboring oncogenic PIK3CA mutations.
2011
·
Katti Jessen
, Linda Kessler
, et al.
·
Molecular Cancer Therapeutics
·
17
Abstract 3753: Potent anti-tumor activity of mTOR kinase inhibitor in combination with anti-angiogenic agents in preclinical models of renal cell cancer
2012
·
Shunyou Wang
, Lucy Lan
, et al.
·
Cancer Research
·
16
Preclinical Evaluation of eFT226, a Novel, Potent and Selective eIF4A Inhibitor with Anti-Tumor Activity in B-Cell Malignancies
2017
·
Peggy A. Thompson
, Boreth Eam
, et al.
·
Blood
·
13
Abstract 5948: FMC-376 a dual inhibitor of ON and OFF states of KRASG12C is broadly active in PDX models of resistance
2024
·
Yan Wang
, Richard M. Neve
, et al.
·
Cancer Research
·
7
Abstract 4501: INK1117: A potent and orally efficacious PI3Kα-selective inhibitor for the treatment of cancer
2011
·
Katayoun A. Jessen
, Linda Kessler
, et al.
·
Cancer Research
·
7
Abstract 596: eFT508, a potent and highly selective inhibitor of MNK1/2 regulates immune checkpoint and cytokine expression promoting anti-tumor immunity
2017
·
Kevin R. Webster
, Vikas K. Goel
, et al.
·
Cancer Research
·
5
Abstract 2698: eFT226, a potent and selective inhibitor of eIF4A, is efficacious in preclinical models of lymphoma
2019
·
Peggy A. Thompson
, Boreth Eam
, et al.
·
Cancer Research
·
4
Abstract B133: eFT226, a first in class inhibitor of eIF4A1, targets FGFR1/2 and HER2 driven cancers
2019
·
Peggy A Thompson
, Nathan P Young
, et al.
·
Molecular Cancer Therapeutics
·
3
Abstract LB-068: Tomivosertib (eFT508), a potent and highly selective inhibitor of MNK1 and MNK2, enhances CAR T cell activity through modulating T cell differentiation
2019
·
Vikas K. Goel
, Rajesh K. Sharma
, et al.
·
Cancer Research
·
3
Abstract 5546: eFT508, a potent and highly selective inhibitor of MNK1 and MNK2, regulates T-cell differentiation promoting an antitumor immune response
2018
·
Rajesh K. Sharma
, Vikas K. Goel
, et al.
·
Cancer Research
·
3
Abstract PR11: eFT508: An oral, potent and highly selective inhibitor of MNK1 and MNK2, promotes anti-tumor immunity as a monotherapy and in combination with immune checkpoint blockade
2017
·
Kevin R. Webster
, Vikas K. Goel
, et al.
·
Cancer Research
·
3
Abstract 4486: INK128, a novel TORC1/2 inhibitor with potent oral antitumor activity in preclinical models of renal cancer
2011
·
Shunyou Wang
, Katti Jessen
, et al.
·
Cancer Research
·
3
Abstract 1302: Targeting hormone receptor-dependent cancers with potent, selective and orally-available small molecule inhibitors of eIF4E
2019
·
Gary G. Chiang
, Gregory S. Parker
, et al.
·
Cancer Research
·
2
Abstract DDT02-05: eFT226: A selective and highly potent inhibitor of eukaryotic initiation factor 4A (eIF4A), a novel approach for the treatment of cancer
2018
·
Siegfried H. Reich
, Peggy A. Thompson
, et al.
·
Cancer Research
·
2
Abstract 5949: The clinical dual KRASG12C inhibitor FMC-376 has demonstrated potential as both a monotherapy and in combination for the treatment of patients with KRASG12C mutation positive NSCLC
2024
·
Yan Wang
, Allison Roberts
, et al.
·
Cancer Research
·
1
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Works count:
45
Citation count:
818
H-index:
13
I10-index:
13
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