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Gillian F. Watt
Observed names:
G F Watt,
G.F. Watt,
Gillian F Watt,
Gillian Watt
Institution:
Pharmaron (United Kingdom)
Observed institutions:
Children's Hospital of Philadelphia,
GlaxoSmithKline (United Kingdom),
Pharmaron (United Kingdom),
UCB Pharma (United Kingdom)
ORCID:
0000-0002-0855-4740
Observed ORCID:
0000-0002-0855-4740
OpenAlex ID:
A5004624072
Extended pharmacodynamic responses observed upon PROTAC-mediated degradation of RIPK2
2020
·
Alina Mares
, Afjal H. Miah
, et al.
·
Communications Biology
·
234
PDF
Discovery and Characterisation of Highly Cooperative FAK‐Degrading PROTACs
2021
·
Robert P. Law
, Joao Nunes
, et al.
·
Angewandte Chemie International Edition
·
122
Structural Insights into PROTAC-Mediated Degradation of Bcl-xL
2020
·
Chun-wa Chung
, Han Dai
, et al.
·
ACS Chemical Biology
·
87
Optimization of a Series of RIPK2 PROTACs
2021
·
Afjal H. Miah
, Ian E. D. Smith
, et al.
·
Journal of Medicinal Chemistry
·
76
Targeted protein degradation in vivo with Proteolysis Targeting Chimeras: Current status and future considerations
2019
·
Gillian F. Watt
, Paul Scott-Stevens
, et al.
·
Drug Discovery Today Technologies
·
73
Design, Synthesis, and Structure−Activity Relationships of Novel Non-Imidazole Histamine H3 Receptor Antagonists
2000
·
Ian D. Linney
, Ildiko M. Buck
, et al.
·
Journal of Medicinal Chemistry
·
65
Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia
2022
·
Yiman Liu
, Qinglan Li
, et al.
·
Cancer Discovery
·
61
PDF
Seletalisib: Characterization of a Novel, Potent, and Selective Inhibitor of PI3Kδ
2017
·
Rodger A. Allen
, Daniel C. Brookings
, et al.
·
Journal of Pharmacology and Experimental Therapeutics
·
45
Evidence for PI-3K-dependent migration of Th17-polarized cells in response to CCR2 and CCR6 agonists
2008
·
Adam Webb
, Andrew Johnson
, et al.
·
Journal of Leukocyte Biology
·
40
Optimization of 1,3,4-Benzotriazepine-Based CCK2 Antagonists to Obtain Potent, Orally Active Inhibitors of Gastrin-Mediated Gastric Acid Secretion
2007
·
Iain M. McDonald
, James W. Black
, et al.
·
Journal of Medicinal Chemistry
·
36
Analysis of the pharmacokinetic/pharmacodynamic relationship of a small molecule CXCR3 antagonist, NBI‐74330, using a murine CXCR3 internalization assay
2007
·
L A Jopling
, G F Watt
, et al.
·
British Journal of Pharmacology
·
20
PDF
Optimization of the in Vitro and in Vivo Properties of a Novel Series of 2,4,5-Trisubstituted Imidazoles as Potent Cholecystokinin-2 (CCK2) Antagonists
2005
·
Ildiko M. Buck
, James W. Black
, et al.
·
Journal of Medicinal Chemistry
·
19
Analysis of the variation in the action of L‐365,260 at CCKB/gastrin receptors in rat, guinea‐pig and mouse isolated gastric tissue assays
1996
·
S.P. Roberts
, E.A. Harper
, et al.
·
British Journal of Pharmacology
·
18
PDF
From histamine to imidazolylalkyl-sulfonamides: The design of a novel series of histamine H3-receptor antagonists
1999
·
Matthew J. Tozer
, Elaine A. Harper
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
Nonpeptide Cholecystokinin-2 Receptor Agonists
2001
·
S. Barret Kalindjian
, David J. Dunstone
, et al.
·
Journal of Medicinal Chemistry
·
16
Discovery and Characterisation of Highly Cooperative FAK‐Degrading PROTACs
2021
·
Robert P. Law
, Joao Nunes
, et al.
·
Angewandte Chemie
·
6
The Discovery of CDP323, a Potent Alpha4 Integrin Antagonist
2012
·
Stuart Bailey
, Roger Palframan
, et al.
·
Current Immunology Reviews
·
1
Discovery of Potent, Orally Bioavailable, and CNS-Penetrant 1,2,3-Triazolopyridinyl Piperazine-Based PARP1-Selective Inhibitors
2026
·
Tammy Ladduwahetty
, Benjamin F. Rahemtulla
, et al.
·
Journal of Medicinal Chemistry
Discovery of a Novel P2X2/3 Allosteric Antagonist as an Efficient Bitter Taste Blocker
2026
·
François Saint-Dizier
, Sebastien Campos
, et al.
·
Journal of Medicinal Chemistry
GB3226, a novel, orally active, first-in-class small molecule inhibitor of ENL-yeats and FLT3 kinase for the treatment of Relapsed/Refractory Acute Myeloid Leukemia
2025
·
Louis Renzetti
, Stacia Kargman
, et al.
·
Blood
Editor’s Note: Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia
2025
·
Yiman Liu
, Qinglan Li
, et al.
·
Cancer Discovery
PDF
Data from Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia
2023
·
Yiman Liu
, Qinglan Li
, et al.
Supplementary Data from Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia
2023
·
Yiman Liu
, Qinglan Li
, et al.
Supplementary Data from Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia
2023
·
Yiman Liu
, Qinglan Li
, et al.
Supplementary Data from Small-Molecule Inhibition of the Acyl-Lysine Reader ENL as a Strategy against Acute Myeloid Leukemia
2023
·
Yiman Liu
, Qinglan Li
, et al.
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Works count:
34
Citation count:
936
H-index:
15
I10-index:
15
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