Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Kristian Birchall
Observed names:
Birchall, K,
Birchall, Kristian,
K. Birchall
Institution:
LifeArc
Observed institutions:
LifeArc,
GlaxoSmithKline (United Kingdom),
Stevenage Bioscience Catalyst,
Medical Research Council,
University of Sheffield
ORCID:
0000-0001-9992-2555
Observed ORCID:
0000-0001-9992-2555
OpenAlex ID:
A5059606387
A potent series targeting the malarial cGMP-dependent protein kinase clears infection and blocks transmission
2017
·
David A. Baker
, Lindsay B. Stewart
, et al.
·
Nature Communications
·
172
PDF
Fragment-based hit identification: thinking in 3D
2013
·
Andrew D. Morley
, Angelo Pugliese
, et al.
·
Drug Discovery Today
·
165
Antitubercular specific activity of ibuprofen and the other 2-arylpropanoic acids using the HT-SPOTi whole-cell phenotypic assay
2013
·
Juan D Guzman
, Dimitrios Evangelopoulos
, et al.
·
BMJ Open
·
95
PDF
Competitive Binding of a Benzimidazole to the Histone-Binding Pocket of the Pygo PHD Finger
2014
·
Thomas C. R. Miller
, Trevor J. Rutherford
, et al.
·
ACS Chemical Biology
·
67
Characterization of Three Druggable Hot-Spots in the Aurora-A/TPX2 Interaction Using Biochemical, Biophysical, and Fragment-Based Approaches
2017
·
Patrick J. McIntyre
, Patrick M. Collins
, et al.
·
ACS Chemical Biology
·
59
Substituted imidazopyridazines are potent and selective inhibitors of Plasmodium falciparum calcium-dependent protein kinase 1 (PfCDPK1)
2013
·
Timothy M. Chapman
, Simon A. Osborne
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
55
PDF
Optimization of an Imidazopyridazine Series of Inhibitors of Plasmodium falciparum Calcium-Dependent Protein Kinase 1 (PfCDPK1)
2014
·
Timothy M. Chapman
, Simon A. Osborne
, et al.
·
Journal of Medicinal Chemistry
·
53
PDF
Synthesis and structure–activity relationships of a novel series of pyrimidines as potent inhibitors of TBK1/IKKε kinases
2012
·
Edward G. McIver
, Justin Bryans
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
51
The serine proteinase hepsin is an activator of pro-matrix metalloproteinases: molecular mechanisms and implications for extracellular matrix turnover
2017
·
David J. Wilkinson
, Antoine Desilets
, et al.
·
Scientific Reports
·
47
PDF
The future of machine learning for small-molecule drug discovery will be driven by data
2024
·
Guy Durant
, Fergus Boyles
, et al.
·
Nature Computational Science
·
46
Design, Synthesis, and Testing of Potent, Selective Hepsin Inhibitors via Application of an Automated Closed-Loop Optimization Platform
2018
·
Shishir M. Pant
, Amanda Mukonoweshuro
, et al.
·
Journal of Medicinal Chemistry
·
45
Biochemical and Antiparasitic Properties of Inhibitors of the Plasmodium falciparum Calcium-Dependent Protein Kinase PfCDPK1
2014
·
Keith H. Ansell
, Hayley M. Jones
, et al.
·
Antimicrobial Agents and Chemotherapy
·
34
Incorporating Target-Specific Pharmacophoric Information into Deep Generative Models for Fragment Elaboration
2022
·
Thomas E. Hadfield
, Fergus Imrie
, et al.
·
Journal of Chemical Information and Modeling
·
33
PDF
Targeted protein degradation in CNS disorders: a promising route to novel therapeutics?
2024
·
Sandra Kuemper
, Andrew G. Cairns
, et al.
·
Frontiers in Molecular Neuroscience
·
32
PDF
Development of a differential scanning fluorimetry based high throughput screening assay for the discovery of affinity binders against an anthrax protein
2010
·
Fiona J. Sorrell
, Gemma K. Greenwood
, et al.
·
Journal of Pharmaceutical and Biomedical Analysis
·
31
Use of Reduced Graphs To Encode Bioisosterism for Similarity-Based Virtual Screening
2009
·
Kristian Birchall
, Valerie J. Gillet
, et al.
·
Journal of Chemical Information and Modeling
·
31
Robustly interrogating machine learning-based scoring functions: what are they learning?
2025
·
Guy Durant
, Fergus Boyles
, et al.
·
Bioinformatics
·
28
Training Similarity Measures for Specific Activities: Application to Reduced Graphs
2006
·
Kristian Birchall
, Valerie J. Gillet
, et al.
·
Journal of Chemical Information and Modeling
·
28
Evolving Interpretable Structure−Activity Relationship Models. 2. Using Multiobjective Optimization To Derive Multiple Models
2008
·
Kristian Birchall
, Valerie J. Gillet
, et al.
·
Journal of Chemical Information and Modeling
·
27
Characterizing the binding and function of TARP γ8-selective AMPA receptor modulators
2020
·
Jan-Niklas Dohrke
, Jake F. Watson
, et al.
·
Journal of Biological Chemistry
·
26
Trisubstituted thiazoles as potent and selective inhibitors of Plasmodium falciparum protein kinase G (PfPKG)
2018
·
Denise J. Tsagris
, Kristian Birchall
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
25
Evolving Interpretable Structure−Activity Relationships. 1. Reduced Graph Queries
2008
·
Kristian Birchall
, Valerie J. Gillet
, et al.
·
Journal of Chemical Information and Modeling
·
22
Potent inhibitors of malarial P. Falciparum protein kinase G: Improving the cell activity of a series of imidazopyridines
2018
·
Jonathan M. Large
, Kristian Birchall
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
20
PDF
Reduced Graphs and Their Applications in Chemoinformatics
2010
·
Kristian Birchall
, Valerie J. Gillet
·
Methods in molecular biology
·
19
Discovery of potent and selective 5-azaindazole inhibitors of leucine-rich repeat kinase 2 (LRRK2) – Part 1
2018
·
Joanne Osborne
, Kristian Birchall
, et al.
·
Bioorganic & Medicinal Chemistry Letters
·
17
PDF
Show more works
View as search
Works count:
42
Citation count:
1,293
H-index:
22
I10-index:
29
Year
Topic
Type