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Belinda Abbott
Belinda Abbott
Email verificata su latrobe.edu.au
Titolo
Citata da
Citata da
Anno
PI 3-kinase p110β: a new target for antithrombotic therapy
SP Jackson, SM Schoenwaelder, I Goncalves, WS Nesbitt, CL Yap, ...
Nature medicine 11 (5), 507-514, 2005
7382005
Inhibition of phosphoinositide 3-kinase β
SP Jackson, AD Robertson, V Kenche, P Thompson, H Prabaharan, ...
US Patent 7,598,377, 2009
882009
Structural determinants defining the allosteric inhibition of an essential antibiotic target
TPS da Costa, S Desbois, C Dogovski, MA Gorman, NE Ketaren, ...
Structure 24 (8), 1282-1291, 2016
432016
PDE2 inhibition by the PI3 kinase inhibitor LY294002 and analogues
BM Abbott, PE Thompson
Bioorganic & medicinal chemistry letters 14 (11), 2847-2851, 2004
342004
A total synthesis of a highly N-methylated cyclodepsipeptide [2S,3S-Hmp]-aureobasidin L using solid-phase methods
R Maharani, RTC Brownlee, AB Hughes, BM Abbott
Tetrahedron 70 (14), 2351-2358, 2014
302014
The Fragment-Based Development of a Benzofuran Hit as a New Class of Escherichia coli DsbA Inhibitors
LF Duncan, G Wang, OV Ilyichova, MJ Scanlon, B Heras, BM Abbott
Molecules 24 (20), 3756, 2019
282019
A 4-cyano-3-methylisoquinoline inhibitor of Plasmodium falciparum growth targets the sodium efflux pump PfATP4
PR Gilson, R Kumarasingha, J Thompson, X Zhang, JS Penington, ...
Scientific Reports 9 (1), 10292, 2019
282019
Quaternary structure analyses of an essential oligomeric enzyme
TPS da Costa, JB Christensen, S Desbois, SE Gordon, R Gupta, ...
Methods in Enzymology 562, 205-223, 2015
282015
A novel small molecule inhibitor of human Drp1
AA Rosdah, BM Abbott, CG Langendorf, Y Deng, JQ Truong, ...
Scientific reports 12 (1), 21531, 2022
262022
Synthesis and biological evaluation of substituted 3-anilino-quinolin-2 (1H)-ones as PDK1 inhibitors
NJ O’Brien, M Brzozowski, DJD Wilson, LW Deady, BM Abbott
Bioorganic & Medicinal Chemistry 22 (14), 3781-3790, 2014
252014
Towards novel herbicide modes of action by inhibiting lysine biosynthesis in plants
TPS da Costa, CJ Hall, S Panjikar, JA Wyllie, RM Christoff, S Bayat, ...
Elife 10, e69444, 2021
242021
Recent progress towards an effective treatment of amyotrophic lateral sclerosis using the SOD1 mouse model in a preclinical setting
EC Browne, BM Abbott
European journal of medicinal chemistry 121, 918-925, 2016
232016
Synthetic studies of the phosphatidylinositol 3-kinase inhibitor LY294002 and related analogues
B Abbott, P Thompson
Australian journal of chemistry 56 (11), 1099-1106, 2003
232003
Molecular evolution of an oligomeric biocatalyst functioning in lysine biosynthesis
TP Soares da Costa, BM Abbott, AR Gendall, S Panjikar, MA Perugini
Biophysical Reviews 10, 153-162, 2018
222018
Synthesis of novel 1, 2, 5-oxadiazoles and evaluation of action against Acinetobacter baumannii
RM Christoff, GL Murray, XP Kostoulias, AY Peleg, BM Abbott
Bioorganic & Medicinal Chemistry 25 (24), 6267-6272, 2017
202017
Antimalarial activity of novel 4-cyano-3-methylisoquinoline inhibitors against Plasmodium falciparum: design, synthesis and biological evaluation
MJ Buskes, KL Harvey, BJ Richards, R Kalhor, RM Christoff, CK Gardhi, ...
Organic & biomolecular chemistry 14 (20), 4617-4639, 2016
182016
Synthesis and biological evaluation of 2-anilino-4-substituted-7H-pyrrolopyrimidines as PDK1 inhibitors
NJ O’Brien, M Brzozowski, MJ Buskes, LW Deady, BM Abbott
Bioorganic & medicinal chemistry 22 (15), 3879-3886, 2014
172014
Potent inhibitors of phosphatidylinositol 3 (PI3) kinase that have antiproliferative activity only when delivered as prodrug forms
NJ O'Brien, S Amran, J Medan, B Cleary, LW Deady, IG Jennings, ...
ChemMedChem 8 (6), 914-918, 2013
162013
Pursuing DHDPS: an enzyme of unrealised potential as a novel antibacterial target
RM Christoff, CK Gardhi, TPS da Costa, MA Perugini, BM Abbott
MedChemComm 10 (9), 1581-1588, 2019
152019
Inhibition of phosphoinositide 3-kinase beta
SP Jackson, AD Robertson, V Kenche, P Thompson, H Prabaharan, ...
PCT Int Appl. WO2004016607, 2004
132004
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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