Lara T. Ward
AstraZeneca, Darwin Building, Cambridge Science Park, 319 Milton Road
Cambridge, ENG CB40WG, United Kingdom
Cambridge, ENG CB40WG, United Kingdom
Last Updated: 09/26/2026
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Found 12 publications
Discovery of a novel aminopyrazine series as selective PI3Kα inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: April 21, 2017
Discovery of a series of 8-(1-phenylpyrrolidin-2-yl)-6-carboxamide-2-morpholino-4H-chromen-4-one as PI3Kβ/δ inhibitors for the treatment of PTEN-deficient tumours.
Journal: Bioorganic & medicinal chemistry letters
Published: February 13, 2017
Optimization of a Series of Bivalent Triazolopyridazine Based Bromodomain and Extraterminal Inhibitors: The Discovery of (3R)-4-[2-[4-[1-(3-Methoxy-[1,2,4]triazolo[4,3-b]pyridazin-6-yl)-4-piperidyl]phenoxy]ethyl]-1,3-dimethyl-piperazin-2-one (AZD5153).
Journal: Journal of medicinal chemistry
Published: August 17, 2016
Discovery of a series of 8-(2,3-dihydro-1,4-benzoxazin-4-ylmethyl)-2-morpholino-4-oxo-chromene-6-carboxamides as PI3Kβ/δ inhibitors for the treatment of PTEN-deficient tumours.
Journal: Bioorganic & medicinal chemistry letters
Published: February 24, 2016
MUFINS: multi-formalism interaction network simulator.
Journal: NPJ systems biology and applications
Published: October 05, 2015
Discovery of 1-(4-(5-(5-amino-6-(5-tert-butyl-1,3,4-oxadiazol-2-yl)pyrazin-2-yl)-1-ethyl-1,2,4-triazol-3-yl)piperidin-1-yl)-3-hydroxypropan-1-one (AZD8835): A potent and selective inhibitor of PI3Kα and PI3Kδ for the treatment of cancers.
Journal: Bioorganic & medicinal chemistry letters
Published: September 11, 2015
Intermittent High-Dose Scheduling of AZD8835, a Novel Selective Inhibitor of PI3Kα and PI3Kδ, Demonstrates Treatment Strategies for PIK3CA-Dependent Breast Cancers.
Journal: Molecular cancer therapeutics
Published: August 19, 2015
Design of selective PI3Kα inhibitors starting from a promiscuous pan kinase scaffold.
Journal: Bioorganic & medicinal chemistry letters
Published: March 04, 2015
Discovery of (R)-8-(1-(3,5-difluorophenylamino)ethyl)-N,N-dimethyl-2-morpholino-4-oxo-4H-chromene-6-carboxamide (AZD8186): a potent and selective inhibitor of PI3Kβ and PI3Kδ for the treatment of PTEN-deficient cancers.
Journal: Journal of medicinal chemistry
Published: December 17, 2014
Inhibition of PI3Kβ signaling with AZD8186 inhibits growth of PTEN-deficient breast and prostate tumors alone and in combination with docetaxel.
Journal: Molecular cancer therapeutics
Published: November 16, 2014
Discovery of 9-(1-anilinoethyl)-2-morpholino-4-oxo-pyrido[1,2-a]pyrimidine-7-carboxamides as PI3Kβ/δ inhibitors for the treatment of PTEN-deficient tumours.
Journal: Bioorganic & medicinal chemistry letters
Published: June 03, 2014
Showing 1-12 of 12
Last Updated: 09/26/2026