Jiangpeng Liao
288 Fute Zhong Road
Waigaoqiao, 200131, China
Waigaoqiao, 200131, China
Last Updated: 09/26/2026
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Found 13 publications
GDC-9545 (Giredestrant): A Potent and Orally Bioavailable Selective Estrogen Receptor Antagonist and Degrader with an Exceptional Preclinical Profile for ER+ Breast Cancer.
Journal: Journal of medicinal chemistry
Published: July 12, 2021
Discovery of GNE-502 as an orally bioavailable and potent degrader for estrogen receptor positive breast cancer.
Journal: Bioorganic & medicinal chemistry letters
Published: May 04, 2021
Discovery of GNE-149 as a Full Antagonist and Efficient Degrader of Estrogen Receptor alpha for ER+ Breast Cancer.
Journal: ACS medicinal chemistry letters
Published: April 28, 2020
Discovery of a C-8 hydroxychromene as a potent degrader of estrogen receptor alpha with improved rat oral exposure over GDC-0927.
Journal: Bioorganic & medicinal chemistry letters
Published: March 20, 2019
Unexpected equivalent potency of a constrained chromene enantiomeric pair rationalized by co-crystal structures in complex with estrogen receptor alpha.
Journal: Bioorganic & medicinal chemistry letters
Published: December 13, 2018
A Unique Approach to Design Potent and Selective Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP) Inhibitors.
Journal: Journal of medicinal chemistry
Published: November 21, 2017
GNE-781, A Highly Advanced Potent and Selective Bromodomain Inhibitor of Cyclic Adenosine Monophosphate Response Element Binding Protein, Binding Protein (CBP).
Journal: Journal of medicinal chemistry
Published: September 12, 2017
Design and synthesis of a biaryl series as inhibitors for the bromodomains of CBP/P300.
Journal: Bioorganic & medicinal chemistry letters
Published: September 01, 2017
From a novel HTS hit to potent, selective, and orally bioavailable KDM5 inhibitors.
Journal: Bioorganic & medicinal chemistry letters
Published: March 24, 2017
Discovery of a Potent and Selective in Vivo Probe (GNE-272) for the Bromodomains of CBP/EP300.
Journal: Journal of medicinal chemistry
Published: September 30, 2016
Lead optimization of a pyrazolo[1,5-a]pyrimidin-7(4H)-one scaffold to identify potent, selective and orally bioavailable KDM5 inhibitors suitable for in vivo biological studies.
Journal: Bioorganic & medicinal chemistry letters
Published: May 31, 2016
Fragment-Based Discovery of a Selective and Cell-Active Benzodiazepinone CBP/EP300 Bromodomain Inhibitor (CPI-637).
Journal: ACS medicinal chemistry letters
Published: February 19, 2016
Last Updated: 09/26/2026