Xishan Wu
No. 190 Kaiyuan Avenue, Guangzhou Science Park
Guangzhou, 510530, China
Guangzhou, 510530, China
Last Updated: 09/26/2026
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Found 19 publications
Discovery of a Highly Potent and Efficient BRD9 Degrader with Strong In Vivo Antitumor Activity.
Journal: Journal of medicinal chemistry
Published: May 28, 2026
PROTAC technology: clinical applications, future challenges, and innovative strategies.
Journal: Bioorganic chemistry
Published: January 31, 2026
Key imidazolyl groups that induce phenylalanine flipping enhance the efficacy of oral BRD9 inhibitors for AML treatment.
Journal: Acta pharmaceutica Sinica. B
Published: January 16, 2025
Discovery of a Potent and Selective GSPT1 Molecular Glue Degrader for the Treatment of Castration-Resistant Prostate Cancer.
Journal: Journal of medicinal chemistry
Published: January 02, 2025
Discovery of the First BRD4 Second Bromodomain (BD2)-Selective Inhibitors.
Journal: Journal of medicinal chemistry
Published: November 27, 2024
Discovery of a Promising CBP/p300 Degrader XYD129 for the Treatment of Acute Myeloid Leukemia.
Journal: Journal of medicinal chemistry
Published: June 03, 2024
Discovery of Highly Potent and Efficient CBP/p300 Degraders with Strong In Vivo Antitumor Activity.
Journal: Journal of medicinal chemistry
Published: April 22, 2024
Optimization of the synthesis of BET BD2 selective inhibitor XY153.
Journal: Chemistry & biodiversity
Published: October 08, 2023
Discovery of a potent and selective CBP bromodomain inhibitor (Y08262) for treating acute myeloid leukemia.
Journal: Bioorganic chemistry
Published: September 24, 2023
Rational design, synthesis and biological evaluation of benzo[d]isoxazole derivatives as potent BET bivalent inhibitors for potential treatment of prostate cancer.
Journal: Bioorganic chemistry
Published: February 17, 2023
Structural insights revealed by the cocrystal structure of CCS1477 in complex with CBP bromodomain.
Journal: Biochemical and biophysical research communications
Published: June 28, 2022
Discovery of a Highly Selective and H435R-Sensitive Thyroid Hormone Receptor β Agonist.
Journal: Journal of medicinal chemistry
Published: May 04, 2022
Last Updated: 09/26/2026