Manuela Sum
Breisacher Str. 66
Freiburg, BW 79106, Germany
Freiburg, BW 79106, Germany
Last Updated: 09/26/2026
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Found 9 publications
Development of High-Affinity CHD1 Chromodomain Inhibitors.
Journal: Journal of medicinal chemistry
Published: May 05, 2026
Structure-Guided Design of a KMT9 Inhibitor Prodrug with Cellular Activity.
Journal: Journal of medicinal chemistry
Published: June 17, 2025
Structure-Activity Studies of 1,2,4-Oxadiazoles for the Inhibition of the NAD+-Dependent Lysine Deacylase Sirtuin 2.
Journal: Journal of medicinal chemistry
Published: June 07, 2024
Lysine Methyltransferase 9 (KMT9) Is an Actionable Target in Muscle-Invasive Bladder Cancer.
Journal: Cancers
Published: February 13, 2024
Mitochondrial KMT9 methylates DLAT to control pyruvate dehydrogenase activity and prostate cancer growth.
Journal: Nature communications
Published: July 27, 2023
Structure-guided design of a selective inhibitor of the methyltransferase KMT9 with cellular activity.
Journal: Nature communications
Published: July 03, 2023
Development of a NanoBRET assay to validate inhibitors of Sirt2-mediated lysine deacetylation and defatty-acylation that block prostate cancer cell migration.
Journal: RSC chemical biology
Published: December 16, 2021
KMT9 monomethylates histone H4 lysine 12 and controls proliferation of prostate cancer cells.
Journal: Nature structural & molecular biology
Published: November 22, 2018
The histone code reader Spin1 controls skeletal muscle development.
Journal: Cell death & disease
Published: May 04, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026