Alexis K. De Haven Brandon
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 33 publications
Correction: AT13148 Is a Novel, Oral Multi-AGC Kinase Inhibitor with Potent Pharmacodynamic and Antitumor Activity.
Journal: Clinical cancer research : an official journal of the American Association for Cancer Research
Published: March 19, 2025
Elucidating molecularly stratified single agent, and combination, therapeutic strategies targeting MCL1 for lethal prostate cancer.
Journal: Nature communications
Published: March 07, 2024
Discovery of an In Vivo Chemical Probe for BCL6 Inhibition by Optimization of Tricyclic Quinolinones.
Journal: Journal of medicinal chemistry
Published: April 07, 2023
Improved Binding Affinity and Pharmacokinetics Enable Sustained Degradation of BCL6 In Vivo.
Journal: Journal of medicinal chemistry
Published: June 02, 2022
Correction: Signalling involving MET and FAK supports cell division independent of the activity of the cell cycle-regulating CDK4/6 kinases.
Journal: Oncogene
Published: February 26, 2020
Identification of ovarian high-grade serous carcinoma cell lines that show estrogen-sensitive growth as xenografts in immunocompromised mice.
Journal: Scientific reports
Published: January 14, 2020
Orally bioavailable CDK9/2 inhibitor shows mechanism-based therapeutic potential in MYCN-driven neuroblastoma.
Journal: The Journal of clinical investigation
Published: October 08, 2019
Signalling involving MET and FAK supports cell division independent of the activity of the cell cycle-regulating CDK4/6 kinases.
Journal: Oncogene
Published: February 16, 2019
Introduction of a Methyl Group Curbs Metabolism of Pyrido[3,4- d]pyrimidine Monopolar Spindle 1 (MPS1) Inhibitors and Enables the Discovery of the Phase 1 Clinical Candidate N2-(2-Ethoxy-4-(4-methyl-4 H-1,2,4-triazol-3-yl)phenyl)-6-methyl- N8-neopentylpyrido[3,4- d]pyrimidine-2,8-diamine (BOS172722).
Journal: Journal of medicinal chemistry
Published: September 11, 2018
Last Updated: 09/26/2026