Anand Divakaran

Affiliations: 
University of California, Berkeley, Berkeley, CA, United States 
Area:
Chemical Biology, Epigenetics
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"Anand Divakaran"
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Parents

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David E Benson research assistant 2010-2013 Calvin College
Daniel A. Harki grad student 2015-2021 UMN
 (Co-advised)
William C. Pomerantz grad student 2015-2021 UMN
 (Co-advised)
Daniel K. Nomura post-doc 2021- UC Berkeley
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Publications

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Hong SH, Divakaran A, Osa A, et al. (2024) Exploiting the Cullin E3 Ligase Adaptor Protein SKP1 for Targeted Protein Degradation. Acs Chemical Biology
Divakaran A, Harki DA, Pomerantz WCK. (2023) Recent progress and structural analyses of domain-selective BET inhibitors. Medicinal Research Reviews
Divakaran A, Scholtz CR, Zahid H, et al. (2022) Development of an N-Terminal BRD4 Bromodomain-Targeted Degrader. Acs Medicinal Chemistry Letters. 13: 1621-1627
Cui H, Divakaran A, Hoell ZJ, et al. (2022) A Structure-based Design Approach for Generating High Affinity BRD4 D1-Selective Chemical Probes. Journal of Medicinal Chemistry
Cui H, Carlson AS, Schleiff MA, et al. (2021) 4-Methyl-1,2,3-Triazoles as -Acetyl-Lysine Mimics Afford Potent BET Bromodomain Inhibitors with Improved Selectivity. Journal of Medicinal Chemistry
Kalra P, McGraw L, Kimbrough JR, et al. (2020) Quantifying the Selectivity of Protein-Protein and Small Molecule Interactions with Fluorinated Tandem Bromodomain Reader Proteins. Acs Chemical Biology
Pomerantz WCK, Cui H, Divakaran A, et al. (2020) Selective N-terminal BRD4 bromodomain inhibitors by targeting non-conserved residues and structured water displacement. Angewandte Chemie (International Ed. in English)
Divakaran A, Kirberger SE, Pomerantz WCK. (2019) SAR by (Protein-Observed) F NMR. Accounts of Chemical Research
Carlson AS, Cui H, Divakaran A, et al. (2019) Systematically Mitigating the p38α Activity of Triazole-based BET Inhibitors. Acs Medicinal Chemistry Letters. 10: 1296-1301
Divakaran A, Talluri SK, Ayoub AM, et al. (2018) Molecular Basis for the N-Terminal Bromodomain and Extra Terminal (BET) Family Selectivity of a Dual Kinase-Bromodomain Inhibitor. Journal of Medicinal Chemistry
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