Inhibitory Properties of ATP-Competitive Coumestrol and Boldine Are Correlated to Different Modulations of CK2 Flexibility-Reference-Cited by-同舟云学术

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Inhibitory Properties of ATP-Competitive Coumestrol and Boldine Are Correlated to Different Modulations of CK2 Flexibility

Published:2019-03-06 Issue:4 Volume:82 Page:1014-1018
ISSN:0163-3864
Container-title:Journal of Natural Products
language:en
Short-container-title:J. Nat. Prod.

Author:

Battistutta Roberto¹^ORCID,Lolli Graziano²^ORCID

Affiliation:

1. Department of Chemical Sciences, University of Padua and Institute of Biomolecular Chemistry, National Research Council (CNR), 35131 Padua, Italy

2. Department of Cellular, Computational and Integrative Biology - CIBIO, University of Trento, Via Sommarive 9, 38123 Povo (TN), Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Complementary and alternative medicine,Drug Discovery,Pharmaceutical Science,Pharmacology,Molecular Medicine,Analytical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.jnatprod.8b00889

Reference36 articles.

1. The Interactome of Protein Kinase CK2

2. Structural Determinants of Protein Kinase CK2 Regulation by Autoinhibitory Polymerization

3. Active Form of the Protein Kinase CK2 α2β2 Holoenzyme Is a Strong Complex with Symmetric Architecture

4. Characterization of the oligomeric states of the CK2 α2β2 holoenzyme in solution

5. Protein kinase CK2 in hematologic malignancies: reliance on a pivotal cell survival regulator by oncogenic signaling pathways

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Anticancer Activity and Molecular Targets of Piper cernuum Substances in Oral Squamous Cell Carcinoma Models;Biomedicines;2023-07-06

2. Strategies of Targeting CK2 in Drug Discovery: Challenges, Opportunities, and Emerging Prospects;Journal of Medicinal Chemistry;2023-02-06

3. Boldine;A Centum of Valuable Plant Bioactives;2021

4. A novel class of selective CK2 inhibitors targeting its open hinge conformation;European Journal of Medicinal Chemistry;2020-06

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