From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: Synthesis and biological evaluation of valproic esters of 3′-C-methyladenosine-Reference-Cited by-同舟云学术

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From the covalent linkage of drugs to novel inhibitors of ribonucleotide reductase: Synthesis and biological evaluation of valproic esters of 3′-C-methyladenosine

Published:2014-11 Issue:22 Volume:24 Page:5304-5309
ISSN:0960-894X
Container-title:Bioorganic & Medicinal Chemistry Letters
language:en
Short-container-title:Bioorganic & Medicinal Chemistry Letters

Author:

Petrelli Riccardo,Meli Maria,Vita Patrizia,Torquati Ilaria,Ferro Arianna,Vodnala Munender,D’Alessandro Natale,Tolomeo Manlio,Del Bello Fabio,Kusumanchi Praveen,Franchetti Palmarisa,Grifantini Mario,Jayaram Hiremagalur N.,Hofer Anders,Cappellacci Loredana

Funder

University of Camerino

Italian MIUR

United States Veterans Affairs Merit Review Award

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry

Reference34 articles.

1. Histone deacetylase inhibitors: Potential in cancer therapy

2. New clinical developments in histone deacetylase inhibitors for epigenetic therapy of cancer

3. Histone Deacetylase Inhibitors in Cancer Therapy

4. Strategies in developing promising histone deacetylase inhibitors

5. Multi-Targeted Histone Deacetylase Inhibitors in Cancer Therapy

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1. Synergistic therapeutics: Co-targeting histone deacetylases and ribonucleotide reductase for enhanced cancer treatment;European Journal of Medicinal Chemistry;2024-04

2. Role of pH in Regulating Cancer Pyrimidine Synthesis;Journal of Xenobiotics;2022-07-06

3. Inhibitors of the Cancer Target Ribonucleotide Reductase, Past and Present;Biomolecules;2022-06-10

4. Recent Progress in Histone Deacetylase Inhibitors as Anticancer Agents;Current Medicinal Chemistry;2020-06-02

5. Development of C-Methyl Branched Purine Ribonucleoside Analogs: Chemistry, Biological Activity and Therapeutic Potential;Current Medicinal Chemistry;2016-10-13

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