Combined Ligand and Fragment‐based Drug Design of Selective Histone Deacetylase

Combined Ligand and Fragment‐based Drug Design of Selective Histone Deacetylase – 6 Inhibitors

Author:

Ruzic Dusan¹,Petkovic Milos²,Agbaba Danica¹,Ganesan A.³,Nikolic Katarina¹¹^ORCID

Affiliation:

1. Department of Pharmaceutical Chemistry, Faculty of PharmacyUniversity of Belgrade Vojvode Stepe 450 11000 Belgrade Serbia

2. Department of Organic Chemistry, Faculty of PharmacyUniversity of Belgrade Vojvode Stepe 450 11000 Belgrade Serbia

3. School of PharmacyUniversity of East Anglia Norwich Research Park NR4 7TJ Norwich United Kingdom

Funder

Ministry of Science and Technological Development of the Republic of Serbia

European COST

Publisher

Wiley

Subject

Organic Chemistry,Computer Science Applications,Drug Discovery,Molecular Medicine,Structural Biology

Link

Reference65 articles.

Cited by 18 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

5. QSAR ANALYSIS OF HDAC6 INHIBITORS;Lomonosov chemistry journal;2023-06-01