HDACiDB: a database for histone deacetylase inhibitors

被引:14
|
作者
Murugan, Kasi [1 ]
Sangeetha, Shanmugasamy [2 ]
Ranjitha, Shanmugasamy [2 ]
Vimala, Antony [2 ]
Al-Sohaibani, Saleh [1 ]
Rameshkumar, Gopal [2 ]
机构
[1] King Saud Univ, Coll Sci, Dept Bot & Microbiol, Riyadh 11451, Saudi Arabia
[2] Anna Univ, KBC Res Ctr, Bioinformat Lab, Madras 600044, Tamil Nadu, India
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2015年 / 9卷
关键词
cancer; drug likeness; histone deacetylase inhibitors; epigenetics; Lipinski's rule; molecular properties; DIFFERENTIATION; RESOURCE;
D O I
10.2147/DDDT.S78276
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
An histone deacetylase (HDAC) inhibitor database (HDACiDB) was constructed to enable rapid access to data relevant to the development of epigenetic modulators (HDAC inhibitors [HDACi]), helping bring precision cancer medicine a step closer. Thousands of HDACi targeting HDACs are in various stages of development and are being tested in clinical trials as monotherapy and in combination with other cancer agents. Despite the abundance of HDACi, information resources are limited. Tools for in silico experiments on specific HDACi prediction, for designing and analyzing the generated data, as well as custom-made specific tools and interactive databases, are needed. We have developed an HDACiDB that is a composite collection of HDACi and currently comprises 1,445 chemical compounds, including 419 natural and 1,026 synthetic ones having the potential to inhibit histone deacetylation. Most importantly, it will allow application of Lipinski's rule of five drug-likeness and other physicochemical property-based screening of the inhibitors. It also provides easy access to information on their source of origin, molecular properties, drug likeness, as well as bioavailability with relevant references cited. Being the first comprehensive database on HDACi that contains all known natural and synthetic HDACi, the HDACiDB may help to improve our knowledge concerning the mechanisms of actions of available HDACi and enable us to selectively target individual HDAC isoforms and establish a new paradigm for intelligent epigenetic cancer drug design. The database is freely available on the http://hdacidb.bioinfo.au-kbc.org.in/hdacidb/website.
引用
收藏
页码:2257 / 2264
页数:8
相关论文
共 50 条
  • [41] Histone Deacetylase Inhibitors in the Treatment of Lymphoma
    Lemoine, Manuela
    Younes, Anas
    DISCOVERY MEDICINE, 2010, 10 (54) : 462 - 470
  • [42] Patent status of histone deacetylase inhibitors
    Miller, TA
    EXPERT OPINION ON THERAPEUTIC PATENTS, 2004, 14 (06) : 791 - 804
  • [43] New patented histone deacetylase inhibitors
    Wang, Haishan
    Dymock, Brian W.
    EXPERT OPINION ON THERAPEUTIC PATENTS, 2009, 19 (12) : 1727 - 1757
  • [44] Histone Deacetylase Inhibitors in Cancer Therapy
    Sun, Yijie
    Sun, Yanyi
    Yue, Saichao
    Wang, Yaohe
    Lu, Fanghui
    CURRENT TOPICS IN MEDICINAL CHEMISTRY, 2018, 18 (28) : 2420 - 2428
  • [45] Histone deacetylase inhibitors and genomic instability
    Eot-Houllier, Gregory
    Fulcrand, Geraldine
    Magnaghi-Jaulin, Laura
    Jaulin, Christian
    CANCER LETTERS, 2009, 274 (02) : 169 - 176
  • [46] Histone Deacetylase Inhibitors in Myelodysplastic Syndrome
    Selene, Insija Ilyas
    Jose, Jemin Aby
    Sardar, Muhammad
    Shah, Zunairah
    Shafqat, Madeeha
    Faridi, Warda
    Malik, Mustafa Nadeem
    Yasir, Muhammad
    Khalil, Muhammad Jahanzeb
    Aslam, Shehroz
    Qureshi, Anum
    Rafiyath, Shamudeen
    Anwer, Faiz
    BLOOD, 2018, 132
  • [47] Histone deacetylase inhibitors in Hodgkin lymphoma
    Buglio, Daniela
    Younes, Anas
    INVESTIGATIONAL NEW DRUGS, 2010, 28 : S21 - S27
  • [48] Histone deacetylase inhibitors in cancer therapy
    Fouladi, Maryam
    CANCER INVESTIGATION, 2006, 24 (05) : 521 - 527
  • [49] Histone deacetylase inhibitors and HIV latency
    Margolis, David M.
    CURRENT OPINION IN HIV AND AIDS, 2011, 6 (01) : 25 - 29
  • [50] Anticancer activities of histone deacetylase inhibitors
    Jessica E. Bolden
    Melissa J. Peart
    Ricky W. Johnstone
    Nature Reviews Drug Discovery, 2006, 5 : 769 - 784