Synthesis and biological evaluation of halogenated curcumin analogs as potential nuclear receptor selective agonists-Reference-Cited by-同舟云学术

Synthesis and biological evaluation of halogenated curcumin analogs as potential nuclear receptor selective agonists

Published:2013-02 Issue:3 Volume:21 Page:693-702
ISSN:0968-0896
Container-title:Bioorganic & Medicinal Chemistry
language:en
Short-container-title:Bioorganic & Medicinal Chemistry

Author:

Batie Shane,Lee Jamie H.,Jama Rabia A.,Browder Drew O.,Montano Luis A.,Huynh Chanh C.,Marcus Lisa M.,Tsosie Dorian G.,Mohammed Zeynab,Trang Vu,Marshall Pamela A.,Jurutka Peter W.,Wagner Carl E.

Publisher

Elsevier BV

Subject

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

Reference54 articles.

1. Biological activities of curcumin and its analogues (Congeners) made by man and Mother Nature

2. Anti-tumour and antioxidant activity of natural curcuminoids

3. Synthesis and biological evaluation of novel curcumin analogs as anti-cancer and anti-angiogenesis agents

4. Novel curcumin analogs targeting TNF-induced NF-κB activation and proliferation in human leukemic KBM-5 cells

5. Active site binding modes of curcumin in HIV-1 protease and integrase

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