| Literature DB >> 12110321 |
Joong Sup Shim1, Dong Hoon Kim, Hye Jin Jung, Jin Hee Kim, Dongyeol Lim, Seok-Ki Lee, Kyu-Won Kim, Jong Woong Ahn, Jong-Shin Yoo, Jung-Rae Rho, Jongheon Shin, Ho Jeong Kwon.
Abstract
Curcumin and some of its derivatives were known as in vivo inhibitors of angiogenesis. In present study, a novel curcumin derivative, named hydrazinocurcumin (HC) was synthesized and examined for its biological activities. HC potently inhibited the proliferation of bovine aortic endothelial cells (BAECs) at a nanomolar concentration (IC(50)=520 nM) without cytotoxicity. In vivo and in vitro angiogenesis experiments showed HC as a new candidate for anti-angiogenic agent.Entities:
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Year: 2002 PMID: 12110321 DOI: 10.1016/s0968-0896(02)00129-3
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641