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Ana S. Leal
Researcher at Michigan State University
Publications - 31
Citations - 689
Ana S. Leal is an academic researcher from Michigan State University. The author has contributed to research in topics: Cancer & Bexarotene. The author has an hindex of 11, co-authored 25 publications receiving 527 citations. Previous affiliations of Ana S. Leal include University of Coimbra & Dartmouth College.
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Journal ArticleDOI
Ursane-type pentacyclic triterpenoids as useful platforms to discover anticancer drugs
TL;DR: This review highlights the potential of natural and semisynthetic ursane-type triterpenoids as candidates for the design of multi-target bioactive compounds, with focus on their anticancer effects.
Journal ArticleDOI
Oleanane-, ursane-, and quinone methide friedelane-type triterpenoid derivatives: Recent advances in cancer treatment
Jorge A. R. Salvador,Ana S. Leal,Ana S. C. Valdeira,Bruno M. F. Gonçalves,Daniela P.S. Alho,Sandra A.C. Figueiredo,Samuel Silvestre,Vanessa I.S. Mendes +7 more
TL;DR: A number of semisynthetic derivatives of oleanane-, ursane- and quinone methide friedelane-type PTs with anticancer activity have been synthetized aiming to improve their therapeutic activity and pharmacokinetic properties, and decrease their toxicity.
Journal ArticleDOI
Bromodomain inhibitors, JQ1 and I-BET 762, as potential therapies for pancreatic cancer
Ana S. Leal,Charlotte R. Williams,Darlene B. Royce,Patricia A. Pioli,Michael B. Sporn,Karen T. Liby,Karen T. Liby +6 more
TL;DR: These drugs suppressed the production of nitric oxide and a variety of inflammatory cytokines, including IL-6, CCL2, and GM-CSF, in both immune and pancreatic cancer cells in vitro.
Journal ArticleDOI
Synthesis of novel ursolic acid heterocyclic derivatives with improved abilities of antiproliferation and induction of p53, p21waf1 and NOXA in pancreatic cancer cells
TL;DR: A series of new heterocyclic derivatives of ursolic acid 1 were synthesized and evaluated for their antiproliferative activity against AsPC-1 pancreatic cancer cells and compound 32 is the most active compound with an IC(50) of 1.9 μM which is sevenfold more active than ursolics acid 1.
Book ChapterDOI
Highlights of Pentacyclic Triterpenoids in the Cancer Settings
Jorge A. R. Salvador,Ana S. Leal,Daniela P.S. Alho,Bruno M. F. Gonçalves,Ana S. C. Valdeira,Vanessa I.S. Mendes,Yongkui Jing +6 more
TL;DR: In this article, the authors presented the most relevant properties that contribute to the antitumor activity of the referred natural triterpenoids and their semisynthetic derivatives and their derivatives.