Abstract
Diversity-oriented construction of new indolizine scaffolds was accomplished by utilizing domino Knoevenagel condensation/intramolecular aldol cyclization. Biological evaluation revealed anticancer activity of these compounds through inhibition of β-catenin and activation of p53.
Original language | English |
---|---|
Pages (from-to) | 110-113 |
Number of pages | 4 |
Journal | Bioorganic and Medicinal Chemistry Letters |
Volume | 26 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2016 Jan 1 |
Bibliographical note
Funding Information:This work was supported by the National Research Foundation of Korea (NRF) Grant funded by the Korea government (MSIP) (2014R1A2A1A11050491) (to I.K.) and the Korea Research Institute of Chemical Technology project grant (SI1505) (to S.K.).
Publisher Copyright:
© 2015 Elsevier Ltd. All rights reserved.
All Science Journal Classification (ASJC) codes
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Pharmaceutical Science
- Drug Discovery
- Clinical Biochemistry
- Organic Chemistry