Guaianolide Sesquiterpene Lactones From Cichorium Intybus (Asteraceae) [1]

Author:

Deng Yonghong1,Scott Lincoln1,Swanson Devin1,Snyder John K.1,Sari Nil2,Dogan Hanzade2

Affiliation:

1. Department of Chemistry, Boston University, 590 Commonwealth Avenue, Boston, MA 02215, USA

2. Department of Medical Ethics and Medical History, Istanbul University, Cerrahpasa Tip Fakultesi, Deontoloji ve Tip Tarihi Anabilim Dali, Cerrahpasa, Istanbul, Turkey

Abstract

Ten guaianolides, including three previously unreported natural products, were isolated from the aerial parts of Cichorium intybus (Asteraceae), more commonly known as chicory. Two of the new compounds ( 8 and 9) were analogues of lactupicrin and 11/β,13-dihydrolactupicrin, respectively, with the C-15 oxidized to the aldehyde state. The third new natural product, which we have called mtybulide A (10), is an isomer of lactucin with the lactone closed to the C-8 oxygen rather than the C-6

Publisher

Walter de Gruyter GmbH

Subject

General Chemistry

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