Structurally novel C17-sesquiterpene lactones from Ainsliaea pertyoides-Reference-Cited by-同舟云学术

Structurally novel C17-sesquiterpene lactones from Ainsliaea pertyoides

Published:2015 Issue:111 Volume:5 Page:91640-91644
ISSN:2046-2069
Container-title:RSC Advances
language:en
Short-container-title:RSC Adv.

Author:

Shi Zhi-Ran¹²³⁴⁵,Shen Yun-Heng⁵⁶⁷⁸⁴,Zhang Xian-Yuan⁹¹⁰⁴,Fang Xin⁵⁶⁷⁸⁴,Zeng Ren-Tao⁵⁶⁷⁸⁴,Liu Qing-Xin¹²³⁴⁵,Zhuo Zhi-Guo⁵⁶⁷⁸⁴,Feng Feng¹²³⁴,Zhang Wei-Dong¹²³⁴⁵

Affiliation:

1. Department of Natural Medicinal Chemistry

2. China Pharmaceutical University

3. Nanjing 210009

4. P. R. China

5. Department of Phytochemistry

6. School of Pharmacy

7. Second Military Medical University

8. Shanghai 200433

9. Shanghai Institute of Pharmaceutical Industry

10. Shanghai 200040

Abstract

Pertyolides A (1) and B (2), two unprecedented C₁₇-eudesmanolides with extended side chains, and one rare C₁₇-guaianolide, pertyolide C (3), along with 15 known sesquiterpene lactones were isolated from the whole plant of Ainsliaea pertyoides.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/RA/C5RA16551B

Reference23 articles.

1. Guaianolides from Ainsliaea fragrans

2. Sesquiterpene lactones from Diaspananthus uniflorus (SCH. BIP.) KITAM.

3. Cytotoxic versus anti-inflammatory effects in HeLa, jurkat t and human peripheral blood cells caused by guaianolide-Type sesquiterpene lactones

4. Ainsliadimer A selectively inhibits IKKα/β by covalently binding a conserved cysteine

5. Probing the Anticancer Mechanism of (−)-Ainsliatrimer A through Diverted Total Synthesis and Bioorthogonal Ligation

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