4.7 Article

Structural and Stereochemical Studies of Laurokamurols A-C, Uncommon Bis-sesquiterpenoids from the Chinese Red Alga Laurencia okamurai Yamada

期刊

JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY
卷 65, 期 8, 页码 1550-1555

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jafc.6b05238

关键词

sesquiterpenoid; laurane; red alga; axial chirality; PTP1B

资金

  1. Natural Science Foundation of China [81520108028, 81273430, 41306130, 81302692, 41676073, 81603022]
  2. SCTSM Project [14431901100, 15431901000]
  3. Institutes for Drug Discovery and Development
  4. Chinese Academy of Sciences [CASIIVIM0120152039]
  5. SKLDR/SIMM Projects [SIMM 1501ZZ-03]
  6. Youth Innovation Promotion Association from the Chinese Academy of Sciences [2016258]
  7. Young Talent Supporting Project from the China Association for Science and Technology [2016QNRC001]
  8. Shanghai Pujiang Program [16PJ1410600]
  9. EU
  10. European Regional Development Fund [GINOP-2.3.2-15-2016-00008]

向作者/读者索取更多资源

Three novel heterodimeric laurane-type sesquiterpenoids, laurokamurols A-C (1-3), along with eight known related monomeric ones (4-11) were isolated from the East China Sea red alga Laurencia okamurai Yamada. The absolute configurations of the new bis-sesquitepenoids, especially their axial chirality, were determined by extensive spectroscopic analyses and TDDFT-ECD method. All of the new compounds showed promising PTP1B inhibitory activities with IC50 values comparable to the positive control, indicating them as potential food additives or pharmaceutical drug leads toward obesity or diabetes.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据