| Literature DB >> 25296343 |
Hui Yang1, Ding-Quan Liu, Tong-Jun Liang, Jia Li, Ai-Hong Liu, Peng Yang, Kun Lin, Xiao-Qing Yu, Yue-Wei Guo, Shui-Chun Mao, Bin Wang.
Abstract
A novel minor bisindole alkaloid, racemosin C (1), characterized by a naturally unprecedented 8-hydroxy-2,4,6-cyclooctatrienone ring fused with two indole systems, was isolated from the green alga Caulerpa racemosa, together with one known related metabolite, caulersin (2). The structure of 1 was elucidated on the basis of extensive spectroscopic analysis, and by comparison with the data of related known compounds. A plausible biosynthetic pathway of 1 was proposed. Compounds 1 and 2 exhibited significant PTP1B inhibitory activity with IC50 values of 5.86 ± 0.57 and 7.14 ± 1.00 μM, respectively, compared with the positive control oleanolic acid (IC50 = 3.03 ± 0.20 μM). On the basis of the data obtained, the Caulerpa bisindole alkaloids may be considered as a new class of PTP1B inhibitors.Entities:
Keywords: Caulerpa racemosa; PTP1B inhibitory activity; bisindole alkaloid; green alga; racemosin C
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Year: 2014 PMID: 25296343 DOI: 10.1080/10286020.2014.965162
Source DB: PubMed Journal: J Asian Nat Prod Res ISSN: 1028-6020 Impact factor: 1.569