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Keywords = norditerpenoid analogues

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23 pages, 3391 KiB  
Article
Synthesis and Biological Evaluation of Diversified Hamigeran B Analogs as Neuroinflammatory Inhibitors and Neurite Outgrowth Stimulators
by Ruo-Xin Li, Rui Han, Guo-Jie Wu, Fu-She Han and Jin-Ming Gao
Mar. Drugs 2020, 18(6), 306; https://doi.org/10.3390/md18060306 - 11 Jun 2020
Cited by 2 | Viewed by 3908
Abstract
We describe the efficient synthesis of a series of new simplified hamigeran B and 1-hydroxy-9-epi-hamigeran B norditerpenoid analogs (23 new members in all), structurally related to cyathane diterpenoid scaffold, and their anti-neuroinflammatory and neurite outgrowth-stimulating (neurotrophic) activity. Compounds 9a, 9h, 9o [...] Read more.
We describe the efficient synthesis of a series of new simplified hamigeran B and 1-hydroxy-9-epi-hamigeran B norditerpenoid analogs (23 new members in all), structurally related to cyathane diterpenoid scaffold, and their anti-neuroinflammatory and neurite outgrowth-stimulating (neurotrophic) activity. Compounds 9a, 9h, 9o, and 9q exhibited moderate nerve growth factor (NGF)-mediated neurite-outgrowth promoting effects in PC-12 cells at the concentration of 20 μm. Compounds 9b, 9c, 9o, 9q, and 9t showed significant nitric oxide (NO) production inhibition in lipopolysaccharide (LPS)-activated BV-2 microglial cells, of which 9c and 9q were the most potent inhibitors, with IC50 values of 5.85 and 6.31 μm, respectively. Two derivatives 9q and 9o as bifunctional agents displayed good activities as NO production inhibitors and neurite outgrowth-inducers. Cytotoxicity experiments, H2O2-induced oxidative injury assay, and ELISA reaction speculated that compounds may inhibit the TNF-α pathway to achieve anti-inflammatory effects on nerve cells. Moreover, molecular docking studies provided a better understanding of the key structural features affecting the anti-neuroinflammatory activity and displayed significant binding interactions of some derivatives (like 9c, 9q) with the active site of iNOS protein. The structure-activity relationships (SARs) were also discussed. These results demonstrated that this structural class compounds offered an opportunity for the development of a new class of NO inhibitors and NGF-like promotors. Full article
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9 pages, 1189 KiB  
Article
Aspidoptoids A–D: Four New Diterpenoids from Aspidopterys obcordata Vine
by Peng Sun, Dong-Hua Cao, Yi-Dian Xiao, Zong-Yi Zhang, Jia-Nan Wang, Xiao-Cui Shi, Chun-Fen Xiao, Hua-Bin Hu and You-Kai Xu
Molecules 2020, 25(3), 529; https://doi.org/10.3390/molecules25030529 - 25 Jan 2020
Cited by 10 | Viewed by 2503
Abstract
Four new diterpenoids, named aspidoptoids A–D (14), together with two known analogues (56) were isolated from Aspidopterys obcordata vine. Aspidoptoids A–B (12) are the first examples of phenylethylene-bearing 20-nor-diterpenoids of which [...] Read more.
Four new diterpenoids, named aspidoptoids A–D (14), together with two known analogues (56) were isolated from Aspidopterys obcordata vine. Aspidoptoids A–B (12) are the first examples of phenylethylene-bearing 20-nor-diterpenoids of which aspidoptoid B (2) possesses a rare 3,10-oxybridge. Their structures and absolute configuration were determined by extensive spectroscopic analyses (IR, HRESIMS, 1D and 2D NMR) and electronic circular dichroism (ECD) calculation. In addition, all the isolates were evaluated for their cytotoxic activities and inhibitory effects on the nitric oxide (NO) production. Full article
(This article belongs to the Section Natural Products Chemistry)
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