Literature DB >> 32419450

Meroapplanins A-E: Five Meroterpenoids with a 2,3,4,5-Tetrahydropyridine Motif from Ganoderma applanatum.

Xing-Rong Peng1, Qing-Qiang Shi1, Jing Yang1, Hai-Guo Su1,2, Lin Zhou1, Ming-Hua Qiu1,2.   

Abstract

Meroapplanins A-E (1-5) with a 2,3,4,5-tetrahydropyridine fragment were isolated from the fruiting bodies of Ganoderma applanatum. Their structures were elucidated by comprehensive spectroscopic analyses. Their absolute configurations were established based on the X-ray diffraction, electronic circular dichroism (ECD), and calculated nuclear magnetic resonance (NMR) with DP4+ analysis. A plausible biosynthetic pathway for 1-5 was proposed. Furthermore, compounds 1-5, together with optically pure compounds 1a-4a and 1b-4b, were evaluated for their protective effects in PC12 cells damaged by H2O2. The results showed that 3b had protective activity with a cell viability of 82.58 ± 1.31%, compared with the model group (cell viability: 65.27 ± 1.48%).

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Year:  2020        PMID: 32419450     DOI: 10.1021/acs.joc.0c00842

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  NMR Assignments of Six Asymmetrical N-Nitrosamine Isomers Determined in an Active Pharmaceutical Ingredient by DFT Calculations.

Authors:  Hao-Yue Guan; Yu-Fei Feng; Bai-Hao Sun; Jian-Zhao Niu; Qing-Sheng Zhang
Journal:  Molecules       Date:  2022-07-25       Impact factor: 4.927

  1 in total

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