| Literature DB >> 32361293 |
Yang Hu1, Hua Yang2, Xiaoqian Ding2, Jian Liu2, Xiachang Wang2, Lihong Hu3, Minyan Liu4, Chaofeng Zhang5.
Abstract
Six pairs of octahydroindolizine-type alkaloid enantiomers (1-6) including three new compounds [(-)-1/(+)-1, 2] were isolated from the stems of Dendrobium crepidatum. Their structures including the absolute configurations were elucidated by extensive spectroscopic analyses and comparison between the experimental and calculated electronic circular dichroism (ECD). All compounds were examined for their inhibitory effects on nitric oxide (NO) production induced by lipopolysaccharide (LPS) in RAW264.7 cells. It was found that compounds (+)-1, 2 and (+)-6 exhibited pronounced inhibition on NO production with IC50 values in the range of 3.62-16.11 µM, being more active than the positive control, dexamethasone (IC50 = 47.04 µM). In vivo, compound 6 (100, 50 and 10 mg/kg) showed protective effects against LPS-induced acute lung injury (ALI) in mice.Entities:
Keywords: Acute lung injury; Dendrobium crepidatum; Enantioselectivity; Indolizine-type alkaloids; Orchidaceae
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Year: 2020 PMID: 32361293 DOI: 10.1016/j.bioorg.2020.103809
Source DB: PubMed Journal: Bioorg Chem ISSN: 0045-2068 Impact factor: 5.275