| Article ID | Journal | Published Year | Pages | File Type | 
|---|---|---|---|---|
| 7584763 | Food Chemistry | 2018 | 7 Pages | 
Abstract
												Eight new ent-kaurane diterpene fatty acid esters, namely caffarolides A-H (1-8), were isolated from green beans of Coffea arabica. Their chemical structures were confirmed by extensive spectroscopic analysis including 1D, 2D NMR (HSQC, HMBC, 1H-1H COSY, and ROESY), HRMS, IR and CD spectra and by GC-FID analysis. Interestingly, the diterpene moiety of these new compounds first occurred in genus Coffea. All the isolates were evaluated for platelet aggregation activity in vitro. As the results, caffarolides C, D and F (3, 4 and 6) showed induction effect for platelet aggregation and the possible structure-activity relationships have been discussed briefly.
											Keywords
												Diterpene esters1D NMR1H–1H COSYPPPTLCGC-FIDHSQCHRMSADPPrP2D NMRadenosine diphosphatePlatelet aggregationROESYtwo-dimensional nuclear magnetic resonancecircular dichroismHigh resolution mass spectrometryInfrared spectroscopyMethanolMeOHHMBC یا Heteronuclear Multiple Bond Correlationplatelet-poor plasmaplatelet-rich plasmaheteronuclear multiple bond connectivityCoffea arabicaColumn chromatographythin layer chromatographyGas chromatography with flame ionization detectorStructure elucidationheteronuclear single quantum coherence
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											Authors
												Xia Wang, QianQian Meng, XingRong Peng, GuiLin Hu, MingHua Qiu, 
											