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Chun-Sheng Fu
Shandong University of Traditional Chinese Medicine
3Publications
2H-index
11Citations
Publications 3
Newest
Published on Jul 1, 2018in Journal of Ethnopharmacology3.41
Yan-Ru Li3
Estimated H-index: 3
(SDU: Shandong University),
Chun-Sheng Fu2
Estimated H-index: 2
(SDUTCM: Shandong University of Traditional Chinese Medicine)
+ 6 AuthorsTao Shen16
Estimated H-index: 16
(SDU: Shandong University)
Abstract Ethnopharmacology relevance Cinnamomum camphora (L.) J. Presl has been used for the traditional medicine as a therapeutic agent of inflammation-related diseases, including sprains, rheumatic arthritis, abdominal pain, cough and bronchitis, for a long history. The aim of the present study was to illustrate anti-inflammatory substances of C. camphora and their mechanism of action, and to establish the correlations between chemical constituents and traditional uses of this plant. Materials...
Published on Jun 1, 2018in Biochemical Systematics and Ecology1.13
Hui Lv1
Estimated H-index: 1
(SDUTCM: Shandong University of Traditional Chinese Medicine),
Chun-Sheng Fu2
Estimated H-index: 2
(SDUTCM: Shandong University of Traditional Chinese Medicine)
+ 4 AuthorsTao Shen16
Estimated H-index: 16
(SDU: Shandong University)
Abstract Phytochemical investigations of the ethanolic extract from the calyxes of Physalis alkekengi L. var. franchetii (Mast.) Makino led to the isolation of n-heptadecanoic acid ( 1 ), n-pentadecanoic acid ( 2 ), n-hexadecoic acid ( 3 ), n-undecanoic acid ( 4 ), hendecane ( 5 ), β-sitosterol ( 6 ), n-octadecanoic acid ( 7 ), isovanillic acid ( 8 ), 4-methylgentisic acid ( 9 ), 2,3,4-trihydroxybenzoic acid ( 10 ), 5,7-di- O -methylquercetin ( 11 ), 8-hydroxy-7-methoxycoumarin ( 12 ), 4,7-dideh...
Published on Nov 18, 2016in Mini-reviews in Medicinal Chemistry2.84
Bang-Jiao Chen3
Estimated H-index: 3
,
Chun-Sheng Fu2
Estimated H-index: 2
+ 4 AuthorsTao Shen16
Estimated H-index: 16
Cinnamaldehyde analogues are a class of chemical substances originated from derivatization of cinnamaldehyde, and are structurally characterized by the presence of cinnamoyl moiety. Due to the presence of highly reactive α,α-unsaturated carbonyl pharmacophore (Michael acceptor) in their structures, these molecules are apt to react with some enzymes and/or receptors as electrophiles, and consequently produce diverse therapeutically relevant pharmacological functions. Naturally occurring molecules...
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