Celamonols A–D, four triterpenoid and catechin conjugates with immunosuppressive activities from the stems of Celastrus monospermus
Literature Information
Publication Date
2019-10-10
DOI
10.1039/C9QO00974D
Impact Factor
5.281
Authors
Yi-Ming Li, Wei-Liang Zhu, Wei-Min Zhao
View Original
Abstract
Celamonols A–D (1–4), featuring an unusual pattern of conjunction between a 24,29-dinorfriedelane-type triterpenoid and a catechin, were isolated from the stems of Celastrus monospermus. Their structures were elucidated by extensive spectroscopic analyses, modified Mosher's method, and ECD calculations. Compounds 1 and 4 exhibited moderate activities against the proliferation of B lymphocytes with IC50 values of 1.46 and 1.35 μM, respectively.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
Recommended Compounds
(S)-1-(3-(Benzyloxy)phenyl)-3-(dimethylamino)-2-methylpropan-1-one (2r,3r)-2,3-bis(benzoyloxy)succinate
CAS Number:
1004315-81-4
Molecular Formula:
C37H37NO10
![(1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid structure](https://static.chemtradehub.com/structs/865/865689-24-3-5fef.webp "(1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid structure")
(1R,6R)-6-({[(2-Methyl-2-propanyl)oxy]carbonyl}amino)-3-cyclohexene-1-carboxylic acid
CAS Number:
865689-24-3
Molecular Formula:
C12H19NO4
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