scholarly journals Melitidin: A Flavanone Glycoside from Citrus grandis ‘Tomentosa’

2013 ◽  
Vol 8 (4) ◽  
pp. 1934578X1300800 ◽  
Author(s):  
Wei Zou ◽  
Yonggang Wang ◽  
Haibin Liu ◽  
Yulong Luo ◽  
Si Chen ◽  
...  

Citrus grandis ‘Tomentosa’ is a traditional Chinese medicine, used as an antitussive. In this research, melitidin, a flavanone glycoside, was isolated from this species for the first time by using chromatographic methods. The structure was confirmed through comprehensive analyses of its ultraviolet, infrared, 1H and 13C NMR, HMBC and HMQC spectroscopic and high-resolution mass spectrometric data. Meliditin showed a good antitussive effect on cough induced by citric acid in Guinea pig, suggesting that it was a contributor to the antitussive effect of C. grandis ‘Tomentosa’.

2010 ◽  
Vol 5 (8) ◽  
pp. 1934578X1000500
Author(s):  
Muhammad Nisar ◽  
Waqar Ahmad Kaleem ◽  
Achyut Adhikari ◽  
Zulfiqar Ali ◽  
Nusrat Hussain ◽  
...  

The structures of (3 S,7 R,13 S)-6-[2-(dimethylamino)-3-phenylpropanoyl]-19-methoxy-2-oxa-6,9,15-triazatetracyclo[16.3.1.03,7. 09,13]docosa-1-(22),16,18,20-tetraene-8,14-dione (1), nummularin-C (2) and nummularin-R (3) have been previously determined mainly based on mass spectrometric data. Stereochemistry and complete 1H and 13C NMR spectroscopic data assignments of these compounds are now described. Compounds 1 and 2 are reported for the first time from


2010 ◽  
Vol 5 (3) ◽  
pp. 1934578X1000500
Author(s):  
Seru Ganapaty ◽  
Desaraju Venkata Rao ◽  
Steve Thomas Pannakal

A new compound, (2 S)- p-hydroxyphenethyl 2-bromo-2-methyldodeconate (1) and 7,3′-dimethoxy-5,4′-dihydroxy flavone, together with lupeol and stigmasterol were isolated from the stem bark of Citharexylum fruticosum (Verbenaceae). The structures of the compounds were established on the basis of the interpretation of NMR (1H, 13C, COSY and HMBC) spectra, as well as low and high-resolution mass spectrometric data. In this paper, we report on the structure elucidation of 1.


Molecules ◽  
2019 ◽  
Vol 24 (19) ◽  
pp. 3498 ◽  
Author(s):  
Klaus Ringsborg Westphal ◽  
Manuela Ilse Helga Werner ◽  
Katrine Amalie Hamborg Nielsen ◽  
Jens Laurids Sørensen ◽  
Valery Andrushchenko ◽  
...  

Chemical analyses of Fusarium avenaceum grown on banana medium resulted in eight novel spiroleptosphols, T1, T2 and U–Z (1–8). The structures were elucidated by a combination of high-resolution mass spectrometric data and 1- and 2-D NMR experiments. The relative stereochemistry was assigned by 1H coupling and NOESY/ROESY experiments. Absolute stereochemistry established for 7 by vibrational circular dichroism was found analogous to that of the putative polyketide spiroleptosphol from Leptosphaeria doliolum.


2019 ◽  
Vol 91 (24) ◽  
pp. 15509-15517 ◽  
Author(s):  
Sadjad Fakouri Baygi ◽  
Sujan Fernando ◽  
Philip K. Hopke ◽  
Thomas M. Holsen ◽  
Bernard S. Crimmins

2006 ◽  
Vol 1 (7) ◽  
pp. 1934578X0600100 ◽  
Author(s):  
Qianliang Chen ◽  
Wenji Sun ◽  
Guangzhong Tu ◽  
Zhangyan Shi ◽  
Yongmin Zhang

A novel amide, qinjiaoamide and a novel iridoid, erythrocentaurin acid, together with seven known compounds [erythrocentaurin (3), roburic acid (4), oleanolic acid (5), gentiopicroside (6), swertiamarine (7), sweroside (8), and 6′-O-β-D-glucosylgentiopicroside (9)], were isolated from the root of Gentiana macrophylla Pall. from Shaanxi Province, China. The novel compounds were identified as N-pentacosyl-2-carboxy-benzoyl amide (1) and 5-carboxyl-3,4-dihydrogen-1H-2-benzopyran-1-one (2), on the basis of spectroscopic (UV, IR, 1D- and 2D-NMR) and mass spectrometric data. Among the known compounds, erythrocentaurin (3) was isolated from the genus Gentiana for the first time.


2016 ◽  
Vol 15 (3) ◽  
pp. 851-867 ◽  
Author(s):  
Kai-Ting Fan ◽  
Aaron K. Rendahl ◽  
Wen-Ping Chen ◽  
Dana M. Freund ◽  
William M. Gray ◽  
...  

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