Spectroscopic analyses and chemical transformation for structure elucidation of two novel indole alkaloids from Gelsemium elegans

2009 ◽  
Vol 50 (26) ◽  
pp. 3341-3344 ◽  
Author(s):  
Yousuke Yamada ◽  
Mariko Kitajima ◽  
Noriyuki Kogure ◽  
Sumphan Wongseripipatana ◽  
Hiromitsu Takayama
2015 ◽  
Vol 10 (1) ◽  
pp. 1934578X1501000
Author(s):  
Mariko Kitajima ◽  
Tetsuya Koyama ◽  
Yuqiu Wu ◽  
Noriyuki Kogure ◽  
Rongping Zhang ◽  
...  

Two new indole alkaloids, kopsiyunnanines J1 and J2, were isolated from Yunnan Kopsia arborea, and their structures were determined by spectroscopic analyses. Kopsiyunnanines J1 and J2 are unprecedented Strychnos-type indole alkaloids having an additional C1 unit in the secologanin moiety of the molecule.


2018 ◽  
Vol 13 (9) ◽  
pp. 1934578X1801300
Author(s):  
Bruna de Falco ◽  
Giuliano Bonanomi ◽  
Virginia Lanzotti

A bioassay guided phytochemical analysis of the bulbs of Allium sativum L. var. Voghiera, typical of Voghiera, Ferrara (Italy), allowed the isolation of six new sulfur compounds with dithiosulfinates and sulfoxides functionalities. Structure elucidation of the isolated compounds was carried out by spectroscopic analyses, including NMR spectroscopy and MS spectrometry. Compounds showed significant antimicrobial activity towards two fungal species, the air-borne pathogen Botrytis cinerea and the beneficial fungus Trichoderma harzianum.


Tetrahedron ◽  
1988 ◽  
Vol 44 (16) ◽  
pp. 5075-5094 ◽  
Author(s):  
Dhavadee Ponglux ◽  
Sumphan Wongseripipatana ◽  
Sanan Subhadhirasakul ◽  
Hiromitsu Takayama ◽  
Masaki Yokota ◽  
...  

ChemInform ◽  
1989 ◽  
Vol 20 (1) ◽  
Author(s):  
D. PONGLUX ◽  
S. WONGSERIPIPATANA ◽  
S. SUBHADHIRASAKUL ◽  
H. TAKAYAMA ◽  
M. YOKOTA ◽  
...  

2003 ◽  
Vol 17 (2) ◽  
pp. 128-133 ◽  
Author(s):  
V. Ivanova ◽  
U. Graefe ◽  
R. Schlegel ◽  
B. Schlegel ◽  
A. Gusterova ◽  
...  

2012 ◽  
Vol 67 (5) ◽  
pp. 417-420 ◽  
Author(s):  
Imene Zendah ◽  
Khaled A. Shaaban ◽  
Elisabeth Helmke ◽  
Armin Maier ◽  
Heinz H. Fiebig ◽  
...  

A new thiazolyl-indole alkaloid, barakacin (1), has been isolated from the ruminal bacterium Pseudomonas aeruginosa strain ZIO. On the basis of detailed spectroscopic analyses and comparison with the data of related compounds, its structure has been determined as 2-{4-[bis-(1H-indol-3- yl)-methyl]-thiazol-2-yl}-phenol. In addition, the known compounds phenazine-1-carboxylic acid, 3-(hydroxyacetyl)-indole, indole-3-carbaldehyde, and glycolipid A were isolated. The discovery of compounds with a new skeleton emphasizes the importance for exploring new ecological niches like the rumen of bovines for the detection of new natural products. This paper describes the fermentation, isolation, structure elucidation and biological activities of compound 1.


2010 ◽  
Vol 48 (9) ◽  
pp. 734-737 ◽  
Author(s):  
Antonia Torres Ávila Pimenta ◽  
Raimundo Braz-Filho ◽  
Piero Giuseppe Delprete ◽  
Elnatan Bezerra de Souza ◽  
Edilberto Rocha Silveira ◽  
...  

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