1H and 13C-NMR studies of the interaction between 1,3,5-trinitrobenzene and 2,6-dimethylnaphthalene

1989 ◽  
Vol 45 (12) ◽  
pp. 1263-1266 ◽  
Author(s):  
M.M. Ayad ◽  
R.M. Issa ◽  
J. Homer
Keyword(s):  
13C Nmr ◽  
Peptides 1990 ◽  
1991 ◽  
pp. 519-520
Author(s):  
Štefica Horvat ◽  
Jaroslav Horvat ◽  
Branimir Klaić

1979 ◽  
Vol 35 (7) ◽  
pp. 733-737 ◽  
Author(s):  
G. Agostini ◽  
F. Coletta ◽  
A. Gambaro ◽  
S. Castellano
Keyword(s):  
13C Nmr ◽  

1986 ◽  
Vol 5 (4) ◽  
pp. 571-584
Author(s):  
L. M. Benzing-purdie ◽  
C. I. Ratcliffe ◽  
J. A. Ripmeester
Keyword(s):  
13C Nmr ◽  

1991 ◽  
Vol 24 (4) ◽  
pp. 509-518 ◽  
Author(s):  
B. Brycki ◽  
B. Brzezinski ◽  
B. Marciniak ◽  
S. Paszyc

1994 ◽  
Vol 13 (4) ◽  
pp. 1404-1410 ◽  
Author(s):  
Makoto Koike ◽  
David G. VanderVelde ◽  
John R. Shapley

Marine Drugs ◽  
2019 ◽  
Vol 17 (9) ◽  
pp. 534 ◽  
Author(s):  
You-Ying Chen ◽  
Lee-Shing Fang ◽  
Yu-Hsin Chen ◽  
Bo-Rong Peng ◽  
Tung-Pin Su ◽  
...  

Three new 8-hydroxybriaranes—fragilides R–T (1–3) were obtained from a sea whip gorgonian coral Junceella fragilis. The structures of briaranes 1–3 were elucidated by using spectroscopic methods, including 1D (1H and 13C NMR), 2D (COSY, HSQC, HMBC, and NOESY experiments) NMR studies, and (+)-HRESIMS. Fragilides S and T (2 and 3) are the only briaranes known to possess 8α-hydroxy and 17β-methyl groups, respectively. Briarane 2 exerted an inhibition effect on iNOS release from RAW264.7; a macrophage cell line that originated from a mouse monocyte macrophage, stimulated with lipopolysaccharides.


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