scholarly journals (+)-Pathylactone A, a New Natural Nor-sesquiterpenoid from the Octocoral Paralemnalia thyrsoides

2018 ◽  
Vol 13 (1) ◽  
pp. 1934578X1801300 ◽  
Author(s):  
Zhi-Jun Zhang ◽  
Wu-Fu Chen ◽  
Bo-Rong Peng ◽  
Zhi-Hong Wen ◽  
Ping-Jyun Sung

A new natural marine nor-sesquiterpenoid, (+)-pathylactone A (1), along with a know nor-sesquiterpenoid, napalilactoe (2), were isolated from the octocoral Paralemnalia thyrsoides. The structure of 1 was established on the basis of spectroscopic methods and by comparison of the spectral data with those of synthetic analogues. Nor-sesquiterpenoid 1 was found to inhibit the protein experssion of pro-inflammatory inducible nitric oxide synthase (iNOS) in a murine macrophage-like cell line.

1995 ◽  
Vol 49 (2) ◽  
pp. 105-115 ◽  
Author(s):  
Salvatore Milano ◽  
Francesco Arcoleo ◽  
Mariella Dieli ◽  
Rita D'Agostino ◽  
Pietro D'Agostino ◽  
...  

1999 ◽  
Vol 126 (5) ◽  
pp. 1253-1261 ◽  
Author(s):  
Peter J Syapin ◽  
Alexia Rendon ◽  
David R Huron ◽  
Julius D Militante

Marine Drugs ◽  
2019 ◽  
Vol 17 (12) ◽  
pp. 706 ◽  
Author(s):  
Tung-Pin Su ◽  
Chien-Han Yuan ◽  
Yi-Ming Jhu ◽  
Bo-Rong Peng ◽  
Zhi-Hong Wen ◽  
...  

Three new 11,20-epoxybriaranes—fragilides U–W (1–3), as well as two known metabolites, junceellonoid D (4) and junceellin (5), were obtained from the octocoral Junceella fragilis. The structures of briaranes 1–3 were elucidated by spectroscopic methods and briaranes 3 and 5 displayed inhibition effects on inducible nitric oxide synthase (iNOS) release from RAW264.7.


1998 ◽  
Vol 275 (5) ◽  
pp. E740-E747 ◽  
Author(s):  
Sidney M. Morris ◽  
Diane Kepka-Lenhart ◽  
Li-Chun Chen

Activated macrophages avidly consume arginine via the action of inducible nitric oxide synthase (iNOS) and/or arginase. In contrast to our knowledge regarding macrophage iNOS expression, the stimuli and mechanisms that regulate expression of the cytosolic type I (arginase I) or mitochondrial type II (arginase II) isoforms of arginase in macrophages are poorly defined. We show that one or both arginase isoforms may be induced in the RAW 264.7 murine macrophage cell line and that arginase expression is regulated independently of iNOS expression. For example, 8-bromo-cAMP strongly induced both arginase I and II mRNAs but not iNOS. Whereas interferon-γ induced iNOS but not arginase, 8-bromo-cAMP and interferon-γ mutually antagonized induction of iNOS and arginase I mRNAs. Dexamethasone, which did not induce either arginase or iNOS, almost completely abolished induction of arginase I mRNA by 8-bromo-cAMP but enhanced induction of arginase II mRNA. Lipopolysaccharide (LPS) induced arginase II mRNA, but 8-bromo-cAMP plus LPS resulted in synergistic induction of both arginase I and II mRNAs. In all cases, increases in arginase mRNAs were sufficient to account for the increases in arginase activity. These complex patterns of expression suggest that the arginase isoforms may play distinct, although partially overlapping, functional roles in macrophage arginine metabolism.


Marine Drugs ◽  
2020 ◽  
Vol 18 (8) ◽  
pp. 383
Author(s):  
Yi-Lin Zhang ◽  
Chih-Chao Chiang ◽  
Yi-Ting Lee ◽  
Zhi-Hong Wen ◽  
Yang-Chang Wu ◽  
...  

Our continuous chemical study of a cultured octocoral Briareum stechei led to the isolation of four new briarane diterpenoids, briarenols Q–T (1–4). The structures of new metabolites 1–4 were established by spectroscopic methods, and compounds 3 and 4 were found to inhibit the generation of inducible nitric oxide synthase (iNOS) from RAW 264.7 stimulated by lipopolysaccharides (LPS).


Sign in / Sign up

Export Citation Format

Share Document