Myriastramides A—C, New Modified Cyclic Peptides from the Philippines Marine Sponge Myriastra clavosa.

ChemInform ◽  
2004 ◽  
Vol 35 (9) ◽  
Author(s):  
Karen L. Erickson ◽  
Kirk R. Gustafson ◽  
Dennis J. Milanowski ◽  
Lewis K. Pannell ◽  
John R. Klose ◽  
...  
Tetrahedron ◽  
2003 ◽  
Vol 59 (51) ◽  
pp. 10231-10238 ◽  
Author(s):  
Karen L Erickson ◽  
Kirk R Gustafson ◽  
Dennis J Milanowski ◽  
Lewis K Pannell ◽  
John R Klose ◽  
...  

1995 ◽  
Vol 50 (9-10) ◽  
pp. 669-674 ◽  
Author(s):  
A. Supriyono ◽  
B. Schwarz ◽  
V. Wray ◽  
L. Witte ◽  
W. E. G. Müller ◽  
...  

Abstract Analysis of the tropical marine sponge Axinella carteri afforded six unusual alkaloids, including the new brominated guanidine derivative 3-bromo-hymenialdisine. The structure elucidation of the new alkaloid is described. The alkaloid patterns of sponges collected in Indonesia or in the Philippines were shown to be qualitatively identical suggesting de novo synthesis by the sponge or by endosymbiontic microorganisms rather than uptake by filterfeeding. All alkaloids were screened for insecticidal activity as well as for cytotoxicity. The guanidine alkaloids hymenialdisine and debromohymenialdisine exhibited insecticidal activity towards neonate larvae of the polyphagous pest insect Spodoptera littoralis (LD50s of 88 and 125 ppm, respectively), when incorporated into artificial diet and offered to the larvae in a chronic feeding bioassay. The remaining alkaloids, including the new compound, were inactive in this bioassay. Cytotoxicity was studied in vitro using L5178y mouse lymphoma cells. Debromohymenialdisine was again the most active compound (ED50 1.8 μg/ml) followed by hymenialdisine and 3-bromohymenialdisine, which were essentially equitoxic and exhibited ED50s of 3.9 μg/ml in both cases. The remaining alkaloids were inactive against this cell line


Marine Drugs ◽  
2021 ◽  
Vol 19 (11) ◽  
pp. 627
Author(s):  
A-Young Shin ◽  
Arang Son ◽  
Changhoon Choi ◽  
Jihoon Lee

The chemical investigation of the marine sponge Dysidea sp., which was collected from Bohol province in the Philippines, resulted in the identification of 15 new scalarane-type sesterterpenoids (1–14, 16), together with 15 known compounds. The chemical structures of the new compounds were elucidated based on NMR spectroscopy and HRMS. The structure of 12-epi-phyllactone D/E (15) isolated during this study was originally identified in 2007. However, careful inspection of our experimental 13C NMR spectrum revealed considerable discrepancies with the reported data at C-9, C-12, C-14, and C-23, leading to the correction of the reported compound to the C-12 epimer of 15, phyllactone D/E. The biological properties of compounds 1–16 were evaluated using the MDA-MB-231 cancer cell line. Compound 7, which bears a pentenone E-ring, exhibits significant cytotoxicity with a GI50 value of 4.21 μM.


2012 ◽  
Vol 75 (8) ◽  
pp. 1451-1458 ◽  
Author(s):  
David E. Williams ◽  
Anne Steinø ◽  
Nicole J. de Voogd ◽  
A. Grant Mauk ◽  
Raymond J. Andersen

2010 ◽  
Vol 18 (14) ◽  
pp. 4947-4956 ◽  
Author(s):  
Sabrin R.M. Ibrahim ◽  
Cho Cho Min ◽  
Franka Teuscher ◽  
Rainer Ebel ◽  
Christel Kakoschke ◽  
...  

2014 ◽  
Vol 77 (12) ◽  
pp. 2678-2684 ◽  
Author(s):  
Kai-Xuan Zhan ◽  
Wei-Hua Jiao ◽  
Fan Yang ◽  
Jing Li ◽  
Shu-Ping Wang ◽  
...  

2012 ◽  
Vol 75 (2) ◽  
pp. 290-294 ◽  
Author(s):  
Miki Kimura ◽  
Toshiyuki Wakimoto ◽  
Yoko Egami ◽  
Karen Co Tan ◽  
Yuji Ise ◽  
...  

Tetrahedron ◽  
2020 ◽  
Vol 76 (10) ◽  
pp. 130997
Author(s):  
Tian Tian ◽  
Kentaro Takada ◽  
Yuji Ise ◽  
Susumu Ohtsuka ◽  
Shigeru Okada ◽  
...  

Planta Medica ◽  
2012 ◽  
Vol 78 (05) ◽  
Author(s):  
X Zhang ◽  
MR Jacob ◽  
RR Rao ◽  
YH Wang ◽  
A Agarwal ◽  
...  

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