Corrigendum to: Structural Variations to the 9-N-Methyladeninium Diterpenoid Hybrid Commonly Isolated from Agelas Sponges

2011 ◽  
Vol 64 (6) ◽  
pp. 846 ◽  
Author(s):  
Laurent Calcul ◽  
Karen Tenney ◽  
Joseline Ratnam ◽  
James H. McKerrow ◽  
Phillip Crews

Four novel 9-N-methyladeninium diterpenoids, agelasine M (3), 2-oxo-agelasine B (4), gelasine A (5), and gelasine B (6) accompanied by the known-agelasine B (1) and F (2) were isolated from the marine sponge Agelas sp. collected in Papua New Guinea. Compounds 3?6 represent higher unsaturated 9-N-methyladeninium bicyclic diterpenoid derivatives including 5 and 6 as unusual norditerpenoid-agelasines. Their structures were elucidated through detailed physical data analyses and comparison with literature properties. All pure compounds were evaluated for inhibitory activity against Trypanosoma brucei as well as for cytotoxicity against Jurkat cells.

2010 ◽  
Vol 63 (6) ◽  
pp. 915 ◽  
Author(s):  
Laurent Calcul ◽  
Karen Tenney ◽  
Joseline Ratnam ◽  
James H. McKerrow ◽  
Phillip Crews

Four novel 9-N-methyladeninium diterpenoids, agelasine M (3), 2-oxo-agelasine B (4), gelasine A (5), and gelasine B (6) accompanied by the known-agelasine B (1) and F (2) were isolated from the marine sponge Agelas sp. collected in Papua New Guinea. Compounds 3–6 represent higher unsaturated 9-N-methyladeninium bicyclic diterpenoid derivatives including 5 and 6 as unusual norditerpenoid-agelasines. Their structures were elucidated through detailed physical data analyses and comparison with literature properties. All pure compounds were evaluated for inhibitory activity against Trypanosoma brucei as well as for cytotoxicity against Jurkat cells.


1999 ◽  
pp. 915-916 ◽  
Author(s):  
George R. Pettit ◽  
Jun-ping Xu ◽  
Diane E. Gingrich ◽  
Michael D. Williams ◽  
Dennis L. Doubek ◽  
...  

ChemInform ◽  
2004 ◽  
Vol 35 (15) ◽  
Author(s):  
Emiliano Manzo ◽  
Rob van Soest ◽  
Lohi Matainaho ◽  
Michel Roberge ◽  
Raymond J. Andersen

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Erica C. Larson ◽  
Christopher D. Pond ◽  
Prem P. Rai ◽  
Teatulohi K. Matainaho ◽  
Pius Piskaut ◽  
...  

The hypothesis underlying this current work is that fresh juice expressed from Papua New Guinea (PNG) medicinal plants (succus) will inhibit human Cytochrome P450s (CYPs). The CYP inhibitory activity identified in fresh material was compared with inhibition in methanol extracts of dried material. Succus is the most common method of traditional medicine (TM) preparation for consumption in PNG. There is increasing concern that TMs might antagonize or complicate drug therapy. We have previously shown that methanol extracts of commonly consumed PNG medicinal plants are able to induce and/or inhibit human CYPsin vitro. In this current work plant succus was prepared from fresh plant leaves. Inhibition of three major CYPs was determined using human liver microsomes and enzyme-selective model substrates. Of 15 species tested, succus from 6/15 was found to inhibit CYP1A2, 7/15 inhibited CYP3A4, and 4/15 inhibited CYP2D6. Chi-squared tests determined differences in inhibitory activity between succus and methanol preparations. Over 80% agreement was found. Thus, fresh juice from PNG medicinal plants does exhibit the potential to complicate drug therapy in at risk populations. Further, the general reproducibility of these findings suggests that methanol extraction of dried material is a reasonable surrogate preparation method for fresh plant samples.


ChemInform ◽  
2010 ◽  
Vol 30 (37) ◽  
pp. no-no
Author(s):  
George R. Pettit ◽  
Jun-ping Xu ◽  
Diane E. Gingrich ◽  
Michael D. Williams ◽  
Dennis L. Doubek ◽  
...  

ChemInform ◽  
2006 ◽  
Vol 37 (33) ◽  
Author(s):  
Camille Chevallier ◽  
Tim S. Bugni ◽  
Xidong Feng ◽  
Mary Kay Harper ◽  
Anita M. Orendt ◽  
...  

1992 ◽  
Vol 57 (26) ◽  
pp. 7217-7220 ◽  
Author(s):  
George R. Pettit ◽  
Jayaram K. Srirangam ◽  
Delbert L. Herald ◽  
Karen L. Erickson ◽  
Dennis L. Doubek ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document