2005
DOI: 10.1002/chin.200524207
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(+)‐Echinobetaine B: Isolation, Structure Elucidation, Synthesis and Preliminary SAR Studies on a New Nematocidal Betaine from a Southern Australian Marine Sponge, Echinodictyum sp.

Abstract: Other bioactive products U 1300 (+)-Echinobetaine B: Isolation, Structure Elucidation, Synthesis and Preliminary SAR Studies on a New Nematocidal Betaine from a Southern Australian Marine Sponge, Echinodictyum sp. -(CAPON*, R. J.; VUONG, D.; MCNALLY, M.; PETERLE, T.; TROTTER, N.; LACEY, E.; GILL, J. H.; Org. Biomol. Chem. 3 (2005) 1, 118-122; Inst. Mol. Biosci.,

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“…Capon and colleagues [27,28] described two novel betaines (−)-echinobetaine A (1) and (+)-echinobetaine B (2), from the Australian sponge Echinodictyum sp. which were nematocidal (LD 99 =83 and 8.3μg/mL, respectively) to the commercial livestock parasite Haemonchus contortus .…”
Section: Marine Compounds With Anthelmintic Antibacterial Anticomentioning
confidence: 99%
“…Capon and colleagues [27,28] described two novel betaines (−)-echinobetaine A (1) and (+)-echinobetaine B (2), from the Australian sponge Echinodictyum sp. which were nematocidal (LD 99 =83 and 8.3μg/mL, respectively) to the commercial livestock parasite Haemonchus contortus .…”
Section: Marine Compounds With Anthelmintic Antibacterial Anticomentioning
confidence: 99%
“…[61], and echinobetaine B (13) from Echinodictyum sp. [62] are anthelmintic compounds from marine sponges. The preliminary SAR of the two latter nematicides revealed the importance of the N-acyl side chain in compound 12 and the importance of 2-OMe and stereopurity of the pharmacophore.…”
Section: Natural Productsmentioning
confidence: 99%