@article {1968,
	title = {Strongylophorine-26, an inhibitor of cancer cell invasion: SAR revealed by synthesis of analogues},
	journal = {Journal of Natural Products},
	volume = {70},
	number = {5},
	year = {2007},
	note = {Warabi, Kaoru Patrick, Brian O. Austin, Pamela Roskelley, Calvin D. Roberge, Michel Andersen, Raymond J.},
	month = {May},
	pages = {736-740},
	abstract = {The absolute configuration of strongylophorine-26 (1) was determined to be 4S, 5R, 8R, 9S, 10S, 13S, 14S by single-crystal X-ray diffraction analysis of the derivative 7 prepared from the co-occurring metabolite strongylophorine-8 (4) and chemical interconversion to the bislactone 8. Synthetic analogues (+)- and (-)-3 have been prepared in order to explore the structure-activity relationship for the anti-invasion pharmacophore of stronglylophorine-26. These studies revealed the unanticipated importance of the A ring lactone moiety for the anti-invasion activity of 1.},
	isbn = {0163-3864},
	url = {<Go to ISI>://000246764300003},
	author = {Warabi, K. and Patrick, B. O. and Austin, P. and Roskelley, C. D. and Roberge, M. and Andersen, R. J.}
}
