@article {44,
	title = {6-Deoxyclitoriacetal from Clitoria macrophylla},
	journal = {PhytochemistryPhytochemistry},
	volume = {31},
	number = {12},
	year = {1992},
	note = {0031-9422},
	pages = {4329-4331},
	abstract = {A new rotenoid, 6-deoxyclitoriacetal, was isolated from the roots of Clitoria macrophylla and its structural assignment was established unambiguously by a series of HETCOR, COLOC and NOE difference experiments. In vitro tests showed that this compound possessed strong cytotoxic activity against cultured P-388 lymphocytic leukemia cells, but was not active with cultured KB cells. However, marginal activity was observed with vinblastine-resistant KB-V1 cells, and this was enhanced by the addition of vinblastine. This rotenoid may, therefore, interact with P-glycoprotein.},
	keywords = {12a-hydroxyrotenoid, 6-deoxyclitoriacetal, Clitoria macrophylla, COLOC NMR spectroscopy, cytotoxic activity., Leguminosae, roots},
	author = {Lin, Lee-Juian and Ruangrungsi, Nijsiri and Cordell, Geoffrey A. and Shieh, Hui-Ling and You, Min and Pezzuto, John M.}
}
