Nitric oxide inhibitory principles from Derris trifoliata stems

Abstract

Nine rotenoids were isolated from the hexane and dichloromethane extracts of Derris trifoliata stems and were tested for nitric oxide (NO) inhibitory activity using RAW264.7 cells. The result indicated that 12a-hydroxyrotenone (7) possessed very potent NO inhibitory activity with an IC(50) value of 0.002 microM, followed by 1 (deguelin, IC(50)=0.008 microM), 9 (12a-hydroxyelliptone, IC(50)=0.010 microM) and 2 (alpha-toxicarol, IC(50)=0.013 microM), respectively. In addition, the DPPH scavenging activity of rotenoids was also investigated. It was found that 6a,12a-dehydrodeguelin (5) possessed the highest activity against DPPH with an IC(50) value of 7.4 microM, followed by deguelin (1, IC(50)=27.4 microM). All compounds did not show any cytotoxicity at their IC(50) values for NO inhibitory activity. Structure-activity relationships (SARs) of these rotenoids against NO release are as follows: (1) hydroxylation at C12a dramatically increased activity, (2) prenylation at furan ring increased activity markedly and (3) hydrogenation of a double bond at C6a-C12a conferred higher activity. For the DPPH radical scavenging effect, it was found that (1) introduction of a double bond at C6a-C12a increased activity and (2) hydroxylation of C11 at the D-ring decreased activity. As regards active compounds of Derris trifoliata stems, the isolated compounds are responsible for the NO inhibitory effect, especially 7, 1, 9 and 2, whereas 5 and 1 are those for the DPPH scavenging activity.