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Strychnos 1990 - 2004 - Crops for the Future

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Author<br />

Title<br />

Year<br />

Source title<br />

Reference<br />

Hattori, M., T. Nakabayashi, Y. A. Lim, H. Miyashiro, M. Kurokawa, K. Shiraki,<br />

Inhibitory effects of various ayurvedic and panamanian medicinal-plants on <strong>the</strong> in<br />

1995<br />

Phyto<strong>the</strong>rapy Research<br />

9(4): 270-276<br />

Abstract<br />

Extracts of 40 Ayurvedic medicines and 39 Panamanian medicinal plants were screened <strong>for</strong> <strong>the</strong>ir<br />

inhibitory activity on <strong>the</strong> plaque <strong>for</strong>mation of herpes simplex virus type I (HSV-1) in cultured cells,<br />

The extracts of II plant species showed potent inhibitory activity at a concentration of 100 mu g/mL,<br />

while those of ten species showed moderate activities, Repeated oral administration of each extract<br />

of Rhus acuminata (galls), Saraca indica (bark), <strong>Strychnos</strong> potatrum (seeds) appreciably suppressed<br />

<strong>the</strong> development of typical skin lesions induced by infection of HSV-1 in BALB/c mice, The extract<br />

of S. potatrum prolonged both development of skin lesion and mean survival time. This indicates<br />

that S. potatrum is a possible candidate <strong>for</strong> <strong>the</strong>rapeutic application <strong>for</strong> HSV-1 infection.<br />

Author<br />

Title<br />

Year<br />

Source title<br />

Reference<br />

Abstract<br />

He, Y. and et al.<br />

Influence of different processing methods on four alkaloid contents in <strong>Strychnos</strong> n<br />

1995<br />

China Journal of Chinese Materia Medica<br />

20(2): 84<br />

-<br />

Author<br />

Title<br />

Year<br />

Source title<br />

Reference<br />

Kizil, M. and J. A. Murphy<br />

Stereoselective preparation of <strong>the</strong> abce tetracycle of aspidospermidine and related<br />

1995<br />

Journal of <strong>the</strong> Chemical Society-Chemical Communications<br />

(14): 1409-1410<br />

Abstract<br />

Tandem radical cyclisation af<strong>for</strong>ds stereoselective access to <strong>the</strong> ABCE tetracyclic substructure of<br />

a s p i d o s p e r m i d i n e a n d r e l a t e d a l k a l o i d s .

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