2-Pyridinethiolate derivatives from branches and leaves of Polyalthia nemoralis and their cytotoxic activities.
- Author:
	        		
		        		
		        		
			        		Ziming LU
			        		
			        		
			        		
			        			1
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Shengjun DAI
			        		
			        		;
		        		
		        		
		        		
			        		Ruoyun CHEN
			        		
			        		;
		        		
		        		
		        		
			        		Dequan YU
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Cell Line, Tumor; Cell Survival; drug effects; Drugs, Chinese Herbal; chemistry; pharmacology; Humans; Magnetic Resonance Spectroscopy; Plant Leaves; chemistry; Plant Stems; chemistry; Polyalthia; chemistry; Pyridines; chemistry
 - From: China Journal of Chinese Materia Medica 2010;35(1):53-57
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo investigate the active constituents of the branches and leaves of Polyalthia nemoralis.
METHODThe compounds were isolated and purified by silica gel, macroporous adsorption resin and Sephadex LH-20 column chromatographic methods. Their chemical structures were elucidated on the basis of physicochemical properties and spectral data.
RESULTEight compounds were isolated and identified as: zincpolyanemin (1), nickel bis-(pyridine-N-oxide-2-thiolate) (2), cupric bis (pyridine-N-oxide-2-thiolate (3), 2-methanesulfonyl-pyridine (4), 2-pyridinethiolate N-oxide (5), 2,2'-dithiodipyridine (6), 2-thiohydroxypyridin-N-oxide-2-S-beta-D-gluco pyranoside (7) and pyridine-N-oxide (8), respectively.
CONCLUSIONCompounds 2, 4-6, 8 were new natural products. The bioassays in vitro against five human tumor cell lines with MTT method showed stronger cytotoxic activities (IC50 0.05-0.09 mg x L(-1)) for compounds 1-3 and 6, and weaker cytotoxic activities (IC50 5.49-7.71 mg x L(-1)) for compound 5.
 
            