Tham khảo Oxyphenisatine

  1. 1 2 3 SciFinder Scholar, version 2004.2; Chemical Abstracts Service, Registry Number 125-13-3, accessed ngày 1 tháng 9 năm 2011
  2. ↑ Farack, U. M.; Nell, G. (1984). “Mechanism of Action of Diphenolic Laxatives: The Role of Adenylate Cyclase and Mucosal Permeability”. Digestion 30 (3): 191–194. PMID 6548720. doi:10.1159/000199105. 
  3. ↑ Kotha, P.; Rake, M. O.; Willatt, D. (1980). “Liver Damage Induced by Oxyphenisatin” (PDF). British Medical Journal 281 (6254): 1530. PMC 1714947. PMID 6893676. doi:10.1136/bmj.281.6254.1530. 
  4. ↑ Baum, H. M.; Sanders, R. G.; Straub, G. J. (1951). “The Occurrence of a Diphenyl Isatin in California Prunes”. Journal of the American Pharmaceutical Association 40 (7): 348–349. PMID 14850362. doi:10.1002/jps.3030400713. 
  5. ↑ Stacewicz-Sapuntzakis, M.; Bowen, P. E.; Hussain, E. A.; Damayanti-Wood, B. I.; Farnsworth, N. R. (2001). “Chemical Composition and Potential Health Effects of Prunes: A Functional Food?”. Critical Reviews in Food Science and Nutrition 41 (4): 251–286. PMID 11401245. doi:10.1080/20014091091814. 
  6. ↑ Baeyer, A.; Lazarus, M. J. (1885). “Ueber Condensationsproducte des Isatins”. Berichte der Deutschen Chemischen Gesellschaft 18 (2): 2637. doi:10.1002/cber.188501802170. 

Tài liệu tham khảo

WikiPedia: Oxyphenisatine http://redpoll.pharmacy.ualberta.ca/drugbank/cgi-b... http://www.bmj.com/highwire/filestream/332472/fiel... http://chemapps.stolaf.edu/jmol/jmol.php?model=OC1... http://chemapps.stolaf.edu/jmol/jmol.php?model=Oc1... http://pubchem.ncbi.nlm.nih.gov/summary/summary.cg... //www.ncbi.nlm.nih.gov/pmc/articles/PMC1714947 //www.ncbi.nlm.nih.gov/pubmed/11401245 //www.ncbi.nlm.nih.gov/pubmed/14850362 //www.ncbi.nlm.nih.gov/pubmed/6548720 //www.ncbi.nlm.nih.gov/pubmed/6893676