69739-21-5Relevant articles and documents
Synthesis and biological evaluation of new naphthoquinone-containing pyrrolo-thiazoles as anticancer agents
Lopes, Susana M. M.,Laranjo, Mafalda,Serra, Armenio C.,Abrantes, Ana Margarida,Rocha Gonsalves, Antonio M. D'A.,Botelho, Maria Filomena,Beja, Ana Matos,Silva, Manuela Ramos,Pinho E Melo, Teresa M. V. D.
experimental part, p. 960 - 966 (2010/10/19)
(Chemical Equation Presented) Naphthoquinones undergo 1,3-dipolar cycloaddition with bicyclic muenchnones generated from thiazolidines affording new pyrrolo-thiazoles with a fused quinone nucleus. The products were obtained as single enantiomers in good yields. These benzo[f]thiazolo[4,3-a] isoindole-6,11(1H,3H)-diones are comprised of four fused rings and present a very planar structure. The evaluation of their anticancer activity against melanoma A375 and colorectal adenocarcinoma WiDr human cell lines showed only moderate activity but gave insight into the modeling of new structures. [Color figure can be viewed in the online issue, which is available at www.interscience.wiley.com.]
KAPPA-OPIOID RECEPTOR AGONIST COMPRISING 2-PHENYLBENZOTHIAZOLINE DERIVATIVE
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Page 32, (2008/06/13)
The present invention provides κ opioid receptor agonists comprising 2-phenylbenzothiazoline derivatives. The present invention relates to κ opioid receptor agonists comprising compounds or salts thereof having the chemical structure represented by the ge