Chemical structure and tumor type specificity of "half-mustard type" phenothiazines
Citation
N. Motohashi et al., Chemical structure and tumor type specificity of "half-mustard type" phenothiazines, ANTICANC R, 19(3A), 1999, pp. 1859-1864
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
ANTICANCER RESEARCH
SICI code
0250-7005(199905/06)19:3A<1859:CSATTS>2.0.ZU;2-E
Abstract
The antiproliferative activity of sir "half-mustard type" phenothiazines ag
ainst a total of 54 tumor cell lines: 4 leukemia, 9 non-small-cell lung, 7
colon; 5 CNS-, 8 melanoma, 6 ovarian; 8 renal; I prostate and 6 breast canc
er was determined by NCI-Information Intensive-Approach. The C-2 position o
f phenothiazines were substituted with H, CI and CF3-groups. The half-musta
rd and ring system was linked either by a propylene or a butylene bridge. C
olon-cancer cell showed the highest sensitivity against "half-mustard type"
phenothiazines, followed by leukemia, melanoma, prostate-, CNS-, breast-,
lung; renal and ovarian cancer cells. These data suggest the "cancer-type-s
pecific" antitumor action of "half-mustard type" phenothiazines.