INHIBITION OF COLLAGENASE BY ARANCIAMYCIN AND ARANCIAMYCIN DERIVATIVES

被引:30
作者
BOLS, M [1 ]
BINDERUP, L [1 ]
HANSEN, J [1 ]
RASMUSSEN, P [1 ]
机构
[1] LEO PHARMACEUT PROD, DK-2750 BALLERUP, DENMARK
关键词
D O I
10.1021/jm00093a008
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Aranciamycin (1), an anthracycline antibiotic, was found to be an inhibitor of Clostridium histolyticum collagenase, with an IC50 = 3.7 x 10(-7) M. Elastase and trypsin were not inhibited at concentrations less-than-or-equal-to 10(-5) M. A number of aranciamycin derivatives 2-13 were prepared and tested for collagenase inhibition. While loss of activity was found for derivatives modified in the sugar ring or rings B and D of the aglycone, increased potency was found when the tertiary alcohol at C-9 was esterified. All compounds 1-13 were found to inhibit DNA synthesis of Yoshida sarcoma tumor cells.
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页码:2768 / 2771
页数:4
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