INHIBITION OF PIG-KIDNEY DIAMINE OXIDASE BY NAZLININ AND NAZLININ DERIVATIVES

被引:3
作者
CHENG, E
DEKKER, HL
VANGELDER, BF
KOOMEN, GJ
机构
[1] UNIV AMSTERDAM,ORGAN CHEM LAB,1018 WS AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,EC SLATER INST BIOCHEM RES,1018 TV AMSTERDAM,NETHERLANDS
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 1995年 / 1253卷 / 02期
关键词
DIAMINE OXIDASE; INHIBITION; ALKALOID; (PORCINE); (KIDNEY);
D O I
10.1016/0167-4838(95)00169-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nazlinin (1-(4-butylamino)-1,2,3,4-tetrahydro-beta-carboline) (1), an alkaloid recently isolated from Nitraria schoberi, and its two derivatives, 1-(4-butylamino)-3,4-dihydro-beta-carboline (2) and 1-(4-butylamino)-beta-carboline (3), were synthesized and their interaction with pig kidney diamine oxidase (PKDO) was studied. Nazlinin appeared to be a very poor substrate while 3 was a good substrate with an apparent K-m of 9.3 10(-5) M. The enzyme was inhibited by 1 and 2. With both compounds the mode of inhibition found was non-competitive and inhibition constants calculated from the slopes and intercepts of double-reciprocal plots show that 2 is a much more potent inhibitor than the natural product. The relationship between the structure of these compounds and the results found is discussed.
引用
收藏
页码:189 / 192
页数:4
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