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Inhibition of pig kidney diamine oxidase by nazlinin and nazlinin derivatives.

作者信息

Cheng E, Dekker H L, van Gelder B F, Koomen G J

机构信息

Laboratory of Organic Chemistry, University of Amsterdam, The Netherlands.

出版信息

Biochim Biophys Acta. 1995 Dec 6;1253(2):189-92. doi: 10.1016/0167-4838(95)00169-5.

Abstract

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 Km 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.

摘要

相似文献

1
Inhibition of pig kidney diamine oxidase by nazlinin and nazlinin derivatives.
Biochim Biophys Acta. 1995 Dec 6;1253(2):189-92. doi: 10.1016/0167-4838(95)00169-5.

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