Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase

被引:24
|
作者
Al Mamun, Abdullah [1 ]
Marikova, Jana [2 ]
Hulcova, Daniela [1 ,3 ]
Janousek, Jiri [1 ,3 ]
Safratova, Marcela [1 ,3 ]
Novakova, Lucie [4 ]
Kucera, Tomas [5 ]
Hrabinova, Martina [6 ,7 ]
Kunes, Jiri [2 ]
Korabecny, Jan [6 ,7 ]
Cahlikova, Lucie [1 ]
机构
[1] Charles Univ Prague, Fac Pharm, Dept Pharmaceut Bot, ADINACO Res Grp, Heyrovskeho 1203, Hradec Kralove 50005, Czech Republic
[2] Charles Univ Prague, Fac Pharm, Dept Organ & Bioorgan Chem, Heyrovskeho 1203, Hradec Kralove 50005, Czech Republic
[3] Charles Univ Prague, Fac Pharm, Dept Pharmacognosy, Heyrovskeho 1203, Hradec Kralove 50005, Czech Republic
[4] Charles Univ Prague, Dept Analyt Chem, Fac Pharm, Heyrovskeho 1203, Hradec Kralove 50005, Czech Republic
[5] Univ Def, Fac Mil Hlth Sci, Dept Mil Med Serv Org & Management, Trebesska 1575, Hradec Kralove 50005, Czech Republic
[6] Univ Def, Fac Mil Hlth Sci, Dept Toxicoloxy & Mil Pharm, Trebesska 1575, Hradec Kralove 50005, Czech Republic
[7] Univ Hosp Hradec Kralove, Biomed Res Ctr, Sokolska 581, Hradec Kralove 50005, Czech Republic
关键词
Amaryllidaceae; Narcissus pseudonarcissus cv; Carlton; alkaloids; carltonine A-C; Alzheimer's disease; butyrylcholinesterase; docking studies; PROLYL OLIGOPEPTIDASE; POTENTIAL CROPS; ACETYLCHOLINESTERASE; CHOLINESTERASES; PATHOPHYSIOLOGY; HAEMANTHAMINE; DAFFODILS; INSIGHTS; COMPLEX; SYSTEM;
D O I
10.3390/biom10050800
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
Thirteen known (1-12 and 16) and three previously undescribed Amaryllidaceae alkaloids of belladine structural type, named carltonine A-C (13-15), were isolated from bulbs of Narcissus pseudonarcissus cv. Carlton (Amaryllidaceae) by standard chromatographic methods. Compounds isolated in sufficient amounts, and not tested previously, were evaluated for their in vitro acetylcholinesterase (AChE; E.C. 3.1.1.7), butyrylcholinesterase (BuChE; E.C. 3.1.1.8) and prolyl oligopeptidase (POP; E.C. 3.4.21.26) inhibition activities. Significant human BuChE (hBUChE) inhibitory activity was demonstrated by newly described alkaloids carltonine A (13) and carltonine B (14) with IC50 values of 913 +/- 20 nM and 31 +/- 1 nM, respectively. Both compounds displayed a selective inhibition pattern for hBuChE with an outstanding selectivity profile over AChE inhibition, higher than 100. The in vitro data were further supported by in silico studies of the active alkaloids 13 and 14 in the active site of hBuChE.
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页数:17
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