Optimization of 8-Hydroxyquinolines as Inhibitors of Catechol O-Methyltransferase.
Optimization of 8-Hydroxyquinolines as Inhibitors of Catechol O-Methyltransferase.
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优化8-羟基喹啉作为儿茶酚O-甲基转移酶的抑制剂。
DOI:
10.1021/acs.jmedchem.8b01126
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发表时间:
2018-11-08
影响因子:
7.3
通讯作者:
Barrow JC
中科院分区:
文献类型:
--
作者:
Buchler I;Akuma D;Au V;Carr G;de León P;DePasquale M;Ernst G;Huang Y;Kimos M;Kolobova A;Poslusney M;Wei H;Swinnen D;Montel F;Moureau F;Jigorel E;Schulze MED;Wood M;Barrow JC
A series of 8-hydroxy quinolines were identified as potent inhibitors of catechol O-methyltransferase (COMT) with selectivity for the membrane-bound form of the enzyme. Small substituents at the 7-position of the quinoline were found to increase metabolic stability without sacrificing potency. Compounds with good pharmacokinetics and brain penetration were identified and demonstrated in vivo modulation of dopamine metabolites in the brain. An X-ray co-crystal structure of compound 21 in the S-COMT active site shows chelation of the active site magnesium similar to catechol-based inhibitors. These compounds should prove useful for treatment of many neurological and psychiatric conditions associated with compromised cortical dopamine signaling.
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DOI:
10.1107/s0907444905036693
发表时间:
2006-01-01
影响因子:
2.2
作者:
Evans, P
通讯作者:
Evans, P
影响因子:
1.8
作者:
Mase, Toshiaki;Itoh, Takahiro
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DOI:
10.1107/s0907444909052925
发表时间:
2010-02
期刊:
Acta crystallographica. Section D, Biological crystallography
影响因子:
--
作者:
Adams PD;Afonine PV;Bunkóczi G;Chen VB;Davis IW;Echols N;Headd JJ;Hung LW;Kapral GJ;Grosse-Kunstleve RW;McCoy AJ;Moriarty NW;Oeffner R;Read RJ;Richardson DC;Richardson JS;Terwilliger TC;Zwart PH
通讯作者:
Zwart PH
影响因子:
56.9
作者:
AXELROD, J
通讯作者:
AXELROD, J
DOI:
10.1107/s0907444909042073
发表时间:
2010-01
期刊:
Acta crystallographica. Section D, Biological crystallography
影响因子:
--
作者:
Chen VB;Arendall WB 3rd;Headd JJ;Keedy DA;Immormino RM;Kapral GJ;Murray LW;Richardson JS;Richardson DC
通讯作者:
Richardson DC