Enaminones-versatile therapeutic pharmacophores. Further advances

被引:126
作者
Eddington, ND
Cox, DS
Roberts, RR
Stables, JP
Powell, CB
Scott, KR [1 ]
机构
[1] Howard Univ, Sch Pharm, Dept Pharmaceut Sci, Washington, DC 20059 USA
[2] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[3] 3M Co, Corp Res, Sci Res Lab, 3M Ctr, St Paul, MN 55144 USA
[4] NINDS, Epilepsy Branch, Div Convuls Dev & Neuromuscular Disorders, Bethesda, MD 20892 USA
[5] Emory Univ, Dept Chem, Atlanta, GA 30054 USA
关键词
D O I
10.2174/0929867003375092
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
Enaminones, enamines of beta-dicarbonyl compounds, have been know for many years. In our initial account (Current Med. Chem. 1994, 1, 159-175), we reported on the anticonvulsant activity of a series of enaminones, notably methyl 4-[(p-chlorophenyl)amino]-6-methyl-2-oxo-cyclohex-3-en-1-oate, 9a (R=CH3, R-1=4-Cl), which, in animal tests, compared favorably to phenytoin and carbamazepine. Since that time, further research in our laboratory and other laboratories have expanded the therapeutic potential of these compounds. In addition to new anticonvulsant derivatives, we have uncovered a novel brain transport mechanism for the enaminones and developed a preliminary regression model for further synthetic direction. These topics will each be presented and elaborated.
引用
收藏
页码:417 / 436
页数:20
相关论文
共 77 条
[2]   BOVINE BRAIN MICROVESSEL ENDOTHELIAL-CELL MONOLAYERS AS A MODEL SYSTEM FOR THE BLOOD-BRAIN-BARRIER [J].
AUDUS, KL ;
BORCHARDT, RT .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 507 :9-18
[3]   CHARACTERIZATION OF AN INVITRO BLOOD-BRAIN-BARRIER MODEL SYSTEM FOR STUDYING DRUG TRANSPORT AND METABOLISM [J].
AUDUS, KL ;
BORCHARDT, RT .
PHARMACEUTICAL RESEARCH, 1986, 3 (02) :81-87
[4]   PEPTIDES AND THE BLOOD-BRAIN-BARRIER - LIPOPHILICITY AS A PREDICTOR OF PERMEABILITY [J].
BANKS, WA ;
KASTIN, AJ .
BRAIN RESEARCH BULLETIN, 1985, 15 (03) :287-292
[5]   Chromatographic indexes on immobilized artificial membranes for local anesthetics: Relationships with activity data on closed sodium channels [J].
Barbato, F ;
La Rotonda, MI ;
Quaglia, F .
PHARMACEUTICAL RESEARCH, 1997, 14 (12) :1699-1705
[6]   Compared reactivity of heterocyclic enaminones: Photochemical and palladium catalyzed synthesis of 6,7,8,9-tetrahydro-5H-pyrido[3,2-b]ind-9-ones [J].
Blache, Y ;
SinibaldiTroin, ME ;
Voldoire, A ;
Chavignon, O ;
Gramain, JC ;
Teulade, JC ;
Chapat, JP .
JOURNAL OF ORGANIC CHEMISTRY, 1997, 62 (24) :8553-8556
[7]   Effects of log P and phenyl ring conformation on the binding of 5-phenylhydantoins to the voltage-dependent sodium channel [J].
Brown, ML ;
Brown, GB ;
Brouillette, WJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (04) :602-607
[8]   Comparative molecular field analysis of hydantoin binding to the neuronal voltage-dependent sodium channel [J].
Brown, ML ;
Zha, CC ;
Van Dyke, CC ;
Brown, GB ;
Brouillette, WJ .
JOURNAL OF MEDICINAL CHEMISTRY, 1999, 42 (09) :1537-1545
[9]   Aroyl(aminoacyl)pyrroles, a new class of anticonvulsant agents [J].
Carson, JR ;
Carmosin, RJ ;
Pitis, PM ;
Vaught, JL ;
Almond, HR ;
Stables, JP ;
Wolf, HH ;
Swinyard, EA ;
White, HS .
JOURNAL OF MEDICINAL CHEMISTRY, 1997, 40 (11) :1578-1584