THE DISCOVERY OF AN UNUSUALLY SELECTIVE AND NOVEL COCAINE ANALOG - DIFLUOROPINE - SYNTHESIS AND INHIBITION OF BINDING AT COCAINE RECOGNITION SITES

被引:98
作者
MELTZER, PC
LIANG, AY
MADRAS, BK
机构
[1] HARVARD UNIV, SCH MED, DEPT PSYCHIAT, SOUTHBOROUGH, MA 01772 USA
[2] NEW ENGLAND REG PRIMATE RES CTR, SOUTHBOROUGH, MA 01772 USA
关键词
D O I
10.1021/jm00039a014
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Cocaine is a stimulant drug with a high abuse liability. Although it inhibits several monamine transporters in the mammalian brain, its primary mechanism of action has been ascribed to its inhibition of the dopamine transporter. The synthesis, characterization, and receptor binding properties of all eight isomers of a unique tropane analog, 2-carbomethoxy-3-[bis(4-fluorophenyl)methoxy]tropane is described. In addition, we report that the S-enantiomer, (S)-(+)-2 beta-carbomethoxy-3 alpha-[bis(4-fluorophenyl)methoxy]tropane, Difluoropine, is a potent (IC50 10.9 nM) and selective (324 [DA/5HT]) ligand for the dopamine transporter.
引用
收藏
页码:2001 / 2010
页数:10
相关论文
共 47 条
[21]   SEVERE DEPLETION OF COCAINE RECOGNITION SITES ASSOCIATED WITH THE DOPAMINE TRANSPORTER IN PARKINSONS-DISEASED STRIATUM [J].
KAUFMAN, MJ ;
MADRAS, BK .
SYNAPSE, 1991, 9 (01) :43-49
[22]   DISTRIBUTION OF COCAINE RECOGNITION SITES IN MONKEY BRAIN .1. INVITRO AUTORADIOGRAPHY WITH [H-3] CFT [J].
KAUFMAN, MJ ;
SPEALMAN, RD ;
MADRAS, BK .
SYNAPSE, 1991, 9 (03) :177-187
[23]  
KENNEDY LT, 1983, J NEUROCHEM, V34, P1137
[24]   UNEVEN PATTERN OF DOPAMINE LOSS IN THE STRIATUM OF PATIENTS WITH IDIOPATHIC PARKINSONS-DISEASE - PATHOPHYSIOLOGIC AND CLINICAL IMPLICATIONS [J].
KISH, SJ ;
SHANNAK, K ;
HORNYKIEWICZ, O .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (14) :876-880
[25]   DOPAMINE TRANSPORTER SITE-DIRECTED MUTATIONS DIFFERENTIALLY ALTER SUBSTRATE TRANSPORT AND COCAINE BINDING [J].
KITAYAMA, S ;
SHIMADA, S ;
XU, HX ;
MARKHAM, L ;
DONOVAN, DM ;
UHL, GR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (16) :7782-7785
[26]   STRUCTURE - ACTIVITY RELATIONSHIP STUDIES OF COCAINE - REPLACEMENT OF THE C-2 ESTER GROUP BY VINYL ARGUES AGAINST H-BONDING AND PROVIDES AN ESTERASE-RESISTANT, HIGH-AFFINITY COCAINE ANALOG [J].
KOZIKOWSKI, AP ;
ROBERTI, M ;
XIANG, L ;
BERGMANN, JS ;
CALLAHAN, PM ;
CUNNINGHAM, KA ;
JOHNSON, KM .
JOURNAL OF MEDICINAL CHEMISTRY, 1992, 35 (25) :4764-4766
[27]   SAR OF COCAINE - FURTHER EXPLORATION OF STRUCTURAL VARIATIONS AT THE C-2 CENTER PROVIDES COMPOUNDS OF SUBNANOMOLAR BINDING POTENCY [J].
KOZIKOWSKI, AP ;
ROBERTI, M ;
JOHNSON, KM ;
BERGMANN, JS ;
BALL, RG .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1993, 3 (06) :1327-1332
[28]   THE DOPAMINE HYPOTHESIS OF THE REINFORCING PROPERTIES OF COCAINE [J].
KUHAR, MJ ;
RITZ, MC ;
BOJA, JW .
TRENDS IN NEUROSCIENCES, 1991, 14 (07) :299-302
[29]   A PRACTICAL SYNTHESIS OF (+)-COCAINE [J].
LEWIN, AH ;
NASEREE, T ;
CARROLL, FI .
JOURNAL OF HETEROCYCLIC CHEMISTRY, 1987, 24 (01) :19-21
[30]  
MADRAS BK, 1989, J PHARMACOL EXP THER, V251, P131