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Enantioselectivity of cocaine recognition sites: binding of (1S)- and (1R)-2 beta-carbomethoxy-3 beta-(4-iodophenyl)tropane (beta-CIT) to monoamine transporters.

作者信息

Wang S, Gao Y, Laruelle M, Baldwin R M, Scanley B E, Innis R B, Neumeyer J L

机构信息

Section of Medicinal Chemistry, Northeastern University, Boston, Massachusetts 02115.

出版信息

J Med Chem. 1993 Jun 25;36(13):1914-7. doi: 10.1021/jm00065a014.

DOI:10.1021/jm00065a014
PMID:8515428
Abstract
摘要

相似文献

1
Enantioselectivity of cocaine recognition sites: binding of (1S)- and (1R)-2 beta-carbomethoxy-3 beta-(4-iodophenyl)tropane (beta-CIT) to monoamine transporters.可卡因识别位点的对映选择性:(1S)-和(1R)-2β-甲氧羰基-3β-(4-碘苯基)托烷(β-CIT)与单胺转运体的结合
J Med Chem. 1993 Jun 25;36(13):1914-7. doi: 10.1021/jm00065a014.
2
Binding of the cocaine analog 2 beta-carbomethoxy-3 beta-(4-[125I]iodophenyl)tropane to serotonin and dopamine transporters: different ionic requirements for substrate and 2 beta-carbomethoxy-3 beta-(4-[125I]iodophenyl)tropane binding.可卡因类似物2β-甲氧羰基-3β-(4-[¹²⁵I]碘苯基)托烷与5-羟色胺及多巴胺转运体的结合:底物与2β-甲氧羰基-3β-(4-[¹²⁵I]碘苯基)托烷结合的不同离子需求
Mol Pharmacol. 1993 Feb;43(2):264-70.
3
N-substituted analogs of 2 beta-carbomethoxy-3 beta- (4'-iodophenyl)tropane (beta-CIT) with selective affinity to dopamine or serotonin transporters in rat forebrain.2β-甲氧羰基-3β-(4'-碘苯基)托烷(β-CIT)的N-取代类似物对大鼠前脑多巴胺或5-羟色胺转运体具有选择性亲和力。
J Med Chem. 1996 Jan 19;39(2):543-8. doi: 10.1021/jm9505324.
4
[3H]beta-CIT: a radioligand for dopamine transporters in rat brain tissue.[3H]β-羧基-3,4-二氢-2β-(4-氯苯基)托品:大鼠脑组织中多巴胺转运体的放射性配体。
Eur J Pharmacol. 1999 Dec 3;385(2-3):291-4. doi: 10.1016/s0014-2999(99)00695-0.
5
Assessment of affinities of beta-CIT, beta-CIT-FE, and beta-CIT-FP for monoamine transporters permanently expressed in cell lines.评估β-CIT、β-CIT-FE和β-CIT-FP对在细胞系中稳定表达的单胺转运体的亲和力。
Nucl Med Biol. 1998 Jan;25(1):53-8. doi: 10.1016/s0969-8051(97)00156-x.
6
Methyl 3 beta-(4-[125I]iodophenyl)tropane-2 beta-carboxylate in vitro binding to dopamine and serotonin transporters under "physiological" conditions.3β-(4-[¹²⁵I]碘苯基)托烷-2β-羧酸甲酯在“生理”条件下与多巴胺和5-羟色胺转运体的体外结合
J Neurochem. 1994 Mar;62(3):978-86. doi: 10.1046/j.1471-4159.1994.62030978.x.
7
3-Aryl-2-(3'-substituted-1',2',4'-oxadiazol-5'-yl)tropane analogues of cocaine: affinities at the cocaine binding site at the dopamine, serotonin, and norepinephrine transporters.可卡因的3-芳基-2-(3'-取代-1',2',4'-恶二唑-5'-基)托烷类似物:在多巴胺、5-羟色胺和去甲肾上腺素转运体的可卡因结合位点的亲和力
J Med Chem. 1993 Oct 1;36(20):2886-90. doi: 10.1021/jm00072a007.
8
N-omega-fluoroalkyl analogs of (1R)-2 beta-carbomethoxy-3 beta-(4-iodophenyl)-tropane (beta-CIT): radiotracers for positron emission tomography and single photon emission computed tomography imaging of dopamine transporters.(1R)-2β-甲氧羰基-3β-(4-碘苯基)-托烷(β-CIT)的N-ω-氟烷基类似物:用于多巴胺转运体正电子发射断层扫描和单光子发射计算机断层扫描成像的放射性示踪剂。
J Med Chem. 1994 May 27;37(11):1558-61. doi: 10.1021/jm00037a004.
9
Studies of the biogenic amine transporters. IV. Demonstration of a multiplicity of binding sites in rat caudate membranes for the cocaine analog [125I]RTI-55.生物胺转运体的研究。IV。大鼠尾状核膜中可卡因类似物[125I]RTI - 55存在多个结合位点的证明。
J Pharmacol Exp Ther. 1994 Jul;270(1):296-309.
10
Comparative in vivo study of iodine-123-labeled beta-CIT and nor-beta-CIT binding to serotonin transporters in rat brain.碘-123标记的β-CIT和去甲β-CIT与大鼠脑内5-羟色胺转运体结合的体内比较研究。
Synapse. 1999 Oct;34(1):77-80. doi: 10.1002/(SICI)1098-2396(199910)34:1<77::AID-SYN9>3.0.CO;2-Y.

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