New Synthesis of Tic-Hydantoins Sigma-1 Ligands and Pharmacological Evaluation on Cocaine-Induced Stimulant Effects
被引:6
作者:
Toussaint, M.
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机构:
CNRS, UMR 8161, F-59021 Lille, France
Univ Lille Nord France, F-59000 Lille, FranceCNRS, UMR 8161, F-59021 Lille, France
Toussaint, M.
[1
,2
]
Debreu-Fontaine, M. -A.
论文数: 0引用数: 0
h-index: 0
机构:
CNRS, UMR 8161, F-59021 Lille, France
Univ Lille Nord France, F-59000 Lille, France
UFR Pharmacie, EA 4481GRIIOT, UDSL, F-59000 Lille, FranceCNRS, UMR 8161, F-59021 Lille, France
Debreu-Fontaine, M. -A.
[1
,2
,3
]
Maurice, T.
论文数: 0引用数: 0
h-index: 0
机构:
INSERM, U710, F-34095 Montpellier, France
Univ Montpellier 2, F-34095 Montpellier, France
EPHE, F-75017 Paris, FranceCNRS, UMR 8161, F-59021 Lille, France
Maurice, T.
[4
,5
,6
]
Melnyk, P.
论文数: 0引用数: 0
h-index: 0
机构:
CNRS, UMR 8161, F-59021 Lille, France
Univ Lille Nord France, F-59000 Lille, France
UFR Pharmacie, EA 4481GRIIOT, UDSL, F-59000 Lille, FranceCNRS, UMR 8161, F-59021 Lille, France
Melnyk, P.
[1
,2
,3
]
机构:
[1] CNRS, UMR 8161, F-59021 Lille, France
[2] Univ Lille Nord France, F-59000 Lille, France
[3] UFR Pharmacie, EA 4481GRIIOT, UDSL, F-59000 Lille, France
[4] INSERM, U710, F-34095 Montpellier, France
[5] Univ Montpellier 2, F-34095 Montpellier, France
Activation of the newly identified sigma(1) chaperone protein is involved in several aspects of the psychostimulant and addictive effects of cocaine. The development of ligands that selectively target the sigma(1) protein may lead to putative potent anti-cocaine agents. We report here a new and more convergent synthetic pathway to amino side chain substituted hydantoins. Twenty new analogs of our lead compound were synthesized. None of them showed better in vitro affinity for sigma(1) receptor than our lead compound. Nevertheless, three of them, obtained as racemates, showed high in vitro affinity and selectivity for sigma(1) receptor. A preliminary in vivo evaluation of their pharmacological activity identified compound (22) under bar as one that increases cocaine-induced locomotor stimulation and therefore acts as a potential efficient sigma(1) agonist.
机构:
University of Pennsylvania, Treatment Research Center, Philadelphia, PA 19104University of Pennsylvania, Treatment Research Center, Philadelphia, PA 19104
机构:
University of Pennsylvania, Treatment Research Center, Philadelphia, PA 19104University of Pennsylvania, Treatment Research Center, Philadelphia, PA 19104