DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
about
Recent advances in ligand-based drug design: relevance and utility of the conformationally sampled pharmacophore approach.Studies of new fused benzazepine as selective dopamine D3 receptor antagonists using 3D-QSAR, molecular docking and molecular dynamicsSingular value decomposition analysis of the torsional angles of dopamine reuptake inhibitor GBR 12909 analogs: effect of force field and charges.Molecular docking and 3D-QSAR studies on the glucocorticoid receptor antagonistic activity of hydroxylated polychlorinated biphenyls.
P2860
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
description
2006 nî lūn-bûn
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2006年の論文
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2006年学术文章
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2006年学术文章
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2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
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2006年學術文章
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name
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@ast
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@en
type
label
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@ast
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@en
prefLabel
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@ast
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@en
P2093
P2860
P1476
DAT/SERT selectivity of flexible GBR 12909 analogs modeled using 3D-QSAR methods.
@en
P2093
Arthur E Jacobson
Carol A Venanzi
Christina M Dersch
David Lewis
Dorota Matecka
Elisabeth Greiner
Kathleen M Gilbert
Kenner C Rice
Richard B Rothman
Terrence L Boos
P2860
P304
P356
10.1016/J.BMC.2006.09.070
P407
P577
2006-10-01T00:00:00Z