Neurosteroid analogues. 17. Inverted binding orientations of androsterone enantiomers at the steroid potentiation site on γ-aminobutyric acid type A receptors
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Anticonvulsant potencies of the enantiomers of the neurosteroids androsterone and etiocholanolone exceed those of the natural formsNeurosteroids, stress and depression: potential therapeutic opportunities.Comparison of Steroid Modulation of Spontaneous Inhibitory Postsynaptic Currents in Cultured Hippocampal Neurons and Steady-State Single-Channel Currents from Heterologously Expressed α1β2γ2L GABA(A) Receptors.Neurosteroid analogues. 18. Structure-activity studies of ent-steroid potentiators of γ-aminobutyric acid type A receptors and comparison of their activities with those of alphaxalone and allopregnanolone.Structural requirements of steroidal agonists of transient receptor potential melastatin 3 (TRPM3) cation channels.Synthesis and pharmacological evaluation of neurosteroid photoaffinity ligands.
P2860
Neurosteroid analogues. 17. Inverted binding orientations of androsterone enantiomers at the steroid potentiation site on γ-aminobutyric acid type A receptors
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2012 nî lūn-bûn
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2012年の論文
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2012年論文
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2012年論文
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2012年論文
@zh-hk
2012年論文
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2012年論文
@zh-tw
2012年论文
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2012年论文
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2012年论文
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name
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@ast
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@en
type
label
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@ast
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@en
prefLabel
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@ast
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@en
P2093
P2860
P356
P1476
Neurosteroid analogues. 17. In ...... obutyric acid type A receptors
@en
P2093
Alex S Evers
Amanda Taylor
Brad D Manion
Charles F Zorumski
Douglas F Covey
John Bracamontes
Joseph H Steinbach
Kathiresan Krishnan
P2860
P304
P356
10.1021/JM2014925
P407
P577
2012-01-18T00:00:00Z