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Albert J Robichaud

Showing results (11-20 of 54) with videos related to

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Bioorganic & Medicinal Chemistry Letters|February 17, 2005
4-(2-Aminoethoxy)-N-(phenylsulfonyl)indoles as novel 5-HT6 receptor ligandsPing Zhou, Yinfa Yan, Ronald Bernotas, et al.
Bioorganic & Medicinal Chemistry Letters|March 18, 2003
Novel, highly potent, selective 5-HT2A/D2 receptor antagonists as potential atypical antipsychoticsTaekyu Lee, Albert J Robichaud, Kristopher E Boyle, et al.
Journal of Medicinal Chemistry|June 22, 2011
Tricyclic thiazolopyrazole derivatives as metabotropic glutamate receptor 4 positive allosteric modulatorsSang-Phyo Hong, Kevin G Liu, Gil Ma, et al.
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
3-(Arylsulfonyl)-1-(azacyclyl)-1H-indoles are 5-HT(6) receptor modulatorsRonald C Bernotas, Schuyler Antane, Rajesh Shenoy, et al.
Journal of Neuroscience Research|August 27, 2015
Rescue of deficient amygdala tonic γ-aminobutyric acidergic currents in the Fmr-/y mouse model of fragile X syndrome by a novel γ-aminobutyric acid type A receptor-positive allosteric modulatorBrandon S Martin, Gabriel Martinez-Botella, Carlos M Loya, et al.
Epilepsy & Behavior : E&B|January 23, 2017
The synthetic neuroactive steroid SGE-516 reduces status epilepticus and neuronal cell death in a rat model of soman intoxicationAlison L Althaus, Hilary S McCarren, Aymen Alqazzaz, et al.
Bioorganic & Medicinal Chemistry Letters|September 1, 2007
Thiophene substituted acylguanidines as BACE1 inhibitorsWilliam F Fobare, William R Solvibile, Albert J Robichaud, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2011
Pyrrolidin-3-yl-N-methylbenzamides as potent histamine 3 receptor antagonistsDahui Zhou, Jonathan L Gross, Jean Y Sze, et al.
Bioorganic & Medicinal Chemistry Letters|November 4, 2009
1-(2-Aminoethyl)-3-(arylsulfonyl)-1H-pyrrolopyridines are 5-HT(6) receptor ligandsRonald C Bernotas, Schuyler A Antane, Steven E Lenicek, et al.
Journal of Medicinal Chemistry|September 18, 2009
Aminoimidazoles as potent and selective human beta-secretase (BACE1) inhibitorsMichael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Pageof 6

Showing results (11-20 of 54) with videos related to

Sort By:
Pageof 6
Bioorganic & Medicinal Chemistry Letters|February 17, 2005
4-(2-Aminoethoxy)-N-(phenylsulfonyl)indoles as novel 5-HT6 receptor ligandsPing Zhou, Yinfa Yan, Ronald Bernotas, et al.
Bioorganic & Medicinal Chemistry Letters|March 18, 2003
Novel, highly potent, selective 5-HT2A/D2 receptor antagonists as potential atypical antipsychoticsTaekyu Lee, Albert J Robichaud, Kristopher E Boyle, et al.
Journal of Medicinal Chemistry|June 22, 2011
Tricyclic thiazolopyrazole derivatives as metabotropic glutamate receptor 4 positive allosteric modulatorsSang-Phyo Hong, Kevin G Liu, Gil Ma, et al.
Bioorganic & Medicinal Chemistry Letters|February 9, 2010
3-(Arylsulfonyl)-1-(azacyclyl)-1H-indoles are 5-HT(6) receptor modulatorsRonald C Bernotas, Schuyler Antane, Rajesh Shenoy, et al.
Journal of Neuroscience Research|August 27, 2015
Rescue of deficient amygdala tonic γ-aminobutyric acidergic currents in the Fmr-/y mouse model of fragile X syndrome by a novel γ-aminobutyric acid type A receptor-positive allosteric modulatorBrandon S Martin, Gabriel Martinez-Botella, Carlos M Loya, et al.
Epilepsy & Behavior : E&B|January 23, 2017
The synthetic neuroactive steroid SGE-516 reduces status epilepticus and neuronal cell death in a rat model of soman intoxicationAlison L Althaus, Hilary S McCarren, Aymen Alqazzaz, et al.
Bioorganic & Medicinal Chemistry Letters|September 1, 2007
Thiophene substituted acylguanidines as BACE1 inhibitorsWilliam F Fobare, William R Solvibile, Albert J Robichaud, et al.
Bioorganic & Medicinal Chemistry Letters|August 17, 2011
Pyrrolidin-3-yl-N-methylbenzamides as potent histamine 3 receptor antagonistsDahui Zhou, Jonathan L Gross, Jean Y Sze, et al.
Bioorganic & Medicinal Chemistry Letters|November 4, 2009
1-(2-Aminoethyl)-3-(arylsulfonyl)-1H-pyrrolopyridines are 5-HT(6) receptor ligandsRonald C Bernotas, Schuyler A Antane, Steven E Lenicek, et al.
Journal of Medicinal Chemistry|September 18, 2009
Aminoimidazoles as potent and selective human beta-secretase (BACE1) inhibitorsMichael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Pageof 6