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Albert J Robichaud

Showing results (21-30 of 54) with videos related to

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Journal of Medicinal Chemistry|December 9, 2009
Design and synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human beta-secretase (BACE1) inhibitorsMichael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Bioorganic & Medicinal Chemistry Letters|April 7, 2009
1-Sulfonylindazoles as potent and selective 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Bioorganic & Medicinal Chemistry Letters|May 13, 2009
Identification of a novel series of 3-piperidinyl-5-sulfonylindazoles as potent 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Journal of Medicinal Chemistry|February 23, 2010
5-Cyclic amine-3-arylsulfonylindazoles as novel 5-HT6 receptor antagonistsSimon N Haydar, Heedong Yun, Patrick M Andrae, et al.
Bioorganic & Medicinal Chemistry|January 5, 2010
Di-substituted pyridinyl aminohydantoins as potent and highly selective human beta-secretase (BACE1) inhibitorsMichael S Malamas, Keith Barnes, Matthew Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|January 21, 2009
Identification of a series of benzoxazoles as potent 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Bioorganic & Medicinal Chemistry Letters|June 28, 2008
A regiospecific synthesis of a series of 1-sulfonyl azepinoindoles as potent 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Bioorganic & Medicinal Chemistry Letters|March 6, 2010
Pyridinyl aminohydantoins as small molecule BACE1 inhibitorsPing Zhou, Yanfang Li, Yi Fan, et al.
Journal of Medicinal Chemistry|February 9, 2012
2-(Pyrrolidin-1-yl)ethyl-3,4-dihydroisoquinolin-1(2H)-one derivatives as potent and selective histamine-3 receptor antagonistsDahui Zhou, Jonathan L Gross, Adedayo B Adedoyin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 1, 2013
The major brain cholesterol metabolite 24(S)-hydroxycholesterol is a potent allosteric modulator of N-methyl-D-aspartate receptorsSteven M Paul, James J Doherty, Albert J Robichaud, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
Journal of Medicinal Chemistry|December 9, 2009
Design and synthesis of 5,5'-disubstituted aminohydantoins as potent and selective human beta-secretase (BACE1) inhibitorsMichael S Malamas, Jim Erdei, Iwan Gunawan, et al.
Bioorganic & Medicinal Chemistry Letters|April 7, 2009
1-Sulfonylindazoles as potent and selective 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Bioorganic & Medicinal Chemistry Letters|May 13, 2009
Identification of a novel series of 3-piperidinyl-5-sulfonylindazoles as potent 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Journal of Medicinal Chemistry|February 23, 2010
5-Cyclic amine-3-arylsulfonylindazoles as novel 5-HT6 receptor antagonistsSimon N Haydar, Heedong Yun, Patrick M Andrae, et al.
Bioorganic & Medicinal Chemistry|January 5, 2010
Di-substituted pyridinyl aminohydantoins as potent and highly selective human beta-secretase (BACE1) inhibitorsMichael S Malamas, Keith Barnes, Matthew Johnson, et al.
Bioorganic & Medicinal Chemistry Letters|January 21, 2009
Identification of a series of benzoxazoles as potent 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Bioorganic & Medicinal Chemistry Letters|June 28, 2008
A regiospecific synthesis of a series of 1-sulfonyl azepinoindoles as potent 5-HT6 ligandsKevin G Liu, Jennifer R Lo, Thomas A Comery, et al.
Bioorganic & Medicinal Chemistry Letters|March 6, 2010
Pyridinyl aminohydantoins as small molecule BACE1 inhibitorsPing Zhou, Yanfang Li, Yi Fan, et al.
Journal of Medicinal Chemistry|February 9, 2012
2-(Pyrrolidin-1-yl)ethyl-3,4-dihydroisoquinolin-1(2H)-one derivatives as potent and selective histamine-3 receptor antagonistsDahui Zhou, Jonathan L Gross, Adedayo B Adedoyin, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|November 1, 2013
The major brain cholesterol metabolite 24(S)-hydroxycholesterol is a potent allosteric modulator of N-methyl-D-aspartate receptorsSteven M Paul, James J Doherty, Albert J Robichaud, et al.
Pageof 6