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Bioorganic & Medicinal Chemistry Letters
|
May 18, 2007
Biaryl cannabinoid mimetics--synthesis and structure-activity relationship
Karin Worm, Q Jean Zhou, Gabriel J Stabley, et al.
Nucleic Acids Research
|
February 13, 2003
A Ca2+-induced mitochondrial permeability transition causes complete release of rat liver endonuclease G activity from its exclusive location within the mitochondrial intermembrane space. Identification of a novel endo-exonuclease activity residing within the mitochondrial matrix
Adrian M Davies, Stuart Hershman, Gabriel J Stabley, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 4, 2003
trans-3,4-dimethyl-4-(3-carboxamidophenyl)piperidines: a novel class of micro-selective opioid antagonists
Bertrand Le Bourdonnec, Serge Belanger, Joel A Cassel, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 5, 2004
(4-Carboxamido)phenylalanine is a surrogate for tyrosine in opioid receptor peptide ligands
Roland E Dolle, Mathieu Machaut, Blanca Martinez-Teipel, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 3, 2005
Arylacetamide kappa opioid receptor agonists with reduced cytochrome P450 2D6 inhibitory activity
Bertrand Le Bourdonnec, Christopher W Ajello, Pamela R Seida, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 3, 2005
Novel phenylamino acetamide derivatives as potent and selective kappa opioid receptor agonists
Guo-Hua Chu, Minghua Gu, Joel A Cassel, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 24, 2008
Sulfamoyl benzamides as novel CB2 cannabinoid receptor ligands
Karin Worm, Q Jean Zhou, Christopher T Saeui, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 4, 2009
Discovery of N-(3-(morpholinomethyl)-phenyl)-amides as potent and selective CB2 agonists
Karin Worm, Damian G Weaver, Rosalyn C Green, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 19, 2008
CB2 selective sulfamoyl benzamides: optimization of the amide functionality
Allan J Goodman, Christopher W Ajello, Karin Worm, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 9) with videos related to
Sort By:
Page
of 1
Bioorganic & Medicinal Chemistry Letters
|
May 18, 2007
Biaryl cannabinoid mimetics--synthesis and structure-activity relationship
Karin Worm, Q Jean Zhou, Gabriel J Stabley, et al.
Nucleic Acids Research
|
February 13, 2003
A Ca2+-induced mitochondrial permeability transition causes complete release of rat liver endonuclease G activity from its exclusive location within the mitochondrial intermembrane space. Identification of a novel endo-exonuclease activity residing within the mitochondrial matrix
Adrian M Davies, Stuart Hershman, Gabriel J Stabley, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 4, 2003
trans-3,4-dimethyl-4-(3-carboxamidophenyl)piperidines: a novel class of micro-selective opioid antagonists
Bertrand Le Bourdonnec, Serge Belanger, Joel A Cassel, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 5, 2004
(4-Carboxamido)phenylalanine is a surrogate for tyrosine in opioid receptor peptide ligands
Roland E Dolle, Mathieu Machaut, Blanca Martinez-Teipel, et al.
Bioorganic & Medicinal Chemistry Letters
|
May 3, 2005
Arylacetamide kappa opioid receptor agonists with reduced cytochrome P450 2D6 inhibitory activity
Bertrand Le Bourdonnec, Christopher W Ajello, Pamela R Seida, et al.
Bioorganic & Medicinal Chemistry Letters
|
November 3, 2005
Novel phenylamino acetamide derivatives as potent and selective kappa opioid receptor agonists
Guo-Hua Chu, Minghua Gu, Joel A Cassel, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 24, 2008
Sulfamoyl benzamides as novel CB2 cannabinoid receptor ligands
Karin Worm, Q Jean Zhou, Christopher T Saeui, et al.
Bioorganic & Medicinal Chemistry Letters
|
August 4, 2009
Discovery of N-(3-(morpholinomethyl)-phenyl)-amides as potent and selective CB2 agonists
Karin Worm, Damian G Weaver, Rosalyn C Green, et al.
Bioorganic & Medicinal Chemistry Letters
|
December 19, 2008
CB2 selective sulfamoyl benzamides: optimization of the amide functionality
Allan J Goodman, Christopher W Ajello, Karin Worm, et al.
Page
of 1