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Organic & Biomolecular Chemistry
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April 20, 2011
Synthesis and evaluation of 1,2,4-methyltriazines as mGluR5 antagonists
Jeremy P Olson, Moses G Gichinga, Elizabeth Butala, et al.
Journal of Medicinal Chemistry
|
August 28, 2014
Diarylureas as allosteric modulators of the cannabinoid CB1 receptor: structure-activity relationship studies on 1-(4-chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea (PSNCBAM-1)
Nadezhda German, Ann M Decker, Brian P Gilmour, et al.
ACS Medicinal Chemistry Letters
|
April 24, 2012
Synthesis and Evaluation of Metabotropic Glutamate Receptor Subtype 5 Antagonists Based on Fenobam()
Moses G Gichinga, Jeremy P Olson, Elizabeth Butala, et al.
Journal of Medicinal Chemistry
|
August 15, 2013
Substituted tetrahydroisoquinolines as selective antagonists for the orexin 1 receptor
David A Perrey, Nadezhda A German, Brian P Gilmour, et al.
Bioorganic & Medicinal Chemistry
|
July 29, 2015
The importance of the 6- and 7-positions of tetrahydroisoquinolines as selective antagonists for the orexin 1 receptor
David A Perrey, Ann M Decker, Jun-Xu Li, et al.
Journal of Medicinal Chemistry
|
June 16, 2007
Synthesis and pharmacological evaluation of phenylethynyl[1,2,4]methyltriazines as analogues of 3-methyl-6-(phenylethynyl)pyridine
F Ivy Carroll, Sharadsrikar V Kotturi, Hernán A Navarro, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 18, 2015
The amide linker in nonpeptide neurotensin receptor ligands plays a key role in calcium signaling at the neurotensin receptor type 2
James B Thomas, Angela M Giddings, Srinivas Olepu, et al.
ACS Chemical Neuroscience
|
May 6, 2014
Synthesis, pharmacological characterization, and structure-activity relationship studies of small molecular agonists for the orphan GPR88 receptor
Chunyang Jin, Ann M Decker, Xi-Ping Huang, et al.
Bioorganic & Medicinal Chemistry
|
November 3, 2007
A new synthesis of the ORL-1 antagonist 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidinyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397) and activity in a calcium mobilization assay
Emilie D Smith, N Ariane Vinson, Desong Zhong, et al.
ACS Chemical Neuroscience
|
February 3, 2015
Effect of 1-substitution on tetrahydroisoquinolines as selective antagonists for the orexin-1 receptor
David A Perrey, Nadezhda A German, Ann M Decker, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 26) with videos related to
Sort By:
Page
of 3
Organic & Biomolecular Chemistry
|
April 20, 2011
Synthesis and evaluation of 1,2,4-methyltriazines as mGluR5 antagonists
Jeremy P Olson, Moses G Gichinga, Elizabeth Butala, et al.
Journal of Medicinal Chemistry
|
August 28, 2014
Diarylureas as allosteric modulators of the cannabinoid CB1 receptor: structure-activity relationship studies on 1-(4-chlorophenyl)-3-{3-[6-(pyrrolidin-1-yl)pyridin-2-yl]phenyl}urea (PSNCBAM-1)
Nadezhda German, Ann M Decker, Brian P Gilmour, et al.
ACS Medicinal Chemistry Letters
|
April 24, 2012
Synthesis and Evaluation of Metabotropic Glutamate Receptor Subtype 5 Antagonists Based on Fenobam()
Moses G Gichinga, Jeremy P Olson, Elizabeth Butala, et al.
Journal of Medicinal Chemistry
|
August 15, 2013
Substituted tetrahydroisoquinolines as selective antagonists for the orexin 1 receptor
David A Perrey, Nadezhda A German, Brian P Gilmour, et al.
Bioorganic & Medicinal Chemistry
|
July 29, 2015
The importance of the 6- and 7-positions of tetrahydroisoquinolines as selective antagonists for the orexin 1 receptor
David A Perrey, Ann M Decker, Jun-Xu Li, et al.
Journal of Medicinal Chemistry
|
June 16, 2007
Synthesis and pharmacological evaluation of phenylethynyl[1,2,4]methyltriazines as analogues of 3-methyl-6-(phenylethynyl)pyridine
F Ivy Carroll, Sharadsrikar V Kotturi, Hernán A Navarro, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 18, 2015
The amide linker in nonpeptide neurotensin receptor ligands plays a key role in calcium signaling at the neurotensin receptor type 2
James B Thomas, Angela M Giddings, Srinivas Olepu, et al.
ACS Chemical Neuroscience
|
May 6, 2014
Synthesis, pharmacological characterization, and structure-activity relationship studies of small molecular agonists for the orphan GPR88 receptor
Chunyang Jin, Ann M Decker, Xi-Ping Huang, et al.
Bioorganic & Medicinal Chemistry
|
November 3, 2007
A new synthesis of the ORL-1 antagonist 1-[(3R,4R)-1-cyclooctylmethyl-3-hydroxymethyl-4-piperidinyl]-3-ethyl-1,3-dihydro-2H-benzimidazol-2-one (J-113397) and activity in a calcium mobilization assay
Emilie D Smith, N Ariane Vinson, Desong Zhong, et al.
ACS Chemical Neuroscience
|
February 3, 2015
Effect of 1-substitution on tetrahydroisoquinolines as selective antagonists for the orexin-1 receptor
David A Perrey, Nadezhda A German, Ann M Decker, et al.
Page
of 3