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Journal of Medicinal Chemistry
|
July 19, 1996
N-heteroaryl-2-phenyl-3-(benzyloxy)piperidines: a novel class of potent orally active human NK1 antagonists
T Ladduwahetty, R Baker, M A Cascieri, et al.
Journal of Medicinal Chemistry
|
October 29, 2000
Discovery of a potent, orally bioavailable beta(3) adrenergic receptor agonist, (R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4 -[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide
R J Mathvink, J S Tolman, D Chitty, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 11, 2000
Synthesis and SAR of benzyl and phenoxymethylene oxadiazole benzenesulfonamides as selective beta3 adrenergic receptor agonist antiobesity agents
T Biftu, D D Feng, G B Liang, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 14, 1999
Human beta3 adrenergic receptor agonists containing imidazolidinone and imidazolone benzenesulfonamides
E M Naylor, E R Parmee, V J Colandrea, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 14, 1999
Human beta3 adrenergic receptor agonists containing cyclic ureidobenzenesulfonamides
E R Parmee, E M Naylor, L Perkins, et al.
Nature Genetics
|
September 6, 2000
Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass
A S Chen, D J Marsh, M E Trumbauer, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
3-Pyridyloxypropanolamine agonists of the beta 3 adrenergic receptor with improved pharmacokinetic properties
A E Weber, H O Ok, R F Alvaro, et al.
Journal of Medicinal Chemistry
|
March 29, 2000
Phosphorylated morpholine acetal human neurokinin-1 receptor antagonists as water-soluble prodrugs
J J Hale, S G Mills, M MacCoss, et al.
The Journal of Clinical Investigation
|
June 17, 1998
A selective human beta3 adrenergic receptor agonist increases metabolic rate in rhesus monkeys
M H Fisher, A M Amend, T J Bach, et al.
Journal of Medicinal Chemistry
|
April 13, 2001
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptor
R J DeVita, T F Walsh, J R Young, et al.
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Search research articles
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Showing results (101-110 of 110) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 110 results.
Journal of Medicinal Chemistry
|
July 19, 1996
N-heteroaryl-2-phenyl-3-(benzyloxy)piperidines: a novel class of potent orally active human NK1 antagonists
T Ladduwahetty, R Baker, M A Cascieri, et al.
Journal of Medicinal Chemistry
|
October 29, 2000
Discovery of a potent, orally bioavailable beta(3) adrenergic receptor agonist, (R)-N-[4-[2-[[2-hydroxy-2-(3-pyridinyl)ethyl]amino]ethyl]phenyl]-4-[4 -[4-(trifluoromethyl)phenyl]thiazol-2-yl]benzenesulfonamide
R J Mathvink, J S Tolman, D Chitty, et al.
Bioorganic & Medicinal Chemistry Letters
|
July 11, 2000
Synthesis and SAR of benzyl and phenoxymethylene oxadiazole benzenesulfonamides as selective beta3 adrenergic receptor agonist antiobesity agents
T Biftu, D D Feng, G B Liang, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 14, 1999
Human beta3 adrenergic receptor agonists containing imidazolidinone and imidazolone benzenesulfonamides
E M Naylor, E R Parmee, V J Colandrea, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 14, 1999
Human beta3 adrenergic receptor agonists containing cyclic ureidobenzenesulfonamides
E R Parmee, E M Naylor, L Perkins, et al.
Nature Genetics
|
September 6, 2000
Inactivation of the mouse melanocortin-3 receptor results in increased fat mass and reduced lean body mass
A S Chen, D J Marsh, M E Trumbauer, et al.
Bioorganic & Medicinal Chemistry Letters
|
January 5, 1999
3-Pyridyloxypropanolamine agonists of the beta 3 adrenergic receptor with improved pharmacokinetic properties
A E Weber, H O Ok, R F Alvaro, et al.
Journal of Medicinal Chemistry
|
March 29, 2000
Phosphorylated morpholine acetal human neurokinin-1 receptor antagonists as water-soluble prodrugs
J J Hale, S G Mills, M MacCoss, et al.
The Journal of Clinical Investigation
|
June 17, 1998
A selective human beta3 adrenergic receptor agonist increases metabolic rate in rhesus monkeys
M H Fisher, A M Amend, T J Bach, et al.
Journal of Medicinal Chemistry
|
April 13, 2001
A potent, nonpeptidyl 1H-quinolone antagonist for the gonadotropin-releasing hormone receptor
R J DeVita, T F Walsh, J R Young, et al.
Page
of 11