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Receptors & Channels
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February 11, 2004
Comparison of the pharmacological properties of rat Na(V)1.8 with rat Na(V)1.2a and human Na(V)1.5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR
R G Vickery, S M Amagasu, R Chang, et al.
Molecular Pharmacology
|
December 13, 2005
Evidence for a multivalent interaction of symmetrical, N-linked, lidocaine dimers with voltage-gated Na+ channels
J A M Smith, S M Amagasu, J Hembrador, et al.
Frontiers in Pharmacology
|
June 21, 2011
The Pharmacology of TD-8954, a Potent and Selective 5-HT(4) Receptor Agonist with Gastrointestinal Prokinetic Properties
David T Beattie, Scott R Armstrong, Ross G Vickery, et al.
British Journal of Pharmacology
|
October 7, 2004
The 5-HT4 receptor agonist, tegaserod, is a potent 5-HT2B receptor antagonist in vitro and in vivo
D T Beattie, J A M Smith, D Marquess, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 12, 2012
Discovery, oral pharmacokinetics and in vivo efficacy of a highly selective 5-HT4 receptor agonist: clinical compound TD-2749
Daniel D Long, Scott R Armstrong, David T Beattie, et al.
Journal of Medicinal Chemistry
|
August 12, 2009
A multivalent approach to the design and discovery of orally efficacious 5-HT4 receptor agonists
R Murray McKinnell, Scott R Armstrong, David T Beattie, et al.
ACS Medicinal Chemistry Letters
|
December 21, 2019
Discovery of Axelopran (TD-1211): A Peripherally Restricted μ-Opioid Receptor Antagonist
Daniel D Long, Scott R Armstrong, David T Beattie, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 11, 2012
Discovery, oral pharmacokinetics and in vivo efficacy of velusetrag, a highly selective 5-HT(4) receptor agonist that has achieved proof-of-concept in patients with chronic idiopathic constipation
Daniel D Long, Scott R Armstrong, David T Beattie, et al.
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of 3
Search research articles
Search
Showing results (21-30 of 28) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 28 results.
Receptors & Channels
|
February 11, 2004
Comparison of the pharmacological properties of rat Na(V)1.8 with rat Na(V)1.2a and human Na(V)1.5 voltage-gated sodium channel subtypes using a membrane potential sensitive dye and FLIPR
R G Vickery, S M Amagasu, R Chang, et al.
Molecular Pharmacology
|
December 13, 2005
Evidence for a multivalent interaction of symmetrical, N-linked, lidocaine dimers with voltage-gated Na+ channels
J A M Smith, S M Amagasu, J Hembrador, et al.
Frontiers in Pharmacology
|
June 21, 2011
The Pharmacology of TD-8954, a Potent and Selective 5-HT(4) Receptor Agonist with Gastrointestinal Prokinetic Properties
David T Beattie, Scott R Armstrong, Ross G Vickery, et al.
British Journal of Pharmacology
|
October 7, 2004
The 5-HT4 receptor agonist, tegaserod, is a potent 5-HT2B receptor antagonist in vitro and in vivo
D T Beattie, J A M Smith, D Marquess, et al.
Bioorganic & Medicinal Chemistry Letters
|
June 12, 2012
Discovery, oral pharmacokinetics and in vivo efficacy of a highly selective 5-HT4 receptor agonist: clinical compound TD-2749
Daniel D Long, Scott R Armstrong, David T Beattie, et al.
Journal of Medicinal Chemistry
|
August 12, 2009
A multivalent approach to the design and discovery of orally efficacious 5-HT4 receptor agonists
R Murray McKinnell, Scott R Armstrong, David T Beattie, et al.
ACS Medicinal Chemistry Letters
|
December 21, 2019
Discovery of Axelopran (TD-1211): A Peripherally Restricted μ-Opioid Receptor Antagonist
Daniel D Long, Scott R Armstrong, David T Beattie, et al.
Bioorganic & Medicinal Chemistry Letters
|
September 11, 2012
Discovery, oral pharmacokinetics and in vivo efficacy of velusetrag, a highly selective 5-HT(4) receptor agonist that has achieved proof-of-concept in patients with chronic idiopathic constipation
Daniel D Long, Scott R Armstrong, David T Beattie, et al.
Page
of 3