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Proceedings of the Western Pharmacology Society
|
January 1, 1987
N-terminal cyclization of a nonsulfated CCK analogue exhibits opioid antagonist activity in vitro
P K Lemcke, E Sugg, M Malarchik, et al.
ACS Chemical Neuroscience
|
September 14, 2016
Discovery of Stable Non-opioid Dynorphin A Analogues Interacting at the Bradykinin Receptors for the Treatment of Neuropathic Pain
Sara M Hall, Lindsay LeBaron, Cyf Ramos-Colon, et al.
Journal of Heterocyclic Chemistry
|
August 19, 2017
Synthesis and Investigation of Mixed μ-Opioid and δ-Opioid Agonists as Possible Bivalent Ligands for Treatment of Pain
Ruben S Vardanyan, James P Cain, Saghar Mowlazadeh Haghighi, et al.
International Journal of Peptide and Protein Research
|
January 1, 1981
H N.M.R. study of the conformation of [Glu4] oxytocin and its lanthanide complexes in aqueous solution
R Walter, C W Smith, K P Sarathy, et al.
Life Sciences
|
March 5, 1984
Synthesis of tritium labeled Ac-[Nle4, D-Phe7]-alpha-MSH4-11-NH2: a superpotent melanotropin with prolonged biological activity
B C Wilkes, V J Hruby, H I Yamamura, et al.
ACS Medicinal Chemistry Letters
|
March 26, 2013
Multivalent Interactions: Synthesis and Evaluation of Melanotropin Multimers - Tools for Melanoma Targeting
Nabila Brabez, Kara Saunders, Kevin L Nguyen, et al.
Journal of Medicinal Chemistry
|
February 17, 1995
Highly kappa receptor-selective dynorphin A analogues with modifications in position 3 of dynorphin A(1-11)-NH2
F D Lung, J P Meyer, G Li, et al.
Journal of Medicinal Chemistry
|
November 1, 1988
Design and synthesis of somatostatin analogues with topographical properties that lead to highly potent and specific mu opioid receptor antagonists with greatly reduced binding at somatostatin receptors
W Kazmierski, W S Wire, G K Lui, et al.
Anesthesiology
|
December 10, 2009
Sex-specific mediation of opioid-induced hyperalgesia by the melanocortin-1 receptor
Aaron Juni, Minying Cai, Magda Stankova, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society
|
March 11, 2004
Biological and conformational study of beta-substituted prolines in MT-II template: steric effects leading to human MC5 receptor selectivity
M Cai, C Cai, A V Mayorov, et al.
Page
of 77
Search research articles
Search
Showing results (621-630 of 762) with videos related to
Sort By:
Page
of 77
Proceedings of the Western Pharmacology Society
|
January 1, 1987
N-terminal cyclization of a nonsulfated CCK analogue exhibits opioid antagonist activity in vitro
P K Lemcke, E Sugg, M Malarchik, et al.
ACS Chemical Neuroscience
|
September 14, 2016
Discovery of Stable Non-opioid Dynorphin A Analogues Interacting at the Bradykinin Receptors for the Treatment of Neuropathic Pain
Sara M Hall, Lindsay LeBaron, Cyf Ramos-Colon, et al.
Journal of Heterocyclic Chemistry
|
August 19, 2017
Synthesis and Investigation of Mixed μ-Opioid and δ-Opioid Agonists as Possible Bivalent Ligands for Treatment of Pain
Ruben S Vardanyan, James P Cain, Saghar Mowlazadeh Haghighi, et al.
International Journal of Peptide and Protein Research
|
January 1, 1981
H N.M.R. study of the conformation of [Glu4] oxytocin and its lanthanide complexes in aqueous solution
R Walter, C W Smith, K P Sarathy, et al.
Life Sciences
|
March 5, 1984
Synthesis of tritium labeled Ac-[Nle4, D-Phe7]-alpha-MSH4-11-NH2: a superpotent melanotropin with prolonged biological activity
B C Wilkes, V J Hruby, H I Yamamura, et al.
ACS Medicinal Chemistry Letters
|
March 26, 2013
Multivalent Interactions: Synthesis and Evaluation of Melanotropin Multimers - Tools for Melanoma Targeting
Nabila Brabez, Kara Saunders, Kevin L Nguyen, et al.
Journal of Medicinal Chemistry
|
February 17, 1995
Highly kappa receptor-selective dynorphin A analogues with modifications in position 3 of dynorphin A(1-11)-NH2
F D Lung, J P Meyer, G Li, et al.
Journal of Medicinal Chemistry
|
November 1, 1988
Design and synthesis of somatostatin analogues with topographical properties that lead to highly potent and specific mu opioid receptor antagonists with greatly reduced binding at somatostatin receptors
W Kazmierski, W S Wire, G K Lui, et al.
Anesthesiology
|
December 10, 2009
Sex-specific mediation of opioid-induced hyperalgesia by the melanocortin-1 receptor
Aaron Juni, Minying Cai, Magda Stankova, et al.
The Journal of Peptide Research : Official Journal of the American Peptide Society
|
March 11, 2004
Biological and conformational study of beta-substituted prolines in MT-II template: steric effects leading to human MC5 receptor selectivity
M Cai, C Cai, A V Mayorov, et al.
Page
of 77