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Journal of Medicinal Chemistry
|
May 5, 2000
Design and synthesis of conformationally constrained glucagon analogues
D Trivedi, Y Lin, J M Ahn, et al.
Advances in Experimental Medicine and Biology
|
April 30, 2009
Novel analogues of bifunctional ligands for opioid and melanocortin 4 receptor
Vinod V Kulkarni, Yeon Sun Lee, Christine Salibay, et al.
Peptides
|
March 1, 1989
The effects of structure-conformation modifications of melanotropin analogs on learning and memory: D-amino acid substituted linear and cyclic analogs
B E Beckwith, T P Tinius, V J Hruby, et al.
Cancer Research
|
October 1, 1985
Prolonged stimulation of S91 melanoma tyrosinase by [Nle4, D-Phe7]-substituted alpha-melanotropins
Z A Abdel Malek, K L Kreutzfeld, M M Marwan, et al.
Bioconjugate Chemistry
|
June 27, 2007
Synthesis and evaluation of bivalent NDP-alpha-MSH(7) peptide ligands for binding to the human melanocortin receptor 4 (hMC4R)
Heather L Handl, Rajesh Sankaranarayanan, Jatinder S Josan, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 24, 2007
Squalene-derived flexible linkers for bioactive peptides
Bhumasamudram Jagadish, Rajesh Sankaranarayanan, Liping Xu, et al.
European Journal of Pharmacology
|
June 9, 1998
Endomorphin-1 and endomorphin-2 are partial agonists at the human mu-opioid receptor
K Hosohata, T H Burkey, J Alfaro-Lopez, et al.
Drug Design and Discovery
|
December 1, 1996
Three-dimensional molecular models of the hMC1R melanocortin receptor: complexes with melanotropin peptide agonists
C Haskell-Luevano, T K Sawyer, S Trumpp-Kallmeyer, et al.
Pigment Cell Research
|
December 1, 1995
The melanotropic peptide, [Nle4,D-Phe7] alpha-MSH, stimulates human melanoma tyrosinase activity and inhibits cell proliferation
J Jiang, S D Sharma, S Nakamura, et al.
Advances in Experimental Medicine and Biology
|
April 30, 2009
Peptide and non-peptide mimetics utilize different pathways for signal transduction
Victor J Hruby, Minying Cai, Matt Dedek, et al.
Page
of 77
Search research articles
Search
Showing results (501-510 of 762) with videos related to
Sort By:
Page
of 77
Journal of Medicinal Chemistry
|
May 5, 2000
Design and synthesis of conformationally constrained glucagon analogues
D Trivedi, Y Lin, J M Ahn, et al.
Advances in Experimental Medicine and Biology
|
April 30, 2009
Novel analogues of bifunctional ligands for opioid and melanocortin 4 receptor
Vinod V Kulkarni, Yeon Sun Lee, Christine Salibay, et al.
Peptides
|
March 1, 1989
The effects of structure-conformation modifications of melanotropin analogs on learning and memory: D-amino acid substituted linear and cyclic analogs
B E Beckwith, T P Tinius, V J Hruby, et al.
Cancer Research
|
October 1, 1985
Prolonged stimulation of S91 melanoma tyrosinase by [Nle4, D-Phe7]-substituted alpha-melanotropins
Z A Abdel Malek, K L Kreutzfeld, M M Marwan, et al.
Bioconjugate Chemistry
|
June 27, 2007
Synthesis and evaluation of bivalent NDP-alpha-MSH(7) peptide ligands for binding to the human melanocortin receptor 4 (hMC4R)
Heather L Handl, Rajesh Sankaranarayanan, Jatinder S Josan, et al.
Bioorganic & Medicinal Chemistry Letters
|
April 24, 2007
Squalene-derived flexible linkers for bioactive peptides
Bhumasamudram Jagadish, Rajesh Sankaranarayanan, Liping Xu, et al.
European Journal of Pharmacology
|
June 9, 1998
Endomorphin-1 and endomorphin-2 are partial agonists at the human mu-opioid receptor
K Hosohata, T H Burkey, J Alfaro-Lopez, et al.
Drug Design and Discovery
|
December 1, 1996
Three-dimensional molecular models of the hMC1R melanocortin receptor: complexes with melanotropin peptide agonists
C Haskell-Luevano, T K Sawyer, S Trumpp-Kallmeyer, et al.
Pigment Cell Research
|
December 1, 1995
The melanotropic peptide, [Nle4,D-Phe7] alpha-MSH, stimulates human melanoma tyrosinase activity and inhibits cell proliferation
J Jiang, S D Sharma, S Nakamura, et al.
Advances in Experimental Medicine and Biology
|
April 30, 2009
Peptide and non-peptide mimetics utilize different pathways for signal transduction
Victor J Hruby, Minying Cai, Matt Dedek, et al.
Page
of 77