Structure-activity study on the Phe side chain arrangement of endomorphins using conformationally constrained analogues

C Tömböly, KE Kövér, A Péter, D Tourwé…

Index: J. Med. Chem., , vol. 47, # 3 p. 735 - 743

Full Text: HTML

Citation Number: 43

Abstract

... Journal of Medicinal Chemistry. ... Budapest, PO Box 370, Hungary. J. Med. Chem. , 2004, 47 (3), pp 735–743. DOI: 10.1021/jm0310028. Publication Date (Web): December 24, 2003. Copyright © 2004 American Chemical Society. ...

Related Articles:

Structure–activity study of endomorphin-2 analogs with C-terminal modifications by NMR spectroscopy and molecular modeling

[Bioorganic and Medicinal Chemistry, , vol. 16, # 12 p. 6415 - 6422]

Receptor Interactions of Synthetic Morphiceptin Analogs Containing Phenylalanine Homologs in Position 4.

[Sakaguchi; Costa; Sakamoto; Shimohigashi Bulletin of the Chemical Society of Japan, 1992 , vol. 65, # 4 p. 1052 - 1056]

Receptor Interactions of Synthetic Morphiceptin Analogs Containing Phenylalanine Homologs in Position 4.

[Bulletin of the Chemical Society of Japan, , vol. 65, # 4 p. 1052 - 1056]

Receptor Interactions of Synthetic Morphiceptin Analogs Containing Phenylalanine Homologs in Position 4.

[Bulletin of the Chemical Society of Japan, , vol. 65, # 4 p. 1052 - 1056]

Receptor Interactions of Synthetic Morphiceptin Analogs Containing Phenylalanine Homologs in Position 4.

[Bulletin of the Chemical Society of Japan, , vol. 65, # 4 p. 1052 - 1056]

More Articles...