Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Steven March Massey"'
Autor:
Joseph P. Tizzano, Trevor J. Howe, Steven March Massey, James A. Monn, Roger L. Robey, Bryan G. Johnson, Rebecca A. Wright, Darryle D. Schoepp, Craig R. Salhoff, Kelly R. Griffey, Charles A. Alt, David R. Helton, Rhodes Gary Anthony, Matthew John Valli, Mary Jeanne Kallman
Publikováno v:
Journal of Medicinal Chemistry. 40:528-537
2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (9) was designed as a conformationally constrained analog of glutamic acid. For 9, the key torsion angles (tau 1 and tau 2) which determine the relative positions of the alpha-amino acid and distal ca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4616fef763f15abbd4bbb61fbc52874e
https://doi.org/10.1021/jm9606756
https://doi.org/10.1021/jm9606756
Autor:
James A. Monn, Charles A. Alt, Rhodes Gary Anthony, Kelly R. Griffey, Bryan G. Johnson, Mary Jeanne Kallman, Roger L. Robey, Darryle D. Schoepp, Craig R. Salhoff, Joseph P. Tizzano, Trevor J. Howe, David R. Helton, Steven March Massey, Rebecca A. Wright, Matthew John Valli
Publikováno v:
ChemInform. 28
2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic acid (9) was designed as a conformationally constrained analog of glutamic acid. For 9, the key torsion angles (τ1 and τ2) which determine the relative positions of the α-amino acid and distal carboxyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d229ce0bb76e8e2a55795617f2bf6af
https://doi.org/10.1002/chin.199722076
https://doi.org/10.1002/chin.199722076