Archer SA / Gartner / Kellogg / ACS / Cochran AG / Beck-Sickinger AG / Kates SA / Boyd SA / /
Country
Germany / /
Currency
pence / / /
Facility
C terminus / University of California / /
IndustryTerm
similar energy / regioisomeric products / low energy conformers / α-chymotrypsin cleavage site / composite products / mRNA display technologies / cyclization product / oligomeric by-products / oligomeric products / energy conformation / resultant product / biological systems / cancer therapeutics / 13C chemical shifts / combinatorial chemical libraries / minor product / 1H chemical shifts / therapeutics for inflammatory diseases / metal ion pair / metal / backbone amide chemical shift temperature dependence / mM solutions / energy minimum / above product / low-energy conformers / interaction networks / nuclear magnetic resonance chemical shift / chemical shifts / phase peptide synthesis protocols / basic solutions / /
Organization
National Cancer Institute / National Science Foundation / J. and Jane M. Cram Endowment / University of California / Los Angeles / Patrick G. Harran1 Department of Chemistry and Biochemistry / /
Person
Robert Peterson / Tristan E. Rose / Comb Sci / Kenneth V. Lawson / Rai V / Huilin Li / Jane M. Cram / Joseph Loo / Kendall N. Houk / Albert Chan / /
Position
prearranged editor / General / Williamson MP / Author / King / Major / /
ProgrammingLanguage
L / /
ProvinceOrState
California / /
PublishedMedium
PLoS ONE / /
RadioStation
Vos AM / Richards FM / /
Technology
combinatorial chemistry / phase peptide synthesis protocols / X-ray / mRNA display technologies / chemical libraries / drug discovery / Web Server / /
PNAS PLUS Template-constrained macrocyclic peptides prepared from native, unprotected precursors Kenneth V. Lawson, Tristan E. Rose, and Patrick G. Harran1 Department of Chemistry and Biochemistry, University of Califor