1.
FEBS Lett
; 344(1): 55-60, 1994 May 09.
Artigo
em Inglês
| MEDLINE
| ID: mdl-8181565
RESUMO
The conformations of three endothelin antagonists, a cyclic pentapeptide, a linear tripeptide and a linear hexapeptide, are compared by 1H NMR and molecular dynamics. The three analogues have a Leu and a DTrp side chain which are oriented parallel, and an acidic group next to the DTrp residue.