105852-64-0Relevant academic research and scientific papers
Synthesis of the hydroxyethylene dipeptide isostere, (2S,4S,5S)-5-amino-6-cyclohexyl-4-hydroxy-2-isopropyl hexanoic acid n-butyl amide
Poss,Reid
, p. 1411 - 1414 (2007/10/02)
A stereoselective synthesis of the hydroxyethylene dipeptide isostere, (2S,4S,5S)-5-amino-6-cyclohexyl-4-hydroxy-2-isopropyl hexanoic acid-n-butyl amide from Boc-L-phenylalanine is described.
5-(HETEROCYCLYLALKANOYL)AMINO-4-HYDROXYPENTANAMIDES
-
, (2008/06/13)
This invention concerns novel nitrogen derivatives of the formula I STR1 (and their pharmaceutically-acceptable salts), together with pharmaceutical compositions containing them. The nitrogen derivatives are inhibitors of the catalytic action of renin. Th
1,2,4-Triazolopyrazine Derivatives with Human Renin Inhibitory Activity. 2. Synthesis, Biological Properties and Molecular Modeling of Hydroxyethylene Isostere Derivatives
Bradbury, Robert H.,Major, John S.,Oldham, Alec A.,Rivett, Janet E.,Roberts, David A.,et al.
, p. 2335 - 2342 (2007/10/02)
A series of inhibitors of human renin have been synthesized, derived from combination of a 2-(8-propyl-6-pyridin-3-yl-1,2,4-triazolopyrazin-3-yl)-3-pyridin-3-ylpropionic acid moiety 6c with the hydroxyethylene isostere of the scissile amide bond (2
THE SYNTHESIS OF (2S,4S,5S)-5-(N-BOC)-AMINO-6-CYCLOHEXYL-4-HYDORXY-2-ISOPROPYL-HEXANOIC ACID LACTONE, AN HYDROXYETHYLENE DIPEPTIDE ISOSTERE PRECURSOR
Chakravarty, Prasun K.,Laszlo, Stephen E. de,Sarnella, Carol S.,Springer, James P.,Schuda, Paul F.
, p. 415 - 418 (2007/10/02)
(2SR,4SR)-5-(S)-(N-Boc)-amino-cyclohexyl-4-hydroxy-2-isopropyl hexanoivc acid from (L)-phenylalanine and the preparation of the n-butyl amide of the 2(S),4(S),5(S) acid is presented.
A Versatile and Stereocontrolled Synthesis of Hydroxyethylene Dipeptide Isosteres
Herold, Peter,Duthaler, Rudolph,Rihs, Grety,Angst, Christof
, p. 1178 - 1185 (2007/10/02)
An asymmetric synthesis of the hydroxyethylene dipeptide isostere unit 1 is described.The synthesis provides excellent stereocontrol over all three chiral centers and is amenable to variation of substituents R1 and R2.Key intermediat
Synthesis and biological activity of some transition-state inhibitors of human renin
Buhlmayer,Caselli,Fuhrer,Goschke,Rasetti,Rueger,Stanton,Criscione,Wood
, p. 1839 - 1846 (2007/10/02)
A series of renin inhibitors containing the dipeptide transition state mimics (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-7-methyloctanoic acid (Leu-(OH)-Val) and (2S,4S,5S)-5-amino-4-hydroxy-2-isopropyl-6-cyclohexylhexanoic acid (Cha-(OH)-Val) was prepared.
