TY - JOUR
T1 - [2,4-Diisoleucine]-oxytocin. An analog of oxytocin with natriuretic and diuretic activities
AU - Hruby, Victor J.
AU - Du Vigneaud, Vincent
AU - Chan, W. Y.
PY - 1970
Y1 - 1970
N2 - [2,4-Diisoleucine]-oxytocin has been synthesized from the requisite protected nonapeptide intermediate which was prepared by the stepwise p-nitrophenyl ester method. In this analog of oxytocin, isoleucine residues replace the tyrosine and glutamine residues at the 2 and 4 positions of the hormone, and thus the isoleucine residue occurs successively at positions 2, 3, and 4. This compound possesses a very low level of avian vasodepressor, oxytocic, and pressor activities, and no antidiuretic activity. However, [2,4-diisoleucine]-oxytocin has a pronounced natriuretic activity and a mild diuretic effect.
AB - [2,4-Diisoleucine]-oxytocin has been synthesized from the requisite protected nonapeptide intermediate which was prepared by the stepwise p-nitrophenyl ester method. In this analog of oxytocin, isoleucine residues replace the tyrosine and glutamine residues at the 2 and 4 positions of the hormone, and thus the isoleucine residue occurs successively at positions 2, 3, and 4. This compound possesses a very low level of avian vasodepressor, oxytocic, and pressor activities, and no antidiuretic activity. However, [2,4-diisoleucine]-oxytocin has a pronounced natriuretic activity and a mild diuretic effect.
UR - https://www.scopus.com/pages/publications/0014749960
UR - https://www.scopus.com/pages/publications/0014749960#tab=citedBy
U2 - 10.1021/jm00296a004
DO - 10.1021/jm00296a004
M3 - Article
C2 - 5418485
AN - SCOPUS:0014749960
SN - 0022-2623
VL - 13
SP - 185
EP - 187
JO - Journal of Medicinal Chemistry
JF - Journal of Medicinal Chemistry
IS - 2
ER -