Synthetic Approaches to Incorporation of Novel Amino Acids into Gonadotropin-Releasing Hormone Peptides

Author(s):  
Fortuna Haviv ◽  
Timothy D. Fitzpatrick
Peptides ◽  
1994 ◽  
pp. 403-405
Author(s):  
G.-C. Jiang ◽  
J. Porter ◽  
C. Rivier ◽  
A. Corrigan ◽  
W. Vale ◽  
...  

1998 ◽  
Vol 112 (3) ◽  
pp. 372-382 ◽  
Author(s):  
Shin-ichi Kawakami ◽  
Masumi Ichikawa ◽  
Kumiko Murahashi ◽  
Kanjun Hirunagi ◽  
Hiroko Tsukamura ◽  
...  

1992 ◽  
Vol 47 (10) ◽  
pp. 1424-1430
Author(s):  
Urszula Słomczyńska ◽  
Tomasz Leplawy ◽  
Mirosław T. Leplawy

We have developed a chemical-enzymatic synthetic approach to gonadotropin releasing hormone Glp1–His-2–Trp3–Ser4–Tyr5–Gly6–Leu7–Arg8—Pro9–Gly10–NH2 (GnRH) which enables one to perform the synthesis efficiently according to minimal protection strategy with all reactive side chains of amino acids unprotected. Five peptide bonds His2–Trp3, Tyr5–Gly6, Leu7–Arg8 and Trp3–Ser4, Ser4–Tyr5 were formed by means of a-chymotrypsin and papain, respectively. The remaining four bonds Glp1–His2, Gly6–Leu7, Arg8—Pro9, Pro9—Gly10 were formed by chemical methods. The synthesis is simple to carry out and there are no problems in scaling up as demonstrated by the final coupling on 2 g scale affording highly pure GnRH in the yield of 84-90%.


2004 ◽  
Vol 171 (4S) ◽  
pp. 49-49
Author(s):  
Christian Schwentner ◽  
Andreas Lunacek ◽  
Josef Oswald ◽  
Georg Bartsch ◽  
Alfons Kreczy ◽  
...  

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