Luteinizing hormone-releasing hormone antagonists containing very hydrophobic amino acids

1984 ◽  
Vol 27 (9) ◽  
pp. 1170-1174 ◽  
Author(s):  
John J. Nestor ◽  
Ram Tahilramani ◽  
Teresa L. Ho ◽  
Georgia I. McRae ◽  
Brian H. Vickery
1982 ◽  
Vol 37 (7) ◽  
pp. 872-876 ◽  
Author(s):  
Karl Folkers ◽  
Cyril Y. Bowers ◽  
Frank Momany ◽  
Klaus J. Friebel ◽  
Teresa Kubiak ◽  
...  

Abstract [N-Ac-Thr 1 ,D-Phe 2,D-Trp 3,6]-LHRH was the model antagonist of LHRH, which was the basis for tho design, synthesis and bioassay of seven peptides having four, five and six D-amino acids, which resulted from three single, three double, and one triple introductions of D-amino acids in positions 4, 5 and 8 of the model. Only the analog with six D-amino acids, [N-Ac-Thr 1,D-Phe 2 ,D-Trp 3,D-Ser 4, D-Tyr 5 ,D-Trp 6 ,D-Arg 8]-LHRH, had antiovulatory activity which was higher than that of the model antagonist, i.e., 70% antiovulatory activity at 25 μg/rat compared with 50% activity at 50 μg/rat, respectively. Empirical energy calculations gave a conformational structure for [N-Ac-Thr 1,D-Phe 2,D-Trp 3, D-Ser 4,D-Tyr 5,D-Arg 6,D-Arg 8]-LHRH which is similar to that calculated for previous potent antagonists. These results are a basis of new designs of antagonists having D-sub-stituents in up to ten positions toward effective inhibitors of ovulation by the parenteral and oral routes of administration.


Amino Acids ◽  
2012 ◽  
Vol 43 (4) ◽  
pp. 1557-1566 ◽  
Author(s):  
Jin-Feng Yao ◽  
Ning Zhou ◽  
Yu-Jian Lv ◽  
Ruifeng Zhang ◽  
Ke-Liang Liu ◽  
...  

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