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Vasopressin antagonist analogs modified at position 7.

作者信息

Moore M L, Greene H, Huffman W F, Stassen F, Stefankiewicz J, Sulat L, Heckman G, Schmidt D, Kinter L, McDonald J

出版信息

Int J Pept Protein Res. 1986 Oct;28(4):379-85. doi: 10.1111/j.1399-3011.1986.tb03269.x.

Abstract

Vasopressin antagonist analogs having alanine or glycine at position 7 were essentially equipotent with analogs with proline, N-methylalanine or sarcosine at position 7. This demonstrates that the conformational constraint imposed by an N-alkyl residue at position 7 is not necessary for binding of antagonist to the receptor, the exact opposite of what is seen in agonists. This suggests that antagonists bind to the receptor in a manner which is very different from that of agonists.

摘要

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