Rapid identification of subtype-selective agonists of the somatostatin receptor through combinatorial chemistry

被引:411
作者
Rohrer, SP
Birzin, ET
Mosley, RT
Berk, SC
Hutchins, SM
Shen, DM
Xiong, YS
Hayes, EC
Parmar, RM
Foor, F
Mitra, SW
Degrado, SJ
Shu, M
Klopp, JM
Cai, SJ
Blake, A
Chan, WWS
Pasternak, A
Yang, LH
Patchett, AA
Smith, RG
Chapman, KT
Schaeffer, JM
机构
[1] Merck Res Labs, Dept Cell Biochem & Physiol, Rahway, NJ 07065 USA
[2] Merck Res Labs, Dept Mol Design & Divers, Rahway, NJ 07065 USA
[3] Merck Res Labs, Dept Med Chem, Rahway, NJ 07065 USA
关键词
D O I
10.1126/science.282.5389.737
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nonpeptide agonists of each of the five somatostatin receptors were identified in combinatorial Libraries constructed on the basis of molecular modeling of known peptide agonists. In vitro experiments using these selective compounds demonstrated the role of the somatostatin subtype-2 receptor in inhibition of glucagon release from mouse pancreatic alpha cells and the somatostatin subtype-5 receptor as a mediator of insulin secretion from pancreatic beta cells. Both receptors regulated growth hormone release from the rat anterior pituitary gland. The availability of high-affinity, subtype-selective agonists for each of the somatostatin receptors provides a direct approach to defining their physiological functions.
引用
收藏
页码:737 / 740
页数:4
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