促肾上腺皮质激素释放因子受体在GtoPdb v.2023.1

F. Dautzenberg, D. Grigoriadis, R. Hauger, V. Risbrough, T. Steckler, W. Vale, R. Valentino
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引用次数: 0

摘要

促肾上腺皮质激素释放因子(CRF,命名由NC-IUPHAR促肾上腺皮质激素释放因子受体小组委员会[34]商定)受体被内源性肽促肾上腺皮质激素释放激素激活,促肾上腺皮质激素释放激素是一种41个氨基酸的肽,有尿皮质素1,40个氨基酸、尿皮质素2,38个氨基酸和尿皮质素3,38个氨基酸。CRF1和CRF2受体被CRH和UCN非选择性激活。CRF2受体被UCN2和UCN3选择性激活。与CRF受体结合的放射性配体可为[125I]Tyr0-CRF或[125I]Tyr0-sauvagine, Kd值为0.1-0.4 nM。CRF1和CRF2受体可被α-螺旋CRF、d - ph -CRF-(12-41)和应激素非选择性拮抗。CRF1受体可被小分子NBI27914、R121919、antalarmin、CP 154,526、CP 376,395选择性拮抗。CRF2受体可被抗索瓦碱和应激素2B选择性拮抗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Corticotropin-releasing factor receptors in GtoPdb v.2023.1
Corticotropin-releasing factor (CRF, nomenclature as agreed by the NC-IUPHAR subcommittee on Corticotropin-releasing Factor Receptors [34]) receptors are activated by the endogenous peptides corticotrophin-releasing hormone, a 41 amino-acid peptide, urocortin 1, 40 amino-acids, urocortin 2, 38 amino-acids and urocortin 3, 38 amino-acids. CRF1 and CRF2 receptors are activated non-selectively by CRH and UCN. CRF2 receptors are selectively activated by UCN2 and UCN3. Binding to CRF receptors can be conducted using radioligands [125I]Tyr0-CRF or [125I]Tyr0-sauvagine with Kd values of 0.1-0.4 nM. CRF1 and CRF2 receptors are non-selectively antagonized by α-helical CRF, D-Phe-CRF-(12-41) and astressin. CRF1 receptors are selectively antagonized by small molecules NBI27914, R121919, antalarmin, CP 154,526, CP 376,395. CRF2 receptors are selectively antagonized by antisauvagine and astressin 2B.
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