Kisspeptin Receptor

The kisspeptin receptor, Kiss1R, also known as GPR54, is a G protein-coupled receptor (GPCR), and it was recognized as canonical receptor for the Kiss1-derived peptides, kisspeptins. Kisspeptins are a family of neuropeptides that are critical for initiating puberty and regulating ovulation in sexually mature females via the central control of the hypothalamic–pituitary–gonadal axis. Recent studies have shown that kisspeptin and Kiss1R are expressed in the mammalian ovary. Convincing evidence indicates that kisspeptins can activate a wide variety of signals via its binding to KISS1R. Experimental data gathered recently suggest a putative role of kisspeptin signaling in the direct control of ovarian function, including follicular development, oocyte maturation, steroidogenesis, and ovulation. Dysregulation or naturally occurring mutations of the kisspeptin/KISS1R system may negatively affect the ovarian function, leading to reproductive pathology or female infertility.

Kisspeptin Receptor 相关产品（7）

货号	产品名	Cas	产品描述
PC11255	Kisspeptin 10 (human)	374675-21-5	Kisspeptin受体（KISS1，GPR54）的内源性配体,Kisspeptin-10 是一种有效的血管收缩剂，抑制血管生成抑制剂及其受体GPR54。
PC10973	Kisspeptin 234	1145998-81-7	kisspeptin受体（KISS1，GPR54）拮抗剂
PL05779	Kisspeptin-10, human TFA		Kisspeptin-10, human TFA 是一种有效的血管收缩剂和血管生成抑制剂。Kisspeptin-10, human TFA 通过其受体 GPR54 来抑制肿瘤转移作用。Kisspeptin-10-GPR54 系统在胚胎肾脏发育中起重要作用。Kisspeptin-10/GPR54 信号通过 NFATc4 介导的 BMP2 表达来诱导成骨细胞分化。
PL05820	Kisspeptin-10, rat TFA		Kisspeptin-10, rat TFA 是一种有效的血管收缩剂和血管生成抑制剂。Kisspeptin-10, rat TFA 是亲吻蛋白受体 GPR54 (也叫 KISS1) 的配体。Kisspeptin-10 TFA 可降低 Methotrexate 诱导的生殖毒性，具有潜在的抗氧化活性。
PC10833	Metastin (human)	374683-24-6	kisspeptin受体(KISS1, GPR54)的内源性配体,Kisspeptin-54(human) (Metastin(human)) 是一种 Kisspeptin 受体 (KISS1，GPR54) 的内源性配体，以高亲和力结合大鼠和人类 GPR54 受体，其 Ki 值分别为 1.81 nM 和 1.45 nM
PL05752	TAK-448 acetate	1470374-22-1	TAK-448 acetate (MVT-602 acetate) 是一种有效的 KISS1R 激动剂，IC50 值为 460 pM，EC50 值为 632 pM。
PL05936	TAK-683 acetate		TAK-683 acetate 是一种有效的完全 KISS1R 激动剂 (IC50=170 pM)，具有改善的代谢稳定性。TAK-683 acetate 是一个九肽 metastin 的类似物，针对人与大鼠 EC50 值分别为 0.96 nM 和 1.6 nM。TAK-683 acetate 消耗下丘脑 GnRH，降低血浆 FSH、LH、睾酮水平，具有研究激素依赖性前列腺癌的潜力。