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非天然氨基酸及其它砌块合成
Hemokinin 1 (human)
名称
Hemokinin 1 (human)
分子结构式
CAS号
491851-53-7
分子式
C54H84N14O14S1
分子量
1185.4
作用靶点
Neurokinin Receptor
序列号
Thr-Gly-Lys-Ala-Ser-Gln-Phe-Phe-Gly-Leu-Met-NH2
短序列号
TGKASQFFGLM-NH2
国际标识符代码
NYBLUYYRUFKGTB-XJCFQSCISA-N
水中溶解度
≥ 50 mg/mL
纯度
95%
引用文献
[1].Cai-Yun Fu, et al. Hemokinin-1(4-11)-induced analgesia selectively up-regulates δ-opioid receptor expression in mice. PLoS One. [2].Francesca Bellucci, et al. Pharmacological profile of the novel mammalian tachykinin, hemokinin 1. Br J Pharmacol. 2002 Jan;135(1):266-74.
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Hemokinin 1, human is a selective tachykinin neurokinin 1 (NK1) receptor full agonist. Hemokinin 1, human is a full agonist at NK2 and NK3 receptor. Hemokinin 1, human can produces an opioid-independent analgesia.

Hemokinin 1 (human) is an endogenous substance P homolog and acts as a selective agonist at the tachykinin NK1 receptor (IC50 = 1.8, 370 and 480 nM for NK1, NK3 and NK2 receptors, respectively). It induces proliferation of B-cells in vitro and exhibits antihypertensive activity in vivo.