您好,欢迎来到试剂仪器网! [登录] [免费注册]
试剂仪器网
位置:首页 > 产品库 > sst2 Receptor agonist-1
立即咨询
咨询类型:
     
*姓名:
*电话:
*单位:
Email:
*留言内容:
请详细说明您的需求。
*验证码:
 
sst2 Receptor agonist-1
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
sst2 Receptor agonist-1图片
CAS NO:1021912-42-4
包装与价格:
包装价格(元)
100mg电议
250mg电议
500mg电议

产品介绍
sst2 Receptor agonist-1 是一种有效的生长抑素 2 型受体 (sst2) 激动剂,Ki为 0.025 nM,cAMPIC50为 4.8 nM。sst2 Receptor agonist-1 可抑制大鼠生长激素 (GH) 分泌和眼部新生血管病变的形成。具有抗血管形成作用。
生物活性

sst2 Receptor agonist-1 is a potentsomatostatin receptorsubtype 2 (sst2)agonist with aKivalue of 0.025 nM and a cAMPIC50value of 4.8 nM. sst2 Receptor agonist-1 can inhibit rat growth hormone (GH) secretion and ocular neovascular lesion formation. Antiangiogenic effect[1].

IC50& Target[1]

SSTR2

0.025 nM (Ki)

SSTR2

4.8 nM (IC50)

体内研究
(In Vivo)

sst2 Receptor agonist-1 (compound 21) (0.2 or 2 mg/kg; IV; single dosage) shows a dose-dependent decrease in growth hormone (GH) secretion[1].
sst2 Receptor agonist-1 (5 or 15 μg/per eye; intraocular; once every 4 days) reduces neovascular lesion area in laser choroidal neovascularization (CNV) rat model[1].
Pharmacokinetic Parameters of sst2 Receptor agonist-1 (compound 21) in dogs and rats[1].

speciesdog (IV 0.125 mg/kg)rat (IV 2 mg/kg or 5 mg/kg)
CLplasma(mL/min/kg)7.152
t1/2(h)112.9
VdSS(L/kg)5.79.4
F (%)ND17

Animal Model:Female Wistar rats (200-250 g; IP injection with 50 mg/kg pentobarbital, then injected with tested compound via jugular cannula, after 40 or 50 min administration, injected with GH secretagogue via jugular cannula)[1]
Dosage:0.2 or 2 mg/kg
Administration:IV; single dosage
Result:Caused a dose-dependent decrease in GH secretion (38 and 91% reduction in plasma GH AUC following administration of 0.2 and 2 mg/kg, respectively).
Animal Model:Male Brown Norway rats (175-225 g; lasered and perfused, a 27G needle was used to make a small hole in the eye 3 mm posterior to iris angled 45° toward the optic nerve)[1]
Dosage:5 or 15 μg/per eye, 5 μL
Administration:Intraocular administration; inject at day 0, 4 and 8
Result:Exhibited a dose-dependent antiangiogenic effect by a 35 and 53% reduction in neovascular lesion area with 5 or 15 μg per eye, respectively.
分子量

432.94

Formula

C26H25ClN2O2

CAS 号

1021912-42-4

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.