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1-(2,3-Dichlorophenyl)ethanamine hydrochloride {[allProObj[0].p_purity_real_show]}

货号:A254512

High affinity inhibitor of phenylethanolamine-N-methyltransferase (PNMT) (Ki = 0.09 μM in vitro). Suppresses the release of growth hormone in an in vivo rat model.

1-(2,3-Dichlorophenyl)ethanamine hydrochloride 化学结构 CAS号:39959-66-5
1-(2,3-Dichlorophenyl)ethanamine hydrochloride 化学结构
CAS号:39959-66-5
1-(2,3-Dichlorophenyl)ethanamine hydrochloride 3D分子结构
CAS号:39959-66-5
1-(2,3-Dichlorophenyl)ethanamine hydrochloride 化学结构 CAS号:39959-66-5
1-(2,3-Dichlorophenyl)ethanamine hydrochloride 3D分子结构 CAS号:39959-66-5
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1-(2,3-Dichlorophenyl)ethanamine hydrochloride 纯度/质量文件 产品仅供科研

货号:A254512 标准纯度: {[allProObj[0].p_purity_real_show]}
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产品名称 Transferase 其他靶点 纯度
Tipifarnib +++

FTase, IC50: 0.6 nM

99%+
Tolcapone +

COMT, Ki: 30 nM

99%+
Lonafarnib +++

H-ras, IC50: 1.9 nM

K-ras-4B, IC50: 2.8 nM

99%+
(E)-Daporinad ++++

NMPRTase, Ki: 0.4 nM

99%+
FTI-277 HCl ++++

FTase, IC50: 500 pM

98%
A 922500 ++

mouse DGAT-1, IC50: 24 nM

human DGAT-1, IC50: 7 nM

98%
Lomeguatrib ++

O6-alkylguanine-DNA-alkyltransferas, IC50: 5 nM

99%+
PF-04620110 +

DGAT1, IC50: 19 nM

98%
LB42708 +++

FTase (K-Ras), IC50: 0.8 nM

FTase (N-ras), IC50: 1.2 nM

98%
GGTI298 Trifluoroacetate 98%+
1. 鼠标悬停在“+”上可以显示相关IC50的具体数值。"+"越多,抑制作用越强。2. "✔"表示该化合物对相应的亚型有抑制作用,但抑制强度暂时没有相关数据。

1-(2,3-Dichlorophenyl)ethanamine hydrochloride 生物活性

描述 Phenylethanolamine-N-methyltransferase (PNMT) is an enzyme that catalyzes the final step of the biosynthesis of epinephrine from norepinephrine. LY 78335 is a PNMT inhibitor with a Ki value of 0.09μM in vitro. The half-life of LY 78335 in rat adrenal glands after injection of a dose of 0.2mmol/kg was 3.4 hours. Treatment of rats with 0.2mmol/kg LY 78335 1 hour before forced exercise led to a significant reduction in the epinephrine level compared with the saline-treated controls[1]. Treatment of mice with 25mg/kg LY 78335 resulted in dose-related reductions in exploratory head-dipping in the hold-board test without affecting locomotor activity[2].

1-(2,3-Dichlorophenyl)ethanamine hydrochloride 参考文献

[1]References are publications that support the biological activity of the product. Fuller et al (1973) Inhibition of phenylethanolamine N-methyltransferase by benzylamines. 2. In vitro and in vivo studies with 2,3-dichloro-α-methylbenzylamine. J.Med.Chem. 16 106 PMID: 4683104 Terry et al (1982) Regulation of episodic GH secretion by the central epinephrine system. J.Clin.Invest. 69 104 PMID: 7054231 Grunewald et al (1988) Synthesis and evaluation of 3-substituted analogues of 1,2,3,4-tetrahydroisoquinoline as inhibitors of phenylethanolamine N-methyltransferase. J.Med.Chem. 31 824 PMID: 3351861 If you know of a relevant reference for LY 78335, please let us know.

[2]Fuller RW, Roush BW, Snoddy HD, Molloy BB. Inhibition of phenylethanolamine N-methyltransferase by benzylamines. 2. In vitro and in vivo studies with 2,3-dichloro-methylbenzylamine. J Med Chem. 1973 Feb;16(2):106-9.

[3]Durcan MJ, Lister RG, Linnoila M. Behavioral effects of the inhibitors of phenylethanolamine-N-methyltransferase, LY 78335 and LY 134046, and their interactions with ethanol. Psychopharmacology (Berl). 1990;101(2):196-202.

1-(2,3-Dichlorophenyl)ethanamine hydrochloride 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

4.41mL

0.88mL

0.44mL

22.07mL

4.41mL

2.21mL

44.14mL

8.83mL

4.41mL

1-(2,3-Dichlorophenyl)ethanamine hydrochloride 技术信息

CAS号39959-66-5
分子式C8H10Cl3N
分子量 226.531
别名
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Sealed in dry,Room Temperature

溶解度

H2O: 100 mg/mL(441.44 mM)

动物实验配方
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