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KHK-IN-1 HCl {[allProObj[0].p_purity_real_show]}

货号:A299396 同义名: KHK-IN-1 hydrochloride

KHK-IN-1 HCl is a potent ketohexokinase (KHK) inhibitor with IC50 of 12 nM, interacts with Asp-27B in the ATP-binding region of KHK.

KHK-IN-1 HCl 化学结构 CAS号:1303470-48-5
KHK-IN-1 HCl 化学结构
CAS号:1303470-48-5
KHK-IN-1 HCl 3D分子结构
CAS号:1303470-48-5
KHK-IN-1 HCl 化学结构 CAS号:1303470-48-5
KHK-IN-1 HCl 3D分子结构 CAS号:1303470-48-5
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KHK-IN-1 HCl 纯度/质量文件 产品仅供科研

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KHK-IN-1 HCl 生物活性

描述 KHK-IN-1 hydrochloride is a specific and cell-permeable inhibitor of ketohexokinase (KHK) (IC50=12 nM; F=34%). It effectively suppresses the generation of F1P in HepG2 cell lysates with an IC50 greater than 400 nM. KHK-IN-1 hydrochloride holds promise for research in the fields of diabetes and obesity[1].
体内研究

KHK-IN-1 hydrochloride (10 mg/kg; pO.; single) demonstrates a rat oral bioavailability of 34%[1].

体外研究

KHK-IN-1 hydrochloride exhibits stability in human and rat liver microsome preparations, with 88% and 72% remaining at 10 minutes, respectively. Furthermore, it does not exert significant inhibition on cytochrome P450 enzymes from human liver microsomes, including 1A2, 2C19, 2D6, 2C9, and 3A4[1].

KHK-IN-1 hydrochloride (0-10 µM; incubate 30 min, then add to 15 mM fructose and incubate for another 3 h) suppresses the generation of F1P in HepG2 cell lysates, exhibiting an IC50 value of 400 nM[1].

KHK-IN-1 HCl 参考文献

[1]Maryanoff BE, et al. Inhibitors of Ketohexokinase: Discovery of Pyrimidinopyrimidines with Specific Substitution that Complements the ATP-Binding Site. ACS Med Chem Lett. 2011 Apr 18;2(7):538-43.

KHK-IN-1 HCl 实验方案

计算器
存储液制备 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.18mL

0.44mL

0.22mL

10.89mL

2.18mL

1.09mL

21.79mL

4.36mL

2.18mL

KHK-IN-1 HCl 技术信息

CAS号1303470-48-5
分子式C21H27ClN8S
分子量 459.011
别名 KHK-IN-1 hydrochloride
运输蓝冰
存储条件

液体 -20°C:3-6个月-80°C:12个月

粉末 Inert atmosphere,2-8°C

溶解度

DMSO: 25 mg/mL(54.46 mM),配合低频超声助溶,注意:DMSO长时间开封后,会吸水并导致溶解能力下降,请避免使用长期开封的DMSO

H2O: 14 mg/mL(30.5 mM),配合低频超声,并水浴加热至45℃助溶

动物实验配方
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