1. Neuronal Signaling
  2. Sigma Receptor
  3. KB-5492 free base

KB-5492 free base 

目录号: HY-47228 纯度: 99.06%
COA 产品使用指南

KB-5492 free base 是一种有效的和选择性的 sigma 受体抑制剂,抑制 [3H]1,3-di(2-tolyl)guanidine (DTG) 与 sigma 受体结合,IC50 值为 3.15 μM。KB-5492 free base 是一种抗溃疡剂。

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KB-5492 free base Chemical Structure

KB-5492 free base Chemical Structure

CAS No. : 113594-64-2

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     可免费申领三个不同产品的试用装。

3.  试用装只面向终端客户

规格 价格 是否有货 数量
Free Sample (0.1 - 0.2 mg)   Apply now  
10 mM * 1 mL in DMSO ¥770
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5 mg ¥700
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10 mg ¥1200
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25 mg ¥2500
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50 mg ¥4000
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100 mg ¥6000
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200 mg   询价  
500 mg   询价  

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Customer Review

Other Forms of KB-5492 free base:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

KB-5492 free base is a potent and selective inhibitor of sigma receptor, inhibits specific [3H]1,3-di(2-tolyl)guanidine (DTG) binding to the sigma receptor with an IC50 of 3.15 μM. KB-5492 free base is an anti-ulcer agent[1][2].

IC50 & Target

IC50: 3.15 μM (sigma receptor)[1]

体外研究
(In Vitro)

KB-5492 (0.001-100 μM) free base inhibits specific [3H]DTG binding in a concentration-dependent manner[1].
KB-5492 (0.1-1 mM) free base significantly and concentration-dependently prevents the ethanol- and acidified aspirin-induced increases in 51Cr release from gastric epithelial cells[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

体内研究
(In Vivo)

KB-5492 (200 mg/kg; p.o.) free base prevents macroscopic lesions in the gastric mucosa[2].

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: Male Sprague-Dawley rats weighing 210-240 g are induced gastric mucosal damage[2]
Dosage: 200 mg/kg
Administration: Oral gavage
Result: Reduced the lesion length as compared with the control.
Prevented the deep mucosal lesions and exfoliation of surface epithelial cells.
分子量

430.49

Formula

C23H30N2O6

CAS 号
性状

固体

颜色

White to off-white

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式
Powder -20°C 3 years
4°C 2 years
In solvent -80°C 6 months
-20°C 1 month
溶解性数据
In Vitro: 

DMSO 中的溶解度 : 100 mg/mL (232.29 mM; 超声助溶; 吸湿的 DMSO 对产品的溶解度有显著影响,请使用新开封的 DMSO)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 2.3229 mL 11.6147 mL 23.2293 mL
5 mM 0.4646 mL 2.3229 mL 4.6459 mL
查看完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

  • 摩尔计算器

  • 稀释计算器

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

质量
=
浓度
×
体积
×
分子量 *

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start)

C1

×
体积 (start)

V1

=
浓度 (final)

C2

×
体积 (final)

V2

动物溶解方案计算器
请输入动物实验的基本信息:

给药剂量

mg/kg

动物的平均体重

g

每只动物的给药体积

μL

动物数量

由于实验过程有损耗,建议您多配一只动物的量
计算结果
工作液所需浓度 : mg/mL
纯度 & 产品资料
参考文献

KB-5492 free base 相关分类

完整储备液配制表

* 请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month。-80°C储存时,请在6个月内使用,-20°C储存时,请在1个月内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.3229 mL 11.6147 mL 23.2293 mL 58.0734 mL
5 mM 0.4646 mL 2.3229 mL 4.6459 mL 11.6147 mL
10 mM 0.2323 mL 1.1615 mL 2.3229 mL 5.8073 mL
15 mM 0.1549 mL 0.7743 mL 1.5486 mL 3.8716 mL
20 mM 0.1161 mL 0.5807 mL 1.1615 mL 2.9037 mL
25 mM 0.0929 mL 0.4646 mL 0.9292 mL 2.3229 mL
30 mM 0.0774 mL 0.3872 mL 0.7743 mL 1.9358 mL
40 mM 0.0581 mL 0.2904 mL 0.5807 mL 1.4518 mL
50 mM 0.0465 mL 0.2323 mL 0.4646 mL 1.1615 mL
60 mM 0.0387 mL 0.1936 mL 0.3872 mL 0.9679 mL
80 mM 0.0290 mL 0.1452 mL 0.2904 mL 0.7259 mL
100 mM 0.0232 mL 0.1161 mL 0.2323 mL 0.5807 mL
Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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产品名称:
KB-5492 free base
目录号:
HY-47228
需求量: