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  3. SC-26196

SC-26196 是一种有效的,具有口服活性的 Delta6 去饱和酶 (D6D, FADS2) 抑制剂 (在大鼠肝微粒体中,IC50=0.2 μM)。具有抗炎活性。

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SC-26196 Chemical Structure

SC-26196 Chemical Structure

CAS No. : 218136-59-5

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规格 价格 是否有货 数量
1 mg ¥522
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5 mg ¥1150
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10 mg ¥1650
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25 mg ¥2860
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50 mg ¥4004
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Customer Review

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

SC-26196 is a potent, orally active Delta6 desaturase (D6D, FADS2) inhibitor (IC50=0.2 μM in a rat liver microsomal assay). Antiinflammatory properties[1].

IC50 & Target

IC50: 0.2 µM (Delta6 desaturase in a rat liver microsomal assay)[1]

体外研究
(In Vitro)

SC-26196 (200 nM) inhibits proliferation of peripheral blood mononuclear cells (PBMCs), but Not Jurkat Cells[2].

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

Cell Proliferation Assay[2]

Cell Line: PBMCs and Jurkat cells
Concentration: 200 nM
Incubation Time: 96 hours for PBMCs; 144 hours for Jurkat cells
Result: Treatment of PBMCs significantly decreased the proportion of cells that underwent division, the division index and proliferation index.
Did not alter cell proliferation significantly in Jurkat cells.
体内研究
(In Vivo)

SC-26196 ( included in the diet at 0, 0.07, 0.21, or 0.7 mg/kg diet to achieve dosages of 0, 10, 30, and 100 mg/kg per day) causes a decrease in the calculated Δ6-desaturase index in both adipose tissue and liver. Feeding 100 mg SC-26196 per kg BW per day inhibits the Δ6-desaturase enzyme[3].

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

Animal Model: Male mice (12- or 15-week-old)[3]
Dosage: 0, 10, 30, and 100 mg/kg per day
Administration: Included in the diet at 0, 0.07, 0.21, or 0.7mg/kg diet to achieve dosages of 0, 10, 30, and 100mg/kg per day.
Result: Caused a decrease in the calculated Δ6-desaturase index in both adipose tissue and liver.
分子量

423.55

Formula

C27H29N5

CAS 号
性状

固体

颜色

Off-white to yellow

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 2 years
-20°C 1 year
溶解性数据
细胞实验: 

DMSO 中的溶解度 : 5 mg/mL (11.80 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 2.3610 mL 11.8050 mL 23.6100 mL
5 mM 0.4722 mL 2.3610 mL 4.7220 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, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

  • 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

动物实验:

以下溶解方案,请直接配制工作液。建议现用现配,在短期内尽快用完。 以下溶剂前显示的百分比是指该溶剂在您配制终溶液中的体积占比; 如在配制过程中出现沉淀、析出现象,可以通过加热和/或超声的方式助溶。

  • 方案 一

    请依序添加每种溶剂: 0.5% CMC-Na/saline water

    Solubility: 5 mg/mL (11.80 mM); 悬浊液; Need ultrasonic and warming and heat to 40°C

  • 方案 二

    请依序添加每种溶剂: 15% Cremophor EL    85% Saline

    Solubility: 10 mg/mL (23.61 mM); 悬浊液; 超声助溶

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

纯度: 99.68%

参考文献

SC-26196 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, 2 years; -20°C, 1 year。-80°C储存时,请在2年内使用, -20°C储存时,请在1年内使用。

可选溶剂 浓度 溶剂体积 质量 1 mg 5 mg 10 mg 25 mg
DMSO 1 mM 2.3610 mL 11.8050 mL 23.6100 mL 59.0249 mL
5 mM 0.4722 mL 2.3610 mL 4.7220 mL 11.8050 mL
10 mM 0.2361 mL 1.1805 mL 2.3610 mL 5.9025 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:
SC-26196
目录号:
HY-107410
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