Scoulerine - CAS:6451-73-6

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Scoulerine (Synonyms:(--Scoulerine; Discretamine))

目录号 : KM20065 CAS No. : 6451-73-6 纯度 : 98%

Data Sheet 产品使用指南

Scoulerine ((-)-Scoulerine) 是一种有效的抗有丝分裂 (antimitotic) 化合物。Scoulerine 也是 BACE1 (淀粉样前体蛋白裂解酶 1) 的抑制剂。Scoulerine 抑制细胞增殖，阻止细胞周期，并诱导癌细胞凋亡。

规格	价格	是否有货	数量
5mg		In-stock

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生物活性

Scoulerine ((-)-Scoulerine), an isoquinoline alkaloid, is a potent antimitotic compound. Scoulerine is also an inhibitor of BACE1 (ß-site amyloid precursor protein cleaving enzyme 1). Scoulerine inhibits proliferation, arrests cell cycle, and induces apoptosis in cancer cells.

体外研究

Scoulerine ((-)-Scoulerine) inhibits mini-panel of human leukemic cells, MOLT-4 (WT), Jurkat (TP53 mutated), Raji (TP53 mutated), HL-60 (TP53 null), U-937 (TP53 mutated), and HEL 92.1.7 (wild-type), with IC₅₀s ranging from 2.7 µM to 6.5 µM.
Scoulerine (2.5-20 µM; 24 hours) decreases proliferation of Jurkat and MOLT-4 cells.
Scoulerine (2.5-20 µM; 24 hours) induces MOLT-4 and Jurkat cells apoptosis.
Scoulerine induces G2 or M cell cycle arrest.
Scoulerine (2.5-5 µM; 24 hours) shows an upregulation of p53 protein in p53 wild-type MOLT-4 cells.
Scoulerine (2.5-5 µM; 24-48 hours) activates caspase-3/7, -8 and -9 in a dose-dependent manner.
Scoulerine (5-10 µM; 24 hours) disrupts microtubule structure of A549 lung carcinoma cells

Cell Proliferation Assay

Cell Line:	Jurkat and MOLT-4 cells
Concentration:	2.5, 5, 10, 15 and 20 µM
Incubation Time:	24 hours
Result:	Significantly reduced the viability and proliferation of Jurkat and MOLT-4 cells in a dose dependent manner.

Apoptosis Analysis

Cell Line:	MOLT-4 and Jurkat cells
Concentration:	2.5, 5, 10, 15 and 20 µM
Incubation Time:	24 hours
Result:	Induced MOLT-4 and Jurkat cells apoptosis.

Cell Cycle Analysis

Cell Line:	Jurkat and MOLT-4 leukemic cells
Concentration:	2.5-20 µM
Incubation Time:	16 hours
Result:	Induced cell cycle arrest at the G2/M transition.

Western Blot Analysis

Cell Line:	MOLT-4 cells
Concentration:	2.5, 5 µM
Incubation Time:	24 hours
Result:	Showed an upregulation of p53 protein in p53 wild-type MOLT-4 cells.

分子式

C₁₉H₂₁NO₄

分子量

327.37

CAS号

6451-73-6

中文名称

金黄紫堇碱

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.

溶解性数据

In Vitro:

DMSO :100 mg/mL (305.46 mM; Need ultrasonic)

配制储备液

浓度溶剂体积质量	1 mg	5 mg	10 mg

1 mM	3.0546 mL	15.2732 mL	30.5465 mL
5 mM	0.6109 mL	3.0546 mL	6.1093 mL
10 mM	0.3055mL	1.5273 mL	3.0546 mL

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。

In Vivo:

请根据您的实验动物和给药方式选择适当的溶解方案。以下溶解方案都请先按照 In Vitro 方式配制澄清的储备液，再依次添加助溶剂：

——为保证实验结果的可靠性，澄清的储备液可以根据储存条件，适当保存；体内实验的工作液，建议您现用现配，当天使用；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

1.

请依序添加每种溶剂： 10% DMSO → 40% PEG300 → 5% Tween-80 → 45% saline

Solubility: ≥ 2.08 mg/mL (6.35 mM); Clear solution

此⽅案可获得 ≥ 2.08 mg/mL (6.35 mM，饱和度未知) 的澄清溶液。

以 1 mL ⼯作液为例，取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 400 μL PEG300 中，混合均匀；向上述体系中加⼊ 50 μ L Tween-80，混合均匀；然后继续加⼊ 450 μL ⽣理盐⽔定容⾄ 1 mL。
2.

请依序添加每种溶剂： 10% DMSO → 90% (20% SBE-β-CD in saline)

Solubility: ≥ 2.08 mg/mL (6.35 mM); Clear solution

此⽅案可获得 ≥ 2.08 mg/mL (6.35 mM，饱和度未知) 的澄清溶液。

以 1 mL ⼯作液为例，取 100 μL 20.8 mg/mL 的澄清 DMSO 储备液加到 900 μL 20% 的 SBE-β-CD ⽣理盐⽔⽔溶液中，混合均匀。

纯度： 98%

Data Sheet

产品使用指南

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