1. Metabolic Enzyme/Protease Apoptosis
  2. Mitochondrial Metabolism Apoptosis
  3. Perhexiline

Perhexiline  (Synonyms: 哌克昔林;双环己哌啶;环己哌啶;环基哌啶)

目录号: HY-B1334
产品使用指南

Perhexiline 是一种具有口服活性的 CPT1CPT2 抑制剂,可减少脂肪酸代谢。Perhexiline 在肝细胞中诱导线粒体功能障碍和细胞凋亡 (apoptosis)。Perhexiline 可穿过血脑屏障 (BBB),并显示出抗肿瘤活性。Perhexiline 可用于癌症和心绞痛等心血管疾病的研究。

该游离形式化合物不稳定,推荐具有相同生物学活性的稳定盐形式 Perhexiline maleate

MCE 的所有产品仅用作科学研究或药证申报,我们不为任何个人用途提供产品和服务

Perhexiline Chemical Structure

Perhexiline Chemical Structure

CAS No. : 6621-47-2

1.  客户无需承担相应的运输费用。

2.  同一机构(单位)同一产品试用装仅限申领一次,同一机构(单位)一年内

     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 是否有货
50 mg   询价  
100 mg   询价  
250 mg   询价  

* Please select Quantity before adding items.

Perhexiline 的其他形式现货产品:

Customer Review

Other Forms of Perhexiline:

  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Perhexiline is an orally active CPT1 and CPT2 inhibitor that reduces fatty acid metabolism. Perhexiline induces mitochondrial dysfunction and apoptosis in hepatic cells. Perhexiline can cross the blood brain barrier (BBB) and shows anti-tumor activity. Perhexiline can be used in the research of cancers, and cardiovascular disease like angina[1][2][5].

体外研究
(In Vitro)

Perhexiline (5-25 μM, 2-6 h) reduces cell viability in HepG2 cells[2].
Perhexiline (5-25 μM, 2-6 h) reduces cellular ATP content and Lactate dehydrogenase (LDH) release in HepG2 cells[2].
Perhexiline (20 μM, 2 h) activates caspase 3/7 in HepG2 cells[2].
Perhexiline (5-25 μM, 4 h) causes mitochondrial dysfunction in HepG2 cells[2].
Perhexiline (5 μM, 48 h) selectively induces massive apoptosis in CLL cells (high expression of CPT)[3].

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

Cell Viability Assay[2]

Cell Line: HepG2 cells
Concentration: 5, 10, 15, 25 μM
Incubation Time: 2, 4, 6 h
Result: Induced time- and concentration-dependent cytotoxicity in hepatic cells.

Western Blot Analysis[2]

Cell Line: HepG2 cells
Concentration: 5, 10, 15, 25 μM
Incubation Time: 2 h
Result: Reduced Bcl-2 and Mcl-1 level, and increased Bad level.
体内研究
(In Vivo)

Perhexiline (200 mg/kg, p.o., daily for 8 weeks) reduces peripheral neural function in female DA rats[4].
Perhexiline (80 mg/kg, oral gavage, for 3 days) demonstrates anti-tumor activity in glioblastoma mouse model[5].

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

Animal Model: Orthotopic glioblastoma mouse model[5]
Dosage: 80 mg/kg
Administration: Oral gavage, for 3 days.
Result: Reduces tumor size (MR imaging) and improves in overall survival.
Clinical Trial
分子量

277.49

Formula

C19H35N

CAS 号
中文名称

哌克昔林;双环己哌啶;环己哌啶;环基哌啶

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.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

The molarity calculator equation

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

质量   浓度   体积   分子量 *
= × ×

The dilution calculator equation

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

This equation is commonly abbreviated as: C1V1 = C2V2

浓度 (start) × 体积 (start) = 浓度 (final) × 体积 (final)
× = ×
C1   V1   C2   V2
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.

您最近查看的产品:

Your information is safe with us. * Required Fields.

   产品名称:

 

* 需求量:

* 客户姓名:

 

* Email:

* 电话:

 

* 公司或机构名称:

   留言给我们:

Bulk Inquiry

Inquiry Information

产品名称:
Perhexiline
目录号:
HY-B1334
需求量: