1. Metabolic Enzyme/Protease Apoptosis
  2. Carnitine Palmitoyltransferase (CPT) Mitochondrial Metabolism Apoptosis
  3. Perhexiline maleate

Perhexiline (maleate)  (Synonyms: ペルヘキシリン マレイン酸塩)

製品番号: HY-B1334A 純度: 99.97%
COA 取扱説明書 Technical Support

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

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CAS 番号 : 6724-53-4

容量 価格(税別) 在庫状況 数量
5 mg $100 在庫あり
10 mg $150 在庫あり
25 mg $270 在庫あり
50 mg $400 在庫あり
100 mg $600 在庫あり
200 mg $840 在庫あり
500 mg   お問い合わせ  
1 g   お問い合わせ  

* アイテムを追加する前、数量をご選択ください

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カスタマーレビュー

Based on 6 publication(s) in Google Scholar

Other Forms of Perhexiline maleate:

Top Publications Citing Use of Products

    Perhexiline maleate purchased from MedChemExpress. Usage Cited in: Nat Genet. 2025 Mar;57(3):680-693.

    Inhibition of CPT1A activity using Perhexiline maleate (0-10 μM, 24 h) and PD-L1 detection by western blotting in A375 cell.

    Perhexiline maleate purchased from MedChemExpress. Usage Cited in: Nat Genet. 2025 Mar;57(3):680-693.

    A375 cells treated with Perhexiline maleate (0-10 μM) for 24 h, then co-cultured with or without activated T cells for 24 h to assess the killing effect.

    Perhexiline maleate purchased from MedChemExpress. Usage Cited in: Acta Pharm Sin B. 2025 Jan;15(1):133-150.

    Results of H&E and Ki67 staining in representative A549 cells tumor sections of vehicle, perhexiline (10 mg/kg, ip, 3 days), and Perhexiline maleate (10 mg/kg) treated naked mice. Scale bar = 200 μm (H&E up).

    Perhexiline maleate purchased from MedChemExpress. Usage Cited in: Acta Pharm Sin B. 2025 Jan;15(1):133-150.

    Perhexiline maleate (0-20 μM, 8 days) exhibited inhibition of colony formation in A549 and NCI-H1975 cells.

    Perhexiline maleate purchased from MedChemExpress. Usage Cited in: Acta Pharm Sin B. 2025 Jan;15(1):133-150.

    Reversal relationship between LUAD GSFM pattern and Perhexiline maleate GSFM pattern.
    • 生物活性

    • 純度とドキュメンテーション

    • 参考文献

    • カスタマーレビュー

    製品説明

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

    IC50 & Target

    CPT-1

     

    CPT-2

     

    体外実験

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

    MedChemExpress (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.
    体内実験

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

    MedChemExpress (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.
    分子量

    393.56

    分子式

    C23H39NO4

    CAS 番号
    Appearance

    Solid

    Color

    White to off-white

    SMILES

    O=C(O)/C=C\C(O)=O.C1(CC(C2CCCCC2)C3CCCCC3)NCCCC1

    輸送条件

    Room temperature in continental US; may vary elsewhere.

    保管条件

    4°C, sealed storage, away from moisture

    *In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

    溶剤 & 溶解度
    体外: 

    DMSO : 16.67 mg/mL (42.36 mM; ultrasonic and adjust pH to 5 with HCl; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

    Preparing
    Stock Solutions
    Concentration Solvent Mass 1 mg 5 mg 10 mg
    1 mM 2.5409 mL 12.7045 mL 25.4091 mL
    5 mM 0.5082 mL 2.5409 mL 5.0818 mL
    10 mM 0.2541 mL 1.2705 mL 2.5409 mL
    View the Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    • Molarity Calculator

    • Dilution Calculator

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

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

    一般には略語で表示されます:C1V1 = C2V2

    濃度 (開始)

    C1

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    体積 (開始)

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    体内:

    For the following dissolution methods, please prepare the working solution directly. It is recommended to prepare fresh solutions and use them promptly within a short period of time.
    The percentages shown for the solvents indicate their volumetric ratio in the final prepared solution. If precipitation or phase separation occurs during preparation, heat and/or sonication can be used to aid dissolution.

    • Protocol 1

      Add each solvent one by one:  0.5% CMC-Na/saline water

      Solubility: 5 mg/mL (12.70 mM); Suspended solution; Need ultrasonic

    In Vivo Dissolution Calculator
    Please enter the basic information of animal experiments:

    Dosage

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    (per animal)

    g

    Dosing volume
    (per animal)

    μL

    Number of animals

    Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.
    Calculation results:
    Working solution concentration: mg/mL
    純度とドキュメンテーション

    純度: 99.97%

    参考文献

    Complete Stock Solution Preparation Table

    * Please refer to the solubility information to select the appropriate solvent. Once prepared, please aliquot and store the solution to prevent product inactivation from repeated freeze-thaw cycles.
    Storage method and period of stock solution: -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture). When stored at -80°C, please use it within 6 months. When stored at -20°C, please use it within 1 month.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 2.5409 mL 12.7045 mL 25.4091 mL 63.5227 mL
    5 mM 0.5082 mL 2.5409 mL 5.0818 mL 12.7045 mL
    10 mM 0.2541 mL 1.2705 mL 2.5409 mL 6.3523 mL
    15 mM 0.1694 mL 0.8470 mL 1.6939 mL 4.2348 mL
    20 mM 0.1270 mL 0.6352 mL 1.2705 mL 3.1761 mL
    25 mM 0.1016 mL 0.5082 mL 1.0164 mL 2.5409 mL
    30 mM 0.0847 mL 0.4235 mL 0.8470 mL 2.1174 mL
    40 mM 0.0635 mL 0.3176 mL 0.6352 mL 1.5881 mL
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    • Molarity Calculator

    • Dilution Calculator

    The molarity calculator equation

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

    質量   濃度   体積   分子量 *
    = × ×

    The dilution calculator equation

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

    一般には略語で表示されます:C1V1 = C2V2

    濃度 (開始) × 体積 (開始) = 濃度 (終了) × 体積 (終了)
    × = ×
    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.

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    製品名:
    Perhexiline maleate
    製品番号:
    HY-B1334A
    数量:
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