1. Cell Cycle/DNA Damage Epigenetics Autophagy Apoptosis
  2. Aurora Kinase Autophagy Apoptosis
  3. Alisertib

Alisertib  (Synonyms: MLN 8237)

製品番号: HY-10971 純度: 99.36%
COA 取扱説明書 Technical Support

Alisertib (MLN 8237) is an orally active and selective Aurora A kinase inhibitor (IC50=1.2 nM), which binds to Aurora A kinase resulting in mitotic spindle abnormalities, mitotic accumulation. Alisertib (MLN 8237) induces apoptosis and autophagy through targeting the AKT/mTOR/AMPK/p38 pathway in leukemic cells. Antitumor activity.

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CAS 番号 : 1028486-01-2

容量 価格(税別) 在庫状況 数量
>無料サンプル (0.1 - 0.2 mg)   今すぐ申し込む  
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
USD 82 在庫あり
Solution
10 mM * 1 mL in DMSO USD 82 在庫あり
Solid
5 mg $72 在庫あり
10 mg $120 在庫あり
25 mg $206 在庫あり
50 mg $290 在庫あり
100 mg $450 在庫あり
200 mg $850 在庫あり
500 mg $1200 在庫あり
1 g $1620 在庫あり
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カスタマーレビュー

Based on 72 publication(s) in Google Scholar

Other Forms of Alisertib:

Top Publications Citing Use of Products

顧客検証

IF
IHC
WB

    Alisertib purchased from MedChemExpress. Usage Cited in: FASEB J. 2018 May;32(5):2735-2746.  [Abstract]

    Representative immunofluorescence (IF) image and graph with frequency of ciliated WT or Pkd12/2 murine renal epithelial cells at 2 h after treatment with vehicle (V), Ganetespib (G), or Alisertib (A) to inhibit AURKA, or (C) combination of Alisertib and Ganetespib. On IF, acetylated a-tubulin (red); g-tubulin (green); DAPI (blue).

    Alisertib purchased from MedChemExpress. Usage Cited in: Drexel University. 2016 Nov.

    Alisertib and combination treatment suppress proliferation in BT474 orthotopic tumors as shown by decrease in Ki-67, which is statistically significantly different between vehicle and combination treatment, FRAX1036 and Alisertib, and FRAX1036 and combination treatment.

    Alisertib purchased from MedChemExpress. Usage Cited in: Drexel University. 2016 Nov.

    Alisertib enhances FRAX1036 inhibitory effect on PAK1 phosphorylation in BT474 xenograft model.

    Aurora Kinase アイソフォーム固有の製品をすべて表示:

    • 生物活性

    • 純度とドキュメンテーション

    • 参考文献

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    製品説明

    Alisertib (MLN 8237) is an orally active and selective Aurora A kinase inhibitor (IC50=1.2 nM), which binds to Aurora A kinase resulting in mitotic spindle abnormalities, mitotic accumulation. Alisertib (MLN 8237) induces apoptosis and autophagy through targeting the AKT/mTOR/AMPK/p38 pathway in leukemic cells. Antitumor activity[1][2][3].

    IC50 & Target[3]

    Aurora A

    1.2 nM (IC50)

    Aurora B

    396.5 nM (IC50)

    Cellular Effect
    Cell Line Type Value Description References
    HCT-116 GI50
    0.03 μM
    Compound: 10, alisertib
    Cytotoxicity against human HCT116 cells assessed as inhibition of cell proliferation by BrdU incorporation assay
    Cytotoxicity against human HCT116 cells assessed as inhibition of cell proliferation by BrdU incorporation assay
    [PMID: 26101564]
    HCT-116 IC50
    1.5 μM
    Compound: 10, alisertib
    Inhibition of aurora kinase B in human HCT116 cells assessed as inhibition of histone H3 phosphorylation by immunofluorescence analysis
    Inhibition of aurora kinase B in human HCT116 cells assessed as inhibition of histone H3 phosphorylation by immunofluorescence analysis
    [PMID: 26101564]
    HCT-116 IC50
    32 μM
    Compound: MLN-8237
    Antiproliferative activity against human HCT116 cells measured after 96 hrs by Brdu incorporation-based ELISA
    Antiproliferative activity against human HCT116 cells measured after 96 hrs by Brdu incorporation-based ELISA
    [PMID: 31381325]
    HCT-116 IC50
    7 nM
    Compound: 10, alisertib
    Inhibition of aurora kinase A autophosphorylation at T288 in human HCT116 cells by immunofluorescence analysis
    Inhibition of aurora kinase A autophosphorylation at T288 in human HCT116 cells by immunofluorescence analysis
    [PMID: 26101564]
    HCT-116 IC50
    95 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human HCT116 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human HCT116 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    HCT-15 IC50
    740 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human HCT15 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human HCT15 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    HL-60 IC50
    74 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human HL60 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human HL60 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    HT-29 IC50
    330 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human HT-29 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human HT-29 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    LC-2-ad IC50
    77 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human LC2/ad cells after 72 hrs by WST8 assay
    Antiproliferative activity against human LC2/ad cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    LU-99A IC50
    62 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human LU99A cells after 72 hrs by WST8 assay
    Antiproliferative activity against human LU99A cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    MIA PaCa-2 IC50
    130 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human MIAPaCa2 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human MIAPaCa2 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    MKN-45 IC50
    93 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human MKN45 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human MKN45 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    MRC5 IC50
    > 10000 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human MRC5 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human MRC5 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    MV4-11 IC50
    1.2 nM
    Compound: 17
    Induction of cell cycle arrest in human MV4-11 cells assessed as accumulation of cells at G2/M phase measured after 12 hrs
    Induction of cell cycle arrest in human MV4-11 cells assessed as accumulation of cells at G2/M phase measured after 12 hrs
    [PMID: 36306471]
    NCI-H358 IC50
    100 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human NCI-H358 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human NCI-H358 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    PC-14 IC50
    170 nM
    Compound: 29, MLN-8237
    Antiproliferative activity against human PC14 cells after 72 hrs by WST8 assay
    Antiproliferative activity against human PC14 cells after 72 hrs by WST8 assay
    [PMID: 25625617]
    Sf9 IC50
    1 nM
    Compound: 10, alisertib
    Inhibition of recombinant mouse aurora kinase A expressed in insect Sf9 cells using biotin-GLRRASLG as substrate in presence of [gamma-33P]ATP
    Inhibition of recombinant mouse aurora kinase A expressed in insect Sf9 cells using biotin-GLRRASLG as substrate in presence of [gamma-33P]ATP
    [PMID: 26101564]
    体外実験

    Alisertib (MLN 8237) leads the MM cells to mitotic spindle abnormalities, mitotic accumulation, as well as inhibition of cell proliferation through apoptosis and senescence. Alisertib up-regulates p53 and tumor suppressor genes p21 and p27[1].
    The decreased activity of Alisertib (MLN 8237) for the T217D/W277E Aurora A/TPX2 complex may reflect the increased affinity for ATP induced by cofactor binding to Aurora A[2].
    Alisertib (MLN 8237) inhibits cell proliferation with IC50s ranging from 15 to 469 nM in different tumer cell lines[4].

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

    体内実験

    Alisertib (MLN 8237) (30 mg/kg, p.o.) significantly reduces tumor burden and increases overall survival in xenograft-murine model of human-MM[1].
    Alisertib (3-30 mg/kg; p.o.; once daily for 3 weeks) causes tumor growth inhibition in solid tumor xenograft models[4].

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

    Animal Model: Nude mice bearing HCT-116 colon tumor xenograft[4]
    Dosage: 3, 10, or 30 mg/kg
    Administration: P.o.; once daily for 3 weeks
    Result: Resulted in a dose-dependent TGI (tumor growth inhibition) of 43.3%, 84.2%, and 94.7% for the 3, 10, and 30 mg/kg groups,respectively.
    臨床実験
    分子量

    518.92

    分子式

    C27H20ClFN4O4

    CAS 番号
    Appearance

    Solid

    Color

    Off-white to yellow

    SMILES

    O=C(C1=CC=C(C=C1OC)NC2=NC=C3CN=C(C4=CC(Cl)=CC=C4C3=N2)C5=C(C=CC=C5F)OC)O

    輸送条件

    Room temperature in continental US; may vary elsewhere.

    保管条件
    Powder -20°C 3 years
      4°C 2 years
    In solvent -80°C 6 months
      -20°C 1 month
    溶剤 & 溶解度
    体外: 

    DMSO : 25 mg/mL (48.18 mM; Need ultrasonic; 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 1.9271 mL 9.6354 mL 19.2708 mL
    5 mM 0.3854 mL 1.9271 mL 3.8542 mL
    10 mM 0.1927 mL 0.9635 mL 1.9271 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, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

    • Molarity Calculator

    • Dilution Calculator

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

    Mass
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    ×
    Volume
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    Molecular Weight *

    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

    ×
    体積 (開始)

    V1

    =
    濃度 (終了)

    C2

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    体積 (終了)

    V2

    体内:

    Select the appropriate dissolution method based on your experimental animal and administration route.

    For the following dissolution methods, please ensure to first prepare a clear stock solution using an In Vitro approach and then sequentially add co-solvents:
    To ensure reliable experimental results, the clarified stock solution can be appropriately stored based on storage conditions. As for the working solution for in vivo experiments, it is recommended to prepare freshly and use it on the same day.
    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:  10% DMSO    40% PEG300    5% Tween-80    45% Saline

      Solubility: 2.08 mg/mL (4.01 mM); Suspended solution; Need ultrasonic

      This protocol yields a suspended solution of 2.08 mg/mL. Suspended solution can be used for oral and intraperitoneal injection.

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 400 μL PEG300, and mix evenly; then add 50 μL Tween-80 and mix evenly; then add 450 μL Saline to adjust the volume to 1 mL.

      Preparation of Saline: Dissolve 0.9 g sodium chloride in ddH₂O and dilute to 100 mL to obtain a clear Saline solution.
    • Protocol 2

      Add each solvent one by one:  10% DMSO    90% Corn Oil

      Solubility: ≥ 2.08 mg/mL (4.01 mM); Clear solution

      This protocol yields a clear solution of ≥ 2.08 mg/mL (saturation unknown). If the continuous dosing period exceeds half a month, please choose this protocol carefully.

      Taking 1 mL working solution as an example, add 100 μL DMSO stock solution (20.8 mg/mL) to 900 μL Corn oil, and mix evenly.

    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:  50% PEG300    50% Saline

      Solubility: 10 mg/mL (19.27 mM); Suspended solution; Need ultrasonic

    • Protocol 2

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

      Solubility: 5 mg/mL (9.64 mM); Suspended solution; Need ultrasonic

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

    Dosage

    mg/kg

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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.
    Please enter your animal formula composition:
    %
    DMSO +
    +
    %
    Tween-80 +
    %
    Saline
    Recommended: Keep the proportion of DMSO in working solution below 2% if your animal is weak.
    The co-solvents required include: DMSO, . All of co-solvents are available by MedChemExpress (MCE). , Tween 80. All of co-solvents are available by MedChemExpress (MCE).
    Calculation results:
    Working solution concentration: mg/mL
    Method for preparing stock solution: mg drug dissolved in μL  DMSO (Stock solution concentration: mg/mL).
    The concentration of the stock solution you require exceeds the measured solubility. The following solution is for reference only. If necessary, please contact MedChemExpress (MCE).
    Method for preparing in vivo working solution for animal experiments: Take μL DMSO stock solution, add μL . μL , mix evenly, next add μL Tween 80, mix evenly, then add μL Saline.
     If the continuous dosing period exceeds half a month, please choose this protocol carefully.
    Please ensure that the stock solution in the first step is dissolved to a clear state, and add co-solvents in sequence. You can use ultrasonic heating (ultrasonic cleaner, recommended frequency 20-40 kHz), vortexing, etc. to assist dissolution.
    純度とドキュメンテーション

    純度: 99.84%

    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, 1 year; -20°C, 6 months. When stored at -80°C, please use it within 1 year. When stored at -20°C, please use it within 6 months.

    Optional Solvent Concentration Solvent Mass 1 mg 5 mg 10 mg 25 mg
    DMSO 1 mM 1.9271 mL 9.6354 mL 19.2708 mL 48.1770 mL
    5 mM 0.3854 mL 1.9271 mL 3.8542 mL 9.6354 mL
    10 mM 0.1927 mL 0.9635 mL 1.9271 mL 4.8177 mL
    15 mM 0.1285 mL 0.6424 mL 1.2847 mL 3.2118 mL
    20 mM 0.0964 mL 0.4818 mL 0.9635 mL 2.4088 mL
    25 mM 0.0771 mL 0.3854 mL 0.7708 mL 1.9271 mL
    30 mM 0.0642 mL 0.3212 mL 0.6424 mL 1.6059 mL
    40 mM 0.0482 mL 0.2409 mL 0.4818 mL 1.2044 mL
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    • Molarity Calculator

    • Dilution Calculator

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

    質量   濃度   体積   分子量 *
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    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
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      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:
    Alisertib
    製品番号:
    HY-10971
    数量:
    MCE 日本正規代理店: