1. PI3K/Akt/mTOR
  2. PIKfyve
  3. MOMIPP

MOMIPP, a macropinocytosis inducer, is a PIKfyve inhibitor. MOMIPP penetrates the blood-brain barrier (BBB).

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MOMIPP

MOMIPP 構造式

CAS 番号 : 1363421-46-8

容量 価格(税別) 在庫状況 数量
Solid + Solvent (Highly Recommended)
10 mM * 1 mL in DMSO
ready for reconstitution
USD 220 在庫あり
Solution
10 mM * 1 mL in DMSO USD 220 在庫あり
Solid
1 mg $142 在庫あり
5 mg $200 在庫あり
10 mg $320 在庫あり
25 mg $580 在庫あり
50 mg $800 在庫あり
100 mg $1200 在庫あり
200 mg   お問い合わせ  
500 mg   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 0 publication(s) in Google Scholar

Other Forms of MOMIPP:

Top Publications Citing Use of Products
  • 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

MOMIPP, a macropinocytosis inducer, is a PIKfyve inhibitor. MOMIPP penetrates the blood-brain barrier (BBB)[1][2].

Cellular Effect
Cell Line Type Value Description References
A-375 IC50
5.02 μM
Compound: 1; MOMIPP
Antiproliferative activity against human A375 cells after 48 hrs by MTS assay
Antiproliferative activity against human A375 cells after 48 hrs by MTS assay
[PMID: 29878764]
A549 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human A549 cells after 48 hrs by MTS assay
Antiproliferative activity against human A549 cells after 48 hrs by MTS assay
[PMID: 29878764]
BGC-823 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human BGC823 cells after 48 hrs by MTS assay
Antiproliferative activity against human BGC823 cells after 48 hrs by MTS assay
[PMID: 29878764]
HCC1806 IC50
> 10 μM
Compound: 1a; MOMIPP
Antiproliferative activity against human HCC1806 cells assessed as inhibition of cell proliferation incubated for 24 hrs by SRB assay
Antiproliferative activity against human HCC1806 cells assessed as inhibition of cell proliferation incubated for 24 hrs by SRB assay
[PMID: 37212861]
HCT-116 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human HCT116 cells after 48 hrs by MTS assay
Antiproliferative activity against human HCT116 cells after 48 hrs by MTS assay
[PMID: 29878764]
HeLa IC50
1.22 μM
Compound: MOMIPP
Antiproliferative activity against human HeLa cells assessed as inhibition of cell viability incubated for 24 hrs by CCK8 assay
Antiproliferative activity against human HeLa cells assessed as inhibition of cell viability incubated for 24 hrs by CCK8 assay
[PMID: 38117948]
HepG2 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human HepG2 cells after 48 hrs by MTS assay
Antiproliferative activity against human HepG2 cells after 48 hrs by MTS assay
[PMID: 29878764]
MCF-10A IC50
> 10 μM
Compound: 1; MOMIPP
Cytotoxicity against human MCF10A cells assessed as reduction in cell viability after 48 hrs by MTS assay
Cytotoxicity against human MCF10A cells assessed as reduction in cell viability after 48 hrs by MTS assay
[PMID: 29878764]
MCF7 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human MCF7 cells after 48 hrs by MTS assay
Antiproliferative activity against human MCF7 cells after 48 hrs by MTS assay
[PMID: 29878764]
MDA-MB-231 IC50
0.88 μM
Compound: MOMIPP
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell viability incubated for 24 hrs by CCK8 assay
Antiproliferative activity against human MDA-MB-231 cells assessed as inhibition of cell viability incubated for 24 hrs by CCK8 assay
[PMID: 38117948]
MDA-MB-231 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human MDA-MB-231 cells after 48 hrs by MTS assay
Antiproliferative activity against human MDA-MB-231 cells after 48 hrs by MTS assay
[PMID: 29878764]
MDA-MB-435S IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human MDA-MB-435S cells after 48 hrs by MTS assay
Antiproliferative activity against human MDA-MB-435S cells after 48 hrs by MTS assay
[PMID: 29878764]
SK-MEL-28 IC50
8.156 μM
Compound: 1; MOMIPP
Antiproliferative activity against human SK-MEL-28 cells after 48 hrs by MTS assay
Antiproliferative activity against human SK-MEL-28 cells after 48 hrs by MTS assay
[PMID: 29878764]
SK-MEL-30 IC50
> 10 μM
Compound: 1; MOMIPP
Antiproliferative activity against human SK-MEL-30 cells after 48 hrs by MTS assay
Antiproliferative activity against human SK-MEL-30 cells after 48 hrs by MTS assay
[PMID: 29878764]
U-251 GI50
2.1 μM
Compound: 1, MOMIPP
Growth inhibition of human U251 cells preincubated for 24 hrs followed by compound-washout measured at 48 hrs by sulforhodamine assay
Growth inhibition of human U251 cells preincubated for 24 hrs followed by compound-washout measured at 48 hrs by sulforhodamine assay
[PMID: 24527179]
U-251 GI50
2.3 μM
Compound: 1a
Induction of methuosis in human U251 cells after 4 to 48 hrs by phase contrast microscopic analysis
Induction of methuosis in human U251 cells after 4 to 48 hrs by phase contrast microscopic analysis
[PMID: 27343855]
U-251 GI50
2.32 μM
Compound: 1a
Growth inhibition of human U251 cells after 48 hrs by sulforhodamine B colorimetric assay
Growth inhibition of human U251 cells after 48 hrs by sulforhodamine B colorimetric assay
[PMID: 27343855]
U-251 GI50
2.32 μM
Compound: 1a, MOMIPP
Growth inhibition of human U251 cells after 24 hrs sulphorhodomine B colorimetric assay
Growth inhibition of human U251 cells after 24 hrs sulphorhodomine B colorimetric assay
[PMID: 25654321]
U-251 IC50
1.9 μM
Compound: 19, MOMIPP
Cytotoxicity against human U251 cells after 24 hrs by MTT assay
Cytotoxicity against human U251 cells after 24 hrs by MTT assay
[PMID: 22335538]
体外実験

MOMIPP can induce intense macropinocytosis, leading to methuosis in cultured glioblastoma cells at low micromolar concentrations[1].
In U373 and Hs683 cell lines, 3 μM for MOMIPP induces cell vacuolization[1].
MOMIPP (10 μM) causes early disruptions of glucose uptake and glycolytic metabolism. MOMIPP selectively activates the JNK1/2 stress kinase pathway, resulting in phosphorylation of c-Jun, Bcl-2 and Bcl-xL[2].

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

Western Blot Analysis[2]

Cell Line: U251 cells
Concentration: 10 μM
Incubation Time: 4 h or 24 h
Result: Activated the JNK stress kinase pathway.
体内実験

MOMIPP (80 mg/kg; i.p.; once daily; for 15 consecutive days) shows moderately effective in suppressing progression of intracerebral glioblastoma xenografts[2].

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

Animal Model: Athymic CrTac:NCR-Foxn1 mice (female, 7-8 weeks)[2]
Dosage: 80 mg/kg
Administration: i.p.; once daily; for 15 consecutive days
Result: Suppressed progression of intracerebral glioblastoma xenografts.
分子量

292.33

分子式

C18H16N2O2

CAS 番号
Appearance

Solid

Color

Yellow to orange

SMILES

O=C(/C=C/C1=C(NC2=C1C=C(C=C2)OC)C)C3=CC=NC=C3

輸送条件

Room temperature in continental US; may vary elsewhere.

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

DMSO : 31.25 mg/mL (106.90 mM; ultrasonic and warming and heat to 60°C; 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 3.4208 mL 17.1040 mL 34.2079 mL
5 mM 0.6842 mL 3.4208 mL 6.8416 mL
10 mM 0.3421 mL 1.7104 mL 3.4208 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. 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)

Mass
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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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濃度 (終了)

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

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Calculation results:
Working solution concentration: mg/mL
純度とドキュメンテーション

純度: 99.00%

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. 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 3.4208 mL 17.1040 mL 34.2079 mL 85.5198 mL
5 mM 0.6842 mL 3.4208 mL 6.8416 mL 17.1040 mL
10 mM 0.3421 mL 1.7104 mL 3.4208 mL 8.5520 mL
15 mM 0.2281 mL 1.1403 mL 2.2805 mL 5.7013 mL
20 mM 0.1710 mL 0.8552 mL 1.7104 mL 4.2760 mL
25 mM 0.1368 mL 0.6842 mL 1.3683 mL 3.4208 mL
30 mM 0.1140 mL 0.5701 mL 1.1403 mL 2.8507 mL
40 mM 0.0855 mL 0.4276 mL 0.8552 mL 2.1380 mL
50 mM 0.0684 mL 0.3421 mL 0.6842 mL 1.7104 mL
60 mM 0.0570 mL 0.2851 mL 0.5701 mL 1.4253 mL
80 mM 0.0428 mL 0.2138 mL 0.4276 mL 1.0690 mL
100 mM 0.0342 mL 0.1710 mL 0.3421 mL 0.8552 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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Inquiry Information

製品名:
MOMIPP
製品番号:
HY-119624
数量:
MCE 日本正規代理店: