1. Cell Cycle/DNA Damage Cytoskeleton Apoptosis
  2. MASTL c-Myc DNA/RNA Synthesis
  3. MKI-2

MKI-2 is a selective MASTL inhibitor with an IC50 of 37.44 nM. MKI-2 induces mitotic catastrophe resulting from the modulation of the MASTL-PP2A axis in breast cancer cells. MKI-2 reduces phospho-ENSA, total, phospho-c-Myc levels. MKI-2 inhibts cancer cells proliferation, migration and induces DNA damage. MKI-2 inhibits germinal vesicle breakdown in mouse oocytes. MKI-2 can be used for the research of cancer, such as breast cancer.

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MKI-2

MKI-2 Chemical Structure

CAS No. : 438204-56-9

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Description

MKI-2 is a selective MASTL inhibitor with an IC50 of 37.44 nM. MKI-2 induces mitotic catastrophe resulting from the modulation of the MASTL-PP2A axis in breast cancer cells. MKI-2 reduces phospho-ENSA, total, phospho-c-Myc levels. MKI-2 inhibts cancer cells proliferation, migration and induces DNA damage. MKI-2 inhibits germinal vesicle breakdown in mouse oocytes. MKI-2 can be used for the research of cancer, such as breast cancer[1].

In Vitro

MKI-2 potently inhibits recombinant MASTL kinase activity with an IC50 of 37.44 nM[1].
MKI-2 (14 h) inhibits cellular MASTL activity in MCF7 breast cancer cells with an IC50 of 142.7 nM, as measured by reduced phospho-ENSA levels[1].
MKI-2 (100 nM) is selective for MASTL, as it does not inhibit recombinant ROCK1, PKACα, or p70S6K kinases and only slightly inhibits AKT1 at a concentration of 100 nM[1].
MKI-2 (250 nM; 12-24 h) modulates the MASTL-PP2A-c-Myc axis in MCF7, BT549, and MDA-MB-468 breast cancer cells by increasing PP2A activity, reducing phospho-ENSA and total, phospho-c-Myc levels[1].
MKI-2 (250 nM; 24 h) induces mitotic catastrophe in MCF7 breast cancer cells at 250 nM for 24 h, as evidenced by mitotic arrest, altered apoptotic and increased DNA damage marker (γ-H2AX) levels, and increased aberrant nuclear cells[1].
MKI-2 (15.63-1000 nM; 72 h) inhibits the proliferation of MCF7, BT549, MDA-MB-468, and 4T1 breast cancer cells with IC50 values ranging from 56.53 nM to 124.6 nM after 72 h of treatment[1].
MKI-2 (6.25-25 nM) inhibits colony, 3D spheroid, and mammosphere formation of MCF7 breast cancer cells[1].
MKI-2 (250 nM; 24 h) inhibits the migration and invasion of BT549 breast cancer cells at 250 nM for 24 h[1].
MKI-2 (250 nM-2 μM; 12-48 h) reduces the percentage of GVBD and has no significant effects on mouse oocytes viability[1].

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

Western Blot Analysis[1]

Cell Line: MCF7, BT549, and MDA-MB-468 breast cancer cells
Concentration: 250 nM
Incubation Time: 12 h
Result: Reduced levels of phospho-ENSA and phospho-c-Myc (Ser62), and decreased total c-Myc protein levels in treated breast cancer cells.

Cell Viability Assay[1]

Cell Line: MCF7, BT549, MDA-MB-468, and 4T1 breast cancer cells
Concentration: 15.63-1000 nM
Incubation Time: 72 h
Result: Inhibited proliferation of all tested breast cancer cell lines with IC50 values of 124.6 nM (MCF7), 58.65 nM (BT549), 56.53 nM (4T1), and 94.22 nM (MDA-MB-468).
Molecular Weight

381.43

Formula

C22H19N7

CAS No.
SMILES

N#CCC1=CC=C(NC2=NC(NC3=NNC(C4CC4)=C3)=C5C=CC=CC5=N2)C=C1

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  • 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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MKI-2
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HY-185310
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