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XMU MP 1

Catalog #: 6482
1 Citation Datasheet / COA / SDS
Catalog # Availability Size / Price Qty
6482/50
6482/10
XMU MP 1 | CAS No. 2061980-01-4 | Other Kinase Inhibitors
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Description: Potent and selective MST1/2 inhibitor; orally bioavailable

Chemical Name: 4-[(6,10-Dihydro-5,10-dimethyl-6-oxo-5H-pyrimido[5,4-b]thieno[3,2-e][1,4]diazepin-2-yl)amino]benzenesulfonamide

Purity: ≥98%

Product Details
Citations (1)
Reviews
Biological Activity Technical Data Additional Information Background Product Datasheets Calculators

Biological Activity

XMU MP 1 is a potent and selective ATP-competitive mammalian sterile 20-like kinase (MST) 1/2 inhibitor (IC50 values are 38.1 and 71.1 nM for MST2 and MST1, respectively). Enhances activity of downstream YAP in vitro. Augments mouse intestinal repair and promotes liver repair and regeneration in a mouse model of acute and chronic liver injury. Orally bioavailable.

Technical Data

M.Wt:
416.48
Formula:
C17H16N6O3S2
Solubility:
Soluble to 100 mM in DMSO
Purity:
≥98%
Storage:
Store at -20°C
CAS No:
2061980-01-4

The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.

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Additional Information

Licensing Caveats:
Sold under license from Dana-Farber Cancer Institute.

Background References

  1. Pharmacological targeting of kinases MST1 and MST2 augments tissue repair and regeneration.
    Fan et al.
    Sci.Transl.Med., 2016;8:352
  2. Therapy: Targeting liver tissue repair and regeneration.
    Ray et al.
    Nat.Rev.Gastroenterol.Hepatol., 2016;13:559
  3. Regenerative medicine: Inhibiting Hippo repairs tissue.
    Crunkhorn et al.
    Nat.Rev.Drug Discov., 2016;15:678

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Citation for XMU MP 1

The citations listed below are publications that use Tocris products. Selected citations for XMU MP 1 include:

1 Citation: Showing 1 - 1

  1. FGFR4 phosphorylates MST1 to confer breast cancer cells resistance to MST1/2-dependent apoptosis.
    Authors: Turunen Et al.
    Cell Death Differ  2019;

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