XMU MP 1
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%
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
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.
Additional Information
Background References
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Pharmacological targeting of kinases MST1 and MST2 augments tissue repair and regeneration.
Fan et al.
Sci.Transl.Med., 2016;8:352 -
Therapy: Targeting liver tissue repair and regeneration.
Ray et al.
Nat.Rev.Gastroenterol.Hepatol., 2016;13:559 -
Regenerative medicine: Inhibiting Hippo repairs tissue.
Crunkhorn et al.
Nat.Rev.Drug Discov., 2016;15:678
Product Datasheets
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Citations for XMU MP 1
The citations listed below are publications that use Tocris products. Selected citations for XMU MP 1 include:
5 Citations: Showing 1 - 5
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The Hippo pathway kinases LATS1 and LATS2 attenuate cellular responses to heavy metals through phosphorylating MTF1.
Authors: Bing Et al.
Nat Cell Biol 2022;24:74-87
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Pulmonary fibrosis distal airway epithelia are dynamically and structurally dysfunctional.
Authors: Hong Wei Et al.
Nat Commun 2021;12:4566
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Yap1-Driven Intestinal Repair Is Controlled by Group 3 Innate Lymphoid Cells.
Authors: Janneke N Et al.
Cell Rep 2020;30:37-45.e3
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Mammalian STE20-Like Kinase 2 Promotes Lipopolysaccharides-Mediated Cardiomyocyte Inflammation and Apoptosis by Enhancing Mitochondrial Fission.
Authors: Ying Et al.
Front Physiol 2020;11:897
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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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