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Chemical Structure| 2061980-01-4 Chemical Structure| 2061980-01-4

Structure of XMU-MP-1
CAS No.: 2061980-01-4

Chemical Structure| 2061980-01-4

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XMU-MP-1 is a reversible and selective MST1/2 inhibitor, with IC50 values of 71.1 and 38.1 nM, respectively.

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Product Details of XMU-MP-1

CAS No. :2061980-01-4
Formula : C17H16N6O3S2
M.W : 416.48
SMILES Code : O=S(C1=CC=C(NC2=NC=C(C(N(C)C3=C4SC=C3)=N2)N(C)C4=O)C=C1)(N)=O
MDL No. :MFCD30377214
InChI Key :YRDHKIFCGOZTGD-UHFFFAOYSA-N
Pubchem ID :121499143

Safety of XMU-MP-1

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Related Pathways of XMU-MP-1

Hippo

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
LX-2 cells 5 µM 24 h Block the Hippo signaling pathway and attenuate the inhibitory effect of ADMSCs on HSCs PMC11515333
C2C12 cells 1 μM 6 h Restores YAP/TAZ nuclear localization in BAG3-depleted cells PMC8478876
NSCLC cell lines H1299 1 mM 24 h XMU-MP-1 treatment partially reversed ACADL-induced YAP phosphorylation and promoted nuclear accumulation of YAP. PMC10894480
NSCLC cell lines A549 1 mM 24 h XMU-MP-1 treatment partially reversed ACADL-induced YAP phosphorylation and promoted nuclear accumulation of YAP. PMC10894480
BMDMs 3μM 6 h After inhibiting MST1/2 activity, RNA-Seq and qRT-PCR results showed increased expression of inflammatory cytokines under LPS stimulation and decreased expression of M2 markers under IL-4+IL-13 stimulation. PMC10797691
RAW 264.7 5μM 4-6 h After pretreatment with XMU-MP-1, RAW 264.7 cells showed inhibited MST1/2 activity and changes in Hippo pathway-related protein expression under LPS or IL-4+IL-13 stimulation. PMC10797691
Huh7 cells 10 μM 12 h XMU-MP-1 significantly reduced HAMP expression in Huh7 cells, even in the presence of BMP6. PMC10687581
Primary hepatocytes 10 μM XMU-MP-1 significantly reduced Hamp expression in primary hepatocytes from both Tmprss6-LKO mice and control littermates. PMC10687581
C3H10T1/2 cells 10 μM 24 h XMU-MP-1 increased the expression of Col2α1 and Col9α2. PMC6962448

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Mice Achilles tendon punch injury model Intraperitoneal 2 mg/kg Three times a week for 3 weeks XMU-MP-1 suppressed ectopic bone formation PMC11739514
Mice DBA/1 mouse model Intraperitoneal injection 2 mg/kg Three times a week for 16 weeks To investigate the effect of XMU-MP-1 on new bone formation in DBA/1 mouse model, results showed that XMU-MP-1 significantly reduced new bone formation. PMC8237173
Nude mice NSCLC xenograft model Intraperitoneal injection 1 mg/kg Twice a week for three weeks XMU-MP-1 partially counteracted the inhibitory effect of ACADL on NSCLC cell growth. PMC10894480
Mice LPS-induced lung injury model Intraperitoneal injection 2 mg/kg Single injection, lungs collected at 12 and 24 hours post-infection Mice treated with XMU-MP-1 in the LPS-induced lung injury model exhibited more severe inflammatory response and tissue damage, increased proportion of CD86-positive cells in lung tissue, and elevated mRNA expression of IL-1β, IL-6, and TNF-α. PMC10797691

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.40mL

0.48mL

0.24mL

12.01mL

2.40mL

1.20mL

24.01mL

4.80mL

2.40mL

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