MS37452

Modify Date: 2024-01-10 19:26:47

MS37452 Structure
MS37452 structure
Common Name MS37452
CAS Number 423748-02-1 Molecular Weight 398.452
Density 1.2±0.1 g/cm3 Boiling Point 628.8±55.0 °C at 760 mmHg
Molecular Formula C22H26N2O5 Melting Point N/A
MSDS Chinese USA Flash Point 334.1±31.5 °C

 Use of MS37452


MS37452 is a potent inhibitor of CBX7 chromodomain binding to H3K27me3, with a Kd of 27.7 μM. MS37452 can derepress transcription of polycomb repressive complex target gene p16/CDKN2A by displacing CBX7 binding to the INK4A/ARF locus in prostate cancer cells[1].

 Names

Name 1-[4-(2,3-Dimethoxy-benzoyl)-piperazin-1-yl]-2-m-tolyloxy-ethanone
Synonym More Synonyms

 MS37452 Biological Activity

Description MS37452 is a potent inhibitor of CBX7 chromodomain binding to H3K27me3, with a Kd of 27.7 μM. MS37452 can derepress transcription of polycomb repressive complex target gene p16/CDKN2A by displacing CBX7 binding to the INK4A/ARF locus in prostate cancer cells[1].
Related Catalog
Target

CBX7[1]

In Vitro MS37452 (125-500 μM; 12 hours) significantly increases INK4A/ARF transcript levels up to 25% and 60% for 250 μM and 500 μM, respectively, as compared to the DMSO control[1]. MS37452 (250 μM; 2 hours) treats human PC3 prostate cancer cells for 2 hours reducing CBX7 occupancy across the INK4A/ARF locus[1]. RT-PCR[1] Cell Line: PC3 cells Concentration: 125-500 μM Incubation Time: 12 hours Result: Up-regulated INK4A/ARF expression up to 25% and 60% for 250 μM and 500 μM, respectively.
References

[1]. Ren C, et al. Small-molecule modulators of methyl-lysine binding for the CBX7 chromodomain. Chem Biol. 2015;22(2):161-168.

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 628.8±55.0 °C at 760 mmHg
Molecular Formula C22H26N2O5
Molecular Weight 398.452
Flash Point 334.1±31.5 °C
Exact Mass 398.184174
LogP 2.29
Vapour Pressure 0.0±1.8 mmHg at 25°C
Index of Refraction 1.575
Storage condition 20°C

 Safety Information

RIDADR NONH for all modes of transport

 Synonyms

1-[4-(2,3-Dimethoxybenzoyl)-1-piperazinyl]-2-(3-methylphenoxy)ethanone
1-[4-(2,3-dimethoxybenzoyl)piperazin-1-yl]-2-(3-methylphenoxy)ethanone
1-[4-(2,3-Dimethoxy-benzoyl)-piperazin-1-yl]-2-m-tolyloxy-ethanone
Ethanone, 1-[4-(2,3-dimethoxybenzoyl)-1-piperazinyl]-2-(3-methylphenoxy)-
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