ChemicalBook--->CAS DataBase List--->1395048-49-3

1395048-49-3

1395048-49-3 Structure

1395048-49-3 Structure
IdentificationBack Directory
[Name]

2-[[3-(4-Morpholinyl)propyl]amino]-4-pyridinecarboxylic acid 2-[1-(4-chloro-2-hydroxyphenyl)propylidene]hydrazide
[CAS]

1395048-49-3
[Synonyms]

M-110
CS-2124
M-110 >=98% (HPLC)
2-[[3-(4-Morpholinyl)propyl]amino]-4-pyridinecarboxylic acid 2-[1-(4-chloro-2-hydroxyphenyl)propylidene]hydrazide
4-Pyridinecarboxylic acid, 2-[[3-(4-morpholinyl)propyl]amino]-, 2-[1-(4-chloro-2-hydroxyphenyl)propylidene]hydrazide
[Molecular Formula]

C22H28ClN5O3
[MOL File]

1395048-49-3.mol
[Molecular Weight]

445.94
Chemical PropertiesBack Directory
[density ]

1.31±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: soluble25mg/mL, clear
[form ]

powder
[pka]

7.46±0.40(Predicted)
[color ]

white to beige
Safety DataBack Directory
[WGK Germany ]

3
Spectrum DetailBack Directory
[Spectrum Detail]

2-[[3-(4-Morpholinyl)propyl]amino]-4-pyridinecarboxylic acid 2-[1-(4-chloro-2-hydroxyphenyl)propylidene]hydrazide(1395048-49-3)1HNMR
Hazard InformationBack Directory
[Biochem/physiol Actions]

M-110 is a highly isoform-selective, cell permeable and potent ATP-competitive inhibitor of the PIM kinase family that prefers PIM-3. M-110 is an inhibitor of Wnt/β-catenin signaling that act downstream of the symb-catenin destruction complex to inhibit both Wnt-induced and cancer associated constitutive Wnt signaling via destabilization of β-catenin. The compound chelates iron in vitro and in intact cells. M-110 inhibits the proliferation of prostate cancer cell lines with IC50s of 0.6 to 0.9 μM, with no activity on normal human peripheral blood mononuclear cells up to 40 μM.
[storage]

Store at -20°C
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