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2421141-51-5

2421141-51-5 Structure

2421141-51-5 Structure
IdentificationBack Directory
[Name]

Benzamide, 2-fluoro-6-methoxy-4-[4-methyl-5-[4-[4-(1-methylethyl)-1-piperazinyl]phenyl]-3-pyridinyl]-
[CAS]

2421141-51-5
[Synonyms]

M4K2234
Benzamide, 2-fluoro-6-methoxy-4-[4-methyl-5-[4-[4-(1-methylethyl)-1-piperazinyl]phenyl]-3-pyridinyl]-
[Molecular Formula]

C27H31FN4O2
[MOL File]

2421141-51-5.mol
[Molecular Weight]

462.56
Chemical PropertiesBack Directory
[Boiling point ]

566.6±50.0 °C(Predicted)
[density ]

1.180±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
[solubility ]

DMSO: 2mg/mL, clear
[form ]

Solid
[pka]

14.55±0.50(Predicted)
[color ]

Light brown to brown
[InChI]

1S/C19H24ClN3/c1-14(2)22-8-10-23(11-9-22)17-6-4-16(5-7-17)18-12-21-13-19(20)15(18)3/h4-7,12-14H,8-11H2,1-3H3
[InChIKey]

UFAWMCANSWTKEG-UHFFFAOYSA-N
[SMILES]

CC(C)N(CC1)CCN1C2=CC=C(C3=C(C)C(Cl)=CN=C3)C=C2
Safety DataBack Directory
[WGK Germany ]

WGK 3
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Uses]

M4K2234 (compound 26b) is an ALK2 inhibitor. M4K2234 inhibits ALK2 and ALK5 with IC50s of 5 and 2144 nM, respectively. M4K2234 can be used as a chemical probe for ALK1 and ALK2 protein kinases. M4K2234 can be used for the research of cancer[1].
[Biological Activity]

M4K2234 is a potent and selective TGF-β type I receptors ALK1/ACVRL1 & ALK2/ACVR1 inhibitor (IC50 = 7/14 nM[ATP] = 10 mM) th at inhibits TNIK and ALK6/BMPR1B only at higher concentrations (IC50 = 41 & 88 nMrespectively) with good kinome selectivity over >370 other kinasesincluding ALK3/BMPR1AALK4/ACVR1BALK5/TGFBR1 (IC50 = 0.1651.661.95 μMrespectively). M4K2234 inhibits cellular phospho-SMAD1/5/8 induction by 10 ng/mL BMP-7 and phospho-SMAD2 induction by either 10 ng/mL activin A or 100 ng/mL TGF-β1 with good target selectivity by cellular NanoBRET assays (ALK1/2 IC50 = 83/13 nM).
[in vivo]

1.19Pharmacokinetic Properties of M4K2234 in Mice [1].
Mice
PO 3 mg/kg
Cmax(ng/mL)1650
AUCinf(ng·h/mL)4630
t1/2(h)2.61
[References]

[1] Ensan D, et al. Targeting ALK2: An Open Science Approach to Developing Therapeutics for the Treatment of Diffuse Intrinsic Pontine Glioma. J Med Chem. 2020 May 14;63(9):4978-4996. DOI:10.1021/acs.jmedchem.0c00395
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