Skip to Content
Merck
CN

SML3569

M4K2234

≥98% (HPLC)

Synonym(s):

2-Fluoro-4-(5-(4-(4-isopropylpiperazin-1-yl)phenyl)-4-methylpyridin-3-yl)-6-methoxybenzamide

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Empirical Formula (Hill Notation):
C27H31FN4O2
CAS Number:
Molecular Weight:
462.56
UNSPSC Code:
12352200
NACRES:
NA.77
Assay:
≥98% (HPLC)
Form:
powder
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


Quality Segment

assay

≥98% (HPLC)

form

powder

color

white to beige

solubility

DMSO: 2 mg/mL, clear

storage temp.

2-8°C

SMILES string

CC(C)N(CC1)CCN1C2=CC=C(C3=C(C)C(Cl)=CN=C3)C=C2

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

InChI key

UFAWMCANSWTKEG-UHFFFAOYSA-N

Biochem/physiol Actions

M4K2234 is a potent and selective TGF-β type I receptors ALK1/ACVRL1 & ALK2/ACVR1 inhibitor (IC50 = 7/14 nM, [ATP] = 10 mM) that inhibits TNIK and ALK6/BMPR1B only at higher concentrations (IC50 = 41 & 88 nM, respectively) with good kinome selectivity over >370 other kinases, including ALK3/BMPR1A, ALK4/ACVR1B, ALK5/TGFBR1 (IC50 = 0.165, 1.66, 1.95 μM, respectively). 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).
Potent and selective TGF-β type I receptors ALK1/ACVRL1 & ALK2/ACVR1 inhibitor.


Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

It looks like we've run into a problem, but you can still download Certificates of Analysis from our Documents section.

If you need assistance, please contact Customer Support

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library