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K02288

Chemical Structure : K02288

CAS No.: 1431985-92-0

K02288 (K 02288;K-02288)

Catalog No.: PC-42940Not For Human Use, Lab Use Only.

K02288 is a potent, selective inhibitor of BMP signaling with IC50 of 1.8/1.1/34.4/6.3 nM for ALK/1/2/3/6, displays 300-fold selectivity for ALK2 over the TGF-β receptor ALK5 and ALK4.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

K02288 is a potent, selective inhibitor of BMP signaling with IC50 of 1.8/1.1/34.4/6.3 nM for ALK/1/2/3/6, displays 300-fold selectivity for ALK2 over the TGF-β receptor ALK5 and ALK4.
K02288 also wekaly inhibits type II BMP receptor ActRIIA (IC50=220 nM).
K02288 specifically inhibits the BMP-induced Smad pathway without affecting TGF-β signaling and induces dorsalization of zebrafish embryos.
K02288 inhibits BMP9-induced phosphorylation of SMAD1/5/8 in HUVECs to reduce both the SMAD and the Notch-dependent transcriptional responses, inhibits functional angiogenesis.

Physicochemical Properties

M.Wt 352.3838
Formula C20H20N2O4
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 58.6 mg/mL

Chemical Name/SMILES

Phenol, 3-[6-amino-5-(3,4,5-trimethoxyphenyl)-3-pyridinyl]-

References

1. Sanvitale CE, et al. PLoS One. 2013 Apr 30;8(4):e62721.

2. Mohedas AH, et al. J Med Chem. 2014 Oct 9;57(19):7900-15.

3. Kerr G, et al. Angiogenesis. 2015 Apr;18(2):209-17.

4. Windhausen T, et al. Molecules. 2015 Apr 24;20(5):7586-601.

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