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K02288

Cat. No. M2789
K02288 Structure
Size Price Availability Quantity
1mg USD 29  USD29 In stock
5mg USD 59  USD59 In stock
10mg USD 105  USD105 In stock
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Quality Control & Documentation
Biological Activity

K02288 is a potent, and selective type I BMP receptor inhibitor with IC50 of 1.1, 1.8, 6.4 nM for ALK2, ALK1 and ALK6, showing weaker inhibition on other ALKs (3, 4, 5) and ActRIIA.

Chemical Information
Molecular Weight 352.38
Formula C20H20N2O4
CAS Number 1431985-92-0
Solubility (25°C) DMSO 50 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
Conversion of different model animals based on BSA (PMID: 27057123)
Species Mouse Rat Rabbit Guinea pig Hamster Dog
Weight (kg) 0.02 0.15 1.8 0.4 0.08 10
Body Surface Area (m2) 0.007 0.025 0.15 0.05 0.02 0.5
Km factor 3 6 12 8 5 20
Animal A (mg/kg) = Animal B (mg/kg) multiplied by  Animal B Km
Animal A Km

For example, to modify the dose of Compound A used for a mouse (20 mg/kg) to a dose based on the BSA for a rat, multiply 20 mg/kg by the Km factor for a mouse and then divide by the Km factor for a rat. This calculation results in a rat equivalent dose for Compound A of 10 mg/kg.

References

[1] D Mattar, et al. Modulatory effects of TGF-β1 and BMP6 on thecal angiogenesis and steroidogenesis in the bovine ovary

[2] Nathan F Denton, et al. Bone morphogenetic protein 2 is a depot-specific regulator of human adipogenesis

[3] Hyoin Kim, et al. Rac1 promotes chondrogenesis by regulating STAT3 signaling pathway

[4] Georgina Kerr, et al. A small molecule targeting ALK1 prevents Notch cooperativity and inhibits functional angiogenesis

[5] Caroline E Sanvitale, et al. A new class of small molecule inhibitor of BMP signaling

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  Catalog
Abmole Inhibitor Catalog




Keywords: K02288 supplier, ALK, inhibitors, activators


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