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BAY-598

Cat. No. M13841
BAY-598 Structure
Size Price Availability Quantity
5mg USD 128  USD128 In stock
10mg USD 205  USD205 In stock
25mg USD 315  USD315 In stock
50mg USD 520  USD520 In stock
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Quality Control & Documentation
Biological Activity

BAY-598 is selective small molecule inhibitor of SMYD2 with an IC50 of 27 nM.

Chemical Information
Molecular Weight 525.34
CAS Number 1906919-67-2
Solubility (25°C) DMSO 90 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] Yi Zhang, et al. Angiogenesis. Targeting SMYD2 inhibits angiogenesis and increases the efficiency of apatinib by suppressing EGFL7 in colorectal cancer

[2] Kezia C L Whatley, et al. PLoS Negl Trop Dis. The repositioning of epigenetic probes/inhibitors identifies new anti-schistosomal lead compounds and chemotherapeutic targets

[3] Hazem Ahmed, et al. J Proteome Res. An Integrative Proteomic Approach Identifies Novel Cellular SMYD2 Substrates

[4] Erik Eggert, et al. J Med Chem. Discovery and Characterization of a Highly Potent and Selective Aminopyrazoline-Based in Vivo Probe (BAY-598) for the Protein Lysine Methyltransferase SMYD2

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  Catalog
Abmole Inhibitor Catalog




Keywords: BAY-598 supplier, Histone Methyltransferase, inhibitors, activators


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