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BET bromodomain inhibitor 

Cat. No. M28548
BET bromodomain inhibitor  Structure
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Biological Activity

BET bromodomain inhibitor is a potent BET inhibitor.

Chemical Information
Molecular Weight 445.9
Formula C24H20ClN5O2
CAS Number 1505453-59-7
Form Solid
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] Guangtong Deng, et al. Theranostics. BET inhibitor suppresses melanoma progression via the noncanonical NF-κB/SPP1 pathway

[2] Elisa Funck-Brentano, et al. Epigenetics. BET bromodomain inhibitor HMBA synergizes with MEK inhibition in treatment of malignant glioma

[3] Emily J Faivre, et al. Nature. Selective inhibition of the BD2 bromodomain of BET proteins in prostate cancer

[4] Jake E Delmore, et al. Cell. BET bromodomain inhibition as a therapeutic strategy to target c-Myc

[5] Panagis Filippakopoulos, et al. Nature. Selective inhibition of BET bromodomains

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