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TM-1 

Cat. No. M30913
TM-1  Structure
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Biological Activity

TM-1 is a potent inhibitor of pyruvate dehydrogenase kinase (PDHK1). TM-1 inhibits PDHK1 and PDHK2 with IC50s of 2.97 μM and 5.2 μM, respectively. TM-1 blocks pyruvate dehydrogenase complex (PDHC) phosphorylation, and inhibits cell proliferation.

Chemical Information
Molecular Weight 468.54
Formula C26H32N2O6
CAS Number 921099-13-0
Form Solid
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] Jinxin Sun, et al. Nanoscale Horiz. Theoretical exploration of the nitrogen fixation mechanism of two-dimensional dual-metal TM1TM2@C9N4 electrocatalysts

[2] Qian Liu, et al. Curr Eye Res. Expression of 14-3-3 Zeta Protein in Dexamethasone-Treated Mice and Human TM-1 Cells

[3] Hui-Chun Ku, et al. Naunyn Schmiedebergs Arch Pharmacol. TM-1-1DP exerts protective effect against myocardial ischemia reperfusion injury via AKT-eNOS pathway

[4] Kazuhiro Ishibashi, et al. Curr Opin Virol. Mechanisms of tomato mosaic virus RNA replication and its inhibition by the host resistance factor Tm-1

[5] Xuan Qiu, et al. Curr Eye Res. Dexamethasone increases Cdc42 expression in human TM-1 cells

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Keywords: TM-1  supplier, PDHK, inhibitors, activators


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