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Splitomicin

Cat. No. M8172
Splitomicin Structure
Size Price Availability Quantity
10mg USD 70  USD70 In stock
25mg USD 140  USD140 In stock
50mg USD 220  USD220 In stock
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Quality Control & Documentation
Biological Activity

Sir2p (silent information regulator) and HDAC inhibitor.

Chemical Information
Molecular Weight 198.22
Formula C13H10O2
CAS Number 5690-03-9
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] Jeong-A Park, et al. Splitomicin, a SIRT1 Inhibitor, Enhances Hematopoietic Differentiation of Mouse Embryonic Stem Cells

[2] Jos M Villalba, et al. Sirtuin activators and inhibitors

[3] Fu-Chao Liu, et al. Splitomicin inhibits fMLP-induced superoxide anion production in human neutrophils by activate cAMP/PKA signaling inhibition of ERK pathway

[4] Fu-Chao Liu, et al. Splitomicin suppresses human platelet aggregation via inhibition of cyclic AMP phosphodiesterase and intracellular Ca++ release

[5] Jeff Posakony, et al. Inhibitors of Sir2: evaluation of splitomicin analogues

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