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Cyclic Pifithrin-α hydrobromide

Cat. No. M8014
Cyclic Pifithrin-α hydrobromide Structure
Synonym:

Cyclic Pifithrin-α hydrobromide; Cyclic PFT-α hydrobromide; PFT-β hydrobromide

Size Price Availability Quantity
10mg USD 100  USD100 In stock
50mg USD 360  USD360 In stock
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Quality Control & Documentation
Biological Activity

Cyclic Pifithrin-α hydrobromide is a stabilized pifithrin-α analog as well as a specific p53 inhibitor with low cytotoxicity.

Chemical Information
Molecular Weight 349.29
Formula C16H16N2S · HBr
CAS Number 511296-88-1
Solubility (25°C) DMSO: 20 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] Eva Vacas, et al. Signalling pathways involved in antitumoral effects of VIP in human renal cell carcinoma A498 cells: VIP induction of p53 expression

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Keywords: Cyclic Pifithrin-α hydrobromide, Cyclic Pifithrin-α hydrobromide; Cyclic PFT-α hydrobromide; PFT-β hydrobromide supplier, p53, inhibitors, activators


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