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Parstatin (mouse) TFA

Cat. No. M31169
Parstatin (mouse) TFA Structure
Size Price Availability Quantity
1mg USD 120  USD120 In stock
5mg USD 380  USD380 In stock
10mg USD 600  USD600 In stock
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Quality Control & Documentation
Biological Activity

Parstatin (mouse) TFA is a peptide formed by protein hydrolysis upon PAR1 receptor activation and is also a PAR-1 agonist with cellular permeability. In addition, Parstatin (mouse) TFA is also a potent inhibitor of angiogenesis. It can be used in studies related to ischemia-reperfusion injury.

Chemical Information
Molecular Weight 4533.18
Formula C191H327F3N58O59S3
CAS Number 1065756-01-5 (free base)
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] P S Gartaganis, et al. Eur Rev Med Pharmacol Sci. Parstatin inhibits viability of human retinal pigment epithelium cells: an in vitro cytotoxicity study

[2] Athanasios Diamantopoulos, et al. Am J Nephrol. Parstatin prevents renal injury following ischemia/reperfusion and radiocontrast administration

[3] Hu Huang, et al. Invest Ophthalmol Vis Sci. Parstatin suppresses ocular neovascularization and inflammation

[4] Jennifer L Strande, et al. Cardiovasc Res. Parstatin: a cryptic peptide involved in cardioprotection after ischaemia and reperfusion injury

[5] Panagiota Zania, et al. J Pharmacol Exp Ther. Parstatin, the cleaved peptide on proteinase-activated receptor 1 activation, is a potent inhibitor of angiogenesis

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