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I-SAP 

Cat. No. M31220
I-SAP  Structure
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Biological Activity

I-SAP is a radioiodinated TXA2/PGH2 receptor antagonist. The bind between I-SAP and the receptors, is inhibited by the histidine modifying reagent diethyl-pyrocarbonate (DEPC).

Chemical Information
Molecular Weight 531.45
Formula C22H30INO4S
CAS Number 133538-58-6
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] Katsuaki Hoshino, et al. Dev Growth Differ. Differential Effects of the Egg Jelly Molecules FSG and SAP-I on Elevation of Intracellular Ca2+ and pH in Sea Urchin Spermatozoa: (FSG/SAP-I/[Ca2+ ]i /pHi )

[2] Takeshi Shimizu, et al. Dev Growth Differ. Identification and Characterization of Putative Receptors for Sperm-Activating Peptide I (SAP-I) in Spermatozoa of the Sea Urchin Hemicentrotus pulcherrimus1

[3] Dorota Rowczenio, et al. Amyloid. Clinical characteristics and SAP scintigraphic findings in 10 patients with AGel amyloidosis

[4] Ying-Zhen Wang, et al. World J Emerg Med. Protective effect of exogenous IGF-I on the intestinalmucosal barrier in rats with severe acute pancreatitis

[5] Wojciech Cytawa, et al. Pol J Radiol. Nuclear imaging of amyloidosis

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Keywords: I-SAP  supplier, Prostaglandin Receptor, inhibitors, activators


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