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Flopropione

Cat. No. M2704
Flopropione Structure
Size Price Availability Quantity
50mg USD 55  USD55 In stock
100mg USD 80  USD80 In stock
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Quality Control & Documentation
Biological Activity

Flopropione is a spasmolytic or antispasmodic agent, and acts as a 5-HT1A receptor antagonist.

Chemical Information
Molecular Weight 182.17
Formula C9H10O4
CAS Number 2295-58-1
Form Solid
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] Meng Zhang, et al. Functional Characterization and Structural Basis of an Efficient Di- C-glycosyltransferase from Glycyrrhiza glabra

[2] Kenji Ohgaki. Efficacy of Naftopidil as a Medical Expulsive Therapy in Japanese Men With Ureteral Stones: A Prospective Randomized Controlled Study

[3] Yasuo Kohjimoto, et al. Naftopidil versus flopropione as medical expulsive therapy for distal ureteral stones: results of a randomized, multicenter, double-blind, controlled trial

[4] Y Aso, et al. Relationship between the crystallization rates of amorphous nifedipine, phenobarbital, and flopropione, and their molecular mobility as measured by their enthalpy relaxation and (1)H NMR relaxation times

[5] A Kondo, et al. Spanate (flopropione), its clinical evaluation for urolithiasis and effects on ureteral peristalsis and blood pressure in dogs

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