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Bepotastine Besilate

Cat. No. M2449
Bepotastine Besilate Structure
Size Price Availability Quantity
10mg USD 50  USD50 In stock
50mg USD 150  USD150 In stock
100mg USD 225  USD225 In stock
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Quality Control & Documentation
Biological Activity

Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7.

Chemical Information
Molecular Weight 547.06
Formula C21H25ClN2O3.C6H6O3S
CAS Number 190786-44-8
Solubility (25°C) DMSO 90 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] Ismael Carrillo-Martin, et al. Bepotastine besilate for the treatment of perennial allergic rhinitis

[2] Leonard Bielory, et al. Bepotastine besilate for the treatment of pruritus

[3] Kyoung-Ah Kim, et al. Pharmacokinetic comparisons of bepotastine besilate and bepotastine salicylate in healthy subjects

[4] Jon I Williams, et al. Non-clinical pharmacology, pharmacokinetics, and safety findings for the antihistamine bepotastine besilate

[5] Tetsuo Kida, et al. Bepotastine besilate, a highly selective histamine H(1) receptor antagonist, suppresses vascular hyperpermeability and eosinophil recruitment in in vitro and in vivo experimental allergic conjunctivitis models

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