Bepotastine Besilate
Bepotastine is a non-sedating, selective antagonist of histamine 1 (H1) receptor with pIC50 of 5.7. (In Vitro) :Bepotastine besilate (10, 100, 1000 μM; preincubates for 120 min) decreases the release of histamine induced by A23187 treatment, which reaches a statistically significant reduces level at 1000 μM.Bepotastine besilate (50 μM; 1 h) suppresses the expression of NGF mRNA in NHEKs. (In Vivo) :Bepotastine besilate (10 g/L; eye drop; 3 times at intervals of 20 min in one eye) demonstrates significant inhibition of PAF-induced conjunctival eosinophil infiltration.Bepotastine besilate (3 mg/kg; p.o.; once) suppresses scratching behavior to a frequency of 59.0 and a duration of 14.57 seconds, which are almost the same levels compares with the control.Bepotastine besilate (10 mg/kg; p.o.; once) significantly suppresses serum LTB 4 levels to 711.3 pg/mL at 1 h and 858.8 pg/mL at 2 h in NC/Nga mice with a rash.
Product Specifications
CAS Number
190786-44-8
Product Name Alternative
Bepotastine besilate | TAU-284
Field of Research
Pharmacology & Drug Discovery
Purity
>98% (HPLC)
Solubility
DMSO:109 mg/mL (199.24 mM) ; Ethanol:<1 mg/mL (<1 mM) ; Water:<1 mg/mL (<1 mM)
Smiles
C1CN (CCC1O[C@@H] (C2=CC=C (C=C2) Cl) C3=CC=CC=N3) CCCC (=O) O.C1=CC=C (C=C1) S (=O) (=O) O
Molecular Formula
C21H25ClN2O3·C6H6O3S
Molecular Weight
547.06
Storage Conditions
Storage temperature: -20°C. Stability: ≥ 2 years
Notes
For research use only.
Available Sizes
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