Bepotastine (besilate)


CAS No. : 190786-44-8

190786-44-8
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Cat. No. : HY-A0015
M.Wt: 547.06
Formula: C27H31ClN2O6S
Purity: >98 %
Solubility: DMSO : ≥ 100 mg/mL
Introduction of 190786-44-8 :

Bepotastine besilate is a selective and orally active second-generation histamine H1 receptor antagonist, can suppress the expression of nerve growth factor (NGF). Bepotastine besilate has the potential for allergic rhinitis, allergic conjunctivitis and urticaria/pruritus research[1][2][3][4]. IC50 & Target: Histamine H1 receptor[1][2][3][4]. 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[1].
Bepotastine besilate (50 µM; 1 h) suppresses the expression of NGF mRNA in NHEKs[2]. 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[1].
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[3].
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[3].

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