Bepotastine
CAS No. 125602-71-3
Bepotastine ( —— )
Catalog No. M21128 CAS No. 125602-71-3
Bepotastine free base is a histamine 1 (H1) receptor antagonis.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 51 | In Stock |
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| 2MG | 29 | In Stock |
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| 5MG | 46 | In Stock |
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| 10MG | 71 | In Stock |
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| 25MG | 144 | In Stock |
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| 50MG | 212 | In Stock |
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| 100MG | 323 | In Stock |
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| 200MG | 479 | In Stock |
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| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
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Biological Information
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Product NameBepotastine
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NoteResearch use only, not for human use.
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Brief DescriptionBepotastine free base is a histamine 1 (H1) receptor antagonis.
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DescriptionBepotastine free base is a histamine 1 (H1) receptor antagonis.
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In VitroBepotastine (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 (50 μM; 1 h) suppresses the expression of NGF mRNA in NHEKs.Cell Viability Assay Cell Line:RPMCs Concentration:10, 100, 1000 μM Incubation Time:120 min (preincubate)Result:Decreased the release of histamine.Western Blot Analysis Cell Line:NHEKs Concentration:50 μM (preincubation)Incubation Time:1 hResult:Suppressed the expression of NGF mRNA in NHEKs.
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In VivoBepotastine (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 (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 (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. Animal Model:Guinea pigs (6-week-old).Dosage:10 g/L (1.0% (w/v)) for 10 μL.Administration:Eye drop; 3 times at intervals of 20 min (in one eye).Result:Inhibited PAF-induced conjunctival eosinophil infiltration.Animal Model:Male BALB/c mice(12-week-old); NC/Nga mice.Dosage:3, 10 mg/kg Administration:Oral administration; once (1 h before induces scratching behavior of Male BALB/c mice).Result:Significantly inhibited histamine-mediated scratching behavior in male BALB/c mice.Significantly suppressed serum LTB 4 levels in NC/Nga mice with a rash.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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Recptorothers
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Research Area——
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Indication——
Chemical Information
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CAS Number125602-71-3
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Formula Weight388.89
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Molecular FormulaC21H25ClN2O3
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Purity>98% (HPLC)
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SolubilityIn Vitro:?DMSO : 100 mg/mL (257.14 mM)
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SMILESO=C(O)CCCN1CCC(OC(c2ccc(Cl)cc2)c2ccccn2)CC1
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Kanzaki S Hashiguchi K Wakabayashi K I et al. Histamine antagonist Bepotastine suppresses nasal symptoms caused by Japanese cedar and cypress pollen exposure[J]. journal of drug assessment 2016 5(1):15-23.
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