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
2MG 29 In Stock
5MG 46 In Stock
10MG 71 In Stock
25MG 144 In Stock
50MG 212 In Stock
100MG 323 In Stock
200MG 479 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Bepotastine
  • Note
    Research use only, not for human use.
  • Brief Description
    Bepotastine free base is a histamine 1 (H1) receptor antagonis.
  • Description
    Bepotastine free base is a histamine 1 (H1) receptor antagonis.
  • In Vitro
    Bepotastine (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.
  • In Vivo
    Bepotastine (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.
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    125602-71-3
  • Formula Weight
    388.89
  • Molecular Formula
    C21H25ClN2O3
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (257.14 mM)
  • SMILES
    O=C(O)CCCN1CCC(OC(c2ccc(Cl)cc2)c2ccccn2)CC1
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • 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.
molnova catalog
related products
  • AS 602801

    AS 602801(Bentamapimod) is a novel, orally active inhibitor of JNK.

  • ETH2120

    Sodium ionophore III (ETH2120) is a Na+ ionophore suitable for the test of sodium activity in plasma, serum, and blood.

  • Dihydroevocarpine

    Dihydroevocarpine shows potent anti-Helicobacter pylori activity with the minimum inhibitory concentration (MIC) value of 10-20 microg/ml. Dihydroevocarpine is a moderate modulator of p-glycoprotein (p-gp) activity; it shows more potent inhibitory effects against MAO-B compared to MAO-A.