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Ciproxifan

Cat. No. M2522
Ciproxifan Structure
Size Price Availability
10mg USD 150 Out of stock
50mg USD 570 Out of stock
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Quality Control
  • Current batch:
  • Purity >99%
  • COA
  • MSDS
Biological Activity

Ciproxifan is a highly potent and selective histamin H3-receptor antagonist with IC50 of 9.2 nM, with low apparent affinity at other receptor subtypes.

Conversion of different model animals based on BSA (Value based on data from FDA Draft Guidelines)
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 resveratrol used for a mouse (22.4 mg/kg) to a dose based on the BSA for a rat, multiply 22.4 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 resveratrol of 11.2 mg/kg.

Chemical Information
Molecular Weight 386.4
Formula C16H18N2O2.C4H4O4
CAS Number 184025-18-1
Purity >99%
Solubility DMSO 40 mg/mL
Storage at -20°C
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Ranitidine HCl

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Mizolastine

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  Catalog
Abmole Inhibitor Catalog 2017




Keywords: Ciproxifan supplier, Histamine Receptor, inhibitors

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