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Carprofen

🥰Excellent
Catalog No. T1325Cas No. 53716-49-7
Alias Rimadyl, Ridamyl, Imadyl

Carprofen (Ridamyl) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic activities.

Carprofen

Carprofen

🥰Excellent
Purity: 99.65%
Catalog No. T1325Alias Rimadyl, Ridamyl, ImadylCas No. 53716-49-7
Carprofen (Ridamyl) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic activities.
Pack SizePriceAvailabilityQuantity
50 mg$36In Stock
100 mg$52In Stock
200 mg$75In Stock
500 mg$125In Stock
1 mL x 10 mM (in DMSO)$50In Stock
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Purity:99.65%
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Product Introduction

Bioactivity
Description
Carprofen (Ridamyl) is a propionic acid derivate and nonsteroidal anti-inflammatory drug (NSAID) with anti-inflammatory, analgesic, and antipyretic activities.
Targets&IC50
COX-2 (canine):30 nM
In vitro
Administration of 4 mg/kg Carprofen significantly elevated peak plasma concentrations in dogs. Compared to buprenorphine, Carprofen treatment resulted in marginally superior analgesic effects with reduced sedative action in canines. Preoperative administration of Carprofen in dogs yielded lower pain scores than other groups, with marked effectiveness observed 2 hours post-extubation. Carprofen provided sustained analgesia for 18 hours in treated canines without adverse side effects and notably improved the speed of recovery in limping birds.
In vivo
Carprofen binds to human serum albumin (HSA) via fluorescence and equilibrium dialysis methods, with two sets of binding constants [K1=5.1 μM (fluorescence) and 3.7 μM (ED), K2=37 μM (fluorescence) and 13 μM (ED)]. It predominantly binds to site II, the benzodiazepine site, while site I, the Warfarin site, exhibits a lower affinity for Carprofen. The carboxyl group of Carprofen plays a significant role in its high-affinity binding with HSA. Additionally, Carprofen (S and R enantiomers) inhibits canine COX2 with an IC50 of 0.102 microM, primarily attributed to the S enantiomer (IC50, 0.0371 μM), which is approximately 200 times more potent than the R enantiomer (IC50, 5.97 microM).
AliasRimadyl, Ridamyl, Imadyl
Chemical Properties
Molecular Weight273.71
FormulaC15H12ClNO2
Cas No.53716-49-7
SmilesClC=1C=C2C=3C(NC2=CC1)=CC(C(C(O)=O)C)=CC3
Relative Density.1.42 g/cm3
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
Ethanol: 51 mg/mL (186.3 mM)
H2O: < 1 mg/mL (insoluble or slightly soluble)
DMSO: 55 mg/mL (200.94 mM)
Solution Preparation Table
Ethanol/DMSO
1mg5mg10mg50mg
1 mM3.6535 mL18.2675 mL36.5350 mL182.6751 mL
5 mM0.7307 mL3.6535 mL7.3070 mL36.5350 mL
10 mM0.3654 mL1.8268 mL3.6535 mL18.2675 mL
20 mM0.1827 mL0.9134 mL1.8268 mL9.1338 mL
50 mM0.0731 mL0.3654 mL0.7307 mL3.6535 mL
100 mM0.0365 mL0.1827 mL0.3654 mL1.8268 mL

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