Chemodex

Naproxen Solution

CHF 75.00
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CDX-N0258-L0055 mlCHF 75.00
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Product Details
Synonyms (S)-Naproxen; (+)-Naproxen; (S)-(+)-6-Methoxy-α-methyl-2-naphthalene acetic acid; Equiproxen; Laraflex
Product Type Chemical
Properties
Formula

C14H14O3

MW 230.26
CAS 22204-53-1
RTECS UF5275000
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (HPLC)
Appearance Liquid. 1mg/ml in methanol.
Solubility Soluble in aqueous buffers.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key CMWTZPSULFXXJA-VIFPVBQESA-N
Smiles C[C@H](C(O)=O)C1=CC2=CC=C(OC)C=C2C=C1
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF
Description

Naproxen is a potent, non-steroidal, non-selective anti-inflammatory cyclooxygenase (COX-1 and COX-2) inhibitor. Inhibits COX-1 expression in HUVECS at a concentration of 5µg/ml. This COX inhibitor is indicated for the treatment of pain, fever, inflammation and stiffness. Research indicates that the S-naproxen is a more active form than the R-naproxen. The S-naproxen enantiomer was observed to inhibit platelet aggregation, and both enantiomers decrease production of thromboxane B2. Naproxen has been demonstrated to block A? fibril growth and form a complex with copper (II).

Product References

(1) W.F. Kean, et al.; J. Pharm. Sci. 78, 324 (1989) | (2) T. Zyglewska, et al.; Biochim. Biophys. Acta 1131, 78 (1992) | (3) J. Barnett, et al.; Biochim. Biophys. Acta 1209, 130 (1994) | (4) O. Laneuville, et al.; J. Pharmacol. Exp. Ther. 271, 927 (1994) | (5) N.M. Davies & K.E. Anderson; Clin. Pharmacokinet. 32, 268 (1997) | (6) N. Monck; IDrugs 6, 593 (2003) | (7) T. Takeda, et al.; J. Phys. Chem. B. 114, 15394 (2010) | (8) K.C. Duggan, et al.; J. Biol. Chem. 285, 34950 (2010)

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