5003-48-5
5003-48-5
Chemical Structure
Benorilate
Synonym(s): Salipran
- CAS No.: 5003-48-5
- Formula:C17H15NO5
- Molecular Weight:313.30
IUPAC Name: 4-acetamidophenyl 2-acetoxybenzoate
InChIKey: FEJKLNWAOXSSNR-UHFFFAOYSA-N
SMILES: O=C(OC1=CC=C(NC(C)=O)C=C1)C2=CC=CC=C2OC(C)=O
Biological Activity: Benorylate (Salipran) is the esterification product of paracetamol and acetylsalicylic acid. Benorylate has anti-inflammatory, analgesic and antipyretic properties. Benorylate could also inhibit prostaglandin (PG) synthesis[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Benorilate | 99.47% | Benorylate (Salipran) is the esterification product of paracetamol and acetylsalicylic acid. Benorylate has anti-inflammatory, analgesic and antipyretic properties. Benorylate could also inhibit prostaglandin (PG) synthesis. | ||||||||||||||||||||
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Benorilate (Standard) | 99.85% | Benorilate (Standard) is the analytical standard of Benorilate. This product is intended for research and analytical applications. Benorylate (Salipran) is the esterification product of paracetamol and acetylsalicylic acid. Benorylate has anti-inflammatory, analgesic and antipyretic properties. Benorylate could also inhibit prostaglandin (PG) synthesis. | ||||||||||||||||||||
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References
- [1]. Croft DN, et al. Gastric bleeding and benorylate, a new aspirin. Br Med J. 1972 Sep 2;3(5826):545-7. [Content Brief]
- [2]. Castell JV, et al. Effects of benorylate and impacina on the metabolism of cultured hepatocytes. Xenobiotica. 1985 Aug-Sep;15(8-9):743-9. [Content Brief]
- [3]. Wright V, et al. A review of benorylate - a new antirheumatic drug. Scand J Rheumatol Suppl. 1975;13:5-8. [Content Brief]
- [4]. A. Bennett , et al. Inhibition of Prostaglandin Synthesis by Benorylate. Rheumatology, Volume XII, Issue suppl, 1 January 1973, Pages 101-105.
Keywords
