Details
Stereochemistry | ACHIRAL |
Molecular Formula | C17H15NO5 |
Molecular Weight | 313.3047 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)NC1=CC=C(OC(=O)C2=C(OC(C)=O)C=CC=C2)C=C1
InChI
InChIKey=FEJKLNWAOXSSNR-UHFFFAOYSA-N
InChI=1S/C17H15NO5/c1-11(19)18-13-7-9-14(10-8-13)23-17(21)15-5-3-4-6-16(15)22-12(2)20/h3-10H,1-2H3,(H,18,19)
Molecular Formula | C17H15NO5 |
Molecular Weight | 313.3047 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
DescriptionSources: http://imr.sagepub.com/content/1/1/65.full.pdfCurator's Comment: description was created based on several sources, including:
www.drugfuture.com/mt/bendazac.pdf
http://pmmp.cnki.net/Resources/CDDPdf/med%5Cbase%5C%E7%A5%9E%E7%BB%8F%E7%B3%BB%E7%BB%9F%E8%8D%AF%E7%89%A9%5C259.pdf
http://ru.medicina-617.medicina.eh.org.ua/42.htm
https://en.wikipedia.org/wiki/Benorilate
Sources: http://imr.sagepub.com/content/1/1/65.full.pdf
Curator's Comment: description was created based on several sources, including:
www.drugfuture.com/mt/bendazac.pdf
http://pmmp.cnki.net/Resources/CDDPdf/med%5Cbase%5C%E7%A5%9E%E7%BB%8F%E7%B3%BB%E7%BB%9F%E8%8D%AF%E7%89%A9%5C259.pdf
http://ru.medicina-617.medicina.eh.org.ua/42.htm
https://en.wikipedia.org/wiki/Benorilate
Benorilate is an aspirin-paracetamol ester with analgesic, antiinflammatory, and antipyretic properties. After absorption, it is rapidly metabolised to salicylate and paracetamol. It has been used orally in the treatment of mild to moderate pain and fever. It has also been used in osteoarthritis, rheumatoid arthritis, and soft-tissue rheumatism. Associated adverse reactions: nausea, diarrhea or constipation, digestive disorders or heartburn, occasionally - a transient skin rash, and sleepiness. Benoral should not be administered concomitantly with probenecid or any other uricosuric agents that decrease tubular reabsorption as any form of salicylate antagonises this effect when given in doses of less than 5 gm per day.
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: GO:0001516 Sources: Rheumatology (1973) XII (suppl): 101-105 doi:10.1093/rheumatology/XII.suppl.101 |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Palliative | Unknown Approved UseBenorylate is indicated in the treatment of rheumatoid arthritis. |
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Palliative | Unknown Approved UseBenorylate is indicated in the treatment of osteoarthritis. |
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Palliative | Unknown Approved UseBenorylate is indicated in the treatment of painful musculoskeletal conditions. |
PubMed
Title | Date | PubMed |
---|---|---|
Comparison of aspirin and benorylate in the treatment of rheumatoid arthritis. | 1972 May 27 |
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Determination of benorilate in pharmaceutical formulations and its metabolite in urine at carbon paste electrode modified by silver nanoparticles. | 2005 Sep 15 |
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Effect of pressure on molecular and ionic motions in ultraviscous acetaminophen-aspirin mixture. | 2006 Nov |
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Overuse of non-prescription analgesics by dental clinic patients. | 2008 Dec 9 |
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Calorimetric relaxation in pharmaceutical molecular glasses and its utility in understanding their stability against crystallization. | 2008 Sep 4 |
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Insights in to the pathogenesis of axial spondyloarthropathy based on gene expression profiles. | 2009 |
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Dielectric study of equimolar acetaminophen-aspirin, acetaminophen-quinidine, and benzoic acid-progesterone molecular alloys in the glass and ultraviscous states and their relevance to solubility and stability. | 2010 Mar |
Patents
Sample Use Guides
In Vivo Use Guide
Sources: http://imr.sagepub.com/content/1/1/65.full.pdf
Curator's Comment: 1,5 g (2 tablets) 4 times per day. In acute phase - 6 g per day
http://ru.medicina-617.medicina.eh.org.ua/42.htm
The dose of benorylate is 6-8 g daily.
Route of Administration:
Oral
In Vitro Use Guide
Sources: http://www.ncbi.nlm.nih.gov/pubmed/2575401
Because of the very rapid hydrolysis of benorylate by liver samples, hydrolysis conditions of 300 uM benorylate plus microsomes (4ug protein equivalent to 0,8 mg liver per incubation) were selected such that benorylate was detectable for 30 min and only 50% disappeared over the first 15 min.
Substance Class |
Chemical
Created
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Record UNII |
W1QX9DV96G
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Validated (UNII)
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QN02BA10
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C257
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N02BA10
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DB13657
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