Drug Information
Drug General Information | |||||
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Drug ID |
D0W9WF
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Former ID |
DAP000623
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Drug Name |
Ketoprofen
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Synonyms |
Actron; Alrheumat; Alrheumum; Alrheumun; Aneol; Capisten; Dexal; Epatec; Fastum; Kefenid; Ketoprofene; Ketoprofeno; Ketoprofenum; Ketopron; Ketoprophene; Lertus; Menamin; Meprofen; Orudis; Orugesic; Oruvail; Oscorel; Profenid; Toprec; Toprek; Benzoylhydratropic Acid; Orudis KT; K 1751; RP 19583; RP19583; RU 4733; Arthril (TN); Fastum (TN); Fastum Gel (TN); Iso-K; Keto (TN); Ketoflam (TN); Ketomex (TN); Ketonal (TN); Ketoprofenas (TN); Ketoprofene (TN); Ketoprofene [INN-French]; Ketoprofeno [INN-Spanish]; Ketoprofenum (TN); Ketoprofenum [INN-Latin]; Ketorin (TN); Ketospray (TN); Lasonil (TN); M-Benzoylhydratropic acid; Oki (TN); Orudis (TN); Oruvail (TN); RP-19583; Racemic-Ketoprofen; Zon (TN); Bi-Profnid (TN); RP, 19,583; Ketoprofen (JP15/USP/INN); Ketoprofen [USAN:INN:BAN:JAN]; Orudis, Oruvail, Ketoflam, Orudis KT, Ketoprofen; Acide (benzoyl-3-phenyl)-2-propionique; Acide (benzoyl-3-phenyl)-2-propionique [French]; L'Acide (benzoyl-3-phenyl)-2-propionique; (+-)-3-Benzoyl-alpha-methylbenzeneacetic acid; (+-)-m-Benzoylhydratropic acid; 2-(3-Benzoylphenyl)propanoic acid; 2-(3-Benzoylphenyl)propionic acid; 2-(m-Benzoylphenyl)propionic acid; 2-[3-(benzoyl)phenyl]propanoic acid; 2-[3-(phenylcarbonyl)phenyl]propanoic acid; 2-[3-Benzoylphenyl]propionic acid; 3-BENZOYL-ALPHA-METHYLBENZENEACETIC ACID; 3-Benzoylhydratropic acid
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Drug Type |
Small molecular drug
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Therapeutic Class |
Analgesics
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Company |
ProEthic Pharmaceuticals
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Structure |
Download2D MOL |
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Formula |
C16H14O3
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InChI |
InChI=1S/C16H14O3/c1-11(16(18)19)13-8-5-9-14(10-13)15(17)12-6-3-2-4-7-12/h2-11H,1H3,(H,18,19)
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InChIKey |
DKYWVDODHFEZIM-UHFFFAOYSA-N
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CAS Number |
CAS 22071-15-4
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PubChem Compound ID | |||||
PubChem Substance ID |
4853, 857801, 5316933, 7847200, 7979680, 8149782, 8152423, 10321584, 10513923, 11335773, 11361012, 11364203, 11366765, 11369327, 11372636, 11373574, 11377489, 11461984, 11466247, 11467367, 11484688, 11485894, 11488772, 11491294, 11491843, 11495123, 11532908, 11533518, 15122326, 17405247, 24278504, 24860779, 24896217, 26612243, 26679814, 26747548, 26747549, 29222944, 46505715, 47216761, 47365167, 47588981, 47588982, 47588983, 47662267, 47736456, 47810738, 48184977, 48413934, 49698784
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ChEBI ID |
ChEBI:6128
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SuperDrug ATC ID |
M01AE03; M02AA10
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SuperDrug CAS ID |
cas=022071154
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Target and Pathway | |||||
Target(s) | Prostaglandin G/H synthase 2 | Target Info | Inhibitor | [536440] | |
KEGG Pathway | Arachidonic acid metabolism | ||||
Metabolic pathways | |||||
NF-kappa B signaling pathway | |||||
VEGF signaling pathway | |||||
TNF signaling pathway | |||||
Retrograde endocannabinoid signaling | |||||
Serotonergic synapse | |||||
Ovarian steroidogenesis | |||||
Oxytocin signaling pathway | |||||
Regulation of lipolysis in adipocytes | |||||
Leishmaniasis | |||||
Pathways in cancer | |||||
Chemical carcinogenesis | |||||
MicroRNAs in cancer | |||||
Small cell lung cancer | |||||
PathWhiz Pathway | Arachidonic Acid Metabolism | ||||
References | |||||
Ref 468024 | (http://www.guidetopharmacology.org/) Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Ligand id: 4795). | ||||
Ref 526212 | Ketoprofen-induced cyclooxygenase inhibition in renal medulla and platelets of rats treated with caffeine. Pharmacology. 2001;63(4):234-9. | ||||
Ref 526261 | Synthesis and biological testing of Acyl-CoA-ketoprofen conjugates as selective irreversible inhibitors of COX-2. Bioorg Med Chem. 2002 Mar;10(3):753-7. | ||||
Ref 538253 | FDA Approved Drug Products from FDA Official Website. 2009. Application Number: (ANDA) 073516. |
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