デクスイブプロフェン
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出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/04/10 21:48:09」(JST)
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Dexibuprofen
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Systematic (IUPAC) name |
(2S)-2-[4-(2-methylpropyl)phenyl]propanoic acid
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Clinical data |
AHFS/Drugs.com |
International Drug Names |
Routes of
administration |
Oral |
Identifiers |
CAS Number |
51146-56-6 Y |
ATC code |
M01AE14 (WHO) |
PubChem |
CID 39912 |
ChemSpider |
36498 Y |
UNII |
671DKG7P5S Y |
KEGG |
D03715 Y |
ChEBI |
CHEBI:43415 Y |
ChEMBL |
CHEMBL175 Y |
Chemical data |
Formula |
C13H18O2 |
Molar mass |
206.28082 g/mol |
SMILES
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C[C@@H](c1ccc(cc1)CC(C)C)C(=O)O
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InChI
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InChI=1S/C13H18O2/c1-9(2)8-11-4-6-12(7-5-11)10(3)13(14)15/h4-7,9-10H,8H2,1-3H3,(H,14,15)/t10-/m0/s1 Y
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Key:HEFNNWSXXWATRW-JTQLQIEISA-N Y
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Dexibuprofen is a non-steroidal anti-inflammatory drug. It is the active dextrorotatory enantiomer of ibuprofen.[1] Most ibuprofen formulations contain a racemic mixture of both isomers.
References
- ^ Hardikar MS (2008). "Chiral non-steroidal anti-inflammatory drugs--a review". J Indian Med Assoc 106 (9): 615–8, 622, 624. PMID 19552094.
Prostanoid signaling
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Receptor
(ligands) |
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Enzyme
(inhibitors) |
COX (PTGS) |
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PGD2 synthase |
- Retinoids
- Selenium (selenium tetrachloride, sodium selenite, selenium disulfide)
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PGE synthase |
HQL-79
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PGF synthase |
Bimatoprost
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PGI2 synthase |
Tranylcypromine
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TXA synthase |
- Camonagrel
- Dazmegrel
- Dazoxiben
- Furegrelate
- Isbogrel
- Midazogrel
- Nafagrel
- Nicogrelate
- Ozagrel
- Picotamide
- Pirmagrel
- Ridogrel
- Rolafagrel
- Samixogrel
- Terbogrel
- U63557A
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Others |
- Precursors: Linoleic acid
- γ-Linolenic acid (gamolenic acid)
- Dihomo-γ-linolenic acid
- Diacylglycerol
- Arachidonic acid
- Prostaglandin G2
- Prostaglandin H2
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See also: Leukotrienergics
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English Journal
- Synthesis, hydrolysis studies and phamacodynamic profiles of amide prodrugs of dexibuprofen with amino acids.
- Rasheed A, Kumar CK, Mishra A.SourceDepartment of Pharmaceutical Chemistry, Sree Vidyanikethan College of Pharmacy, Sree Sainath Nagar, Tirupati, Andhra Pradesh, India.
- Journal of enzyme inhibition and medicinal chemistry.J Enzyme Inhib Med Chem.2011 Oct;26(5):688-95. Epub 2011 Jan 21.
- The present investigation deals with the synthesis of novel prodrugs of dexibuprofen with amino acids with an aim to achieve potent anti-inflammatory activity and less gastrointestinal toxicity. Structures of synthesized compounds were confirmed by spectral and elemental analyses. In vitro hydrolyti
- PMID 21250819
- Single dose oral analgesics for acute postoperative pain in adults.
- Moore RA, Derry S, McQuay HJ, Wiffen PJ.SourcePain Research and Nuffield Department of Clinical Neurosciences (Nuffield Division of Anaesthetics), University of Oxford, Pain Research Unit, Churchill Hospital, Oxford, Oxfordshire, UK, OX3 7LJ.
- Cochrane database of systematic reviews (Online).Cochrane Database Syst Rev.2011 Sep 7;9:CD008659.
- BACKGROUND: Thirty-five Cochrane Reviews of randomised trials testing the analgesic efficacy of individual drug interventions in acute postoperative pain have been published. This overview brings together the results of all those reviews and assesses the reliability of available data.OBJECTIVES: To
- PMID 21901726
Japanese Journal
- Aseptic meningo-encephalitis related to dexibuprofen use in a patient with systemic lupus erythematosus : a case report with MR findings
Related Links
- Dexibuprofen is a non-steroidal anti-inflammatory drug. It is the active dextrorotatory enantiomer of ibuprofen. Most ibuprofen formulations contain a racemic mixture of dexibuprofen [(+)-iboprofen] and (?)-ibuprofen. ...
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