| 词条 | Dexibuprofen |
| 释义 |
| Watchedfields = changed | verifiedrevid = 443586803 | IUPAC_name = (2S)-2-[4-(2-methylpropyl)phenyl]propanoic acid | image = Dexibuprofen Structural Formulae V.1.svg | image2 = (S)-ibuprofen-3D-balls.png | tradename = Ibusoft, Monactil, Seractil | Drugs.com = {{drugs.com|international|dexibuprofen}} | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_status = | routes_of_administration = Oral | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion = | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 51146-56-6 | ATC_prefix = M01 | ATC_suffix = AE14 | PubChem = 39912 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 36498 | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 671DKG7P5S | KEGG_Ref = {{keggcite|correct|kegg}} | KEGG = D03715 | ChEBI_Ref = {{ebicite|correct|EBI}} | ChEBI = 43415 | ChEMBL_Ref = {{ebicite|correct|EBI}} | ChEMBL = 175 | C=13 | H=18 | O=2 | molecular_weight = 206.28082 g/mol | smiles = C[C@@H](c1ccc(cc1)CC(C)C)C(=O)O | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 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 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = HEFNNWSXXWATRW-JTQLQIEISA-N }} Dexibuprofen is a nonsteroidal anti-inflammatory drug (NSAID). It is the active dextrorotatory enantiomer of ibuprofen.[1] Most ibuprofen formulations contain a racemic mixture of both isomers. References1. ^{{cite journal |vauthors=Hardikar MS |title=Chiral non-steroidal anti-inflammatory drugs--a review |journal=J Indian Med Assoc |volume=106 |issue=9 |pages=615–8, 622, 624 |year=2008 |pmid=19552094 |doi= |url=}} {{Anti-inflammatory products}}{{Prostanoid signaling modulators}}{{Musculoskeletal-drug-stub}} 3 : Enantiopure drugs|Nonsteroidal anti-inflammatory drugs|Propionic acids |
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