Oxaceprol
{{Short description|Chemical compound}}
{{Drugbox
| verifiedrevid = 447917039
| IUPAC_name = (4R)-1-acetyl-4-hydroxy-L-proline
| image = Oxaceprol.svg
| image_class = skin-invert-image
| width = 200px
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| Drugs.com = {{drugs.com|international|oxaceprol}}
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| CAS_number_Ref = {{cascite|correct|??}}
| CAS_number = 33996-33-7
| ATC_prefix = D11
| ATC_suffix = AX09
| ATC_supplemental = {{ATC|M01|AX24}}
| PubChem = 65784
| DrugBank_Ref = {{drugbankcite|correct|drugbank}}
| DrugBank =
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = Q0XV76B96L
| KEGG_Ref = {{keggcite|correct|kegg}}
| KEGG = D07215
| ChemSpiderID = 59203
| ChEMBL = 1407356
| ChEBI = 233149
| C=7 | H=11 | N=1 | O=4
| smiles = CC(=O)N1C[C@@H](C[C@H]1C(=O)O)O
| StdInChI = 1S/C7H11NO4/c1-4(9)8-3-5(10)2-6(8)7(11)12/h5-6,10H,2-3H2,1H3,(H,11,12)/t5-,6+/m1/s1
| StdInChIKey = BAPRUDZDYCKSOQ-RITPCOANSA-N
| synonyms = (2S,4R)-1-acetyl-4-hydroxypyrrolidine-2-carboxylic acid
}}
Oxaceprol is an anti-inflammatory drug used in the treatment of osteoarthritis.{{cite journal | vauthors = Herrmann G, Steeger D, Klasser M, Wirbitzky J, Fürst M, Venbrocks R, Rohde H, Jungmichel D, Hildebrandt HD, Parnham MJ, Gimbel W, Dirschedl H | display-authors = 6 | title = Oxaceprol is a well-tolerated therapy for osteoarthritis with efficacy equivalent to diclofenac | journal = Clinical Rheumatology | volume = 19 | issue = 2 | pages = 99–104 | year = 2000 | pmid = 10791619 | doi = 10.1007/s100670050025 | s2cid = 25654850 }} It is derived from L-proline, a DNA-encoded amino acid. The active effect of Oxaceprol is to inhibit the adhesion and migration of white blood cells.
References
External links
- {{cite web | url = https://druginfo.nlm.nih.gov/drugportal/name/oxaceprol | publisher = U.S. National Library of Medicine | work = Drug Information Portal | title = Oxaceprol }}
{{Other dermatological preparations}}
{{Anti-inflammatory and antirheumatic products}}
Category:Amino acid derivatives
{{musculoskeletal-drug-stub}}
{{dermatologic-drug-stub}}