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{{Short description|Nonsteroidal anti-inflammatory drug (NSAID)}} |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| Verifiedfields = changed |
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| UNII = V7DXN0M42R |
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| Watchedfields = changed |
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| verifiedrevid = 444429984 |
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| verifiedrevid = 451725338 |
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| ImageFile = Clonixin.png |
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| ImageFile = Clonixin.png |
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| PIN = 2-(3-Chloro-2-methylanilino)pyridine-3-carboxylic acid |
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| ImageSize = 200px |
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| OtherNames = Clonixic acid; CBA 93626<ref name="Clinical">{{cite journal|url=http://onlinelibrary.wiley.com/doi/10.1177/009127007101100508/abstract|title=Clonixin: A Clinical Evaluation of a New Oral Analgesic |journal=The Journal of Clinical Pharmacology and New Drugs |volume=11 |issue=5 |pages=371–377 |access-date=2015-05-21|doi=10.1177/009127007101100508|pmid=4935715 |year=1971 |last1=Finch |first1=Jay S. |last2=Dekornfeld |first2=Thomas J. |hdl=2027.42/67636 |s2cid=38883141 |hdl-access=free }}</ref> |
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| IUPACName = 2-(3-chloro-2-methylanilino)pyridine-3-carboxylic acid |
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|Section1={{Chembox Identifiers |
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| OtherNames = Clonixic acid; CBA 93626<ref name="Clinical">{{cite web|url=http://jcp.sagepub.com/cgi/content/abstract/11/5/371|title=Clonixin: A Clinical Evaluation of a New Oral Analgesic |last=The Journal of Clinical Pharmacology|accessdate=2010-06-16}}</ref> |
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| Section1 = {{Chembox Identifiers |
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| Abbreviations = |
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| Abbreviations = |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo = 17737-65-4 |
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| CASNo = 17737-65-4 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| UNII = V7DXN0M42R |
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| PubChem = 28718 |
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| PubChem = 28718 |
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| SMILES = O=C(O)C1=CC=CN=C1NC2=C(C)C(Cl)=CC=C2 |
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| SMILES = O=C(O)C1=CC=CN=C1NC2=C(C)C(Cl)=CC=C2 |
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| MeSHName = |
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| MeSHName = |
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| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| ChemSpiderID = |
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| ChemSpiderID = 26711 |
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| ChEBI_Ref = {{ebicite|correct|EBI}} |
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| ChEMBL_Ref = {{ebicite|changed|EBI}} |
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| ChEBI = |
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| ChEMBL = 1332971 |
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| InChI = 1/C13H11ClN2O2/c1-8-10(14)5-2-6-11(8)16-12-9(13(17)18)4-3-7-15-12/h2-7H,1H3,(H,15,16)(H,17,18) |
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| ATCCode_prefix = |
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| InChIKey = CLOMYZFHNHFSIQ-UHFFFAOYAG |
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| ATCCode_suffix = |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| ATC_Supplemental = |
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| StdInChI = 1S/C13H11ClN2O2/c1-8-10(14)5-2-6-11(8)16-12-9(13(17)18)4-3-7-15-12/h2-7H,1H3,(H,15,16)(H,17,18) |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChIKey = CLOMYZFHNHFSIQ-UHFFFAOYSA-N |
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| ChEBI_Ref = {{ebicite|changed|???}} |
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| ChEBI = 76200 |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank_Ref = {{drugbankcite|correct|drugbank}} |
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| DrugBank = |
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| DrugBank = |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG_Ref = {{keggcite|correct|kegg}} |
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| KEGG = D03555 |
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| KEGG = D03555 |
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}} |
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| DCB = 05349 (clonixinato de lisina) <!-- this is brazilian data, pt:Denominação Comum Brasileira //--> |
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|Section2={{Chembox Properties |
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| Medicamento_de_referência = |
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}} |
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| Section2 = {{Chembox Properties |
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| C=13 | H=11 | Cl=1 | N=2 | O=2 |
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| C=13 | H=11 | Cl=1 | N=2 | O=2 |
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| Appearance = |
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| Appearance = |
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| Density = |
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| Density = |
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| MeltingPt = |
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| Solubility = |
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| Solvent = |
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| Solvent = |
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| Section3 = {{Chembox Pharmacology |
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|Section3={{Chembox Pharmacology |
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| AdminRoutes = ] |
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| AdminRoutes = ] |
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| Bioavail = |
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| Bioavail = |
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| Metabolism = |
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| Metabolism = Glucuronidation via UGT2B7 |
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| HalfLife = |
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| Legal_US = Not sold in the U.S. |
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| Legal_BR = |
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|Section4={{Chembox Hazards |
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| LD50 = |
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| Section4 = {{Chembox Hazards |
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| LD50 = }} |
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|Section5 = |
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|fundo = fármaco |
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}} |
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'''Clonixin''' is a ]. It also has ], ], and ] actions. It is used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation. |
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'''Clonixin''' is a ] (NSAID). It also has ], ], and ] actions. It is used primarily in the treatment of chronic arthritic conditions and certain soft tissue disorders associated with pain and inflammation. |
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==Synthesis== |
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]).]] |
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==Clonixeril== |
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The glyceryl ester of clonixin, clonixeril, is also an NSAID. It was prepared by a somewhat roundabout method. |
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Clonixin was reacted with ] and ] to give '''2'''. Heating with ] and ] displaced the ] to produce ester '''3''', which was deblocked in ] to produce clonixeril ('''4'''). |
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==See also== |
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*] |
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== References == |
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== References == |
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{{reflist}} |
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{{reflist}} |
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{{Prostanoidergics}} |
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{{musculoskeletal-drug-stub}} |
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{{musculoskeletal-drug-stub}} |
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] |
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