- Cinchophen
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Cinchophen Systematic (IUPAC) name 2-phenylquinoline-4-carboxylic acid Clinical data AHFS/Drugs.com International Drug Names Pregnancy cat. ? Legal status ? Identifiers CAS number 132-60-5 ATC code M04AC02 PubChem CID 8593 ChemSpider 8274 UNII 39Y533Z02M KEGG D07280 ChEMBL CHEMBL348000 Chemical data Formula C16H11NO2 Mol. mass 249.264 g/mol SMILES eMolecules & PubChem (what is this?) (verify) Cinchophen (trade names Atophan, Quinophan, and Phenaquin) is an analgesic drug that was introduced in 1910 and frequently used to treat gout. This drug is still used, in combination with Prednisolone, by veterinarians to treat arthritis in animals.
Use of this drug in humans ceased in the 1930s due to the discovery that cinchophen can cause serious liver damage.[1]
There is some evidence that it stimulates C-Fos.[2]
References
- ^ Cutrín Prieto C, Nieto Pol E, Batalla Eiras A, Casal Iglesias L, Pérez Becerra E, Lorenzo Zúñiga V (1991). "[Toxic hepatitis from cinchophen: report of 3 cases]" (in Spanish; Castilian). Medicina clínica 97 (3): 104–6. PMID 1679861.
- ^ Takayama K, Xiong Y, Miura M (May 1994). "Neuronal expression of Fos protein in the paraventricular nucleus of the hypothalamus after i.p. injection of ulcergenic cinchophen". Neurosci. Lett. 172 (1–2): 55–8. doi:10.1016/0304-3940(94)90661-0. PMID 7916144. http://linkinghub.elsevier.com/retrieve/pii/0304-3940(94)90661-0.
Antigout preparations (M04) Uricosurics primary: Probenecid • Sulfinpyrazone • Benzbromarone • Isobromindione
secondary: Amlodipine • Atorvastatin • Fenofibrate • Guaifenesin • LosartanXanthine oxidase inhibitors purine analogues: Allopurinol# • Oxypurinol • Tisopurine
other: Febuxostat • Inositols (Phytic acid, Myo-inositol)Mitotic inhibitors Other M: JNT
anat(h/c, u, t, l)/phys
noco(arth/defr/back/soft)/cong, sysi/epon, injr
proc, drug(M01C, M4)
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