Amflutizole |
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| ATC code | |
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4-Amino-3-[3-(trifluoromethyl)phenyl]-1,2-thiazole-5-carboxylic acid
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| KEGG | |
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| ChEMBL | |
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| Formula | C11H7F3N2O2S |
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| Molar mass | 288.24 g·mol−1 |
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| 3D model (JSmol) | |
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FC(F)(F)c1cccc(c1)c2nsc(c2N)C(=O)O
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InChI=1S/C11H7F3N2O2S/c12-11(13,14)6-3-1-2-5(4-6)8-7(15)9(10(17)18)19-16-8/h1-4H,15H2,(H,17,18) Y Key:KVMCEGAWQYTFKC-UHFFFAOYSA-N Y
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Amflutizole is a xanthine oxidase inhibitor[1] used for the treatment of gout.
References
- ^ O'Regan MH, Smith-Barbour M, Perkins LM, Cao X, Phillis JW (October 1994). "The effect of amflutizole, a xanthine oxidase inhibitor, on ischemia-evoked purine release and free radical formation in the rat cerebral cortex". Neuropharmacology. 33 (10): 1197–201. doi:10.1016/S0028-3908(05)80010-3. PMID 7862255. S2CID 37262919.
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Receptor (ligands) | | P0 (adenine) |
- Agonists: 8-Aminoadenine
- Adenine
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P1 (adenosine) |
- Agonists: 2-(1-Hexynyl)-N-methyladenosine
- 2-Cl-IB-MECA
- 2-Chloroadenosine
- 2'-MeCCPA
- 4'-O-β-D-Glucosyl-9-O-(6''-deoxysaccharosyl)olivil
- 5'-N-ethylcarboxamidoadenosine
- Adenosine
- ADP
- AMP
- Apadenoson
- ATL-146e
- ATP
- BAY 60–6583
- Binodenoson
- Capadenoson
- CCPA
- CGS-21680
- CP-532,903
- CV-1808
- Evodenoson
- GR 79236
- HENECA
- LUF-5835
- LUF-5845
- N6-Cyclopentyladenosine
- Namodenoson
- NECA
- Neladenoson dalanate
- Piclidenoson
- Regadenoson
- SDZ WAG 994
- Selodenoson
- Sonedenoson
- Tecadenoson
- Trabodenoson
- UK-432,097
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P2 (nucleotide) | |
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Transporter (blockers) | | CNTsTooltip Concentrative nucleoside transporters | |
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| ENTsTooltip Equilibrative nucleoside transporters | |
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| PMATTooltip Plasma membrane monoamine transporter | |
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Enzyme (inhibitors) | | XOTooltip Xanthine oxidase | |
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| Others | |
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| Others |
- Precursors: Adenine
- Adenosine
- AMP
- ADP
- ATP
- Cytosine
- Cytidine
- CMP
- CDP
- CTP
- Guanine
- Guanosine
- GMP
- GDP
- GTP
- Hypoxanthine
- Inosine
- IMP
- IDP
- ITP
- Ribose
- Uracil
- Uridine
- UMP
- UDP
- UTP
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See also: Receptor/signaling modulators |