Alminoprofen
Chemical compound
- M01AE16 (WHO)
- 2-{4-[(2-Methylprop-2-en-1-yl)amino]phenyl}propanoic acid
- 39718-89-3 N
- 2097
- 2013 Y
- 0255AHR9GJ
- D01513 Y
- CHEBI:31190 N
- ChEMBL1765293 N
- DTXSID90865968
- Interactive image
- O=C(O)C(c1ccc(NC/C(=C)C)cc1)C
InChI
- InChI=1S/C13H17NO2/c1-9(2)8-14-12-6-4-11(5-7-12)10(3)13(15)16/h4-7,10,14H,1,8H2,2-3H3,(H,15,16) Y
- Key:FPHLBGOJWPEVME-UHFFFAOYSA-N Y
Alminoprofen is a non-steroidal anti-inflammatory drug.[1]
References
- ^ Raguenes-Nicol C, Russo-Marie F, Domage G, Diab N, Solito E, Dray F, Mace JL, Streichenberger G (February 1999). "Anti-inflammatory mechanism of alminoprofen: action on the phospholipid metabolism pathway". Biochemical Pharmacology. 57 (4): 433–43. doi:10.1016/s0006-2952(98)00312-8. PMID 9933032.
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pyrazolidines
and related substances
- Ampiroxicam
- Droxicam
- Isoxicam
- Lornoxicam
- Meloxicam
- Piroxicam
- Pivoxicam
- Tenoxicam
derivatives (profens)
- Alminoprofen
- Benoxaprofen†
- Carprofen‡
- Dexibuprofen
- Dexketoprofen
- Fenbufen
- Fenoprofen
- Flunoxaprofen
- Flurbiprofen
- Ibuprofen#
- Ibuproxam
- Indoprofen†
- Ketoprofen
- Loxoprofen
- Miroprofen
- Naproxen
- Oxaprozin
- Pelubiprofen
- Piketoprofen
- Pirprofen
- Suprofen
- Tarenflurbil
- Tepoxalin‡
- Tiaprofenic acid
- Vedaprofen‡
- Zaltoprofen
- COX-inhibiting nitric oxide donator: Naproxcinod
acids (fenamates)
(coxibs)
combinations
Key: underline indicates initially developed first-in-class compound of specific group; #WHO-Essential Medicines; †withdrawn drugs; ‡veterinary use.
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