Chemistry:Alminoprofen

Alminoprofen
Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	M01AE16 (WHO) ;
Identifiers
	IUPAC name 2-{4-[(2-Methylprop-2-en-1-yl)amino]phenyl}propanoic acid;
CAS Number	39718-89-3 ;
PubChem CID	2097;
ChemSpider	2013 ;
UNII	0255AHR9GJ;
KEGG	D01513 ;
ChEBI	CHEBI:31190 ;
ChEMBL	ChEMBL1765293 ;
Chemical and physical data
Formula	C13H17NO2
Molar mass	219.284 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES 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) ; Key:FPHLBGOJWPEVME-UHFFFAOYSA-N ;
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Short description: Chemical compound

Alminoprofen is a non-steroidal anti-inflammatory drug.^[1]

References

↑ "Anti-inflammatory mechanism of alminoprofen: action on the phospholipid metabolism pathway". Biochemical Pharmacology 57 (4): 433–43. February 1999. doi:10.1016/s0006-2952(98)00312-8. PMID 9933032.

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Original source: https://en.wikipedia.org/wiki/Alminoprofen. Read more

[pmid9933032-1] "Anti-inflammatory mechanism of alminoprofen: action on the phospholipid metabolism pathway". Biochemical Pharmacology 57 (4): 433–43. February 1999. doi:10.1016/s0006-2952(98)00312-8. PMID 9933032.

[1]

v t e Nonsteroidal anti-inflammatory drugs (NSAIDs) (primarily M01A and M02A, also N02BA)
Pyrazolones / Pyrazolidines	Aminophenazone Ampyrone Azapropazone Clofezone Difenamizole Famprofazone Feprazone Kebuzone Metamizole Mofebutazone Morazone Nifenazone Oxyphenbutazone Phenazone Phenylbutazone Propyphenazone Sulfinpyrazone Suxibuzone^‡
Salicylates	Aspirin (acetylsalicylic acid)^# Aloxiprin Benorylate Carbasalate calcium Diflunisal Dipyrocetyl Ethenzamide Guacetisal Magnesium salicylate Methyl salicylate Salsalate Salicin Salicylamide Salicylic acid (salicylate) Sodium salicylate
Acetic acid derivatives and related substances	Aceclofenac Acemetacin Alclofenac Amfenac Bendazac Bromfenac Bumadizone Bufexamac Diclofenac Difenpiramide Etodolac Felbinac Fenclozic acid Fentiazac Indometacin Indometacin farnesil Isoxepac Ketorolac Lonazolac Oxametacin Prodolic acid Proglumetacin Sulindac Tiopinac Tolmetin Zomepirac^†
Oxicams	Ampiroxicam Droxicam Isoxicam Lornoxicam Meloxicam Piroxicam Tenoxicam
Propionic acid derivatives (profens)	Alminoprofen Benoxaprofen^† Carprofen^‡ Dexibuprofen Dexketoprofen Fenbufen Fenoprofen Flunoxaprofen Flurbiprofen Ibuprofen^# Ibuproxam Indoprofen^† Ketoprofen Loxoprofen Miroprofen Naproxen Oxaprozin Pirprofen Suprofen Tarenflurbil Tepoxalin^‡ Tiaprofenic acid Vedaprofen^‡ Zaltoprofen COX-inhibiting nitric oxide donator: Naproxcinod
N-Arylanthranilic acids (fenamates)	Azapropazone Clonixin Etofenamate Flufenamic acid Flunixin Meclofenamic acid Mefenamic acid Morniflumate Niflumic acid Tolfenamic acid Flutiazin
Coxibs	Apricoxib Celecoxib Cimicoxib^‡ Deracoxib^‡ Etoricoxib Firocoxib^‡ Lumiracoxib^† Mavacoxib^‡ Parecoxib Robenacoxib^‡ Rofecoxib^† Valdecoxib^†
Other	Aminopropionitrile Benzydamine Chondroitin sulfate Diacerein Fluproquazone Glucosamine Glycosaminoglycan Hyperforin Nabumetone Nimesulide Oxaceprol Proquazone Superoxide dismutase/Orgotein Tenidap
Items listed in bold indicate initially developed compounds of specific groups. ^#WHO-EM ^†Withdrawn drugs. ^‡Veterinary use medications.

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