Ethenzamide

Ethenzamide
Clinical data
ATC code	N02BA07 (WHO) ;
Identifiers
	IUPAC name 2-ethoxybenzamide;
CAS Number	938-73-8 ;
PubChem CID	3282;
ChemSpider	3167 ;
UNII	L929ZCK4BF;
KEGG	D01466 ;
ChEMBL	ChEMBL1483877;
CompTox Dashboard (EPA)	DTXSID4020581 ;
ECHA InfoCard	100.012.133
Chemical and physical data
Formula	C9H11NO2
Molar mass	165.189 g/mol g·mol−1
3D model (JSmol)	Interactive image;
	SMILES O=C(c1ccccc1OCC)N;
	InChI InChI=1S/C9H11NO2/c1-2-12-8-6-4-3-5-7(8)9(10)11/h3-6H,2H2,1H3,(H2,10,11) ; Key:SBNKFTQSBPKMBZ-UHFFFAOYSA-N ;
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Ethenzamide (2-ethoxybenzamide) is a common analgesic and anti-inflammatory drug that is used for the relief of fever, headaches, and other minor aches and pains.[1][2] It is an ingredient in numerous cold medications and many prescription analgesics.[3]

References

Darias, V.; Bravo, L.; Abdallah, S. S.; Sánchez Mateo, C. C.; Expósito-Orta, M. A.; Lissavetsky, J.; Manzanares, J. (1992). "Synthesis and preliminary pharmacological study of thiophene analogues of the antipyretic and analgesic agent ethenzamide". Archiv der Pharmazie. 325 (2): 83–87. doi:10.1002/ardp.19923250206. PMID 1605721.
Wang, P. J.; Guo, H. R. (2004). "Frequent analgesics consumption in migraineurs: Comparison between chronic and episodic migraineurs". The Journal of Headache and Pain. 5: 30–35. doi:10.1007/s10194-004-0065-x. PMC 3452147.
ChemChart

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[1] Darias, V.; Bravo, L.; Abdallah, S. S.; Sánchez Mateo, C. C.; Expósito-Orta, M. A.; Lissavetsky, J.; Manzanares, J. (1992). "Synthesis and preliminary pharmacological study of thiophene analogues of the antipyretic and analgesic agent ethenzamide". Archiv der Pharmazie. 325 (2): 83–87. doi:10.1002/ardp.19923250206. PMID 1605721.

[2] Wang, P. J.; Guo, H. R. (2004). "Frequent analgesics consumption in migraineurs: Comparison between chronic and episodic migraineurs". The Journal of Headache and Pain. 5: 30–35. doi:10.1007/s10194-004-0065-x. PMC 3452147.

[3] ChemChart

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.