acetamide

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Related to Acetamides: acetic amide

ac·et·a·mide

(as-et-am'īd, ă-set'ă-mīd),
CH3CONH2; used in biomedical research.
Synonym(s): acetic amide

acetamide

(ă″set-ă-m′īd″, as″ĕt-am′īd″) [L. acetum, vinegar + amide]
Acetic acid amide, CH3CONH2, used in industry for synthesis of chemicals and as a solvent.
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References in periodicals archive ?
Hashim, "Anticancer, anti-inflammatory, and analgesic activities of synthesized 2(substituted phenoxy) acetamide derivatives," BioMed Research International, vol.
Marzocco et al., "Acetamide derivatives with antioxidant activity and potential anti-inflammatory activity," Molecules, vol.
Jawed et al., "N-(2-hydroxyphenyl) acetamide (NA-2) and Temozolomide synergistically induce apoptosis in human glioblastoma cell line U87," Cancer Cell International, vol.
TABLE 1: Normal modes assignments and scaled frequencies for 2-(2,6-dichlorophenyl)-N-(1,3-thiazol-2yl) acetamide. For comparison, observed FTIR bands are also given.
Simjee, N-(2-Hydroxy Phenyl) Acetamide Inhibits Inflammation-Related Cytokines and ROS in Adjuvant-Induced Arthritic (AIA) Rats, Int.
Ejaz, Synthesis, Characterization and Biological Screening of 5-Substituted-1,3,4- Oxadiazole-2yl-N-(2-Methoxy-5-Chlorophenyl)- 2-Sulfanyl Acetamide, Pak.
Sinha, Synthesis and evaluation of antitubercular activity of glycosyl thio- and sulfonyl acetamide derivatives, Bioorg.
Sorensen et al., "Discovery and metabolic stabilization of potent and selective 2-amino-N-(adamant-2-yl) acetamide 11[beta]-hydroxysteroid dehydrogenase type 1 inhibitors," Journal of Medicinal Chemistry, vol.
General procedure for the synthesis of N-substituted-5-(4-chlorophenyl)-1,3,4-Oxadiazol-2-yl-2-sulfanyl acetamide derivatives (6a-o)
2-[{5-(4-Chlorophenyl)-1,3,4-Oxadiazol-2- yl}sulfanyl]-N-(2-(methoxycarbonyl)phenyl) acetamide (6n):
The outstanding activity of these compounds is probably due to N-substitution of electrophiles in these molecules containing acetamide groups.
The received solid was filtered, washed with water and dried to yield the corresponding N-substituted derivatives of N-(4-(N- (5-chloro-2-methoxyphenyl) sulfamoyl)phenyl) acetamide (5a-k).