Some polyamides from dicarboxylic acids containing aromatic ether groups

Tyler, G. J.; Whittaker, K.

doi:10.1002/jbt.2570091105

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-Acetylphenoxyacetic Acid (14a)1

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2005

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“…The residue was purified by recrystallization (hexane/EtOAc, 8:2), giving 0.44 g (63%) of 14a as a white solid. Mp 172-1741C (mp 176-1781C [Tyler and Whittaker, 1959]); R f 0.46 (hexane/EtOAc/AcOH, 1:1:0.1); IR (CH 2 Cl 2 ) 3700-2280, 1758, 1610, 1583, 1483, 1456, 1422, 1295, 1253, 1232, 1158, 1092, …”

Section: -Acetylphenoxyacetic Acid (14a)mentioning

confidence: 99%

Design of new potent hypolipidemic agents with the synergistic structural properties of α‐asarone and fibrates

Zúñiga¹,

Garduño‐Siciliano²,

Cruz³

et al. 2005

Drug Development Research

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The series of bioisosteric analogs 9-17 were designed based on the potential pharmacophores of the highly hypolipidemic agents, a-asarone (1), and fibrates such as clofibrate (2) and fenofibrate (3). These compounds are characterized by their simplicity, in terms of functional group diversity, because most of them are phenoxyacetic acids or their methyl and ethyl esters monosubstituted by an ethyl side-chain at the ortho, meta, and para positions of the benzene ring. Despite this structural simplicity, these derivatives exhibited potent hypocholesterolemic activity, lowering the mice serum cholesterol and low-density lipoprotein cholesterol levels up to 40% at the lowest dose of 25 mg/kg. These results supported the concept that the phenoxyacetic frame and the ethyl side-chain can be considered as potent pharmacophores for the preparation of potential hypocholesterolemic drugs. Drug Dev. Res. 64:28-40, 2005.

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Section: -Acetylphenoxyacetic Acid (14a)mentioning

confidence: 99%