Antimalarial activity enhancement in hydroxymethylcarbonyl (HMC) isostere-based dipeptidomimetics targeting malarial aspartic protease plasmepsin. [Erratum to document cited in CA150:047339] was written by Hidaka, Koushi;Kimura, Tooru;Ruben, Adam J.;Uemura, Tsuyoshi;Kamiya, Mami;Kiso, Aiko;Okamoto, Tetsuya;Tsuchiya, Yumi;Hayashi, Yoshio;Freire, Ernesto;Kiso, Yoshiaki. And the article was included in Bioorganic & Medicinal Chemistry in 2009.Category: ethers-buliding-blocks This article mentions the following:
On page 10050, in the left column, in paragraph 1, in lines 22 and 25, “S1′ pocket”, was incorrectly given, and should read: “S2 pocket” and “S2‘ pocket”, resp. In the experiment, the researchers used many compounds, for example, 2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4Category: ethers-buliding-blocks).
2-(4-Methoxyphenoxy)acetic acid (cas: 1877-75-4) belongs to ethers. Ether is less polar than esters, alcohols or amines because of the oxygen atom that is unable to participate in hydrogen bonding due to the presence of bulky alkyl groups on both sides of the oxygen atom. Ethers are good solvents partly because they are not very reactive. Most ethers can be cleaved, however, by hydrobromic acid (HBr) to give alkyl bromides or by hydroiodic acid (HI) to give alkyl iodides.Category: ethers-buliding-blocks
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem