Design, Synthesis, and Biological Evaluation of Potent Thiazine- and Thiazepine-Based Matrix Metalloproteinase Inhibitors was written by Almstead, Neil G.;Bradley, Rimma S.;Pikul, Stanislaw;De, Biswanath;Natchus, Michael G.;Taiwo, Yetunde O.;Gu, Fei;Williams, Lisa E.;Hynd, Barbara A.;Janusz, Michael J.;Dunaway, C. Michelle;Mieling, Glen E.. And the article was included in Journal of Medicinal Chemistry in 1999.HPLC of Formula: 1138-56-3 This article mentions the following:
The synthesis and enzyme inhibition data for a series of thiazine- and thiazepine-based matrix metalloproteinase (MMP) inhibitors are described. The thiazine- and thiazepine-based inhibitors were discovered by optimization of hetererocyclic sulfonamide-based inhibitors. The most potent series of inhibitors was obtained by modification of the amino acid
4-Butoxybenzene-1-sulfonyl chloride (cas: 1138-56-3) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.HPLC of Formula: 1138-56-3
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics