Discovery of C10H10O3

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 2879-20-1. In my other articles, you can also check out more blogs about 2879-20-1

Related Products of 2879-20-1, In homogeneous catalysis, catalysts are in the same phase as the reactants. Enzymes are biological catalysts that produce large increases in reaction rates and tend to be specific for certain reactants and products. In a document type is Article, and a compound is mentioned, CAS :2879-20-1, Name is 1-(2,3-Dihydrobenzo[b][1,4]dioxin-6-yl)ethanone, molecular weight is 178.1846, introducing its new discovery.

HIV protease inhibitors possessing a novel, high-affinity, and achiral P1?/P2? ligand with a unique pattern of in vitro resistance. Importance of a conformationally-restricted template in the design of enzyme inhibitors

Achiral pyran-2-one analogs possessing a 3-S-(2-alkylphenyl) group were determined to be high-affinity inhibitors for human immunodeficiency virus (HIV) protease (PR). Crystallographic, modeling, and structure-activity studies led to the 3-S-(2-tert-butylphenyl) moiety as an apparent optimal group to access the S2?/S1? pockets of the enzyme. Further optimization led to an inhibitor, 3-[(2-tert-butylphenyl)sulfanyl]-4-hydroxy-6-(3-methylphenyl)-pyran-2-one (14), possessing a Ki of 3 nM. An X-ray crystallographic structure of an inhibitor, 4-hydroxy-3-[(2-isopropylphenyl)sulfanyl]-6-phenylpyran-2-one (8), bound to HIV PR showed that the 3-S-(2-isopropylphenyl) group occupied the P2? and P1? pockets, while other crucial interactions were common to those found with other pyran-2-one analogs. The high potency observed for this series may be due, in part, to the restrictions on the intramolecular collapsibility of these molecules in aqueous solution, leading to a highly favorable hydrophobic effect on binding. Herein we report a novel P2?/P1? achiral ligand which results in a tight-binding inhibitor that occupies only three pockets in the enzyme and exhibits a unique pattern of in vitro resistance.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Related Products of 2879-20-1. In my other articles, you can also check out more blogs about 2879-20-1

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem