mycobactin and thiazoline-2-thione

mycobactin has been researched along with thiazoline-2-thione* in 1 studies

Other Studies

1 other study(ies) available for mycobactin and thiazoline-2-thione

Article	Year
Synthesis and stereochemical assignment of brasilibactin A. Organic letters, 2007, Apr-26, Volume: 9, Issue:9 [structure: see text] Brasilibactin A, a naturally occurring siderophore related to the mycobactins, has been synthesized in six steps. Use of asymmetric titanium-mediated aldol reactions allowed the preparation of both diastereomers from a common synthetic intermediate, thus allowing the relative stereochemistry of the natural product to be assigned. Brasilibactin A exhibits no inhibition of histone deacetylases (HDACs) in spite of the N-formyl-N-hydroxy lysine moiety that is expected to affect the activity of these metal-dependent lysine-modifying enzymes. Topics: Amides; Enzyme Inhibitors; Histone Deacetylase Inhibitors; Histone Deacetylases; Histones; Hydroxylation; Lysine; Metals; Molecular Structure; Oxazoles; Stearic Acids; Stereoisomerism; Thiazolidines	2007

Article

Year

Synthesis and stereochemical assignment of brasilibactin A.

Organic letters, 2007, Apr-26, Volume: 9, Issue:9

[structure: see text] Brasilibactin A, a naturally occurring siderophore related to the mycobactins, has been synthesized in six steps. Use of asymmetric titanium-mediated aldol reactions allowed the preparation of both diastereomers from a common synthetic intermediate, thus allowing the relative stereochemistry of the natural product to be assigned. Brasilibactin A exhibits no inhibition of histone deacetylases (HDACs) in spite of the N-formyl-N-hydroxy lysine moiety that is expected to affect the activity of these metal-dependent lysine-modifying enzymes.

Topics: Amides; Enzyme Inhibitors; Histone Deacetylase Inhibitors; Histone Deacetylases; Histones; Hydroxylation; Lysine; Metals; Molecular Structure; Oxazoles; Stearic Acids; Stereoisomerism; Thiazolidines

2007