75812-49-6

Upstream product

• 108-24-7 acetic anhydride 
• 418785-09-8 Acetic acid (1S,2S,3S,4R,5S,6S)-2,3,4-triacetoxy-5-benzyloxy-6-((2R,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-azido-tetrahydro-pyran-2-yloxy)-cyclohexyl ester 
• 75802-23-2 1L-1-O-(2-amino-2-deoxy-α-D-glucopyranosyl)-myo-inositol 

Downstream Products

• 526201-68-3 D-myo-inosityl 2-N-acetamido-2-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

Synthesis of 1-D- and 1-L-myo-inosityl 2-N-acetamido-2-deoxy-α-D-glucopyranoside establishes substrate specificity of the Mycobacterium tuberculosis enzyme AcGI deacetylase

Mycothiol (MSH, 1-D-myo-inosityl 2-(N-acetyl-L-cysteinyl)amido-2-deoxy-α-D-glucopyranoside) is the principal low molecular weight thiol in actinomycetes. The enzyme 1-D-myo-inosityl 2-N-acetamido-2-deoxy-α-D-glucopyranoside deacetylase (AcGI deacetylase)

Microbial Products. 5. Absolute Configuration of Aminoglycoside X-14847

Analysis of the 1H NMR spectrum of X-14847 nonaacetate reduces the number of possible structures for X-14847 to two.A study involving multiple cuprammonium complexation of the N-acetyl derivative which contains eight hydroxyl groups, generating five vicinal glycol groupings, permits the identification of X-14847 as 2-amino-2-deoxy-α-D-glucopyranosyl-1-O-D-myo-inositol.This assignment is confirmed by single-crystal Roentgen analysis of 2--2-deoxy-α-D-glucopyranosyl-1-O-D-myo-inositol octaacetate prepared from X-14847 with 1-bromo-3-fluoro-4,6-dinitrobenzene and subsequent peracetylation.