12040-70-9

Upstream product

• 83948-71-4 N-[3-(Acetyl-benzyloxy-amino)-propyl]-2-{[3-(acetyl-benzyloxy-amino)-propylcarbamoyl]-methyl}-2-hydroxy-succinamic acid benzyl ester 
• 83948-78-1 Sodium; 3-[3-(acetyl-benzyloxy-amino)-propylcarbamoyl]-2-{[3-(acetyl-benzyloxy-amino)-propylcarbamoyl]-methyl}-2-hydroxy-propionate 
• 114340-53-3 2-tert-butyl-1,3-di-N-(hydroxyl) succinimidyl citrate 
• 114340-56-6 N-(3-Benzyloxyamino-propyl)-2-[(3-benzyloxyamino-propylcarbamoyl)-methyl]-2-hydroxy-succinamic acid tert-butyl ester 
• 83966-25-0 2-isopropyl citrate 
• 83948-73-6 N-[3-(Acetyl-benzyloxy-amino)-propyl]-2-{[3-(acetyl-benzyloxy-amino)-propylcarbamoyl]-methyl}-2-hydroxy-succinamic acid isopropyl ester 
• 83948-69-0 3-Benzyloxycarbonyl-3-hydroxy-pentanedioic acid bis-(4-nitro-phenyl) ester 
• 83948-61-2 1-Amino-3-propane Hydrochloride 
• 83948-68-9 2-Hydroxy-1,2,3-propanetricarboxylic Acid 2-Benzyl Ester 
• 83966-24-9 2-Hydroxy-1,2,3-propanetricarboxylic Acid 2-Isopropyl Ester 
• 83948-50-9 1-<(tert-Butoxycarbonyl)amino>-3-propane 
• 144-16-1 5-oxo-1,3-dioxolan-4-ylidenedi(acetic acid) 
• 114340-58-8 N-[3-(Acetyl-benzyloxy-amino)-propyl]-2-{[3-(acetyl-benzyloxy-amino)-propylcarbamoyl]-methyl}-2-hydroxy-succinamic acid tert-butyl ester 
• 114340-51-1 2-tert-butyl 1,3-dimethyl 2-hydroxypropane-1,2,3-tricarboxylate 

Relevant academic research and scientific papers

Synthesis and iron coordination properties of schizokinen and its imide derivative

The iron(iii) affinity constants for schizokinen and its imide derivative are reported for the first time. Surprisingly, schizokinen possesses a higher affinity for iron(iii) than desferrioxamine B; log?KFeIII (FeL), 36.2 and 30.6, respectively. This incr

Synthesis, structure, and molecular dynamics of gallium complexes of schizokinen and the amphiphilic siderophore acinetoferrin

A new general synthesis of the citrate-based siderophores acinetoferrin (Af) and schizokinen (Sz) and their analogues is described. The molecular structure of gallium schizokinen, GaSz, was determined by combined 1H NMR, Hartree-Fock ab initio

Synthesis of Schizokinen, Homoschizokinen, Its Imide and the Detection of Imide with 13C-N.M.R.-Spectroscopy

A new method for the synthesis of homoschizokinen 1 and schizokinen 2 is described. 2-tert-Butyl-1,3-di-N-hydroxysuccinimidyl citrate has been applied as the key substrate.The method excludes the possibility of imide formation.The imide of compound 1 has