74272-80-3

Upstream product

• 69146-58-3 2,3-bis(benzyloxy)benzoyl chloride 
• 56-40-6 glycine 
• 81254-86-6 2,3-bis(benzyloxy)-1-((2-thioxothiazolidin-1-yl)carbonyl)benzene 
• 945496-82-2 dibenzyloxybenzoyl glycine methyl ester 
• 904916-47-8 (2,3-bis-benzyloxy-benzoylamino)-acetic acid ethyl ester 
• 303-38-8 2,3-Dihydroxybenzoic acid 
• 74272-78-9 2,3-dibenzyloxybenzoic acid 
• 100-39-0 benzyl bromide 
• 2411-83-8 methyl-2,3-dihydroxybenzoate 
• 2169-27-9 Methyl 2,3-bis(benzyloxy)benzoate 

Downstream Products

• 945496-83-3 C₄₆H₆₅N₃O₈ 
• 1026961-63-6 C₄₅H₆₃N₃O₈ 
• 945496-86-6 C₅₅H₇₉N₅O₁₁ 
• 945496-85-5 C₅₅H₇₉N₅O₁₁ 
• 74272-84-7 N,N-bis(2,3-dihydroxybenzamidopropyl)-(2,3-dihydroxybenzoyl)glycinamide 
• 78217-89-7 N⁴--N¹,N⁸-bis(2,3-dihydroxybenzoyl)spermidine 
• 416843-20-4 2,3-bis(benzyloxy)glycinylfluoride benzoylamide 
• 114482-48-3 N-<3-(2,3-dibenzyloxybenzoylamino)propyl>-N-<4-(2,3-dibenzyloxybenzoylamino)butyl>-N-2,3-dibenzyloxybenzoylglycylamide 
• 74272-83-6 N,N-bis(2,3-dibenzyloxybenzamidopropyl)-(2,3-dibenzyloxybenzoyl)glycinamide 

Relevant academic research and scientific papers

COMPOUNDS, COMPLEXES, AND METHODS USEFUL FOR DETECTING AND/OR TREATING BACTERIAL PATHOGENS

Compounds and complexes that can be useful as enterobactin probes not necessary are disclosed herein. Methods of detecting bacteria and/or methods of determining susceptibility of bacteria to an antibiotic using such compounds and complexes are also disclosed herein.

Synthesis and studies of catechol-containing mycobactin S and T analogs

The syntheses of catechol-containing mycobactin S and T analogs are described. These analogs incorporate a catechol-glycine moiety in place of the phenol-oxazoline of the naturally occurring mycobactins S and T. Studies indicated that the new siderophore

Corynebactin and enterobactin: Related siderophores of opposite chirality

Most species of bacteria employ siderophores to acquire iron. The chirality of the ferric siderophore complex plays an important role in cell recognition, uptake, and utilization. Corynebactin, isolated from Gram-positive bacteria, is structurally similar

New synthetic probes of the iron transport system of Paracoccus denitrificans

A range of analogues of parabactin A 4 and agrobactin A 5 have been synthesised. All these compounds were able to chelate iron, and to promote the growth of iron-starved Paracoccus denitrificans to varying degrees. A degree of flexibility in the sideropho

Synthesis of Parabactin Analogues and Formation of Transition Metal Complexes of Parabactin and Related Compounds

Transition metal complexes of parabactin and its related synthetic spermidine catecholamides which lack the central o-hydroxyphenyloxazoline were studied by the potentiometric titration method, e.s.r. spectroscopy, and fast atom bombardment mass spectrometry (FAB-MS).Direct mass spectral sampling of the parabactin-Fe(III) complex in glycerol solution was first achieved by FAB-MS spectrometry, confirming that the composition of the parabactin-Fe(III) complex is (2-)*2Na(1+) and that the iron(III) ion binds with two catechols and an o-hydroxyphenyl-Δ2-oxazoline moiety in NaOH solution.The e.s.r. g value (4.5) of the parabactin-Fe(III) complex differed from those (4.3) of the 3:1 catechol-Fe(III) complex and other parabactin-related catecholamide-Fe(III) complexes.These results suggest that the structure of the parabactin-Fe(III) complex differs considerably from the regular octahedral structure of the 3:1 catechol-Fe(III) complex and may have a structure similar to the ferrimycobactin P-Fe(III) complex, in which the iron(III) lies exposed in a splayed V-shaped cleft and binds with five oxygens and one nitrogen in a very strained octahedron.