39007-57-3

Basic information

• Product Name: arthrobactin
• Synonyms: arthrobactin;4-[5-(Acetylhydroxyamino)pentylamino]-2-[2-[5-(acetylhydroxyamino)pentylamino]-2-oxoethyl]-2-hydroxy-4-oxobutyric acid;Terregens factor
• CAS NO: 39007-57-3
• Molecular Formula: C20H36 N4 O9
• Molecular Weight: 0
• Mol File: 39007-57-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: °Cat760mmHg
• Flash Point: °C
• Appearance: /
• Density: 1.3g/cm³
• Refractive Index: 1.543
• CAS DataBase Reference: arthrobactin(CAS DataBase Reference)
• NIST Chemistry Reference: arthrobactin(39007-57-3)
• EPA Substance Registry System: arthrobactin(39007-57-3)

Safety Data

• Hazardous Substances Data: 39007-57-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C20H36N4O9/c1-15(25)23(32)11-7-3-5-9-21-17(27)13-20(31,19(29)30)14-18(28)22-10-6-4-8-12-24(33)16(2)26/h31-33H,3-14H2,1-2H3,(H,21,27)(H,22,28)(H,29,30)

Upstream product

• 83948-79-2 Sodium; 3-[5-(acetyl-benzyloxy-amino)-pentylcarbamoyl]-2-{[5-(acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-2-hydroxy-propionate 
• 83948-75-8 Tribenzylarthrobactin 
• 83948-69-0 3-Benzyloxycarbonyl-3-hydroxy-pentanedioic acid bis-(4-nitro-phenyl) ester 
• 83948-51-0 1-<(tert-Butoxycarbonyl)amino>-5-pentane 
• 83948-68-9 2-Hydroxy-1,2,3-propanetricarboxylic Acid 2-Benzyl Ester 
• 83966-23-8 1-Amino-5-pentane 
• 83948-54-3 tert-butyl (5-bromopentyl)carbamate 
• 75178-90-4 N-(tert-butyloxycarbonyl)-5-aminopentanol 
• 144-16-1 5-oxo-1,3-dioxolan-4-ylidenedi(acetic acid) 
• 2508-29-4 5-hydroxypentylamine 
• 153492-05-8 N-[5-(Acetyl-benzyloxy-amino)-pentyl]-2-{[5-(acetyl-benzyloxy-amino)-pentylcarbamoyl]-methyl}-2-hydroxy-succinamic acid tert-butyl ester 

Relevant articles and documents

Synthesis of Novel Citrate-Based Siderophores and Siderophore-β-Lactam Conjugates. Iron Transport-Mediated Drug Delivery Systems

The synthesis of analogs of arthrobactin (5), a microbial iron chelator, and its imide 8 are described.The differentially protected citric acid residue 31 served as the key intermediate in making conjugates having a generalized structure 14 with two representative carbacephalosporin units, 15 and 16.Both conjugates, 49 and 51, showed antibiotic activity, while conjugate 51 obtained from β-lactam 16 bearing a phenylglycyl side chain was shown to be more effective.