Enterobactin from Escherichia coli

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Names

[ CAS No. ]:
28384-96-5

[ Name ]:
Enterobactin from Escherichia coli

[Synonym ]:
N-[(3S,7S,11S)-7,11-bis[(2,3-dihydroxybenzoyl)amino]-2,6,10-trioxo-1,5,9-trioxacyclododec-3-yl]-2,3-dihydroxybenzamide
Enterobactin

Chemical & Physical Properties

[ Density]:
1.72g/cm3

[ Boiling Point ]:
1109.1ºC at 760 mmHg

[ Melting Point ]:
202-203°C (lit.)

[ Molecular Formula ]:
C30H27N3O15

[ Molecular Weight ]:
669.54600

[ Flash Point ]:
624.6ºC

[ Exact Mass ]:
669.14400

[ PSA ]:
298.05000

[ LogP ]:
0.98340

[ Vapour Pressure ]:
0mmHg at 25°C

[ Index of Refraction ]:
1.732

[ Storage condition ]:
20°C

Safety Information

[ RIDADR ]:
NONH for all modes of transport

Articles

The C-glycosyltransferase IroB from pathogenic Escherichia coli: identification of residues required for efficient catalysis.

Biochim. Biophys. Acta 1844(9) , 1619-30, (2014)

Escherichia coli C-glycosyltransferase IroB catalyzes the formation of a CC bond between enterobactin and the glucose moiety of UDP-glucose, resulting in the production of mono-, di- and tri-glucosyla...

Human Urinary Composition Controls Antibacterial Activity of Siderocalin.

J. Biol. Chem. 290 , 15949-60, (2015)

During Escherichia coli urinary tract infections, cells in the human urinary tract release the antimicrobial protein siderocalin (SCN; also known as lipocalin 2, neutrophil gelatinase-associated lipoc...

AhpC is required for optimal production of enterobactin by Escherichia coli.

J. Bacteriol. 194(24) , 6748-57, (2012)

Escherichia coli alkyl hydroperoxide reductase subunit C (AhpC) is a peroxiredoxin that detoxifies peroxides. Here we show an additional role for AhpC in cellular iron metabolism of E. coli. Deletion ...


More Articles


Related Compounds

  • 2-({[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)cycloheptyl]formamido}oxy)propanoic acid
  • 2-({[4-chloro-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)phenyl]formamido}oxy)propanoic acid
  • 2-({[4-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-iodophenyl]formamido}oxy)propanoic acid
  • 2-[({4-[2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)ethyl]phenyl}formamido)oxy]propanoic acid
  • 3-[N-benzyl-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-(1H-pyrrol-2-yl)propanamido]propanoic acid
  • 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-(3-hydroxy-3-propylpiperidin-1-yl)-4-oxobutanoic acid
  • 3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-[3-hydroxy-3-(propan-2-yl)piperidin-1-yl]-4-oxobutanoic acid
  • 2-({3-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]oxan-3-yl}formamido)-3-hydroxy-2-methylpropanoic acid
  • (2S,3R)-2-({3-[({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)methyl]oxan-3-yl}formamido)-3-hydroxybutanoic acid
  • 3-{[(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)propanamido]methyl}oxane-3-carboxylic acid
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