| Identification | Back Directory | [Name]
4-[[1-[4-[[(1R)-1-[[(1S)-4-(acetyl-hydroxy-amino)-1-[[(2R)-2-[[(2S,3R) -2-[[(2S)-2,6-diaminohexanoyl]amino]-3-hydroxy-butanoyl]amino]-3-hydro xy-propanoyl]carbamoyl]butyl]-(1-hydroxy-2-oxo-3-piperidyl)carbamoyl]e thyl]carbamoyl]-3,4,5,6-tetrahydropyrimidin-2-yl]-2-(4-hydroxyphenyl)e thyl]carbamoyl]-2-amino-butanoic acid | [CAS]
140198-04-5 | [Synonyms]
desferriferribactin
4-[[1-[4-[[(1R)-1-[[(1S)-4-(acetyl-hydroxy-amino)-1-[[(2R)-2-[[(2S,3R) -2-[[(2S)-2,6-diaminohexanoyl]amino]-3-hydroxy-butanoyl]amino]-3-hydro xy-propanoyl]carbamoyl]butyl]-(1-hydroxy-2-oxo-3-piperidyl)carbamoyl]e thyl]carbamoyl]-3,4,5,6-tetrahydropyrimidin-2-yl]-2-(4-hydroxyphenyl)e thyl]carbamoyl]-2-amino-butanoic acid | [Molecular Formula]
C46H73N13O16 | [MOL File]
140198-04-5.mol | [Molecular Weight]
1064.15 |
| Hazard Information | Back Directory | [Description]
Desferriferribactin is a biogenetic precursor of pyoverdin. | [Uses]
Desferriferribactin is a cyclic peptide containing a thirteen-membered ring. Desferriferribactin is a precursor of pyoverdins[1]. | [References]
[1] Caroline Linget, et al. Bacterial siderophores: the structure of a desferriferribactin produced by pseudomonas fluorescens ATCC 13525. Tetrahedron Letters. 1992, 33, 27. |
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