Molecule

Fimsbactin C

AlkaPlorer ID: AK077152

Synonym: None

IUPAC Name: [(2R,3S)-4-[4-[acetyl(hydroxy)amino]butylamino]-3-[[(4S,5R)-2-(2,3-dihydroxyphenyl)-5-methyl-4,5-dihydro-1,3-oxazole-4-carbonyl]amino]-4-oxobutan-2-yl] 2,3-dihydroxybenzoate

Structure

SMILES: CC(=O)N(O)CCCCN=C(O)[C@@H](N=C(O)[C@H]1N=C(C2=CC=CC(O)=C2O)O[C@@H]1C)[C@@H](C)OC(=O)C1=CC=CC(O)=C1O

InChI: InChI=1S/C28H34N4O11/c1-14-22(31-27(42-14)17-8-6-10-19(34)23(17)36)26(39)30-21(25(38)29-12-4-5-13-32(41)16(3)33)15(2)43-28(40)18-9-7-11-20(35)24(18)37/h6-11,14-15,21-22,34-37,41H,4-5,12-13H2,1-3H3,(H,29,38)(H,30,39)/t14-,15-,21+,22+/m1/s1

InChIKey: RUWXGLOMCAWQQD-SDVFQCAASA-N

Reference

Structure and Biosynthesis of Fimsbactins A–F, Siderophores from <i>Acinetobacter baumannii</i> and <i>Acinetobacter baylyi</i>

PubChem CID: 139586811

LOTUS: LTS0130597

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NPAtlas: NPA013418

Source

Species	Genus	Family	Order	Class	Phylum	Kingdom	Domain
Acinetobacter baumannii	Acinetobacter	Moraxellaceae	Moraxellales	Gammaproteobacteria	Pseudomonadota	None	Bacteria

Properties Information

Molecule Weight: 602.5970000000004

TPSA？: 234.53

MolLogP？: 2.587900000000002

Number of H-Donors: 7

Number of H-Acceptors: 12

RingCount: 3

Activities Information

Organism	Target Name	Standard Type	Standard Value	Standard Units	doi