Staphyloferrin B
AlkaPlorer ID: AK073983
Synonym: None
IUPAC Name: (2S)-2-[2-[[(2S)-2-amino-2-carboxyethyl]amino]-2-oxoethyl]-4-[2-[(4-carboxy-4-oxobutanoyl)amino]ethylamino]-2-hydroxy-4-oxobutanoic acid
Structure
SMILES: N[C@@H](CN=C(O)C[C@@](O)(CC(O)=NCCN=C(O)CCC(=O)C(=O)O)C(=O)O)C(=O)O
InChI: InChI=1S/C16H24N4O11/c17-8(13(25)26)7-20-12(24)6-16(31,15(29)30)5-11(23)19-4-3-18-10(22)2-1-9(21)14(27)28/h8,31H,1-7,17H2,(H,18,22)(H,19,23)(H,20,24)(H,25,26)(H,27,28)(H,29,30)/t8-,16-/m0/s1
InChIKey: SIAZVTIHOHTZDD-PWJLMRLQSA-N
Reference
Staphyloferrin B, a Citrate Siderophore of Ralstonia eutropha
PubChem CID: 46861568
LOTUS: LTS0183593
{NPAtlas: NPA012996
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Cupriavidus necator | Cupriavidus | Burkholderiaceae | Burkholderiales | Betaproteobacteria | Pseudomonadota | None | Bacteria |
Properties Information
Molecule Weight: 448.3850000000002
TPSA？: 272.98999999999995
MolLogP？: -1.7023999999999946
Number of H-Donors: 8
Number of H-Acceptors: 9
RingCount: 0
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|