nocardicin A
AlkaPlorer ID: AK012935
Synonym: 'Antibiotic FR 2458', 'Nocardicin A', 'Antibiotic FR 1923', 'Nocardicin B'
IUPAC Name: (2S)-2-amino-4-[4-[(E)-C-[[(3S)-1-[(S)-carboxy-(4-hydroxyphenyl)methyl]-2-oxoazetidin-3-yl]carbamoyl]-N-hydroxycarbonimidoyl]phenoxy]butanoic acid
Structure
SMILES: N[C@@H](CCOC1=CC=C(/C(=N/O)C(O)=N[C@H]2CN([C@H](C(=O)O)C3=CC=C(O)C=C3)C2=O)C=C1)C(=O)O
InChI: InChI=1S/C23H24N4O9/c24-16(22(31)32)9-10-36-15-7-3-12(4-8-15)18(26-35)20(29)25-17-11-27(21(17)30)19(23(33)34)13-1-5-14(28)6-2-13/h1-8,16-17,19,28,35H,9-11,24H2,(H,25,29)(H,31,32)(H,33,34)/b26-18-/t16-,17-,19-/m0/s1
InChIKey: CTNZOGJNVIFEBA-JATCHWAJSA-N
Reference
The role of nocardicin G in nocardicin A biosynthesis
PubChem CID: 12831262
LOTUS: LTS0258588
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| Streptomyces clavuligerus | Streptomyces | Streptomycetaceae | Kitasatosporales | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 500.4640000000002
TPSA?: 215.57
MolLogP?: 0.7444999999999999
Number of H-Donors: 6
Number of H-Acceptors: 9
RingCount: 3
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|
