Foroxymithine
AlkaPlorer ID: AK033326
Synonym: None
IUPAC Name: (2S)-2-acetamido-5-[formyl(hydroxy)amino]-N-[(2S)-1-[3-[(2S,5S)-5-[3-[formyl(hydroxy)amino]propyl]-3,6-dioxopiperazin-2-yl]propyl-hydroxyamino]-3-hydroxy-1-oxopropan-2-yl]pentanamide
Structure
SMILES: CC(O)=N[C@@H](CCCN(O)C=O)C(O)=N[C@@H](CO)C(=O)N(O)CCC[C@@H]1N=C(O)[C@H](CCCN(O)C=O)N=C1O
InChI: InChI=1S/C22H37N7O11/c1-14(33)23-15(5-2-8-27(38)12-31)19(34)26-18(11-30)22(37)29(40)10-4-7-17-21(36)24-16(20(35)25-17)6-3-9-28(39)13-32/h12-13,15-18,30,38-40H,2-11H2,1H3,(H,23,33)(H,24,36)(H,25,35)(H,26,34)/t15-,16-,17-,18-/m0/s1
InChIKey: IQMHGRIOYXVPSE-XSLAGTTESA-N
Reference
Foroxymithine, a new inhibitor of angiotensin-converting enzyme, produced by actinomycetes.
PubChem CID: 13648082
LOTUS: LTS0252128
{NPAtlas: NPA020865
Source
| Species | Genus | Family | Order | Class | Phylum | Kingdom | Domain |
|---|---|---|---|---|---|---|---|
| None | None | None | None | Actinomycetes | Actinomycetota | None | Bacteria |
Properties Information
Molecule Weight: 575.5760000000004
TPSA？: 272.21000000000004
MolLogP？: -0.4337999999999944
Number of H-Donors: 8
Number of H-Acceptors: 11
RingCount: 1
Activities Information
| Organism | Target Name | Standard Type | Standard Value | Standard Units | doi |
|---|