Structure via PubChem · Public domain (PubChem)
Chemical data
- Formula
- C25H37NO4
- Molecular weight
- 415.6 g/mol
- IUPAC name
- 2-[(2E,5E,7E,9R,10R,11E)-10-hydroxy-3,7,9,11-tetramethyltrideca-2,5,7,11-tetraenyl]-5,6-dimethoxy-3-methyl-1H-pyridin-4-one
- SMILES
- C/C=C(\C)/[C@@H]([C@H](C)/C=C(\C)/C=C/C/C(=C/CC1=C(C(=O)C(=C(N1)OC)OC)C)/C)O
- InChIKey
- BBLGCDSLCDDALX-LKGBESRRSA-N
- XLogP
- 6.1
- Polar surface area
- 67.8 Ų
- H-bond donors
- 2
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
162 papers- Piericidin A aggravates Tau pathology in P301S transgenic mice.PloS one · 2014
- Iakyricidins A-D, Antiproliferative Piericidin Analogues Bearing a Carbonyl Group or Cyclic Skeleton from Streptomyces iakyrus SCSIO NS104.The Journal of organic chemistry · 2019
- New piericidin glucosides, glucopiericidins A and B.The Journal of antibiotics · 1987
- Piericidin A: a new inhibitor of mitochondrial electron transport.Biochemical and biophysical research communications · 1966
- Efficacies of quorum sensing inhibitors, piericidin A and glucopiericidin A, produced by Streptomyces xanthocidicus KPP01532 for the control of potato soft rot caused by Erwinia carotovora subsp. atroseptica.Microbiological research · 2016
via PubMed
Wikidata facts
- Mass
- 415.272
Show 4 more facts
- chemical formula
- C₂₅H₃₇NO₄
- canonical SMILES
- CC=C(C)C(C(C)C=C(C)C=CCC(=CCC1=C(C(=O)C(=C(N1)OC)OC)C)C)O
- subject has role
- antibiotic
- isomeric SMILES
- C/C=C(\C)/[C@@H]([C@H](C)/C=C(\C)/C=C/C/C(=C/CC1=C(C(=O)C(=C(N1)OC)OC)C)/C)O
Sources (2)
via Wikidata · CC0