Structure via PubChem · Public domain (PubChem)
actinonin
Sign in to saveAlso known as 2-[(Formyl-Hydroxy-Amino)-Methyl]-Heptanoic Acid [1-(2-Hydroxymethyl-Pyrrolidine-1-Carbonyl)-2-Methyl-Propyl]-Amide
Actinonin is a naturally occurring antibacterial agent that has demonstrated anti-tumor activity.
In the Vinony graph
Vinony's link graph records 2 inbound references to actinonin, and connects out to bacteria, enzyme and antibiotic.
It sits within the topics Chembox image size set and Hydroxamic acids.
Vinony links it to 5 Wikipedia language editions.
Chemical data
- Formula
- C19H35N3O5
- Molecular weight
- 385.5 g/mol
- IUPAC name
- (2R)-N'-hydroxy-N-[(2S)-1-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl]-2-pentylbutanediamide
- SMILES
- CCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1CO
- InChIKey
- XJLATMLVMSFZBN-VYDXJSESSA-N
- XLogP
- 1.5
- Polar surface area
- 119 Ų
- H-bond donors
- 4
- H-bond acceptors
- 5
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- chemical compound
- Mass
- 385.258
Show 5 more facts
- chemical formula
- C₁₉H₃₅N₃O₅
- canonical SMILES
- CCCCCC(CC(=O)NO)C(=O)NC(C(C)C)C(=O)N1CCCC1CO
- isomeric SMILES
- CCCCC[C@H](CC(=O)NO)C(=O)N[C@@H](C(C)C)C(=O)N1CCC[C@H]1CO
- subject has role
- antibiotic
- found in taxon
- Streptomyces
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
1 sectionsContents
- References
{{Chembox | Verifiedfields = changed | verifiedrevid = 477241675 | ImageFile = Actinonin.svg | ImageSize = 200px | PIN = (2R)-N4-Hydroxy-N1-{(2S)-1-[(2S)-2-(hydroxymethyl)pyrrolidin-1-yl]-3-methyl-1-oxobutan-2-yl}-2-pentylbutanediamide | OtherNames = HONH-Val-Pro-OH (IUPAC peptide linear) |Section1= |Section2= |Section3= }} Actinonin is a naturally occurring antibacterial agent that has demonstrated anti-tumor activity.
Actiononin has been shown to inhibit the enzyme peptide deformylase, which is essential in bacteria.
Excerpted from Wikipedia’s “actinonin” article, available under the CC BY-SA 4.0 licence.