o-F-amidine   Click here for help

GtoPdb Ligand ID: 8625

Synonyms: compound 17 [PMID: 21882827]
Compound class: Synthetic organic
Comment: This compound is an irreversible inhibitor of protein arginine deiminases, with selectivity for PADI1 and PADI4 [1]. It can be used to study protein arginine deiminase function.
Our structure was drawn from [1]. PubChem CID 54669783 represents an alternative tautomer, and both CHEMBL1962643 and the PDB ligand (YFF&sid=3B1U) have defined stereochemistry which we don't include.
Click here for help

Ligand Activity Visualisation Charts

These are box plot that provide a unique visualisation, summarising all the activity data for a ligand taken from ChEMBL and GtoPdb across multiple targets and species. Click on a plot to see the median, interquartile range, low and high data points. A value of zero indicates that no data are available. A separate chart is created for each target, and where possible the algorithm tries to merge ChEMBL and GtoPdb targets by matching them on name and UniProt accession, for each available species. However, please note that inconsistency in naming of targets may lead to data for the same target being reported across multiple charts.

✖

View interactive charts of activity data across species
2D Structure
Click here for help

2D Structure

An image of the ligand's 2D structure. For small molecules with SMILES these are drawn using the NCI/CADD Chemical Identifier Resolver. Click on the image to access the chemical structure search tool with the ligand pre-loaded in the structure editor. For other types of ligands, e.g. longer nucleotides and peptides, a manually drawn representation of the molecule may be provided.

✖
Click here for structure editor
Physico-chemical Properties
Click here for help

Physico-chemical Properties

Calculated molecular properties are available for small molecules and natural products (not peptides). Properties were generated using the Chemistry Development Kit (CDK) (Willighagen EL et al. Journal of Cheminformatics vol. 9:33. 2017, doi:10.1186/s13321-017-0220-4; https://cdk.github.io/). All properties were selected to enable the prediction of the Lipinski Rule-of-Five profile or ‘druglikeness’ for each ligand. For more info on each category see the help pages.

✖
Hydrogen bond acceptors 8
Hydrogen bond donors 5
Rotatable bonds 11
Topological polar surface area 145.37
Molecular weight 338.14
XLogP 0.78
No. Lipinski's rules broken 0

Generated using the Chemistry Development Kit (CDK) (Willighagen EL et al. Journal of Cheminformatics vol. 9:33. 2017, doi:10.1186/s13321-017-0220-4; https://cdk.github.io/)
SMILES / InChI / InChIKey
Click here for help

SMILES / InChI / InChIKey

SMILES (Simplified Molecular Input Line Entry Specification) A specification for unambiguously describing the structure of chemical molecules using short ASCII strings. Canonical SMILES specify a unique representation of the 2D structure without chiral or isotopic specifications. Isomeric SMILES include chiral specification and isotopes.

Standard InChI (IUPAC International Chemical Identifier) and InChIKey InChI is a non-proprietary, standard, textual identifier for chemical substances designed to facilitate linking of information and database searching. An InChIKey is a simplified version of a full InChI, designed for easier web searching.

Generated using the Chemistry Development Kit (CDK) (Willighagen EL et al. Journal of Cheminformatics vol. 9:33. 2017, doi:10.1186/s13321-017-0220-4; https://cdk.github.io/)

✖
Canonical SMILES FCC(=N)NCCCC(C(=O)N)NC(=O)c1ccccc1C(=O)O
Isomeric SMILES FCC(=N)NCCCC(C(=O)N)NC(=O)c1ccccc1C(=O)O
InChI InChI=1S/C15H19FN4O4/c16-8-12(17)19-7-3-6-11(13(18)21)20-14(22)9-4-1-2-5-10(9)15(23)24/h1-2,4-5,11H,3,6-8H2,(H2,17,19)(H2,18,21)(H,20,22)(H,23,24)
InChI Key HBEIARVCIYYMOR-UHFFFAOYSA-N

Generated using the Chemistry Development Kit (CDK) (Willighagen EL et al. Journal of Cheminformatics vol. 9:33. 2017, doi:10.1186/s13321-017-0220-4; https://cdk.github.io/)
Bioactivity Comments
Note that bioactivity data maps to the trifluoroacetic acid salt (CHEMBL1910970). Note also that because these compounds are time dependent irreversible inactivators, the IC50 values should be considered 'apparent' measures of affinity rather than absolute values.
Selectivity at enzymes
Key to terms and symbols Click column headers to sort
Target Sp. Type Action Value Parameter Concentration range (M) Reference
peptidyl arginine deiminase 1 Primary target of this compound Hs Inhibitor Irreversible inhibition 5.8 pIC50 - 1
⤷ pIC50 5.8 (IC50 1.4x10-6 M) [1]
peptidyl arginine deiminase 4 Primary target of this compound Hs Inhibitor Irreversible inhibition 5.7 pIC50 - 1
⤷ pIC50 5.7 (IC50 1.9x10-6 M) [1]