STK16-IN-1   Click here for help

GtoPdb Ligand ID: 9692

Compound class: Synthetic organic
Comment: STK16-IN-1 is a selective inhibitor of serine/threonine kinase 16 (STK16) that can be used as a pharmacological tool to investigate the biological functions of STK16 [2]. It is compound 219 in a 2010 patent claiming mTOR inhibitors [1].
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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.

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View interactive charts of activity data across species

STK16-IN-1 is commercially available from our sponsors

2D Structure
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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.

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Physico-chemical Properties
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Physico-chemical Properties

Calculated molecular properties are available for small molecules and natural products (not peptides). Properties were generated using the CDK toolkit. 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.

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Hydrogen bond acceptors 2
Hydrogen bond donors 1
Rotatable bonds 1
Topological polar surface area 50.16
Molecular weight 293.1
XLogP 4.22
No. Lipinski's rules broken 0
SMILES / InChI / InChIKey
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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.

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Canonical SMILES Fc1ccc(cc1C)n1c(=O)ccc2c1c1cc[nH]c1nc2
Isomeric SMILES Fc1ccc(cc1C)n1c(=O)ccc2c1c1cc[nH]c1nc2
InChI InChI=1S/C17H12FN3O/c1-10-8-12(3-4-14(10)18)21-15(22)5-2-11-9-20-17-13(16(11)21)6-7-19-17/h2-9H,1H3,(H,19,20)
InChI Key WQNRDXHKVSKUPI-UHFFFAOYSA-N
Bioactivity Comments
In kinase selectivity profiling STK16-IN-1 only potently inhibited STK16 and mTOR at a concentration of 10 μM, but enzymatic inhibition assays indicate much less effective inhibition of mTOR than STK16 by STK16-IN-1 [2]. Despite exhibiting inhibitory activity against PI3K isoforms in enzymatic assays, this was not replicated in cell-based assays.
Selectivity at enzymes
Key to terms and symbols Click column headers to sort
Target Sp. Type Action Value Parameter Concentration range (M) Reference
serine/threonine kinase 16 Primary target of this compound Hs Inhibitor Inhibition 6.5 pIC50 - 2
⤷ pIC50 6.5 (IC50 2.95x10-7 M) [2]
Description: In an in vitro enzymatic inhibition assay.
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta Hs Inhibitor Inhibition 6.1 pIC50 - 2
⤷ pIC50 6.1 (IC50 8.56x10-7 M) [2]
Description: In an in vitro enzymatic assay.
phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma Hs Inhibitor Inhibition 6.1 pIC50 - 2
⤷ pIC50 6.1 (IC50 8.67x10-7 M) [2]
Description: In an in vitro enzymatic assay.
mechanistic target of rapamycin kinase Hs Inhibitor Inhibition 5.3 pIC50 - 2
⤷ pIC50 5.3 (IC50 5.56x10-6 M) [2]
Description: In an in vitro enzymatic assay.