TrxR1 inhibitor 6a   Click here for help

GtoPdb Ligand ID: 13699

Compound class: Synthetic organic
Comment: Compound 6a is a covalent inhibitor of thioredoxin reductase 1 (TrxR1) [1]. It is generated in cells via the action of reactive oxygen species (ROS) on TrxR1 prodrug 5u. Inhibition of TrxR1 by compound 6a further elevates intracellular ROS, which activates apoptotic and ferroptotic cell death pathways in NSCLC cells. The covalent pharmacophore in 6a is a previously identified α-methylene-γ-lactone moiety that interacts with Cys475 and Sec498 of TrxR1.
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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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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 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.

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Hydrogen bond acceptors 7
Hydrogen bond donors 1
Rotatable bonds 5
Topological polar surface area 90.93
Molecular weight 361.39
XLogP 1.62
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
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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.

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/)

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Canonical SMILES CCCNC(=O)O[C@@H]1/C=C(/C)\C[C@H]2C=C(C[C@H]3[C@H]1C(=C)C(=O)O3)C(=O)O2
Isomeric SMILES CCCNC(=O)O[C@@H]1/C=C(/C)\C[C@@H]2OC(=O)C(C[C@@H]3OC(=O)C(=C)[C@@H]13)=C2
InChI InChI=1S/C19H23NO6/c1-4-5-20-19(23)26-14-7-10(2)6-13-8-12(18(22)24-13)9-15-16(14)11(3)17(21)25-15/h7-8,13-16H,3-6,9H2,1-2H3,(H,20,23)/b10-7-/t13-,14+,15-,16-/m0/s1
InChI Key HDMARTJIELVTHW-KGQQZJRTSA-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/)

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Similar Ligands Click here for help
TrxR1 prodrug 5u
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lactucopicrin
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Targets
TAS2R43; TAS2R46