ChemGrid

CHEMGRID MOLECULE CARD

Lidocaine N-methyl hydrochloride

Lidocaine N-methyl hydrochloride in ChemGrid: 24 screened assays, 0 with significant responses. Explore chemical identifiers, strain activity and target evidence.

LOPAC 01003

Explore activity & SONAR
Chemical structure of Lidocaine N-methyl hydrochloride
Stored molecular structure
24Screened assays
0Significant assay responses
7Source-labelled target records

Identity and chemistry

ChemGrid identifier
LOPAC 01003
Molecular formula
C13ClH22N2O
Libraries
Lopac
Stored SMILES[ClH-].Cc1cccc(C)c1NC(=O)C[N+](C)(C)C

Matched external records: PubChem 9795082

Chemical identifiers and library names are reproduced from ChemGrid records. Missing values are omitted.

Measured chemical–genetic activity

24 measurements across 24 distinct library–species–strain assays; 0 assays have at least one significant response (|Z| ≥ 4, p ≤ 0.001, excluding flagged outliers).

Responses are indirect screening phenotypes. They do not establish that a strain gene is a direct molecular target. Strains and timepoints are retained as recorded; these counts are not counts of unique ORFs.

Recorded target evidence and yeast matches

Source annotations are shown separately from SONAR hypotheses. Evidence type and identity matching can vary; consult the linked source and interactive evidence panel.

TargetSourceYeast ORF / orthologue
BLM · RecQ-like DNA helicase BLMChEMBL analogueSGS1 YMR190C (ortholog_one2one)
GAA · Lysosomal alpha-glucosidaseChEMBL analogueROT2 YBR229C (ortholog_one2many)
HDAC6 · Protein deacetylase HDAC6ChEMBL analogueHDA1 YNL021W (ortholog_one2one)
LMNA · Prelamin-A/CChEMBL analogueNo stored yeast mapping
MAPT · Microtubule-associated protein tauChEMBL analogueNo stored yeast mapping
rep · Replicase polyprotein 1abChEMBL analogueNo stored yeast mapping
BlockerChemGrid bioactivity_infoNo stored yeast mapping

Structural activity predictions and SONAR

Stored structural activity predictions are available in the interactive profile, with assay-specific cutoffs and applicability-domain assessments.

SONAR ranks candidate targets through genetic and physical interaction evidence. Structural SONAR uses predicted strain responses; measured SONAR uses experimental responses. These are experimental hypotheses, not confirmed binding targets. Outside-domain predictions are treated as unknown.

Open the complete Lidocaine N-methyl hydrochloride research profile →

Sources and provenance

Screening measurements: ChemGrid chemical-genetic datasets. Wildenhain et al., Cell Systems (2015). Target annotations: sources named in the evidence table. Structure and library metadata: stored ChemGrid catalogue records.

Card snapshot: 2026-11-02. Linked interactive views may contain newer data.