ChemGrid

CHEMGRID MOLECULE CARD

Fluoxetine hydrochloride

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

LOPAC 00510

Explore activity & SONAR
Chemical structure of Fluoxetine hydrochloride
Stored molecular structure
24Screened assays
0Significant assay responses
19Source-labelled target records

Identity and chemistry

ChemGrid identifier
LOPAC 00510
Molecular formula
C17ClF3H19NO
InChIKey
GIYXAJPCNFJEHY-UHFFFAOYSA-N
Libraries
Lopac
Other recorded names
Reconcile
Stored SMILESCl.CNCCC(Oc1ccc(cc1)C(F)(F)F)c1ccccc1

Matched external records: PubChem 62857

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
CX3CR1 · CX3C chemokine receptor 1ChEMBLNo stored yeast mapping
GPR65 · G-protein coupled receptor 65ChEMBLNo stored yeast mapping
HTR2C · 5-hydroxytryptamine receptor 2CChEMBLNo stored yeast mapping
LMNA · Prelamin-A/CChEMBLNo stored yeast mapping
RAN · GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1ChEMBLGSP1 YLR293C (ortholog_one2many); GSP2 YOR185C (ortholog_one2many)
Slc6a2 · TransporterChEMBLNo stored yeast mapping
Slc6a3 · Sodium-dependent dopamine transporterChEMBLNo stored yeast mapping
Slc6a4 · Sodium-dependent serotonin transporterChEMBLNo stored yeast mapping
UBE2N · Ubiquitin-conjugating enzyme E2 NChEMBLNo stored yeast mapping
CX3CR1 · CX3C chemokine receptor 1ChEMBL analogueNo stored yeast mapping
GPR65 · G-protein coupled receptor 65ChEMBL analogueNo stored yeast mapping
HTR2C · 5-hydroxytryptamine receptor 2CChEMBL analogueNo stored yeast mapping
LMNA · Prelamin-A/CChEMBL analogueNo stored yeast mapping
RAN · GTP-binding nuclear protein Ran/Importin subunit beta-1/Snurportin-1ChEMBL analogueGSP1 YLR293C (ortholog_one2many); GSP2 YOR185C (ortholog_one2many)
Slc6a2 · TransporterChEMBL analogueNo stored yeast mapping
Slc6a3 · Sodium-dependent dopamine transporterChEMBL analogueNo stored yeast mapping
Slc6a4 · Sodium-dependent serotonin transporterChEMBL analogueNo stored yeast mapping
UBE2N · Ubiquitin-conjugating enzyme E2 NChEMBL analogueNo stored yeast mapping
ReuptakeChemGrid 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 Fluoxetine 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.