ChemGrid

CHEMGRID MOLECULE CARD

Hydrocortisone base

Hydrocortisone base in ChemGrid: 3 screened assays, 0 with significant responses. Explore chemical identifiers, strain activity and target evidence.

Prest265

Explore activity & SONAR
Chemical structure of Hydrocortisone base
Stored molecular structure
3Screened assays
0Significant assay responses
4Source-labelled target records

Identity and chemistry

ChemGrid identifier
Prest265
Molecular formula
C21H30O5
CAS registry number
50-23-7
InChIKey
JYGXADMDTFJGBT-UHFFFAOYSA-N
Libraries
Prestwick
Other recorded names
11,17,21-Trihydroxypregn-4-ene-3,20-dione
Stored SMILESCC12CCC(=O)C=C1CCC1C3CCC(O)(C(=O)CO)C3(C)CC(O)C12

Matched external records: PubChem 3640

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

Measured chemical–genetic activity

3 measurements across 3 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
Luciferin 4-monooxygenaseChEMBLNo stored yeast mapping
ERG · Transcriptional regulator ERGChEMBLNo stored yeast mapping
NFE2L2 · Nuclear factor erythroid 2-related factor 2ChEMBLNo stored yeast mapping
TDP1 · Tyrosyl-DNA phosphodiesterase 1ChEMBLTDP1 YBR223C (ortholog_one2one)

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 Hydrocortisone base 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.