Start with Friedreich ataxia, then reuse UniProt Q16236 as the stable protein anchor across project notes and exports.
CHEMBL1075094 Target Snapshot
Nuclear factor erythroid 2-related factor 2 · SINGLE PROTEIN · Homo sapiens
Research home keeps recent targets
This target will appear in recent viewed items on this browser. Use the demo workspace to preview watch rules and decision queues.
Switch target
Move to another high-traffic target or paste a specific ChEMBL target ID.
Frame the target before identity details
Structured disease, protein, and project context should read before the lower-level identity rail.
As of 2026-09-13Nuclear factor erythroid 2-related factor 2 shows approved-linked disease relevance led by Friedreich ataxia. 3 more disease programs remain visible in the same review block. 1 linked drug keeps the current disease frame grounded. Protein identity stays anchored to UniProt Q16236. Start with Friedreich ataxia, then reuse UniProt Q16236 as the stable protein anchor across project notes and exports.
Nuclear factor erythroid 2-related factor 2 shows approved-linked disease relevance led by Friedreich ataxia. 3 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.
Start review with Friedreich ataxia because it currently carries approved-linked support. Linked drugs include OMAVELOXOLONE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Disease source · ChEMBL drug mechanism + indication proxyNuclear factor erythroid 2-related factor 2
Review this target as Nuclear factor erythroid 2-related factor 2, mapped to UniProt Q16236. Sequence length is 605 aa.
Protein source · UniProt accession via ChEMBL component mappingCross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Nuclear factor erythroid 2-related factor 2 as ChEMBL target CHEMBL1075094, mapped to UniProt Q16236. Disease framing currently uses the Open Targets-ready proxy contract.
Reuse the same identifiers in notes, watch rules, exports, and review packs so provenance stays stable across surfaces.
Start with the right source
Choose the first block or source based on the question you are trying to answer.
Start here when your first question is whether Nuclear factor erythroid 2-related factor 2 is the right protein anchor across sources, using UniProt Q16236 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why Friedreich ataxia is currently framed as approved-linked support. It currently carries 1 linked drug in the same disease frame.
Jump to Disease ContextOpen the one-page evidence card when you want the rationale, activity base, and attribution together.
Open Review-ready CardBasic Information
Verify identity, organism, and the fastest next research jumps from the same page.
| Preferred Name | Nuclear factor erythroid 2-related factor 2 |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | Q16236 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Nuclear factor erythroid 2-related factor 2 |
| UniProt Accession | Q16236 |
| Component Type | Protein |
| Sequence Length | 605 aa |
Nuclear factor erythroid 2-related factor 2
How to read this target
Review this target as Nuclear factor erythroid 2-related factor 2, mapped to UniProt Q16236. Sequence length is 605 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Nuclear factor erythroid 2-related factor 2 shows approved-linked disease relevance led by Friedreich ataxia. 3 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with Friedreich ataxia because it currently carries approved-linked support. Linked drugs include OMAVELOXOLONE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Clinical Phase Distribution
Activity Type Distribution
Top Inhibitors (by pChEMBL)
| ChEMBL ID | pChEMBL | Type | Value (nM) | Phase |
|---|---|---|---|---|
| CHEMBL4643134 | 8.04 | EC50 | 9.2 | Preclinical |
| CHEMBL4776211 | 8.0 | EC50 | 10.0 | Preclinical |
| CHEMBL4450921 | 7.96 | EC50 | 11.0 | Preclinical |
| CHEMBL5437928 | 7.7 | EC50 | 20.0 | Preclinical |
| CHEMBL1197091 | 7.65 | IC50 | 22.3 | Clinical |
| CHEMBL4793600 | 7.58 | EC50 | 26.0 | Preclinical |
| CHEMBL459546 | 7.54 | IC50 | 29.19 | Preclinical |
| CHEMBL4447060 | 7.52 | EC50 | 30.0 | Preclinical |
| CHEMBL4757795 | 7.52 | EC50 | 30.0 | Preclinical |
| CHEMBL5418829 | 7.52 | EC50 | 30.0 | Preclinical |
pChEMBL Value Distribution
Assay Landscape
Binding — 511 assays, 557 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 463 | 320 | 5.8 |
| assay format | 25 | 233 | 5.5 |
| single protein format | 11 | 4 | 5.9 |
| tissue-based format | 11 | 0 | — |
| subcellular format | 1 | 0 | — |
Functional — 49 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 41 | 0 | — |
| assay format | 8 | 0 | — |