Start with Autosomal dominant polycystic kidney disease, then reuse UniProt O14920 as the stable protein anchor across project notes and exports.
CHEMBL1991 Target Snapshot
Inhibitor of nuclear factor kappa-B kinase subunit beta · SINGLE PROTEIN · Homo sapiens
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As of 2026-09-13Inhibitor of nuclear factor kappa-B kinase subunit beta shows late clinical disease relevance led by Autosomal dominant polycystic kidney disease. 5 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 O14920. Start with Autosomal dominant polycystic kidney disease, then reuse UniProt O14920 as the stable protein anchor across project notes and exports.
Inhibitor of nuclear factor kappa-B kinase subunit beta shows late clinical disease relevance led by Autosomal dominant polycystic kidney disease. 5 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.
Start review with Autosomal dominant polycystic kidney disease because it currently carries late clinical support. Linked drugs include BARDOXOLONE METHYL. 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 proxyInhibitor of nuclear factor kappa-B kinase subunit beta
Review this target as Inhibitor of nuclear factor kappa-B kinase subunit beta, mapped to UniProt O14920. Sequence length is 756 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 Inhibitor of nuclear factor kappa-B kinase subunit beta as ChEMBL target CHEMBL1991, mapped to UniProt O14920. 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.
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Start here when your first question is whether Inhibitor of nuclear factor kappa-B kinase subunit beta is the right protein anchor across sources, using UniProt O14920 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why Autosomal dominant polycystic kidney disease is currently framed as late clinical 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
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| Preferred Name | Inhibitor of nuclear factor kappa-B kinase subunit beta |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | O14920 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Inhibitor of nuclear factor kappa-B kinase subunit beta |
| UniProt Accession | O14920 |
| Component Type | Protein |
| Sequence Length | 756 aa |
Inhibitor of nuclear factor kappa-B kinase subunit beta
How to read this target
Review this target as Inhibitor of nuclear factor kappa-B kinase subunit beta, mapped to UniProt O14920. Sequence length is 756 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Inhibitor of nuclear factor kappa-B kinase subunit beta shows late clinical disease relevance led by Autosomal dominant polycystic kidney disease. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with Autosomal dominant polycystic kidney disease because it currently carries late clinical support. Linked drugs include BARDOXOLONE METHYL. 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 |
|---|---|---|---|---|
| CHEMBL3897289 | 10.1 | IC50 | 0.08 | Preclinical |
| CHEMBL5919378 | 10.0 | IC50 | 0.1 | Preclinical |
| CHEMBL5878871 | 9.7 | IC50 | 0.2 | Preclinical |
| CHEMBL5883781 | 9.7 | IC50 | 0.2 | Preclinical |
| CHEMBL5997512 | 9.7 | IC50 | 0.2 | Preclinical |
| CHEMBL384467 | 9.3 | IC50 | 0.5 | Approved |
| CHEMBL1669569 | 9.3 | IC50 | 0.5 | Preclinical |
| CHEMBL1669608 | 9.3 | IC50 | 0.5 | Preclinical |
| CHEMBL1669562 | 9.22 | IC50 | 0.6 | Preclinical |
| CHEMBL1669563 | 9.22 | IC50 | 0.6 | Preclinical |
pChEMBL Value Distribution
Approved Drugs
Assay Landscape
Binding — 793 assays, 1,154 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 566 | 1,035 | 6.6 |
| cell-based format | 127 | 75 | 5.6 |
| assay format | 79 | 42 | 6.5 |
| subcellular format | 17 | 0 | — |
| tissue-based format | 4 | 2 | 5.3 |
ADME — 5 assays, 15 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 4 | 15 | 5.7 |
| assay format | 1 | 0 | — |
Functional — 4 assays, 44 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| assay format | 2 | 34 | 5.9 |
| cell-based format | 2 | 10 | 5.8 |