Start with myelodysplastic syndrome, then reuse UniProt P04637 as the stable protein anchor across project notes and exports.
CHEMBL4096 Target Snapshot
Cellular tumor antigen p53 · SINGLE PROTEIN · Homo sapiens
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As of 2026-09-14Cellular tumor antigen p53 shows late clinical disease relevance led by myelodysplastic syndrome. 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 P04637. Start with myelodysplastic syndrome, then reuse UniProt P04637 as the stable protein anchor across project notes and exports.
Cellular tumor antigen p53 shows late clinical disease relevance led by myelodysplastic syndrome. 5 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.
Start review with myelodysplastic syndrome because it currently carries late clinical support. Linked drugs include EPRENETAPOPT. 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 proxyCellular tumor antigen p53
Review this target as Cellular tumor antigen p53, mapped to UniProt P04637. Sequence length is 393 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 Cellular tumor antigen p53 as ChEMBL target CHEMBL4096, mapped to UniProt P04637. 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
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Start here when your first question is whether Cellular tumor antigen p53 is the right protein anchor across sources, using UniProt P04637 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why myelodysplastic syndrome 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 | Cellular tumor antigen p53 |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | P04637 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Cellular tumor antigen p53 |
| UniProt Accession | P04637 |
| Component Type | Protein |
| Sequence Length | 393 aa |
Cellular tumor antigen p53
How to read this target
Review this target as Cellular tumor antigen p53, mapped to UniProt P04637. Sequence length is 393 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Cellular tumor antigen p53 shows late clinical disease relevance led by myelodysplastic syndrome. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with myelodysplastic syndrome because it currently carries late clinical support. Linked drugs include EPRENETAPOPT. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Activity Type Distribution
Top Inhibitors (by pChEMBL)
| ChEMBL ID | pChEMBL | Type | Value (nM) | Phase |
|---|---|---|---|---|
| CHEMBL4248974 | 8.7 | EC50 | 2.0 | Preclinical |
| CHEMBL4238053 | 8.4 | EC50 | 4.0 | Preclinical |
| CHEMBL4246320 | 8.4 | EC50 | 4.0 | Preclinical |
| CHEMBL4243509 | 8.05 | EC50 | 9.0 | Preclinical |
| CHEMBL4240212 | 7.92 | EC50 | 12.0 | Preclinical |
| CHEMBL4244338 | 7.19 | EC50 | 65.0 | Preclinical |
| CHEMBL4240141 | 7.13 | EC50 | 74.0 | Preclinical |
| CHEMBL2436173 | 7.1 | EC50 | 80.0 | Preclinical |
| CHEMBL4240977 | 6.82 | EC50 | 152.0 | Preclinical |
| CHEMBL4243377 | 6.8 | EC50 | 158.0 | Preclinical |
pChEMBL Value Distribution
Assay Landscape
Binding — 453 assays, 62 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 409 | 31 | 6.0 |
| assay format | 29 | 26 | 4.5 |
| single protein format | 14 | 5 | 5.8 |
| mitochondrion format | 1 | 0 | — |
ADME — 83 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 83 | 0 | — |
Functional — 9 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| assay format | 7 | 0 | — |
| cell-based format | 2 | 0 | — |
Toxicity — 1 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 1 | 0 | — |