Start with cancer, then reuse UniProt P04049 as the stable protein anchor across project notes and exports.
CHEMBL1906 Target Snapshot
RAF proto-oncogene serine/threonine-protein kinase · SINGLE PROTEIN · Homo sapiens
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As of 2026-09-13RAF proto-oncogene serine/threonine-protein kinase shows approved-linked disease relevance led by cancer. 5 more disease programs remain visible in the same review block. 3 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P04049. Start with cancer, then reuse UniProt P04049 as the stable protein anchor across project notes and exports.
RAF proto-oncogene serine/threonine-protein kinase shows approved-linked disease relevance led by cancer. 5 more disease programs remain visible in the same review block. 3 linked drugs remain visible in the same block.
Start review with cancer because it currently carries approved-linked support. Linked drugs include REGORAFENIB, SORAFENIB TOSYLATE, XL-281. 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 proxyRAF proto-oncogene serine/threonine-protein kinase
Review this target as RAF proto-oncogene serine/threonine-protein kinase, mapped to UniProt P04049. Sequence length is 648 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 RAF proto-oncogene serine/threonine-protein kinase as ChEMBL target CHEMBL1906, mapped to UniProt P04049. 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 RAF proto-oncogene serine/threonine-protein kinase is the right protein anchor across sources, using UniProt P04049 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why cancer is currently framed as approved-linked support. It currently carries 3 linked drugs 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 | RAF proto-oncogene serine/threonine-protein kinase |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | P04049 |
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UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | RAF proto-oncogene serine/threonine-protein kinase |
| UniProt Accession | P04049 |
| Component Type | Protein |
| Sequence Length | 648 aa |
RAF proto-oncogene serine/threonine-protein kinase
How to read this target
Review this target as RAF proto-oncogene serine/threonine-protein kinase, mapped to UniProt P04049. Sequence length is 648 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
RAF proto-oncogene serine/threonine-protein kinase shows approved-linked disease relevance led by cancer. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with cancer because it currently carries approved-linked support. Linked drugs include REGORAFENIB, SORAFENIB TOSYLATE, XL-281. 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 |
|---|---|---|---|---|
| CHEMBL3924812 | 10.62 | IC50 | 0.024 | Preclinical |
| CHEMBL3961999 | 10.52 | IC50 | 0.03 | Preclinical |
| CHEMBL3933272 | 10.41 | IC50 | 0.039 | Preclinical |
| CHEMBL6023111 | 10.4 | IC50 | 0.04 | Preclinical |
| CHEMBL3951474 | 10.25 | IC50 | 0.056 | Preclinical |
| CHEMBL4776565 | 10.22 | Ki | 0.06 | Preclinical |
| CHEMBL5094514 | 10.22 | Ki | 0.06 | Preclinical |
| CHEMBL4778419 | 10.21 | Ki | 0.062 | Preclinical |
| CHEMBL3577124 | 10.21 | Ki | 0.061 | Preclinical |
| CHEMBL4780060 | 10.21 | Ki | 0.061 | Preclinical |
pChEMBL Value Distribution
Approved Drugs
Assay Landscape
Binding — 761 assays, 3,876 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 601 | 2,459 | 7.9 |
| assay format | 86 | 1,175 | 8.9 |
| cell-based format | 73 | 242 | 6.5 |
| subcellular format | 1 | 0 | — |
Functional — 24 assays, 1 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 23 | 1 | 6.2 |
| assay format | 1 | 0 | — |
ADME — 5 assays, 0 compounds
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 4 | 0 | — |
| single protein format | 1 | 0 | — |