ALK tyrosine kinase receptor · SINGLE PROTEIN · Homo sapiens
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As of 2026-09-13ALK tyrosine kinase receptor shows approved-linked disease relevance led by non-small cell lung carcinoma. 5 more disease programs remain visible in the same review block. 9 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt Q9UM73. Start with non-small cell lung carcinoma, then reuse UniProt Q9UM73 as the stable protein anchor across project notes and exports.
Start with non-small cell lung carcinoma, then reuse UniProt Q9UM73 as the stable protein anchor across project notes and exports.
ALK tyrosine kinase receptor shows approved-linked disease relevance led by non-small cell lung carcinoma. 5 more disease programs remain visible in the same review block. 9 linked drugs remain visible in the same block.
Start review with non-small cell lung carcinoma because it currently carries approved-linked support. Linked drugs include ALECTINIB HYDROCHLORIDE, BRIGATINIB, CERITINIB, CONTELTINIB. 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 proxyALK tyrosine kinase receptor
Review this target as ALK tyrosine kinase receptor, mapped to UniProt Q9UM73. Sequence length is 1620 aa.
Protein source · UniProt accession via ChEMBL component mappingKeep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats ALK tyrosine kinase receptor as ChEMBL target CHEMBL4247, mapped to UniProt Q9UM73. 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 ALK tyrosine kinase receptor is the right protein anchor across sources, using UniProt Q9UM73 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why non-small cell lung carcinoma is currently framed as approved-linked support. It currently carries 9 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 CardVerify identity, organism, and the fastest next research jumps from the same page.
| Preferred Name | ALK tyrosine kinase receptor |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | Q9UM73 |
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | ALK tyrosine kinase receptor |
| UniProt Accession | Q9UM73 |
| Component Type | Protein |
| Sequence Length | 1620 aa |
ALK tyrosine kinase receptor
Review this target as ALK tyrosine kinase receptor, mapped to UniProt Q9UM73. Sequence length is 1620 aa.
Open Targets-ready disease context using the current target-indication evidence contract.
ALK tyrosine kinase receptor shows approved-linked disease relevance led by non-small cell lung carcinoma. 5 more disease programs remain visible in the same review block.
Start review with non-small cell lung carcinoma because it currently carries approved-linked support. Linked drugs include ALECTINIB HYDROCHLORIDE, BRIGATINIB, CERITINIB, CONTELTINIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
| ChEMBL ID | pChEMBL | Type | Value (nM) | Phase |
|---|---|---|---|---|
| CHEMBL3397300 | 10.15 | IC50 | 0.07 | Preclinical |
| CHEMBL3286823 | 10.0 | Ki | 0.1 | Preclinical |
| CHEMBL3286825 | 10.0 | Ki | 0.1 | Preclinical |
| CHEMBL5593687 | 10.0 | IC50 | 0.1 | Preclinical |
| CHEMBL3286826 | 9.96 | IC50 | 0.11 | Preclinical |
| CHEMBL3286828 | 9.92 | Ki | 0.12 | Preclinical |
| CHEMBL3824308 | 9.92 | IC50 | 0.12 | Preclinical |
| CHEMBL509032 | 9.82 | IC50 | 0.15 | Preclinical |
| CHEMBL3892880 | 9.78 | IC50 | 0.168 | Preclinical |
| CHEMBL3687205 | 9.77 | IC50 | 0.17 | Preclinical |
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 762 | 1,629 | 7.6 |
| cell-based format | 386 | 592 | 6.9 |
| assay format | 183 | 317 | 7.5 |
| organism-based format | 4 | 0 | — |
| subcellular format | 1 | 2 | 8.6 |
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| cell-based format | 4 | 2 | 7.4 |
| organism-based format | 3 | 0 | — |
| assay format | 1 | 259 | 6.1 |
| BAO Format | Assays | Compounds | Avg pChEMBL |
|---|---|---|---|
| single protein format | 1 | 0 | — |