Proto-oncogene tyrosine-protein kinase ROS
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Proto-oncogene tyrosine-protein kinase ROS as ChEMBL target CHEMBL5568, mapped to UniProt P08922. 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.
Why Proto-oncogene tyrosine-protein kinase ROS matters
Proto-oncogene tyrosine-protein kinase ROS is reviewed as Proto-oncogene tyrosine-protein kinase ROS (UniProt P08922); Proto-oncogene tyrosine-protein kinase ROS shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block.; 4 linked drugs keep this evidence frame grounded.; the current evidence base includes 21 approved drugs, 1772 compounds, and 412 assays, with lead potency reaching pChEMBL 10.7.
Proto-oncogene tyrosine-protein kinase ROS Sequence length is 2347 aa.
Review this target as Proto-oncogene tyrosine-protein kinase ROS, mapped to UniProt P08922. Sequence length is 2347 aa.
Protein source · UniProt accession via ChEMBL component mappingProto-oncogene tyrosine-protein kinase ROS shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 4 linked drugs keep the rationale reviewable. 5 additional disease programs remain visible in the same card. Linked drugs include CRIZOTINIB, ENTRECTINIB, REPOTRECTINIB.
Start review with neoplasm because it currently carries approved-linked support. Linked drugs include CRIZOTINIB, ENTRECTINIB, REPOTRECTINIB, TALETRECTINIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
ChEMBL target recordChEMBL currently tracks 21 approved drugs, 1772 compounds, and 412 assays for this target. The dominant activity type is KI. CHEMBL3128069 is the current potency anchor at pChEMBL 10.7.
Use CHEMBL3128069 as the tractability anchor when discussing potency (pChEMBL 10.7).
Activity source · ChEMBL 36 via Core EngineStart with the right source
Pick the first block or linked source that matches the review question in front of you.
Start with the review rationale when you need to explain why Proto-oncogene tyrosine-protein kinase ROS matters before drilling into raw source blocks.
Jump to Review RationaleGo back to the target snapshot when you need the naming and mapping contract behind UniProt P08922, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need to see why neoplasm is currently treated as approved-linked support.
Open Disease ContextSnapshot State
No project snapshot selected. Export uses the live evidence card state.
pChEMBL Activity Distribution
Top 5 Inhibitors (by pChEMBL)
| Structure | Compound | pChEMBL | Type | Phase |
|---|---|---|---|---|
|
|
No preferred name
CHEMBL3128069
|
10.7 | Ki | — |
|
|
No preferred name
CHEMBL388978
|
10.2 | IC50 | — |
|
|
No preferred name
CHEMBL4298138
|
10.2 | IC50 | Approved |
|
|
No preferred name
CHEMBL3286830
|
10.0 | Ki | Approved |
|
|
No preferred name
CHEMBL5712062
|
10.0 | Ki | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
REPOTRECTINIB
CHEMBL4298138
|
2023 |
|
|
ENTRECTINIB
CHEMBL1983268
|
2019 |
|
|
FEDRATINIB
CHEMBL1287853
|
2019 |
|
|
LORLATINIB
CHEMBL3286830
|
2018 |
|
|
GILTERITINIB
CHEMBL3301622
|
2018 |
|
|
BRIGATINIB
CHEMBL3545311
|
2017 |
|
|
MIDOSTAURIN
CHEMBL608533
|
2017 |
|
|
CERITINIB
CHEMBL2403108
|
2014 |
|
|
CRIZOTINIB
CHEMBL601719
|
2011 |
|
|
PAZOPANIB
CHEMBL477772
|
2009 |