Tyrosine-protein kinase JAK1
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Tyrosine-protein kinase JAK1 as ChEMBL target CHEMBL2835, mapped to UniProt P23458. 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 Tyrosine-protein kinase JAK1 matters
Tyrosine-protein kinase JAK1 is reviewed as Tyrosine-protein kinase JAK1 (UniProt P23458); Tyrosine-protein kinase JAK1 shows approved-linked disease relevance led by rheumatoid arthritis. 5 more disease programs remain visible in the same review block.; 6 linked drugs keep this evidence frame grounded.; the current evidence base includes 37 approved drugs, 14221 compounds, and 1194 assays, with lead potency reaching pChEMBL 11.0.
Tyrosine-protein kinase JAK1 Sequence length is 1154 aa.
Review this target as Tyrosine-protein kinase JAK1, mapped to UniProt P23458. Sequence length is 1154 aa.
Protein source · UniProt accession via ChEMBL component mappingTyrosine-protein kinase JAK1 shows approved-linked disease relevance led by rheumatoid arthritis. 5 more disease programs remain visible in the same review block. 6 linked drugs keep the rationale reviewable. 5 additional disease programs remain visible in the same card. Linked drugs include BARICITINIB, FILGOTINIB, FILGOTINIB MALEATE.
Start review with rheumatoid arthritis because it currently carries approved-linked support. Linked drugs include BARICITINIB, FILGOTINIB, FILGOTINIB MALEATE, INCB-047986. 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 37 approved drugs, 14221 compounds, and 1194 assays for this target. The dominant activity type is IC50. CHEMBL5945428 is the current potency anchor at pChEMBL 11.0.
Use CHEMBL5945428 as the tractability anchor when discussing potency (pChEMBL 11.0).
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 Tyrosine-protein kinase JAK1 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 P23458, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need to see why rheumatoid arthritis 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
CHEMBL5945428
|
11.0 | IC50 | — |
|
|
No preferred name
CHEMBL3896068
|
11.0 | IC50 | — |
|
|
No preferred name
CHEMBL6031741
|
11.0 | IC50 | — |
|
|
No preferred name
CHEMBL6017191
|
11.0 | IC50 | — |
|
|
No preferred name
CHEMBL5942656
|
11.0 | IC50 | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
MOMELOTINIB
CHEMBL1078178
|
2023 |
|
|
DEUCRAVACITINIB
CHEMBL4435170
|
2022 |
|
|
PACRITINIB
CHEMBL2035187
|
2022 |
|
|
ABROCITINIB
CHEMBL3655081
|
2021 |
|
|
FILGOTINIB
CHEMBL3301607
|
2020 |
|
|
FEDRATINIB
CHEMBL1287853
|
2019 |
|
|
ENTRECTINIB
CHEMBL1983268
|
2019 |
|
|
PEFICITINIB
CHEMBL3137308
|
2019 |
|
|
UPADACITINIB
CHEMBL3622821
|
2019 |
|
|
MIDOSTAURIN
CHEMBL608533
|
2017 |
|
|
BARICITINIB
CHEMBL2105759
|
2017 |
|
|
NINTEDANIB
CHEMBL502835
|
2014 |
|
|
TOFACITINIB
CHEMBL221959
|
2012 |
|
|
TOFACITINIB CITRATE
CHEMBL2103743
|
2012 |
|
|
PONATINIB
CHEMBL1171837
|
2012 |
|
|
RUXOLITINIB PHOSPHATE
CHEMBL1795071
|
2011 |
|
|
RUXOLITINIB
CHEMBL1789941
|
2011 |
|
|
CRIZOTINIB
CHEMBL601719
|
2011 |
|
|
SUNITINIB
CHEMBL535
|
2006 |