Autotaxin
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Autotaxin as ChEMBL target CHEMBL3691, mapped to UniProt Q13822. 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 Autotaxin matters
Autotaxin is reviewed as Autotaxin (UniProt Q13822); Autotaxin shows late clinical disease relevance led by idiopathic pulmonary fibrosis. 2 more disease programs remain visible in the same review block.; 1 linked drug keep this evidence frame grounded.; the current evidence base includes 5 approved drugs, 3479 compounds, and 292 assays, with lead potency reaching pChEMBL 11.0.
Autotaxin Sequence length is 863 aa.
Review this target as Autotaxin, mapped to UniProt Q13822. Sequence length is 863 aa.
Protein source · UniProt accession via ChEMBL component mappingAutotaxin shows late clinical disease relevance led by idiopathic pulmonary fibrosis. 2 more disease programs remain visible in the same review block. 1 linked drug keep the rationale reviewable. 2 additional disease programs remain visible in the same card. Linked drugs include ZIRITAXESTAT.
Start review with idiopathic pulmonary fibrosis because it currently carries late clinical support. Linked drugs include ZIRITAXESTAT. 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 5 approved drugs, 3479 compounds, and 292 assays for this target. The dominant activity type is IC50. CHEMBL3828074 is the current potency anchor at pChEMBL 11.0.
Use CHEMBL3828074 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 Autotaxin 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 Q13822, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need to see why idiopathic pulmonary fibrosis is currently treated as late clinical 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
CHEMBL3828074
|
11.0 | IC50 | Clinical |
|
|
No preferred name
CHEMBL5183599
|
9.4 | IC50 | — |
|
|
No preferred name
CHEMBL4640012
|
9.4 | IC50 | — |
|
|
No preferred name
CHEMBL5766179
|
9.0 | IC50 | — |
|
|
No preferred name
CHEMBL5759407
|
9.0 | IC50 | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
DRONABINOL
CHEMBL465
|
1985 |
|
|
EVANS BLUE
CHEMBL1200712
|
1982 |