Ephrin type-A receptor 6
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Ephrin type-A receptor 6 as ChEMBL target CHEMBL4526, mapped to UniProt Q9UF33. 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 Ephrin type-A receptor 6 matters
Ephrin type-A receptor 6 is reviewed as Ephrin type-A receptor 6 (UniProt Q9UF33); the current evidence base includes 15 approved drugs, 339 compounds, and 127 assays, with lead potency reaching pChEMBL 9.0.
Ephrin type-A receptor 6 Sequence length is 1036 aa.
Review this target as Ephrin type-A receptor 6, mapped to UniProt Q9UF33. Sequence length is 1036 aa.
Protein source · UniProt accession via ChEMBL component mappingDisease relevance is not yet populated for this evidence card.
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 15 approved drugs, 339 compounds, and 127 assays for this target. The dominant activity type is KD. CHEMBL1230609 is the current potency anchor at pChEMBL 9.0.
Use CHEMBL1230609 as the tractability anchor when discussing potency (pChEMBL 9.0).
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 Ephrin type-A receptor 6 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 Q9UF33, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need the disease program and supporting signals, not only the card summary.
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
CHEMBL1230609
|
9.0 | Kd | Clinical |
|
|
No preferred name
CHEMBL388978
|
7.9 | IC50 | — |
|
|
No preferred name
CHEMBL1738757
|
7.8 | IC50 | Clinical |
|
|
No preferred name
CHEMBL249097
|
7.7 | Kd | — |
|
|
No preferred name
CHEMBL491473
|
7.4 | Kd | Clinical |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
NINTEDANIB
CHEMBL502835
|
2014 |
|
|
AFATINIB
CHEMBL1173655
|
2013 |
|
|
AFATINIB DIMALEATE
CHEMBL2105712
|
2013 |
|
|
VANDETANIB
CHEMBL24828
|
2011 |
|
|
CRIZOTINIB
CHEMBL601719
|
2011 |
|
|
NILOTINIB
CHEMBL255863
|
2007 |
|
|
SUNITINIB
CHEMBL535
|
2006 |
|
|
SORAFENIB
CHEMBL1336
|
2005 |
|
|
ERLOTINIB
CHEMBL553
|
2004 |
|
|
GEFITINIB
CHEMBL939
|
2003 |