Vasopressin V1a receptor
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Vasopressin V1a receptor as ChEMBL target CHEMBL1889, mapped to UniProt P37288. 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 Vasopressin V1a receptor matters
Vasopressin V1a receptor is reviewed as Vasopressin V1a receptor (UniProt P37288); Vasopressin V1a receptor shows approved-linked disease relevance led by heart failure. 5 more disease programs remain visible in the same review block.; 2 linked drugs keep this evidence frame grounded.; the current evidence base includes 17 approved drugs, 3847 compounds, and 414 assays, with lead potency reaching pChEMBL 10.5.
Vasopressin V1a receptor Sequence length is 418 aa.
Review this target as Vasopressin V1a receptor, mapped to UniProt P37288. Sequence length is 418 aa.
Protein source · UniProt accession via ChEMBL component mappingVasopressin V1a receptor shows approved-linked disease relevance led by heart failure. 5 more disease programs remain visible in the same review block. 2 linked drugs keep the rationale reviewable. 5 additional disease programs remain visible in the same card. Linked drugs include CONIVAPTAN HYDROCHLORIDE, PECAVAPTAN.
Start review with heart failure because it currently carries approved-linked support. Linked drugs include CONIVAPTAN HYDROCHLORIDE, PECAVAPTAN. 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 17 approved drugs, 3847 compounds, and 414 assays for this target. The dominant activity type is KI. CHEMBL394602 is the current potency anchor at pChEMBL 10.5.
Use CHEMBL394602 as the tractability anchor when discussing potency (pChEMBL 10.5).
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 Vasopressin V1a receptor 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 P37288, not just the summarized rationale.
Open Protein ContextUse the target snapshot disease block when you need to see why heart failure 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
CHEMBL394602
|
10.5 | Ki | — |
|
|
No preferred name
CHEMBL4094454
|
10.5 | EC50 | — |
|
|
No preferred name
CHEMBL1807272
|
10.4 | Ki | — |
|
|
No preferred name
CHEMBL1807267
|
10.4 | Ki | — |
|
|
No preferred name
CHEMBL1083094
|
10.3 | Ki | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
VASOPRESSIN
CHEMBL373742
|
2014 |
|
|
TOLVAPTAN
CHEMBL344159
|
2009 |
|
|
MOZAVAPTAN
CHEMBL420762
|
2006 |
|
|
CONIVAPTAN
CHEMBL1755
|
2005 |
|
|
ATOSIBAN
CHEMBL382301
|
2000 |
|
|
OXYTOCIN
CHEMBL395429
|
1980 |
|
|
DESMOPRESSIN
CHEMBL1429
|
1978 |