Vasopressin V2 receptor
Cross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Vasopressin V2 receptor as ChEMBL target CHEMBL3766, mapped to UniProt Q00788. 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 V2 receptor matters
Vasopressin V2 receptor is reviewed as Vasopressin V2 receptor (UniProt Q00788); the current evidence base includes 7 approved drugs, 634 compounds, and 75 assays, with lead potency reaching pChEMBL 10.7.
Vasopressin V2 receptor Sequence length is 371 aa.
Review this target as Vasopressin V2 receptor, mapped to UniProt Q00788. Sequence length is 371 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 7 approved drugs, 634 compounds, and 75 assays for this target. The dominant activity type is IC50. CHEMBL4468523 is the current potency anchor at pChEMBL 10.7.
Use CHEMBL4468523 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 Vasopressin V2 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 Q00788, 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
CHEMBL4468523
|
10.7 | EC50 | — |
|
|
No preferred name
CHEMBL1429
|
10.5 | EC50 | Approved |
|
|
No preferred name
CHEMBL4539370
|
10.3 | EC50 | — |
|
|
No preferred name
CHEMBL375324
|
9.7 | Ki | — |
|
|
No preferred name
CHEMBL435323
|
9.6 | Ki | — |
Approved Drugs
| Structure | Compound | First Approval |
|---|---|---|
|
|
VASOPRESSIN
CHEMBL373742
|
2014 |
|
|
MOZAVAPTAN
CHEMBL420762
|
2006 |
|
|
CONIVAPTAN
CHEMBL1755
|
2005 |
|
|
OXYTOCIN
CHEMBL395429
|
1980 |
|
|
DESMOPRESSIN
CHEMBL1429
|
1978 |