Start with dry eye syndrome, then reuse UniProt P0DMS8 as the stable protein anchor across project notes and exports.
CHEMBL256 Target Snapshot
Adenosine receptor A3 · SINGLE PROTEIN · Homo sapiens
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As of 2026-09-13Adenosine receptor A3 shows late clinical disease relevance led by dry eye syndrome. 5 more disease programs remain visible in the same review block. 1 linked drug keeps the current disease frame grounded. Protein identity stays anchored to UniProt P0DMS8. Start with dry eye syndrome, then reuse UniProt P0DMS8 as the stable protein anchor across project notes and exports.
Adenosine receptor A3 shows late clinical disease relevance led by dry eye syndrome. 5 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.
Start review with dry eye syndrome because it currently carries late clinical support. Linked drugs include PICLIDENOSON. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Disease source · ChEMBL drug mechanism + indication proxyAdenosine receptor A3
Review this target as Adenosine receptor A3, mapped to UniProt P0DMS8. Sequence length is 318 aa.
Protein source · UniProt accession via ChEMBL component mappingCross-source identity
Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.
This review treats Adenosine receptor A3 as ChEMBL target CHEMBL256, mapped to UniProt P0DMS8. 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.
Start with the right source
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Start here when your first question is whether Adenosine receptor A3 is the right protein anchor across sources, using UniProt P0DMS8 as the stable mapping.
Jump to Protein ContextUse this block first when you need to confirm why dry eye syndrome is currently framed as late clinical support. It currently carries 1 linked drug in the same disease frame.
Jump to Disease ContextOpen the one-page evidence card when you want the rationale, activity base, and attribution together.
Open Review-ready CardBasic Information
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| Preferred Name | Adenosine receptor A3 |
| Target Type | SINGLE PROTEIN |
| Organism | Homo sapiens |
| UniProt | P0DMS8 |
Next Actions
UniProt Target Context
Reviewable protein naming and mapping context for this target snapshot.
| Protein Label | Adenosine receptor A3 |
| UniProt Accession | P0DMS8 |
| Component Type | Protein |
| Sequence Length | 318 aa |
Adenosine receptor A3
How to read this target
Review this target as Adenosine receptor A3, mapped to UniProt P0DMS8. Sequence length is 318 aa.
Disease Relevance & Evidence Level
Open Targets-ready disease context using the current target-indication evidence contract.
Adenosine receptor A3 shows late clinical disease relevance led by dry eye syndrome. 5 more disease programs remain visible in the same review block.
How to read disease relevance
Start review with dry eye syndrome because it currently carries late clinical support. Linked drugs include PICLIDENOSON. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.
Clinical Phase Distribution
Activity Type Distribution
Top Inhibitors (by pChEMBL)
| ChEMBL ID | pChEMBL | Type | Value (nM) | Phase |
|---|---|---|---|---|
| CHEMBL332091 | 11.0 | Ki | 0.01 | Preclinical |
| CHEMBL118923 | 11.0 | Ki | 0.01 | Preclinical |
| CHEMBL1771603 | 11.0 | Ki | 0.01 | Preclinical |
| CHEMBL119709 | 10.84 | IC50 | 0.01445 | Preclinical |
| CHEMBL5558289 | 10.79 | EC50 | 0.01622 | Preclinical |
| CHEMBL3754229 | 10.57 | Ki | 0.027 | Preclinical |
| CHEMBL1098108 | 10.21 | IC50 | 0.061 | Preclinical |
| CHEMBL4464176 | 10.2 | EC50 | 0.0631 | Preclinical |
| CHEMBL88147 | 10.11 | Kd | 0.07762 | Preclinical |
| CHEMBL119709 | 10.1 | Ki | 0.08 | Preclinical |