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Target Snapshot

CHEMBL2095169 Target Snapshot

Dopamine receptors; D2 & D3 · SELECTIVITY GROUP · Homo sapiens

531Compounds
43Assays
0Approved Drugs
0Activities
Free Research Context

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Broader Open DB context

Frame the target before identity details

Structured disease, protein, and project context should read before the lower-level identity rail.

As of 2026-09-14

Dopamine receptors; D2 & D3 shows approved-linked disease relevance led by Nausea and vomiting. 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 P14416. Start with Nausea and vomiting, then reuse UniProt P14416 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with Nausea and vomiting, then reuse UniProt P14416 as the stable protein anchor across project notes and exports.

ChEMBL component mapping + Open Targets-ready proxy + ChEMBL 36 via Core Engine 2026-09-14 1 linked drug
Open source guide
Disease program
Nausea and vomiting

Dopamine receptors; D2 & D3 shows approved-linked disease relevance led by Nausea and vomiting. 5 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with Nausea and vomiting because it currently carries approved-linked support. Linked drugs include AMISULPRIDE. 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 proxy
Approved-linked Open Targets-ready proxy 1 linked drug
Open disease block
Identity Layer

Cross-source identity

Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.

This review treats Dopamine receptors; D2 & D3 as ChEMBL target CHEMBL2095169, mapped to UniProt P14416. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Dopamine receptors; D2 & D3
SELECTIVITY GROUP · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL2095169
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
P14416
D(2) dopamine receptor
UniProt accession via ChEMBL component mapping As of 2026-09-14
www.uniprot.org
Disease evidence contract
Open Targets-ready proxy
ChEMBL drug mechanism + indication proxy
ChEMBL drug mechanism + indication proxy As of 2026-09-14
www.ebi.ac.uk

Reuse the same identifiers in notes, watch rules, exports, and review packs so provenance stays stable across surfaces.

Source Guidance

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Need stable target naming and protein identity?
UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether Dopamine receptors; D2 & D3 is the right protein anchor across sources, using UniProt P14416 as the stable mapping.

Jump to Protein Context
Need disease fit before discussing compounds?
Disease Relevance & Evidence Level
ChEMBL drug mechanism + indication proxy

Use this block first when you need to confirm why Nausea and vomiting is currently framed as approved-linked support. It currently carries 1 linked drug in the same disease frame.

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Evidence Card
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Overview

Basic Information

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UniProt Context

UniProt Target Context

Reviewable protein naming and mapping context for this target snapshot.

Protein LabelD(2) dopamine receptor
UniProt AccessionP14416
Component TypeProtein
Sequence Length443 aa

D(2) dopamine receptor

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Dopamine receptors; D2 & D3, mapped to UniProt P14416. ChEMBL maps the protein component as D(2) dopamine receptor. Sequence length is 443 aa.

Mapped IDP14416
Review nameDopamine receptors; D2 & D3
OrganismHomo sapiens
Disease Relevance

Disease Relevance & Evidence Level

Open Targets-ready disease context using the current target-indication evidence contract.

Approved-linked Open Targets-ready proxy

Dopamine receptors; D2 & D3 shows approved-linked disease relevance led by Nausea and vomiting. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
Nausea and vomiting
1 linked drug · 1 direct · 1 efficacy
Linked drugAMISULPRIDE
Approved-linked Approved
post operative nausea and vomiting
1 linked drug · 1 direct · 1 efficacy
Linked drugAMISULPRIDE
Approved-linked Approved
psychosis
1 linked drug · 1 direct · 1 efficacy
Linked drugAMISULPRIDE
Late clinical Phase III
anxiety
1 linked drug · 1 direct · 1 efficacy
Linked drugAMISULPRIDE
Late clinical Phase III
Dementia
1 linked drug · 1 direct · 1 efficacy
Linked drugAMISULPRIDE
Late clinical Phase III
depressive disorder
1 linked drug · 1 direct · 1 efficacy
Linked drugAMISULPRIDE
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with Nausea and vomiting because it currently carries approved-linked support. Linked drugs include AMISULPRIDE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaseNausea and vomiting
Strongest levelApproved-linked
Block modeOpen Targets-ready proxy
Distribution

pChEMBL Value Distribution

0
5.0
0
5.5
0
6.0
0
6.5
0
7.0
0
7.5
0
8.0
0
8.5
0
9.0
0
9.5
pChEMBL
Assay Landscape

Assay Landscape

43
Total Assays
0
Tested Compounds
2
Assay Types
Binding — 36 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
protein format 36 0
Functional — 7 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 6 0
cell-based format 1 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine