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Target Snapshot

CHEMBL5451 Target Snapshot

Sodium channel protein type 10 subunit alpha · SINGLE PROTEIN · Homo sapiens

897Compounds
107Assays
2Approved Drugs
832.0Activities
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

Sodium channel protein type 10 subunit alpha shows clinical signal disease relevance led by overactive bladder. 2 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 Q9Y5Y9. Start with overactive bladder, then reuse UniProt Q9Y5Y9 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with overactive bladder, then reuse UniProt Q9Y5Y9 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
overactive bladder

Sodium channel protein type 10 subunit alpha shows clinical signal disease relevance led by overactive bladder. 2 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with overactive bladder because it currently carries clinical signal support. Linked drugs include AFACIFENACIN. 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
Clinical signal 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 Sodium channel protein type 10 subunit alpha as ChEMBL target CHEMBL5451, mapped to UniProt Q9Y5Y9. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Sodium channel protein type 10 subunit alpha
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL5451
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
Q9Y5Y9
Sodium channel protein type 10 subunit alpha
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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UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether Sodium channel protein type 10 subunit alpha is the right protein anchor across sources, using UniProt Q9Y5Y9 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 overactive bladder is currently framed as clinical signal support. It currently carries 1 linked drug in the same disease frame.

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Evidence Card
Review-ready rationale with source-aware context

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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 LabelSodium channel protein type 10 subunit alpha
UniProt AccessionQ9Y5Y9
Component TypeProtein
Sequence Length1956 aa

Sodium channel protein type 10 subunit alpha

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Sodium channel protein type 10 subunit alpha, mapped to UniProt Q9Y5Y9. Sequence length is 1956 aa.

Mapped IDQ9Y5Y9
Review nameSodium channel protein type 10 subunit alpha
OrganismHomo sapiens
Disease Relevance

Disease Relevance & Evidence Level

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

Clinical signal Open Targets-ready proxy

Sodium channel protein type 10 subunit alpha shows clinical signal disease relevance led by overactive bladder. 2 more disease programs remain visible in the same review block.

Clinical signal Phase II
overactive bladder
1 linked drug · 1 direct · 1 efficacy
Linked drugAFACIFENACIN
Clinical signal Phase II
toothache
1 linked drug · 1 direct · 1 efficacy
Linked drugPF-04531083
Clinical signal Phase I
Chronic pain
1 linked drug · 1 direct · 1 efficacy
Linked drugPF-04531083
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with overactive bladder because it currently carries clinical signal support. Linked drugs include AFACIFENACIN. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaseoveractive bladder
Strongest levelClinical signal
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

2
Approved
2
Phase III
2
Phase II
1
Phase I
Assay Mix

Activity Type Distribution

IC50812.0
KI1.0
EC5019.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL4760292 9.52 IC50 0.3 Preclinical
CHEMBL4798938 9.4 IC50 0.4 Preclinical
CHEMBL4777598 9.3 IC50 0.5 Preclinical
CHEMBL4753280 9.1 IC50 0.8 Preclinical
CHEMBL5845128 9.1 IC50 0.8 Preclinical
CHEMBL4781110 9.05 IC50 0.9 Preclinical
CHEMBL1277958 9.0 IC50 1.0 Preclinical
CHEMBL3678273 9.0 IC50 1.0 Preclinical
CHEMBL4745699 9.0 IC50 1.0 Preclinical
CHEMBL4744908 8.89 IC50 1.3 Preclinical
Distribution

pChEMBL Value Distribution

88
5.0
130
5.5
127
6.0
91
6.5
110
7.0
88
7.5
54
8.0
40
8.5
11
9.0
2
9.5
pChEMBL
Assay Landscape

Assay Landscape

107
Total Assays
759
Tested Compounds
2
Assay Types
Binding — 103 assays, 759 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 76 235 6.6
single protein format 14 251 7.2
assay format 13 273 6.2
ADME — 4 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 4 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine