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Target Snapshot

CHEMBL2095173 Target Snapshot

Potassium-transporting ATPase · PROTEIN COMPLEX · Homo sapiens

336Compounds
17Assays
5Approved Drugs
327.0Activities
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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 2026-09-13

Potassium-transporting ATPase shows approved-linked disease relevance led by gastroesophageal reflux disease. 5 more disease programs remain visible in the same review block. 13 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P20648. Start with gastroesophageal reflux disease, then reuse UniProt P20648 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with gastroesophageal reflux disease, then reuse UniProt P20648 as the stable protein anchor across project notes and exports.

ChEMBL component mapping + Open Targets-ready proxy + ChEMBL 36 via Core Engine 2026-09-13 13 linked drugs
Open source guide
Disease program
gastroesophageal reflux disease

Potassium-transporting ATPase shows approved-linked disease relevance led by gastroesophageal reflux disease. 5 more disease programs remain visible in the same review block. 13 linked drugs remain visible in the same block.

Start review with gastroesophageal reflux disease because it currently carries approved-linked support. Linked drugs include ABEPRAZAN, DEXLANSOPRAZOLE, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE SODIUM. 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 13 linked drugs
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 Potassium-transporting ATPase as ChEMBL target CHEMBL2095173, mapped to UniProt P20648. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Potassium-transporting ATPase
PROTEIN COMPLEX · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL2095173
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P20648
Potassium-transporting ATPase alpha chain 1
UniProt accession via ChEMBL component mapping As of 2026-09-13
www.uniprot.org
Disease evidence contract
Open Targets-ready proxy
ChEMBL drug mechanism + indication proxy
ChEMBL drug mechanism + indication proxy As of 2026-09-13
www.ebi.ac.uk

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

Source Guidance

Start with the right source

Choose the first block or source based on the question you are trying to answer.

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

Start here when your first question is whether Potassium-transporting ATPase is the right protein anchor across sources, using UniProt P20648 as the stable mapping.

Jump to Protein Context
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Disease Relevance & Evidence Level
ChEMBL drug mechanism + indication proxy

Use this block first when you need to confirm why gastroesophageal reflux disease is currently framed as approved-linked support. It currently carries 13 linked drugs 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 LabelPotassium-transporting ATPase alpha chain 1
UniProt AccessionP20648
Component TypeProtein
Sequence Length1035 aa

Potassium-transporting ATPase alpha chain 1

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Potassium-transporting ATPase, mapped to UniProt P20648. ChEMBL maps the protein component as Potassium-transporting ATPase alpha chain 1. Sequence length is 1035 aa.

Mapped IDP20648
Review namePotassium-transporting ATPase
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

Potassium-transporting ATPase shows approved-linked disease relevance led by gastroesophageal reflux disease. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
gastroesophageal reflux disease
13 linked drugs · 13 direct · 13 efficacy
Linked drugABEPRAZAN
Linked drugDEXLANSOPRAZOLE
Linked drugESOMEPRAZOLE MAGNESIUM
Linked drugESOMEPRAZOLE SODIUM
Approved-linked Approved
duodenal ulcer
9 linked drugs · 9 direct · 9 efficacy
Linked drugESOMEPRAZOLE MAGNESIUM
Linked drugESOMEPRAZOLE SODIUM
Linked drugESOMEPRAZOLE STRONTIUM
Linked drugILAPRAZOLE
Approved-linked Approved
gastric ulcer
6 linked drugs · 6 direct · 6 efficacy
Linked drugESOMEPRAZOLE MAGNESIUM
Linked drugESOMEPRAZOLE STRONTIUM
Linked drugLANSOPRAZOLE
Linked drugOMEPRAZOLE
Approved-linked Approved
Peptic ulcer
6 linked drugs · 6 direct · 6 efficacy
Linked drugABEPRAZAN
Linked drugDEXLANSOPRAZOLE
Linked drugILAPRAZOLE
Linked drugLANSOPRAZOLE
Approved-linked Approved
Esophagitis
5 linked drugs · 5 direct · 5 efficacy
Linked drugDEXLANSOPRAZOLE
Linked drugESOMEPRAZOLE MAGNESIUM
Linked drugOMEPRAZOLE
Linked drugPANTOPRAZOLE SODIUM
Approved-linked Approved
Zollinger-Ellison Syndrome
5 linked drugs · 5 direct · 5 efficacy
Linked drugESOMEPRAZOLE MAGNESIUM
Linked drugESOMEPRAZOLE STRONTIUM
Linked drugOMEPRAZOLE
Linked drugPANTOPRAZOLE SODIUM
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with gastroesophageal reflux disease because it currently carries approved-linked support. Linked drugs include ABEPRAZAN, DEXLANSOPRAZOLE, ESOMEPRAZOLE MAGNESIUM, ESOMEPRAZOLE SODIUM. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseasegastroesophageal reflux disease
Strongest levelApproved-linked
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

5
Approved
Assay Mix

Activity Type Distribution

IC50327.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL1202672 7.7 IC50 20.0 Preclinical
CHEMBL1202661 7.52 IC50 30.0 Preclinical
CHEMBL1790041 7.4 IC50 40.0 Approved
CHEMBL1202621 7.3 IC50 50.0 Preclinical
CHEMBL1202647 7.3 IC50 50.0 Preclinical
CHEMBL47529 7.19 IC50 65.0 Preclinical
CHEMBL296482 7.19 IC50 64.0 Preclinical
CHEMBL1202681 7.1 IC50 80.0 Preclinical
CHEMBL1202667 7.05 IC50 90.0 Preclinical
CHEMBL1202658 6.96 IC50 110.0 Preclinical
Distribution

pChEMBL Value Distribution

59
5.0
58
5.5
66
6.0
55
6.5
9
7.0
2
7.5
0
8.0
0
8.5
0
9.0
0
9.5
pChEMBL
Approved Drugs

Approved Drugs

PANTOPRAZOLE
CHEMBL1502
Approved 2000
LANSOPRAZOLE
CHEMBL480
Approved 1995
OMEPRAZOLE
CHEMBL1503
Approved 1989
RANITIDINE
CHEMBL1790041
Approved 1983
CIMETIDINE
CHEMBL30
Approved 1977
Assay Landscape

Assay Landscape

17
Total Assays
185
Tested Compounds
2
Assay Types
Binding — 13 assays, 185 compounds
BAO Format Assays Compounds Avg pChEMBL
tissue-based format 7 55 5.5
protein complex format 5 126 5.3
organism-based format 1 4 6.0
Functional — 4 assays, 68 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 4 68 6.4

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine