Skip to main content
Free research Free research Free target review with research home and workspace preview
Quick search ChEMBL 36
Loading Target Snapshot...
Querying ChEMBL database. This may take a few seconds.
Target Snapshot

CHEMBL3974 Target Snapshot

Proteinase-activated receptor 1 · SINGLE PROTEIN · Homo sapiens

1,296Compounds
175Assays
2Approved Drugs
1,382.0Activities
Free Research Context

Research home keeps recent targets

This target will appear in recent viewed items on this browser. Use the demo workspace to preview watch rules and decision queues.

Navigation

Switch target

Move to another high-traffic target or paste a specific ChEMBL target ID.

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

Proteinase-activated receptor 1 shows approved-linked disease relevance led by myocardial infarction. 4 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 P25116. Start with myocardial infarction, then reuse UniProt P25116 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with myocardial infarction, then reuse UniProt P25116 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
myocardial infarction

Proteinase-activated receptor 1 shows approved-linked disease relevance led by myocardial infarction. 4 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with myocardial infarction because it currently carries approved-linked support. Linked drugs include VORAPAXAR SULFATE. 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 Proteinase-activated receptor 1 as ChEMBL target CHEMBL3974, mapped to UniProt P25116. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Proteinase-activated receptor 1
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL3974
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
P25116
Proteinase-activated receptor 1
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

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 Proteinase-activated receptor 1 is the right protein anchor across sources, using UniProt P25116 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 myocardial infarction is currently framed as approved-linked support. It currently carries 1 linked drug in the same disease frame.

Jump to Disease Context
Need a meeting-ready explanation of why this target matters?
Evidence Card
Review-ready rationale with source-aware context

Open the one-page evidence card when you want the rationale, activity base, and attribution together.

Open Review-ready Card
Overview

Basic Information

Verify identity, organism, and the fastest next research jumps from the same page.

UniProt Context

UniProt Target Context

Reviewable protein naming and mapping context for this target snapshot.

Protein LabelProteinase-activated receptor 1
UniProt AccessionP25116
Component TypeProtein
Sequence Length425 aa

Proteinase-activated receptor 1

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Proteinase-activated receptor 1, mapped to UniProt P25116. Sequence length is 425 aa.

Mapped IDP25116
Review nameProteinase-activated receptor 1
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

Proteinase-activated receptor 1 shows approved-linked disease relevance led by myocardial infarction. 4 more disease programs remain visible in the same review block.

Approved-linked Approved
myocardial infarction
1 linked drug · 1 direct · 1 efficacy
Linked drugVORAPAXAR SULFATE
Approved-linked Approved
peripheral arterial disease
1 linked drug · 1 direct · 1 efficacy
Linked drugVORAPAXAR SULFATE
Approved-linked Approved
stroke
1 linked drug · 1 direct · 1 efficacy
Linked drugVORAPAXAR SULFATE
Clinical signal Phase II
acute coronary syndrome
2 linked drugs · 2 direct · 2 efficacy
Linked drugATOPAXAR
Linked drugVORAPAXAR SULFATE
Clinical signal Phase II
coronary artery disease
2 linked drugs · 2 direct · 2 efficacy
Linked drugATOPAXAR
Linked drugPZ-128
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

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

Lead diseasemyocardial infarction
Strongest levelApproved-linked
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

2
Approved
2
Phase II
Assay Mix

Activity Type Distribution

IC501,162.0
KI82.0
EC50123.0
KD15.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL267059 10.4 Kd 0.04 Preclinical
CHEMBL7642 9.82 Kd 0.15 Preclinical
CHEMBL275003 9.36 Kd 0.44 Preclinical
CHEMBL275946 9.15 Kd 0.7 Preclinical
CHEMBL428311 9.09 Kd 0.82 Preclinical
CHEMBL3954641 9.05 IC50 0.9 Preclinical
CHEMBL4111522 9.05 IC50 0.9 Preclinical
CHEMBL3939323 9.0 IC50 0.99 Preclinical
CHEMBL3942006 9.0 IC50 1.0 Preclinical
CHEMBL493982 8.96 IC50 1.1 Approved
Distribution

pChEMBL Value Distribution

131
5.0
162
5.5
186
6.0
164
6.5
137
7.0
175
7.5
95
8.0
53
8.5
7
9.0
1
9.5
pChEMBL
Approved Drugs

Approved Drugs

VORAPAXAR
CHEMBL493982
Approved 2014
Assay Landscape

Assay Landscape

175
Total Assays
786
Tested Compounds
3
Assay Types
Binding — 89 assays, 786 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 32 333 7.2
single protein format 20 150 7.0
cell-free format 16 39 6.1
cell membrane format 12 170 7.0
cell-based format 8 94 5.7
tissue-based format 1 0
Functional — 82 assays, 331 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 43 255 5.8
cell-based format 36 75 6.4
cell-free format 3 1 6.5
ADME — 4 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-free format 4 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine