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Target Snapshot

CHEMBL4323 Target Snapshot

Phospholipase A2 group V · SINGLE PROTEIN · Homo sapiens

222Compounds
25Assays
0Approved Drugs
74.0Activities
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 2026-09-15

Phospholipase A2 group V shows late clinical disease relevance led by acute coronary syndrome. 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 P39877. Start with acute coronary syndrome, then reuse UniProt P39877 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with acute coronary syndrome, then reuse UniProt P39877 as the stable protein anchor across project notes and exports.

ChEMBL component mapping + Open Targets-ready proxy + ChEMBL 36 via Core Engine 2026-09-15 1 linked drug
Open source guide
Disease program
acute coronary syndrome

Phospholipase A2 group V shows late clinical disease relevance led by acute coronary syndrome. 2 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with acute coronary syndrome because it currently carries late clinical support. Linked drugs include VARESPLADIB METHYL. 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
Late clinical 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 Phospholipase A2 group V as ChEMBL target CHEMBL4323, mapped to UniProt P39877. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Phospholipase A2 group V
SINGLE PROTEIN · Homo sapiens
As of 2026-09-15
ChEMBL target ID
CHEMBL4323
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-15
www.ebi.ac.uk
UniProt accession
P39877
Phospholipase A2 group V
UniProt accession via ChEMBL component mapping As of 2026-09-15
www.uniprot.org
Disease evidence contract
Open Targets-ready proxy
ChEMBL drug mechanism + indication proxy
ChEMBL drug mechanism + indication proxy As of 2026-09-15
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 Phospholipase A2 group V is the right protein anchor across sources, using UniProt P39877 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 acute coronary syndrome is currently framed as late clinical 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 LabelPhospholipase A2 group V
UniProt AccessionP39877
Component TypeProtein
Sequence Length138 aa

Phospholipase A2 group V

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Phospholipase A2 group V, mapped to UniProt P39877. Sequence length is 138 aa.

Mapped IDP39877
Review namePhospholipase A2 group V
OrganismHomo sapiens
Disease Relevance

Disease Relevance & Evidence Level

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

Late clinical Open Targets-ready proxy

Phospholipase A2 group V shows late clinical disease relevance led by acute coronary syndrome. 2 more disease programs remain visible in the same review block.

Late clinical Phase III
acute coronary syndrome
1 linked drug · 1 direct · 1 efficacy
Linked drugVARESPLADIB METHYL
Clinical signal Phase II
coronary artery disease
1 linked drug · 1 direct · 1 efficacy
Linked drugVARESPLADIB METHYL
Clinical signal Phase I
kidney disease
1 linked drug · 1 direct · 1 efficacy
Linked drugVARESPLADIB METHYL
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with acute coronary syndrome because it currently carries late clinical support. Linked drugs include VARESPLADIB METHYL. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaseacute coronary syndrome
Strongest levelLate clinical
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

1
Phase II
Assay Mix

Activity Type Distribution

IC5074.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5172164 8.0 IC50 10.0 Preclinical
CHEMBL515637 7.46 IC50 35.0 Preclinical
CHEMBL148649 7.36 IC50 44.0 Preclinical
CHEMBL332993 7.0 IC50 100.0 Preclinical
CHEMBL514692 7.0 IC50 100.0 Preclinical
CHEMBL444450 6.96 IC50 110.0 Preclinical
CHEMBL148674 6.91 IC50 124.0 Clinical
CHEMBL446349 6.85 IC50 140.0 Preclinical
CHEMBL4205008 6.75 IC50 180.0 Preclinical
CHEMBL357979 6.57 IC50 270.0 Preclinical
Distribution

pChEMBL Value Distribution

6
5.0
17
5.5
13
6.0
5
6.5
4
7.0
0
7.5
1
8.0
0
8.5
0
9.0
0
9.5
pChEMBL
Assay Landscape

Assay Landscape

25
Total Assays
49
Tested Compounds
1
Assay Types
Binding — 25 assays, 49 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 21 38 6.0
assay format 3 10 5.9
cell-based format 1 1 8.0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine