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Target Snapshot

CHEMBL4342 Target Snapshot

Group 10 secretory phospholipase A2 · SINGLE PROTEIN · Homo sapiens

166Compounds
24Assays
0Approved Drugs
193.0Activities
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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 2026-09-14

Group 10 secretory phospholipase A2 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 O15496. Start with acute coronary syndrome, then reuse UniProt O15496 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with acute coronary syndrome, then reuse UniProt O15496 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
acute coronary syndrome

Group 10 secretory phospholipase A2 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 Group 10 secretory phospholipase A2 as ChEMBL target CHEMBL4342, mapped to UniProt O15496. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Group 10 secretory phospholipase A2
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL4342
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
O15496
Group 10 secretory phospholipase A2
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 Group 10 secretory phospholipase A2 is the right protein anchor across sources, using UniProt O15496 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 LabelGroup 10 secretory phospholipase A2
UniProt AccessionO15496
Component TypeProtein
Sequence Length165 aa

Group 10 secretory phospholipase A2

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Group 10 secretory phospholipase A2, mapped to UniProt O15496. Sequence length is 165 aa.

Mapped IDO15496
Review nameGroup 10 secretory phospholipase A2
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

Group 10 secretory phospholipase A2 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

IC50193.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL477548 8.15 IC50 7.0 Preclinical
CHEMBL514705 8.0 IC50 10.0 Preclinical
CHEMBL514656 7.96 IC50 11.0 Preclinical
CHEMBL4215835 7.85 IC50 14.0 Preclinical
CHEMBL474874 7.85 IC50 14.0 Preclinical
CHEMBL4210991 7.82 IC50 15.0 Preclinical
CHEMBL514692 7.82 IC50 15.0 Preclinical
CHEMBL515637 7.7 IC50 20.0 Preclinical
CHEMBL148649 7.66 IC50 22.0 Preclinical
CHEMBL4171084 7.58 IC50 26.0 Preclinical
Distribution

pChEMBL Value Distribution

21
5.0
18
5.5
33
6.0
27
6.5
18
7.0
13
7.5
3
8.0
0
8.5
0
9.0
0
9.5
pChEMBL
Assay Landscape

Assay Landscape

24
Total Assays
120
Tested Compounds
1
Assay Types
Binding — 24 assays, 120 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 19 85 6.3
assay format 4 34 6.0
cell-based format 1 1 4.6

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine