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Target Snapshot

CHEMBL3588738 Target Snapshot

Histone-lysine N-methyltransferase, H3 lysine-36 specific · SINGLE PROTEIN · Homo sapiens

90Compounds
86Assays
2Approved Drugs
47.0Activities
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

Protein identity stays anchored to UniProt Q96L73. Use UniProt Q96L73 as the stable identity anchor, then attach disease evidence before program review.

Review focus
Protein anchor ready

Use UniProt Q96L73 as the stable identity anchor, then attach disease evidence before program review.

ChEMBL component mapping + Open Targets-ready proxy + ChEMBL 36 via Core Engine 2026-09-14
Open source guide
Identity Layer

Cross-source identity

Keep the review anchor, source IDs, and context contract aligned before reusing this target elsewhere.

This review treats Histone-lysine N-methyltransferase, H3 lysine-36 specific as ChEMBL target CHEMBL3588738, mapped to UniProt Q96L73. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Histone-lysine N-methyltransferase, H3 lysine-36 specific
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL3588738
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
Q96L73
Histone-lysine N-methyltransferase, H3 lysine-36 specific
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 Histone-lysine N-methyltransferase, H3 lysine-36 specific is the right protein anchor across sources, using UniProt Q96L73 as the stable mapping.

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Disease Relevance & Evidence Level
ChEMBL drug mechanism + indication proxy

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Evidence Card
Review-ready rationale with source-aware context

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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 LabelHistone-lysine N-methyltransferase, H3 lysine-36 specific
UniProt AccessionQ96L73
Component TypeProtein
Sequence Length2696 aa

Histone-lysine N-methyltransferase, H3 lysine-36 specific

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Histone-lysine N-methyltransferase, H3 lysine-36 specific, mapped to UniProt Q96L73. Sequence length is 2696 aa.

Mapped IDQ96L73
Review nameHistone-lysine N-methyltransferase, H3 lysine-36 specific
OrganismHomo sapiens
Clinical Profile

Clinical Phase Distribution

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

Activity Type Distribution

IC5041.0
KD6.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL337173 6.96 IC50 110.0 Preclinical
CHEMBL5408212 6.8 IC50 160.0 Preclinical
CHEMBL5438312 6.67 IC50 214.0 Preclinical
CHEMBL5419719 6.65 IC50 225.0 Preclinical
CHEMBL5396709 6.61 IC50 248.0 Preclinical
CHEMBL5432302 6.57 IC50 270.0 Preclinical
CHEMBL5422549 6.16 IC50 690.0 Preclinical
CHEMBL5438496 5.92 Kd 1200.0 Preclinical
CHEMBL554190 5.85 Kd 1400.0 Preclinical
CHEMBL3137309 5.62 IC50 2400.0 Approved
Distribution

pChEMBL Value Distribution

4
5.0
3
5.5
1
6.0
8
6.5
0
7.0
0
7.5
0
8.0
0
8.5
0
9.0
0
9.5
pChEMBL
Assay Landscape

Assay Landscape

86
Total Assays
25
Tested Compounds
1
Assay Types
Binding — 86 assays, 25 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 64 15 6.0
cell-based format 12 4 5.6
assay format 10 6 4.0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine