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Target Snapshot

CHEMBL2637 Target Snapshot

Mitogen-activated protein kinase 10 · SINGLE PROTEIN · Homo sapiens

3,105Compounds
670Assays
18Approved Drugs
2,745.0Activities
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 2026-09-13

Mitogen-activated protein kinase 10 shows late clinical disease relevance led by hearing loss. 3 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 P53779. Start with hearing loss, then reuse UniProt P53779 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with hearing loss, then reuse UniProt P53779 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 1 linked drug
Open source guide
Disease program
hearing loss

Mitogen-activated protein kinase 10 shows late clinical disease relevance led by hearing loss. 3 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with hearing loss because it currently carries late clinical support. Linked drugs include BRIMAPITIDE, C-TERMINAL ACID. 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 Mitogen-activated protein kinase 10 as ChEMBL target CHEMBL2637, mapped to UniProt P53779. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Mitogen-activated protein kinase 10
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL2637
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P53779
Mitogen-activated protein kinase 10
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

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UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether Mitogen-activated protein kinase 10 is the right protein anchor across sources, using UniProt P53779 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 hearing loss 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 LabelMitogen-activated protein kinase 10
UniProt AccessionP53779
Component TypeProtein
Sequence Length464 aa

Mitogen-activated protein kinase 10

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Mitogen-activated protein kinase 10, mapped to UniProt P53779. Sequence length is 464 aa.

Mapped IDP53779
Review nameMitogen-activated protein kinase 10
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

Mitogen-activated protein kinase 10 shows late clinical disease relevance led by hearing loss. 3 more disease programs remain visible in the same review block.

Late clinical Phase III
hearing loss
1 linked drug · 1 direct · 1 efficacy
Linked drugBRIMAPITIDE, C-TERMINAL ACID
Clinical signal Phase II
idiopathic pulmonary fibrosis
1 linked drug · 1 direct · 1 efficacy
Linked drugTANZISERTIB
Clinical signal Phase I
inflammation
1 linked drug · 1 direct · 1 efficacy
Linked drugBRIMAPITIDE
Clinical signal Phase I
myeloid leukemia
1 linked drug · 1 direct · 1 efficacy
Linked drugCC-401
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with hearing loss because it currently carries late clinical support. Linked drugs include BRIMAPITIDE, C-TERMINAL ACID. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseasehearing loss
Strongest levelLate clinical
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

18
Approved
5
Phase III
27
Phase II
13
Phase I
Assay Mix

Activity Type Distribution

IC502,039.0
KI178.0
KD528.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL210618 10.17 IC50 0.068 Preclinical
CHEMBL4546504 9.97 IC50 0.107 Preclinical
CHEMBL3220502 9.8 IC50 0.16 Preclinical
CHEMBL3220499 9.6 IC50 0.25 Preclinical
CHEMBL3220493 9.55 IC50 0.28 Preclinical
CHEMBL3220497 9.55 IC50 0.28 Preclinical
CHEMBL3220496 9.52 IC50 0.3 Preclinical
CHEMBL4077018 9.52 IC50 0.3 Preclinical
CHEMBL3220498 9.51 IC50 0.31 Preclinical
CHEMBL5403678 9.42 IC50 0.379 Preclinical
Distribution

pChEMBL Value Distribution

268
5.0
184
5.5
275
6.0
255
6.5
263
7.0
151
7.5
89
8.0
53
8.5
29
9.0
12
9.5
pChEMBL
Approved Drugs

Approved Drugs

FEDRATINIB
CHEMBL1287853
Approved 2019
GILTERITINIB
CHEMBL3301622
Approved 2018
ABEMACICLIB
CHEMBL3301610
Approved 2017
NINTEDANIB
CHEMBL502835
Approved 2014
GEFITINIB
CHEMBL939
Approved 2003
IMATINIB
CHEMBL941
Approved 2001
Assay Landscape

Assay Landscape

670
Total Assays
1,656
Tested Compounds
3
Assay Types
Binding — 666 assays, 1,656 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 546 1,498 6.3
assay format 55 95 6.6
cell-based format 52 44 6.3
subcellular format 13 19 6.5
Functional — 3 assays, 23 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 1 21 7.1
cell-based format 1 1 6.0
subcellular format 1 1 6.7
ADME — 1 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 1 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine