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Target Snapshot

CHEMBL3553 Target Snapshot

Non-receptor tyrosine-protein kinase TYK2 · SINGLE PROTEIN · Homo sapiens

10,420Compounds
889Assays
42Approved Drugs
17,179.0Activities
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

Non-receptor tyrosine-protein kinase TYK2 shows approved-linked disease relevance led by alopecia areata. 5 more disease programs remain visible in the same review block. 3 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P29597. Start with alopecia areata, then reuse UniProt P29597 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with alopecia areata, then reuse UniProt P29597 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 3 linked drugs
Open source guide
Disease program
alopecia areata

Non-receptor tyrosine-protein kinase TYK2 shows approved-linked disease relevance led by alopecia areata. 5 more disease programs remain visible in the same review block. 3 linked drugs remain visible in the same block.

Start review with alopecia areata because it currently carries approved-linked support. Linked drugs include BREPOCITINIB, DEUCRAVACITINIB, DEURUXOLITINIB PHOSPHATE. 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 3 linked drugs
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 Non-receptor tyrosine-protein kinase TYK2 as ChEMBL target CHEMBL3553, mapped to UniProt P29597. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Non-receptor tyrosine-protein kinase TYK2
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL3553
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P29597
Non-receptor tyrosine-protein kinase TYK2
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

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 Non-receptor tyrosine-protein kinase TYK2 is the right protein anchor across sources, using UniProt P29597 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 alopecia areata is currently framed as approved-linked support. It currently carries 3 linked drugs in the same disease frame.

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Evidence Card
Review-ready rationale with source-aware context

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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 LabelNon-receptor tyrosine-protein kinase TYK2
UniProt AccessionP29597
Component TypeProtein
Sequence Length1187 aa

Non-receptor tyrosine-protein kinase TYK2

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Non-receptor tyrosine-protein kinase TYK2, mapped to UniProt P29597. Sequence length is 1187 aa.

Mapped IDP29597
Review nameNon-receptor tyrosine-protein kinase TYK2
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

Non-receptor tyrosine-protein kinase TYK2 shows approved-linked disease relevance led by alopecia areata. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
alopecia areata
3 linked drugs · 3 direct · 3 efficacy
Linked drugBREPOCITINIB
Linked drugDEUCRAVACITINIB
Linked drugDEURUXOLITINIB PHOSPHATE
Approved-linked Approved
psoriasis
3 linked drugs · 3 direct · 3 efficacy
Linked drugBREPOCITINIB
Linked drugDEUCRAVACITINIB
Linked drugROPSACITINIB
Approved-linked Approved
rheumatoid arthritis
3 linked drugs · 3 direct · 3 efficacy
Linked drugFILGOTINIB
Linked drugFILGOTINIB MALEATE
Linked drugUPADACITINIB HEMIHYDRATE
Approved-linked Approved
psoriasis vulgaris
1 linked drug · 1 direct · 1 efficacy
Linked drugDEUCRAVACITINIB
Late clinical Phase III
ulcerative colitis
4 linked drugs · 4 direct · 4 efficacy
Linked drugBREPOCITINIB
Linked drugDEUCRAVACITINIB
Linked drugFILGOTINIB
Linked drugROPSACITINIB
Late clinical Phase III
psoriatic arthritis
3 linked drugs · 3 direct · 3 efficacy
Linked drugBREPOCITINIB
Linked drugDEUCRAVACITINIB
Linked drugFILGOTINIB
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with alopecia areata because it currently carries approved-linked support. Linked drugs include BREPOCITINIB, DEUCRAVACITINIB, DEURUXOLITINIB PHOSPHATE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseasealopecia areata
Strongest levelApproved-linked
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

42
Approved
10
Phase III
37
Phase II
11
Phase I
Assay Mix

Activity Type Distribution

IC506,307.0
KI2,745.0
EC50304.0
KD7,823.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5427107 11.0 IC50 0.01 Preclinical
CHEMBL4460368 10.82 Ki 0.015 Preclinical
CHEMBL5427277 10.8 IC50 0.016 Preclinical
CHEMBL4442827 10.74 Ki 0.018 Preclinical
CHEMBL5422022 10.74 IC50 0.018 Preclinical
CHEMBL5424497 10.72 Kd 0.019 Preclinical
CHEMBL5433700 10.72 Kd 0.019 Preclinical
CHEMBL4435170 10.7 Ki 0.02 Approved
CHEMBL4789639 10.7 Ki 0.02 Preclinical
CHEMBL5398548 10.64 Kd 0.023 Preclinical
Distribution

pChEMBL Value Distribution

267
5.0
399
5.5
1070
6.0
1004
6.5
1925
7.0
850
7.5
1928
8.0
277
8.5
2129
9.0
543
9.5
pChEMBL
Approved Drugs

Approved Drugs

MOMELOTINIB
CHEMBL1078178
Approved 2023
CRAVACITINIB
CHEMBL4596392
Approved 2022
DEUCRAVACITINIB
CHEMBL4435170
Approved 2022
PACRITINIB
CHEMBL2035187
Approved 2022
ABROCITINIB
CHEMBL3655081
Approved 2021
FILGOTINIB
CHEMBL3301607
Approved 2020
FEDRATINIB
CHEMBL1287853
Approved 2019
UPADACITINIB
CHEMBL3622821
Approved 2019
PEFICITINIB
CHEMBL3137308
Approved 2019
BARICITINIB
CHEMBL2105759
Approved 2017
MIDOSTAURIN
CHEMBL608533
Approved 2017
NINTEDANIB
CHEMBL502835
Approved 2014
TOFACITINIB
CHEMBL221959
Approved 2012
TOFACITINIB CITRATE
CHEMBL2103743
Approved 2012
RUXOLITINIB PHOSPHATE
CHEMBL1795071
Approved 2011
RUXOLITINIB
CHEMBL1789941
Approved 2011
CRIZOTINIB
CHEMBL601719
Approved 2011
SUNITINIB
CHEMBL535
Approved 2006
DASATINIB
CHEMBL5416410
Approved 2006
Assay Landscape

Assay Landscape

889
Total Assays
6,932
Tested Compounds
3
Assay Types
Binding — 849 assays, 6,932 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 628 5,170 7.5
cell-based format 107 1,439 8.8
assay format 86 190 6.9
subcellular format 19 11 6.5
tissue-based format 9 122 7.0
Functional — 39 assays, 90 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 25 2 6.8
tissue-based format 13 2 6.9
assay format 1 86 6.6
ADME — 1 assays, 8 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 1 8 5.8

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine