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Target Snapshot

CHEMBL2148 Target Snapshot

Tyrosine-protein kinase JAK3 · SINGLE PROTEIN · Homo sapiens

11,611Compounds
1,278Assays
48Approved Drugs
14,852.0Activities
Free Research Context

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Broader Open DB context

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Structured disease, protein, and project context should read before the lower-level identity rail.

As of 2026-09-13

Tyrosine-protein kinase JAK3 shows approved-linked disease relevance led by rheumatoid arthritis. 5 more disease programs remain visible in the same review block. 5 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P52333. Start with rheumatoid arthritis, then reuse UniProt P52333 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with rheumatoid arthritis, then reuse UniProt P52333 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 5 linked drugs
Open source guide
Disease program
rheumatoid arthritis

Tyrosine-protein kinase JAK3 shows approved-linked disease relevance led by rheumatoid arthritis. 5 more disease programs remain visible in the same review block. 5 linked drugs remain visible in the same block.

Start review with rheumatoid arthritis because it currently carries approved-linked support. Linked drugs include DECERNOTINIB, FILGOTINIB, FILGOTINIB MALEATE, RITLECITINIB. 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 5 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 Tyrosine-protein kinase JAK3 as ChEMBL target CHEMBL2148, mapped to UniProt P52333. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Tyrosine-protein kinase JAK3
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL2148
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P52333
Tyrosine-protein kinase JAK3
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 Tyrosine-protein kinase JAK3 is the right protein anchor across sources, using UniProt P52333 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 rheumatoid arthritis is currently framed as approved-linked support. It currently carries 5 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 LabelTyrosine-protein kinase JAK3
UniProt AccessionP52333
Component TypeProtein
Sequence Length1124 aa

Tyrosine-protein kinase JAK3

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Tyrosine-protein kinase JAK3, mapped to UniProt P52333. Sequence length is 1124 aa.

Mapped IDP52333
Review nameTyrosine-protein kinase JAK3
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

Tyrosine-protein kinase JAK3 shows approved-linked disease relevance led by rheumatoid arthritis. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
rheumatoid arthritis
5 linked drugs · 5 direct · 5 efficacy
Linked drugDECERNOTINIB
Linked drugFILGOTINIB
Linked drugFILGOTINIB MALEATE
Linked drugRITLECITINIB
Approved-linked Approved
alopecia areata
3 linked drugs · 3 direct · 3 efficacy
Linked drugDEURUXOLITINIB PHOSPHATE
Linked drugRITLECITINIB
Linked drugRITLECITINIB TOSYLATE
Late clinical Phase III
Crohn's disease
2 linked drugs · 2 direct · 2 efficacy
Linked drugFILGOTINIB
Linked drugRITLECITINIB
Late clinical Phase III
ulcerative colitis
2 linked drugs · 2 direct · 2 efficacy
Linked drugFILGOTINIB
Linked drugRITLECITINIB
Late clinical Phase III
Vitiligo
2 linked drugs · 2 direct · 2 efficacy
Linked drugCERDULATINIB
Linked drugRITLECITINIB
Late clinical Phase III
ankylosing spondylitis
1 linked drug · 1 direct · 1 efficacy
Linked drugFILGOTINIB
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with rheumatoid arthritis because it currently carries approved-linked support. Linked drugs include DECERNOTINIB, FILGOTINIB, FILGOTINIB MALEATE, RITLECITINIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaserheumatoid arthritis
Strongest levelApproved-linked
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

48
Approved
16
Phase III
41
Phase II
11
Phase I
Assay Mix

Activity Type Distribution

IC5011,998.0
KI2,400.0
EC50226.0
KD228.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL3335689 10.98 Ki 0.01046 Preclinical
CHEMBL3335699 10.98 Ki 0.01055 Preclinical
CHEMBL3665184 10.98 IC50 0.01051 Preclinical
CHEMBL3665122 10.98 IC50 0.01047 Preclinical
CHEMBL3665173 10.97 Ki 0.01074 Preclinical
CHEMBL3665213 10.97 Ki 0.01081 Preclinical
CHEMBL3665193 10.97 IC50 0.01071 Preclinical
CHEMBL3665200 10.96 IC50 0.01096 Preclinical
CHEMBL3665167 10.93 Ki 0.01179 Preclinical
CHEMBL3665172 10.93 IC50 0.01175 Preclinical
Distribution

pChEMBL Value Distribution

1276
5.0
585
5.5
1478
6.0
1269
6.5
1963
7.0
858
7.5
950
8.0
589
8.5
1043
9.0
416
9.5
pChEMBL
Approved Drugs

Approved Drugs

MOMELOTINIB
CHEMBL1078178
Approved 2023
RITLECITINIB
CHEMBL4085457
Approved 2023
DEUCRAVACITINIB
CHEMBL4435170
Approved 2022
PACRITINIB
CHEMBL2035187
Approved 2022
ABROCITINIB
CHEMBL3655081
Approved 2021
FILGOTINIB
CHEMBL3301607
Approved 2020
FEDRATINIB
CHEMBL1287853
Approved 2019
ZANUBRUTINIB
CHEMBL3936761
Approved 2019
UPADACITINIB
CHEMBL3622821
Approved 2019
PEFICITINIB
CHEMBL3137308
Approved 2019
ENTRECTINIB
CHEMBL1983268
Approved 2019
BARICITINIB
CHEMBL2105759
Approved 2017
MIDOSTAURIN
CHEMBL608533
Approved 2017
PALBOCICLIB
CHEMBL189963
Approved 2015
NINTEDANIB
CHEMBL502835
Approved 2014
IBRUTINIB
CHEMBL1873475
Approved 2013
TOFACITINIB
CHEMBL221959
Approved 2012
TOFACITINIB CITRATE
CHEMBL2103743
Approved 2012
RUXOLITINIB PHOSPHATE
CHEMBL1795071
Approved 2011
RUXOLITINIB
CHEMBL1789941
Approved 2011
CRIZOTINIB
CHEMBL601719
Approved 2011
DASATINIB
CHEMBL5416410
Approved 2006
ERLOTINIB
CHEMBL553
Approved 2004
Assay Landscape

Assay Landscape

1,278
Total Assays
7,328
Tested Compounds
4
Assay Types
Binding — 1,225 assays, 7,328 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 941 6,385 7.3
cell-based format 151 474 7.0
assay format 120 460 7.5
organism-based format 7 8 6.7
subcellular format 5 0
tissue-based format 1 1 5.7
Functional — 37 assays, 238 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 35 2 7.1
assay format 2 236 6.3
ADME — 14 assays, 37 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 10 7 7.6
assay format 2 29 6.7
cell-based format 2 1 5.6
Toxicity — 2 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 1 0
tissue-based format 1 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine