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Target Snapshot

CHEMBL4895 Target Snapshot

Tyrosine-protein kinase receptor UFO · SINGLE PROTEIN · Homo sapiens

5,070Compounds
646Assays
25Approved Drugs
4,934.0Activities
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

Tyrosine-protein kinase receptor UFO shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 4 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P30530. Start with neoplasm, then reuse UniProt P30530 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with neoplasm, then reuse UniProt P30530 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 4 linked drugs
Open source guide
Disease program
neoplasm

Tyrosine-protein kinase receptor UFO shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 4 linked drugs remain visible in the same block.

Start review with neoplasm because it currently carries approved-linked support. Linked drugs include BEMCENTINIB, BPI-9016, GILTERITINIB, MECBOTAMAB VEDOTIN. 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 4 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 receptor UFO as ChEMBL target CHEMBL4895, mapped to UniProt P30530. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Tyrosine-protein kinase receptor UFO
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL4895
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P30530
Tyrosine-protein kinase receptor UFO
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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Need stable target naming and protein identity?
UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether Tyrosine-protein kinase receptor UFO is the right protein anchor across sources, using UniProt P30530 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 neoplasm is currently framed as approved-linked support. It currently carries 4 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 receptor UFO
UniProt AccessionP30530
Component TypeProtein
Sequence Length894 aa

Tyrosine-protein kinase receptor UFO

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Tyrosine-protein kinase receptor UFO, mapped to UniProt P30530. Sequence length is 894 aa.

Mapped IDP30530
Review nameTyrosine-protein kinase receptor UFO
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 receptor UFO shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
neoplasm
4 linked drugs · 4 direct · 4 efficacy
Linked drugBEMCENTINIB
Linked drugBPI-9016
Linked drugGILTERITINIB
Linked drugMECBOTAMAB VEDOTIN
Approved-linked Approved
acute myeloid leukemia
3 linked drugs · 3 direct · 3 efficacy
Linked drugBEMCENTINIB
Linked drugGILTERITINIB
Linked drugGILTERITINIB FUMARATE
Approved-linked Approved
myeloid leukemia
2 linked drugs · 2 direct · 2 efficacy
Linked drugGILTERITINIB
Linked drugGILTERITINIB FUMARATE
Clinical signal Phase II
non-small cell lung carcinoma
4 linked drugs · 4 direct · 4 efficacy
Linked drugBEMCENTINIB
Linked drugBPI-9016
Linked drugGILTERITINIB
Linked drugNINGETINIB
Clinical signal Phase II
myelodysplastic syndrome
2 linked drugs · 2 direct · 2 efficacy
Linked drugBEMCENTINIB
Linked drugGILTERITINIB
Clinical signal Phase II
COVID-19
1 linked drug · 1 direct · 1 efficacy
Linked drugBEMCENTINIB
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with neoplasm because it currently carries approved-linked support. Linked drugs include BEMCENTINIB, BPI-9016, GILTERITINIB, MECBOTAMAB VEDOTIN. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

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

Clinical Phase Distribution

25
Approved
15
Phase III
24
Phase II
6
Phase I
Assay Mix

Activity Type Distribution

IC503,869.0
KI883.0
EC5039.0
KD143.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5758853 11.0 Ki 0.01 Preclinical
CHEMBL5935453 10.92 Ki 0.012 Preclinical
CHEMBL5932919 10.92 Ki 0.012 Preclinical
CHEMBL5792035 10.85 Ki 0.014 Preclinical
CHEMBL5923596 10.82 Ki 0.015 Preclinical
CHEMBL5930737 10.82 Ki 0.015 Preclinical
CHEMBL5906788 10.8 Ki 0.016 Preclinical
CHEMBL5931969 10.8 Ki 0.016 Preclinical
CHEMBL6041852 10.8 Ki 0.016 Preclinical
CHEMBL5819606 10.74 Ki 0.018 Preclinical
Distribution

pChEMBL Value Distribution

246
5.0
351
5.5
402
6.0
462
6.5
475
7.0
311
7.5
343
8.0
210
8.5
117
9.0
53
9.5
pChEMBL
Approved Drugs

Approved Drugs

ENTRECTINIB
CHEMBL1983268
Approved 2019
FEDRATINIB
CHEMBL1287853
Approved 2019
GILTERITINIB
CHEMBL3301622
Approved 2018
NERATINIB
CHEMBL180022
Approved 2017
MIDOSTAURIN
CHEMBL608533
Approved 2017
NINTEDANIB
CHEMBL502835
Approved 2014
CABOZANTINIB
CHEMBL2105717
Approved 2012
BOSUTINIB
CHEMBL288441
Approved 2012
AXITINIB
CHEMBL1289926
Approved 2012
CRIZOTINIB
CHEMBL601719
Approved 2011
VANDETANIB
CHEMBL24828
Approved 2011
SUNITINIB
CHEMBL535
Approved 2006
SORAFENIB
CHEMBL1336
Approved 2005
Assay Landscape

Assay Landscape

646
Total Assays
2,667
Tested Compounds
2
Assay Types
Binding — 643 assays, 2,667 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 485 1,914 6.7
cell-based format 84 256 7.6
assay format 58 495 8.5
subcellular format 16 2 8.0
Functional — 3 assays, 169 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 2 168 7.0
cell-based format 1 1 6.8

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine