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Target Snapshot

CHEMBL2041 Target Snapshot

Proto-oncogene tyrosine-protein kinase receptor Ret · SINGLE PROTEIN · Homo sapiens

6,476Compounds
1,417Assays
65Approved Drugs
26,466.0Activities
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

Proto-oncogene tyrosine-protein kinase receptor Ret shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 9 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P07949. Start with neoplasm, then reuse UniProt P07949 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with neoplasm, then reuse UniProt P07949 as the stable protein anchor across project notes and exports.

ChEMBL component mapping + Open Targets-ready proxy + ChEMBL 36 via Core Engine 2026-09-14 9 linked drugs
Open source guide
Disease program
neoplasm

Proto-oncogene tyrosine-protein kinase receptor Ret shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 9 linked drugs remain visible in the same block.

Start review with neoplasm because it currently carries approved-linked support. Linked drugs include CEP-32496, PRALSETINIB, QUIZARTINIB, REGORAFENIB. 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 9 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 Proto-oncogene tyrosine-protein kinase receptor Ret as ChEMBL target CHEMBL2041, mapped to UniProt P07949. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Proto-oncogene tyrosine-protein kinase receptor Ret
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL2041
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
P07949
Proto-oncogene tyrosine-protein kinase receptor Ret
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 Proto-oncogene tyrosine-protein kinase receptor Ret is the right protein anchor across sources, using UniProt P07949 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 9 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 LabelProto-oncogene tyrosine-protein kinase receptor Ret
UniProt AccessionP07949
Component TypeProtein
Sequence Length1114 aa

Proto-oncogene tyrosine-protein kinase receptor Ret

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Proto-oncogene tyrosine-protein kinase receptor Ret, mapped to UniProt P07949. Sequence length is 1114 aa.

Mapped IDP07949
Review nameProto-oncogene tyrosine-protein kinase receptor Ret
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

Proto-oncogene tyrosine-protein kinase receptor Ret shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
neoplasm
9 linked drugs · 9 direct · 9 efficacy
Linked drugCEP-32496
Linked drugPRALSETINIB
Linked drugQUIZARTINIB
Linked drugREGORAFENIB
Approved-linked Approved
non-small cell lung carcinoma
8 linked drugs · 8 direct · 8 efficacy
Linked drugALECTINIB HYDROCHLORIDE
Linked drugMOTESANIB
Linked drugPRALSETINIB
Linked drugSELPERCATINIB
Approved-linked Approved
cancer
7 linked drugs · 7 direct · 7 efficacy
Linked drugPRALSETINIB
Linked drugREGORAFENIB
Linked drugSELPERCATINIB
Linked drugSORAFENIB TOSYLATE
Approved-linked Approved
gastrointestinal stromal tumor
5 linked drugs · 5 direct · 5 efficacy
Linked drugREGORAFENIB
Linked drugSORAFENIB TOSYLATE
Linked drugSUNITINIB
Linked drugSUNITINIB MALATE
Approved-linked Approved
hepatocellular carcinoma
5 linked drugs · 5 direct · 5 efficacy
Linked drugREGORAFENIB
Linked drugSORAFENIB TOSYLATE
Linked drugSUNITINIB
Linked drugSUNITINIB MALATE
Approved-linked Approved
thyroid cancer
5 linked drugs · 5 direct · 5 efficacy
Linked drugREGORAFENIB
Linked drugSELPERCATINIB
Linked drugSORAFENIB TOSYLATE
Linked drugSUNITINIB MALATE
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 CEP-32496, PRALSETINIB, QUIZARTINIB, REGORAFENIB. 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

65
Approved
27
Phase III
55
Phase II
33
Phase I
Assay Mix

Activity Type Distribution

IC5025,018.0
KI749.0
EC507.0
KD692.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5962713 10.77 IC50 0.017 Preclinical
CHEMBL4067871 10.4 IC50 0.04 Preclinical
CHEMBL5944764 10.4 IC50 0.04 Preclinical
CHEMBL5916213 10.15 IC50 0.07 Preclinical
CHEMBL5838635 10.05 IC50 0.09 Preclinical
CHEMBL4218013 10.0 IC50 0.1 Preclinical
CHEMBL5619652 10.0 IC50 0.1 Preclinical
CHEMBL5786997 10.0 IC50 0.1 Preclinical
CHEMBL5902423 10.0 IC50 0.1 Preclinical
CHEMBL5913548 10.0 IC50 0.1 Preclinical
Distribution

pChEMBL Value Distribution

976
5.0
1350
5.5
2759
6.0
4535
6.5
5759
7.0
5633
7.5
2248
8.0
732
8.5
463
9.0
234
9.5
pChEMBL
Approved Drugs

Approved Drugs

QUIZARTINIB
CHEMBL576982
Approved 2023
SELPERCATINIB
CHEMBL4559134
Approved 2020
PRALSETINIB
CHEMBL4582651
Approved 2020
FEDRATINIB
CHEMBL1287853
Approved 2019
ENTRECTINIB
CHEMBL1983268
Approved 2019
GILTERITINIB
CHEMBL3301622
Approved 2018
BRIGATINIB
CHEMBL3545311
Approved 2017
TIVOZANIB
CHEMBL1289494
Approved 2017
MIDOSTAURIN
CHEMBL608533
Approved 2017
BARICITINIB
CHEMBL2105759
Approved 2017
LENVATINIB
CHEMBL1289601
Approved 2015
ALECTINIB
CHEMBL1738797
Approved 2015
NINTEDANIB
CHEMBL502835
Approved 2014
CERITINIB
CHEMBL2403108
Approved 2014
IBRUTINIB
CHEMBL1873475
Approved 2013
CABOZANTINIB
CHEMBL2105717
Approved 2012
REGORAFENIB
CHEMBL1946170
Approved 2012
AXITINIB
CHEMBL1289926
Approved 2012
PONATINIB
CHEMBL1171837
Approved 2012
VEMURAFENIB
CHEMBL1229517
Approved 2011
VANDETANIB
CHEMBL24828
Approved 2011
RUXOLITINIB
CHEMBL1789941
Approved 2011
PAZOPANIB
CHEMBL477772
Approved 2009
NILOTINIB
CHEMBL255863
Approved 2007
SUNITINIB
CHEMBL535
Approved 2006
DASATINIB
CHEMBL5416410
Approved 2006
DASATINIB ANHYDROUS
CHEMBL1421
Approved 2006
SORAFENIB
CHEMBL1336
Approved 2005
ERLOTINIB
CHEMBL553
Approved 2004
CYCLOBENZAPRINE
CHEMBL669
Approved 1977
AMITRIPTYLINE
CHEMBL629
Approved 1961
Assay Landscape

Assay Landscape

1,418
Total Assays
4,122
Tested Compounds
3
Assay Types
Binding — 1,414 assays, 4,122 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 984 3,598 7.2
assay format 214 193 6.9
cell-based format 202 176 6.6
organism-based format 13 63 7.0
subcellular format 1 92 6.6
ADME — 3 assays, 0 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 2 0
assay format 1 0
Functional — 1 assays, 339 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 1 339 6.6

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine