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Target Snapshot

CHEMBL3717 Target Snapshot

Hepatocyte growth factor receptor · SINGLE PROTEIN · Homo sapiens

8,731Compounds
1,914Assays
37Approved Drugs
10,540.0Activities
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

Hepatocyte growth factor receptor shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 25 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P08581. Start with neoplasm, then reuse UniProt P08581 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with neoplasm, then reuse UniProt P08581 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 25 linked drugs
Open source guide
Disease program
neoplasm

Hepatocyte growth factor receptor shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 25 linked drugs remain visible in the same block.

Start review with neoplasm because it currently carries approved-linked support. Linked drugs include ALTIRATINIB, AMG-208, AMG-337, AMIVANTAMAB. 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 25 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 Hepatocyte growth factor receptor as ChEMBL target CHEMBL3717, mapped to UniProt P08581. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Hepatocyte growth factor receptor
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL3717
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P08581
Hepatocyte growth factor receptor
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

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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 Hepatocyte growth factor receptor is the right protein anchor across sources, using UniProt P08581 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 25 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 LabelHepatocyte growth factor receptor
UniProt AccessionP08581
Component TypeProtein
Sequence Length1390 aa

Hepatocyte growth factor receptor

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Hepatocyte growth factor receptor, mapped to UniProt P08581. Sequence length is 1390 aa.

Mapped IDP08581
Review nameHepatocyte growth factor receptor
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

Hepatocyte growth factor receptor shows approved-linked disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
neoplasm
25 linked drugs · 25 direct · 25 efficacy
Linked drugALTIRATINIB
Linked drugAMG-208
Linked drugAMG-337
Linked drugAMIVANTAMAB
Approved-linked Approved
cancer
18 linked drugs · 18 direct · 18 efficacy
Linked drugALTIRATINIB
Linked drugAMG-208
Linked drugAMG-337
Linked drugCAPMATINIB
Approved-linked Approved
non-small cell lung carcinoma
16 linked drugs · 16 direct · 16 efficacy
Linked drugAMIVANTAMAB
Linked drugBPI-9016
Linked drugCABOZANTINIB S-MALATE
Linked drugCAPMATINIB
Approved-linked Approved
hepatocellular carcinoma
7 linked drugs · 7 direct · 7 efficacy
Linked drugAMIVANTAMAB
Linked drugCABOZANTINIB S-MALATE
Linked drugCAPMATINIB
Linked drugFORETINIB
Approved-linked Approved
papillary renal cell carcinoma
4 linked drugs · 4 direct · 4 efficacy
Linked drugCABOZANTINIB S-MALATE
Linked drugCRIZOTINIB
Linked drugSAVOLITINIB
Linked drugTIVANTINIB
Approved-linked Approved
renal cell carcinoma
3 linked drugs · 3 direct · 3 efficacy
Linked drugCABOZANTINIB S-MALATE
Linked drugFORETINIB
Linked drugSAVOLITINIB
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 ALTIRATINIB, AMG-208, AMG-337, AMIVANTAMAB. 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

37
Approved
18
Phase III
47
Phase II
24
Phase I
Assay Mix

Activity Type Distribution

IC508,429.0
KI1,400.0
EC50112.0
KD599.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5184459 10.72 IC50 0.019 Preclinical
CHEMBL5174958 10.46 IC50 0.035 Preclinical
CHEMBL3668200 10.0 Ki 0.1 Preclinical
CHEMBL3797911 9.92 IC50 0.12 Preclinical
CHEMBL3582305 9.89 IC50 0.13 Preclinical
CHEMBL3188267 9.89 IC50 0.13 Approved
CHEMBL5095061 9.85 IC50 0.14 Clinical
CHEMBL1236107 9.72 Kd 0.19 Preclinical
CHEMBL3674521 9.7 IC50 0.2 Preclinical
CHEMBL1802904 9.7 IC50 0.2 Preclinical
Distribution

pChEMBL Value Distribution

388
5.0
414
5.5
743
6.0
792
6.5
1297
7.0
1371
7.5
1437
8.0
751
8.5
254
9.0
27
9.5
pChEMBL
Approved Drugs

Approved Drugs

ENSARTINIB
CHEMBL4113131
Approved 2024
CAPMATINIB
CHEMBL3188267
Approved 2020
TEPOTINIB
CHEMBL3402762
Approved 2020
ENTRECTINIB
CHEMBL1983268
Approved 2019
TIVOZANIB
CHEMBL1289494
Approved 2017
BRIGATINIB
CHEMBL3545311
Approved 2017
MIDOSTAURIN
CHEMBL608533
Approved 2017
CERITINIB
CHEMBL2403108
Approved 2014
NINTEDANIB
CHEMBL502835
Approved 2014
AFATINIB
CHEMBL1173655
Approved 2013
AXITINIB
CHEMBL1289926
Approved 2012
CABOZANTINIB S-MALATE
CHEMBL2103868
Approved 2012
CABOZANTINIB
CHEMBL2105717
Approved 2012
CRIZOTINIB
CHEMBL601719
Approved 2011
ERLOTINIB
CHEMBL553
Approved 2004
Assay Landscape

Assay Landscape

1,914
Total Assays
5,050
Tested Compounds
3
Assay Types
Binding — 1,906 assays, 5,050 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 1,290 3,908 7.5
cell-based format 412 751 7.0
assay format 192 357 7.2
subcellular format 10 34 6.9
mitochondrion format 2 0
Functional — 4 assays, 248 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 3 38 7.3
assay format 1 210 6.2
ADME — 4 assays, 9 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 2 9 6.9
assay format 1 0
cell-based format 1 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine