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Target Snapshot

CHEMBL2842 Target Snapshot

Serine/threonine-protein kinase mTOR · SINGLE PROTEIN · Homo sapiens

10,263Compounds
1,037Assays
10Approved Drugs
7,302.0Activities
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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 2026-09-14

Serine/threonine-protein kinase mTOR shows late clinical disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 13 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P42345. Start with neoplasm, then reuse UniProt P42345 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with neoplasm, then reuse UniProt P42345 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 13 linked drugs
Open source guide
Disease program
neoplasm

Serine/threonine-protein kinase mTOR shows late clinical disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block. 13 linked drugs remain visible in the same block.

Start review with neoplasm because it currently carries late clinical support. Linked drugs include AZD-8055, DACTOLISIB, DS-7423, GEDATOLISIB. 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
Late clinical Open Targets-ready proxy 13 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 Serine/threonine-protein kinase mTOR as ChEMBL target CHEMBL2842, mapped to UniProt P42345. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Serine/threonine-protein kinase mTOR
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL2842
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
P42345
Serine/threonine-protein kinase mTOR
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 Serine/threonine-protein kinase mTOR is the right protein anchor across sources, using UniProt P42345 as the stable mapping.

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Disease Relevance & Evidence Level
ChEMBL drug mechanism + indication proxy

Use this block first when you need to confirm why neoplasm is currently framed as late clinical support. It currently carries 13 linked drugs in the same disease frame.

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Evidence Card
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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 LabelSerine/threonine-protein kinase mTOR
UniProt AccessionP42345
Component TypeProtein
Sequence Length2549 aa

Serine/threonine-protein kinase mTOR

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Serine/threonine-protein kinase mTOR, mapped to UniProt P42345. Sequence length is 2549 aa.

Mapped IDP42345
Review nameSerine/threonine-protein kinase mTOR
OrganismHomo sapiens
Disease Relevance

Disease Relevance & Evidence Level

Open Targets-ready disease context using the current target-indication evidence contract.

Late clinical Open Targets-ready proxy

Serine/threonine-protein kinase mTOR shows late clinical disease relevance led by neoplasm. 5 more disease programs remain visible in the same review block.

Late clinical Phase III
neoplasm
13 linked drugs · 13 direct · 13 efficacy
Linked drugAZD-8055
Linked drugDACTOLISIB
Linked drugDS-7423
Linked drugGEDATOLISIB
Late clinical Phase III
cancer
12 linked drugs · 12 direct · 12 efficacy
Linked drugAPITOLISIB
Linked drugAZD-8055
Linked drugBGT-226
Linked drugDACTOLISIB
Late clinical Phase III
breast cancer
11 linked drugs · 11 direct · 11 efficacy
Linked drugAPITOLISIB
Linked drugBGT-226
Linked drugDACTOLISIB
Linked drugGEDATOLISIB
Late clinical Phase III
osteosarcoma
2 linked drugs · 2 direct · 2 efficacy
Linked drugCC-115
Linked drugRIDAFOROLIMUS
Late clinical Phase III
soft tissue sarcoma
2 linked drugs · 2 direct · 2 efficacy
Linked drugRIDAFOROLIMUS
Linked drugSAPANISERTIB
Late clinical Phase III
bone sarcoma
1 linked drug · 1 direct · 1 efficacy
Linked drugRIDAFOROLIMUS
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with neoplasm because it currently carries late clinical support. Linked drugs include AZD-8055, DACTOLISIB, DS-7423, GEDATOLISIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaseneoplasm
Strongest levelLate clinical
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

10
Approved
10
Phase III
34
Phase II
10
Phase I
Assay Mix

Activity Type Distribution

IC506,423.0
KI612.0
EC501.0
KD266.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL413 10.3 IC50 0.05 Approved
CHEMBL3645910 10.15 IC50 0.07 Preclinical
CHEMBL558955 10.1 IC50 0.08 Preclinical
CHEMBL3545097 10.04 Kd 0.092 Clinical
CHEMBL1091714 10.0 IC50 0.1 Preclinical
CHEMBL1098245 10.0 IC50 0.1 Preclinical
CHEMBL566004 10.0 IC50 0.1 Preclinical
CHEMBL566216 10.0 IC50 0.1 Preclinical
CHEMBL585480 10.0 IC50 0.1 Preclinical
CHEMBL573157 9.96 IC50 0.11 Preclinical
Distribution

pChEMBL Value Distribution

365
5.0
389
5.5
529
6.0
754
6.5
928
7.0
896
7.5
766
8.0
502
8.5
282
9.0
85
9.5
pChEMBL
Approved Drugs

Approved Drugs

COPANLISIB
CHEMBL3218576
Approved 2017
EVEROLIMUS
CHEMBL1908360
Approved 2009
SIROLIMUS
CHEMBL413
Approved 1999
TACROLIMUS ANHYDROUS
CHEMBL269732
Approved 1994
CHLOROQUINE
CHEMBL76
Approved 1949
Assay Landscape

Assay Landscape

1,037
Total Assays
5,041
Tested Compounds
4
Assay Types
Binding — 997 assays, 5,041 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 598 4,261 7.3
cell-based format 296 407 7.4
assay format 74 303 7.0
subcellular format 21 1 8.2
organism-based format 5 68 5.8
protein complex format 2 0
tissue-based format 1 1 6.7
Functional — 37 assays, 2 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 27 2 7.5
assay format 6 0
organism-based format 4 0
ADME — 2 assays, 9 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 1 1 7.6
single protein format 1 8 5.9
Toxicity — 1 assays, 3 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 1 3 6.2

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine