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Target Snapshot

CHEMBL5443 Target Snapshot

Cell division cycle 7-related protein kinase · SINGLE PROTEIN · Homo sapiens

1,227Compounds
108Assays
0Approved Drugs
1,304.0Activities
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

Cell division cycle 7-related protein kinase shows clinical signal disease relevance led by neoplasm. 2 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt O00311. Start with neoplasm, then reuse UniProt O00311 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with neoplasm, then reuse UniProt O00311 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 2 linked drugs
Open source guide
Disease program
neoplasm

Cell division cycle 7-related protein kinase shows clinical signal disease relevance led by neoplasm. 2 linked drugs remain visible in the same block.

Start review with neoplasm because it currently carries clinical signal support. Linked drugs include NMS-1116354, SIMUROSERTIB. 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
Clinical signal Open Targets-ready proxy 2 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 Cell division cycle 7-related protein kinase as ChEMBL target CHEMBL5443, mapped to UniProt O00311. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Cell division cycle 7-related protein kinase
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL5443
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
O00311
Cell division cycle 7-related protein kinase
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 Cell division cycle 7-related protein kinase is the right protein anchor across sources, using UniProt O00311 as the stable mapping.

Jump to Protein Context
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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 clinical signal support. It currently carries 2 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 LabelCell division cycle 7-related protein kinase
UniProt AccessionO00311
Component TypeProtein
Sequence Length574 aa

Cell division cycle 7-related protein kinase

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Cell division cycle 7-related protein kinase, mapped to UniProt O00311. Sequence length is 574 aa.

Mapped IDO00311
Review nameCell division cycle 7-related protein kinase
OrganismHomo sapiens
Disease Relevance

Disease Relevance & Evidence Level

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

Clinical signal Open Targets-ready proxy

Cell division cycle 7-related protein kinase shows clinical signal disease relevance led by neoplasm.

Clinical signal Phase I
neoplasm
2 linked drugs · 2 direct · 2 efficacy
Linked drugNMS-1116354
Linked drugSIMUROSERTIB
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with neoplasm because it currently carries clinical signal support. Linked drugs include NMS-1116354, SIMUROSERTIB. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

Lead diseaseneoplasm
Strongest levelClinical signal
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

8
Phase II
1
Phase I
Assay Mix

Activity Type Distribution

IC50399.0
KI763.0
KD142.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL1964519 9.9 Ki 0.1259 Preclinical
CHEMBL244793 9.9 Ki 0.1259 Preclinical
CHEMBL2062936 9.8 Ki 0.1585 Preclinical
CHEMBL1986943 9.8 Ki 0.1585 Preclinical
CHEMBL2005509 9.8 Ki 0.1585 Preclinical
CHEMBL1992220 9.7 Ki 0.1995 Preclinical
CHEMBL1965660 9.7 Ki 0.1995 Preclinical
CHEMBL1980562 9.6 Ki 0.2512 Preclinical
CHEMBL1958408 9.55 Ki 0.28 Preclinical
CHEMBL1969151 9.5 Ki 0.3162 Preclinical
Distribution

pChEMBL Value Distribution

17
5.0
30
5.5
100
6.0
107
6.5
108
7.0
97
7.5
111
8.0
64
8.5
51
9.0
19
9.5
pChEMBL
Assay Landscape

Assay Landscape

108
Total Assays
432
Tested Compounds
2
Assay Types
Binding — 107 assays, 432 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 63 345 7.5
cell-based format 41 56 6.4
assay format 2 29 7.6
subcellular format 1 2 5.8
Functional — 1 assays, 247 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 1 247 7.7

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine