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Target Snapshot

CHEMBL6093 Target Snapshot

Calmodulin-1 · SINGLE PROTEIN · Homo sapiens

53Compounds
21Assays
6Approved Drugs
52.0Activities
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

Calmodulin-1 shows approved-linked disease relevance led by cardiovascular disease. 2 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P0DP23. Start with cardiovascular disease, then reuse UniProt P0DP23 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with cardiovascular disease, then reuse UniProt P0DP23 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
cardiovascular disease

Calmodulin-1 shows approved-linked disease relevance led by cardiovascular disease. 2 linked drugs remain visible in the same block.

Start review with cardiovascular disease because it currently carries approved-linked support. Linked drugs include BENZIODARONE, PRENYLAMINE. 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 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 Calmodulin-1 as ChEMBL target CHEMBL6093, mapped to UniProt P0DP23. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Calmodulin-1
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL6093
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P0DP23
Calmodulin-1
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

Choose the first block or source based on the question you are trying to answer.

Need stable target naming and protein identity?
UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether Calmodulin-1 is the right protein anchor across sources, using UniProt P0DP23 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 cardiovascular disease is currently framed as approved-linked support. It currently carries 2 linked drugs in the same disease frame.

Jump to Disease Context
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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 LabelCalmodulin-1
UniProt AccessionP0DP23
Component TypeProtein
Sequence Length149 aa

Calmodulin-1

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Calmodulin-1, mapped to UniProt P0DP23. Sequence length is 149 aa.

Mapped IDP0DP23
Review nameCalmodulin-1
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

Calmodulin-1 shows approved-linked disease relevance led by cardiovascular disease.

Approved-linked Approved
cardiovascular disease
2 linked drugs · 2 direct · 2 efficacy
Linked drugBENZIODARONE
Linked drugPRENYLAMINE
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with cardiovascular disease because it currently carries approved-linked support. Linked drugs include BENZIODARONE, PRENYLAMINE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

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

Clinical Phase Distribution

6
Approved
2
Phase III
Assay Mix

Activity Type Distribution

IC5040.0
KI3.0
KD9.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL3337496 9.0 Kd 1.0 Preclinical
CHEMBL495235 7.75 Kd 18.0 Preclinical
CHEMBL2408940 7.74 Kd 18.25 Preclinical
CHEMBL2408939 7.71 Kd 19.4 Preclinical
CHEMBL3752910 6.96 Kd 110.36 Preclinical
CHEMBL5653589 6.67 Kd 212.52 Preclinical
CHEMBL3798296 6.07 Kd 850.0 Preclinical
CHEMBL422 6.0 Kd 1000.0 Approved
CHEMBL71 5.91 Kd 1240.0 Approved
CHEMBL138649 5.29 IC50 5170.0 Preclinical
Distribution

pChEMBL Value Distribution

7
5.0
1
5.5
2
6.0
2
6.5
0
7.0
3
7.5
0
8.0
0
8.5
1
9.0
0
9.5
pChEMBL
Approved Drugs

Approved Drugs

TRIFLUOPERAZINE
CHEMBL422
Approved 1959
Assay Landscape

Assay Landscape

21
Total Assays
43
Tested Compounds
1
Assay Types
Binding — 21 assays, 43 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 14 36 5.0
assay format 7 7 5.5

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine