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Target Snapshot

CHEMBL3833484 Target Snapshot

VP1 capsid protein · SINGLE PROTEIN · Human rhinovirus sp.

23Compounds
30Assays
0Approved Drugs
56.0Activities
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

VP1 capsid protein shows clinical signal disease relevance led by asthma. 3 more disease programs remain visible in the same review block. 1 linked drug keeps the current disease frame grounded. Protein identity stays anchored to UniProt Q7T664. Start with asthma, then reuse UniProt Q7T664 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with asthma, then reuse UniProt Q7T664 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 1 linked drug
Open source guide
Disease program
asthma

VP1 capsid protein shows clinical signal disease relevance led by asthma. 3 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with asthma because it currently carries clinical signal support. Linked drugs include VAPENDAVIR. 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 1 linked drug
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 VP1 capsid protein as ChEMBL target CHEMBL3833484, mapped to UniProt Q7T664. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
VP1 capsid protein
SINGLE PROTEIN · Human rhinovirus sp.
As of 2026-09-13
ChEMBL target ID
CHEMBL3833484
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
Q7T664
Genome polyprotein
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.

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UniProt Target Context
UniProt accession via ChEMBL component mapping

Start here when your first question is whether VP1 capsid protein is the right protein anchor across sources, using UniProt Q7T664 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 asthma is currently framed as clinical signal support. It currently carries 1 linked drug 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 LabelGenome polyprotein
UniProt AccessionQ7T664
Component TypeProtein
Sequence Length287 aa

Genome polyprotein

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as VP1 capsid protein, mapped to UniProt Q7T664. ChEMBL maps the protein component as Genome polyprotein. Sequence length is 287 aa.

Mapped IDQ7T664
Review nameVP1 capsid protein
OrganismHuman rhinovirus sp.
Disease Relevance

Disease Relevance & Evidence Level

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

Clinical signal Open Targets-ready proxy

VP1 capsid protein shows clinical signal disease relevance led by asthma. 3 more disease programs remain visible in the same review block.

Clinical signal Phase II
asthma
1 linked drug · 1 direct · 1 efficacy
Linked drugVAPENDAVIR
Clinical signal Phase II
Enterovirus infectious disease
1 linked drug · 1 direct · 1 efficacy
Linked drugPLECONARIL
Clinical signal Phase II
type 1 diabetes mellitus
1 linked drug · 1 direct · 1 efficacy
Linked drugPLECONARIL
Clinical signal Phase II
viral disease
1 linked drug · 1 direct · 1 efficacy
Linked drugPLECONARIL
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

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

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

Clinical Phase Distribution

1
Phase II
Assay Mix

Activity Type Distribution

EC5056.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL29609 8.4 EC50 4.0 Clinical
CHEMBL4208180 7.77 EC50 17.0 Preclinical
CHEMBL4208286 7.3 EC50 50.0 Preclinical
CHEMBL4209270 6.89 EC50 128.0 Preclinical
CHEMBL4215079 6.75 EC50 180.0 Preclinical
CHEMBL4203308 6.72 EC50 190.0 Preclinical
CHEMBL4214859 6.7 EC50 200.0 Preclinical
CHEMBL4211585 6.6 EC50 250.0 Preclinical
CHEMBL4214159 6.6 EC50 250.0 Preclinical
CHEMBL4202881 6.4 EC50 400.0 Preclinical
Distribution

pChEMBL Value Distribution

2
5.0
5
5.5
6
6.0
7
6.5
3
7.0
5
7.5
1
8.0
0
8.5
0
9.0
0
9.5
pChEMBL
Assay Landscape

Assay Landscape

30
Total Assays
19
Tested Compounds
1
Assay Types
Binding — 30 assays, 19 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 25 19 6.7
single protein format 5 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine