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Target Snapshot

CHEMBL3776 Target Snapshot

Caspase-8 · SINGLE PROTEIN · Homo sapiens

886Compounds
114Assays
0Approved Drugs
584.0Activities
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 2026-09-14

Caspase-8 shows clinical signal disease relevance led by hepatitis C virus infection. 1 more disease program remain visible in the same review block. 1 linked drug keeps the current disease frame grounded. Protein identity stays anchored to UniProt Q14790. Start with hepatitis C virus infection, then reuse UniProt Q14790 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with hepatitis C virus infection, then reuse UniProt Q14790 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 1 linked drug
Open source guide
Disease program
hepatitis C virus infection

Caspase-8 shows clinical signal disease relevance led by hepatitis C virus infection. 1 more disease program remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with hepatitis C virus infection because it currently carries clinical signal support. Linked drugs include NIVOCASAN. 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 Caspase-8 as ChEMBL target CHEMBL3776, mapped to UniProt Q14790. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Caspase-8
SINGLE PROTEIN · Homo sapiens
As of 2026-09-14
ChEMBL target ID
CHEMBL3776
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-14
www.ebi.ac.uk
UniProt accession
Q14790
Caspase-8
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

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 Caspase-8 is the right protein anchor across sources, using UniProt Q14790 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 hepatitis C virus infection 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 LabelCaspase-8
UniProt AccessionQ14790
Component TypeProtein
Sequence Length479 aa

Caspase-8

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Caspase-8, mapped to UniProt Q14790. Sequence length is 479 aa.

Mapped IDQ14790
Review nameCaspase-8
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

Caspase-8 shows clinical signal disease relevance led by hepatitis C virus infection. 1 more disease program remain visible in the same review block.

Clinical signal Phase II
hepatitis C virus infection
1 linked drug · 1 direct · 1 efficacy
Linked drugNIVOCASAN
Clinical signal Phase II
non-alcoholic steatohepatitis
1 linked drug · 1 direct · 1 efficacy
Linked drugNIVOCASAN
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

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

Lead diseasehepatitis C virus infection
Strongest levelClinical signal
Block modeOpen Targets-ready proxy
Clinical Profile

Clinical Phase Distribution

1
Phase II
Assay Mix

Activity Type Distribution

IC50457.0
KI104.0
EC5023.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5569363 9.92 IC50 0.12 Preclinical
CHEMBL5723373 9.04 Ki 0.92 Preclinical
CHEMBL5822466 9.0 IC50 1.0 Preclinical
CHEMBL3934331 8.89 Ki 1.3 Preclinical
CHEMBL91281 8.89 Ki 1.3 Preclinical
CHEMBL5723323 8.8 Ki 1.6 Preclinical
CHEMBL315868 8.72 Ki 1.9 Preclinical
CHEMBL194207 8.68 Ki 2.1 Preclinical
CHEMBL3914770 8.6 Ki 2.5 Preclinical
CHEMBL3917557 8.59 Ki 2.6 Preclinical
Distribution

pChEMBL Value Distribution

88
5.0
60
5.5
48
6.0
29
6.5
27
7.0
29
7.5
46
8.0
9
8.5
2
9.0
1
9.5
pChEMBL
Assay Landscape

Assay Landscape

114
Total Assays
354
Tested Compounds
2
Assay Types
Binding — 104 assays, 354 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 89 312 6.4
assay format 9 42 5.3
cell-based format 5 0
biochemical format 1 0
Functional — 10 assays, 9 compounds
BAO Format Assays Compounds Avg pChEMBL
assay format 5 4 8.6
cell-based format 5 5

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine