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Target Snapshot

CHEMBL4191 Target Snapshot

Monoglyceride lipase · SINGLE PROTEIN · Homo sapiens

3,193Compounds
327Assays
1Approved Drugs
3,574.0Activities
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

Monoglyceride lipase shows clinical signal disease relevance led by tic disorder. 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 Q99685. Start with tic disorder, then reuse UniProt Q99685 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with tic disorder, then reuse UniProt Q99685 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
tic disorder

Monoglyceride lipase shows clinical signal disease relevance led by tic disorder. 3 more disease programs remain visible in the same review block. 1 linked drug remains visible in the same block.

Start review with tic disorder because it currently carries clinical signal support. Linked drugs include ELCUBRAGISTAT. 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 Monoglyceride lipase as ChEMBL target CHEMBL4191, mapped to UniProt Q99685. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Monoglyceride lipase
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL4191
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
Q99685
Monoglyceride lipase
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 Monoglyceride lipase is the right protein anchor across sources, using UniProt Q99685 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 tic disorder 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 LabelMonoglyceride lipase
UniProt AccessionQ99685
Component TypeProtein
Sequence Length303 aa

Monoglyceride lipase

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Monoglyceride lipase, mapped to UniProt Q99685. Sequence length is 303 aa.

Mapped IDQ99685
Review nameMonoglyceride lipase
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

Monoglyceride lipase shows clinical signal disease relevance led by tic disorder. 3 more disease programs remain visible in the same review block.

Clinical signal Phase II
tic disorder
1 linked drug · 1 direct · 1 efficacy
Linked drugELCUBRAGISTAT
Clinical signal Phase II
Tourette syndrome
1 linked drug · 1 direct · 1 efficacy
Linked drugELCUBRAGISTAT
Clinical signal Phase I
dyspepsia
1 linked drug · 1 direct · 1 efficacy
Linked drugELCUBRAGISTAT
Clinical signal Phase I
pain
1 linked drug · 1 direct · 1 efficacy
Linked drugELCUBRAGISTAT
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

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

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

Clinical Phase Distribution

1
Approved
2
Phase II
1
Phase I
Assay Mix

Activity Type Distribution

IC503,553.0
KI17.0
EC501.0
KD3.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL5785193 10.85 IC50 0.014 Preclinical
CHEMBL5283351 10.72 IC50 0.019 Preclinical
CHEMBL5569248 10.68 IC50 0.021 Preclinical
CHEMBL5074982 10.62 IC50 0.024 Preclinical
CHEMBL5832941 10.57 IC50 0.027 Preclinical
CHEMBL4749516 10.52 IC50 0.03 Preclinical
CHEMBL5618354 10.52 IC50 0.03 Preclinical
CHEMBL5282368 10.47 IC50 0.034 Preclinical
CHEMBL5892322 10.41 IC50 0.039 Preclinical
CHEMBL4759880 10.4 IC50 0.04 Preclinical
Distribution

pChEMBL Value Distribution

270
5.0
205
5.5
417
6.0
262
6.5
334
7.0
291
7.5
229
8.0
151
8.5
90
9.0
34
9.5
pChEMBL
Approved Drugs

Approved Drugs

DISULFIRAM
CHEMBL964
Approved 1951
Assay Landscape

Assay Landscape

327
Total Assays
2,133
Tested Compounds
3
Assay Types
Binding — 322 assays, 2,133 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 217 931 6.6
assay format 63 860 7.1
cell-based format 38 215 7.2
subcellular format 2 34 7.7
cell membrane format 1 0
organism-based format 1 93 6.6
ADME — 3 assays, 1 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 3 1 5.5
Functional — 2 assays, 1 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 2 1 8.8

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine