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Target Snapshot

CHEMBL213 Target Snapshot

Beta-1 adrenergic receptor · SINGLE PROTEIN · Homo sapiens

4,459Compounds
662Assays
74Approved Drugs
4,103.0Activities
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

Beta-1 adrenergic receptor shows approved-linked disease relevance led by hypertension. 5 more disease programs remain visible in the same review block. 10 linked drugs keep the current disease frame grounded. Protein identity stays anchored to UniProt P08588. Start with hypertension, then reuse UniProt P08588 as the stable protein anchor across project notes and exports.

Review focus
Review-ready target frame

Start with hypertension, then reuse UniProt P08588 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 10 linked drugs
Open source guide
Disease program
hypertension

Beta-1 adrenergic receptor shows approved-linked disease relevance led by hypertension. 5 more disease programs remain visible in the same review block. 10 linked drugs remain visible in the same block.

Start review with hypertension because it currently carries approved-linked support. Linked drugs include ACEBUTOLOL HYDROCHLORIDE, ATENOLOL, BETAXOLOL HYDROCHLORIDE, BISOPROLOL FUMARATE. 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 10 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 Beta-1 adrenergic receptor as ChEMBL target CHEMBL213, mapped to UniProt P08588. Disease framing currently uses the Open Targets-ready proxy contract.

Review anchor
Beta-1 adrenergic receptor
SINGLE PROTEIN · Homo sapiens
As of 2026-09-13
ChEMBL target ID
CHEMBL213
Primary anchor for compounds, assays, approvals, and exports
ChEMBL 36 via Core Engine As of 2026-09-13
www.ebi.ac.uk
UniProt accession
P08588
Beta-1 adrenergic receptor
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 Beta-1 adrenergic receptor is the right protein anchor across sources, using UniProt P08588 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 hypertension is currently framed as approved-linked support. It currently carries 10 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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Open Review-ready Card
Overview

Basic Information

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UniProt Context

UniProt Target Context

Reviewable protein naming and mapping context for this target snapshot.

Protein LabelBeta-1 adrenergic receptor
UniProt AccessionP08588
Component TypeProtein
Sequence Length477 aa

Beta-1 adrenergic receptor

Source · UniProt accession via ChEMBL component mapping
Review Cue

How to read this target

Review this target as Beta-1 adrenergic receptor, mapped to UniProt P08588. Sequence length is 477 aa.

Mapped IDP08588
Review nameBeta-1 adrenergic receptor
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

Beta-1 adrenergic receptor shows approved-linked disease relevance led by hypertension. 5 more disease programs remain visible in the same review block.

Approved-linked Approved
hypertension
10 linked drugs · 10 direct · 10 efficacy
Linked drugACEBUTOLOL HYDROCHLORIDE
Linked drugATENOLOL
Linked drugBETAXOLOL HYDROCHLORIDE
Linked drugBISOPROLOL FUMARATE
Approved-linked Approved
cardiovascular disease
9 linked drugs · 9 direct · 9 efficacy
Linked drugATENOLOL
Linked drugCELIPROLOL
Linked drugDOBUTAMINE HYDROCHLORIDE
Linked drugLANDIOLOL
Approved-linked Approved
atrial fibrillation
8 linked drugs · 8 direct · 8 efficacy
Linked drugATENOLOL
Linked drugBUCINDOLOL HYDROCHLORIDE
Linked drugLANDIOLOL
Linked drugLANDIOLOL HYDROCHLORIDE
Approved-linked Approved
stroke
6 linked drugs · 6 direct · 6 efficacy
Linked drugATENOLOL
Linked drugMETOPROLOL SUCCINATE
Linked drugMETOPROLOL TARTRATE
Linked drugNADOLOL
Approved-linked Approved
angina pectoris
5 linked drugs · 5 direct · 5 efficacy
Linked drugATENOLOL
Linked drugMETOPROLOL SUCCINATE
Linked drugMETOPROLOL TARTRATE
Linked drugNADOLOL
Approved-linked Approved
heart failure
5 linked drugs · 5 direct · 5 efficacy
Linked drugATENOLOL
Linked drugMETOPROLOL SUCCINATE
Linked drugMETOPROLOL TARTRATE
Linked drugPROPAFENONE HYDROCHLORIDE
Source · ChEMBL drug mechanism + indication proxy
Review Cue

How to read disease relevance

Start review with hypertension because it currently carries approved-linked support. Linked drugs include ACEBUTOLOL HYDROCHLORIDE, ATENOLOL, BETAXOLOL HYDROCHLORIDE, BISOPROLOL FUMARATE. This disease block keeps the Open Targets-ready contract explicit while current evidence comes from ChEMBL mechanism and indication mappings.

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

Clinical Phase Distribution

74
Approved
3
Phase III
39
Phase II
1
Phase I
Assay Mix

Activity Type Distribution

IC501,510.0
KI1,342.0
EC501,097.0
KD154.0
Lead Set

Top Inhibitors (by pChEMBL)

ChEMBL IDpChEMBLTypeValue (nM)Phase
CHEMBL2012522 10.64 Ki 0.023 Preclinical
CHEMBL2011218 10.4 IC50 0.04 Preclinical
CHEMBL2011227 10.3 IC50 0.05 Preclinical
CHEMBL2011226 10.3 IC50 0.05 Preclinical
CHEMBL5207281 10.12 Kd 0.075 Preclinical
CHEMBL5201074 10.12 Kd 0.075 Preclinical
CHEMBL4860528 10.12 Kd 0.075 Preclinical
CHEMBL5206565 10.12 Kd 0.075 Preclinical
CHEMBL2011216 10.1 IC50 0.08 Preclinical
CHEMBL434 10.08 EC50 0.084 Approved
Distribution

pChEMBL Value Distribution

201
5.0
243
5.5
313
6.0
296
6.5
242
7.0
174
7.5
153
8.0
106
8.5
33
9.0
23
9.5
pChEMBL
Approved Drugs

Approved Drugs

BREXPIPRAZOLE
CHEMBL2105760
Approved 2015
CARIPRAZINE HYDROCHLORIDE
CHEMBL2024517
Approved 2015
OLODATEROL
CHEMBL605846
Approved 2014
OLODATEROL HYDROCHLORIDE
CHEMBL2105743
Approved 2014
INDACATEROL
CHEMBL1095777
Approved 2009
ARFORMOTEROL
CHEMBL1363
Approved 2006
DARIFENACIN
CHEMBL1346
Approved 2004
FORMOTEROL
CHEMBL1256786
Approved 2001
CARVEDILOL
CHEMBL723
Approved 1995
SALMETEROL
CHEMBL1263
Approved 1994
SOTALOL
CHEMBL471
Approved 1992
PROPAFENONE
CHEMBL631
Approved 1989
CARTEOLOL
CHEMBL839
Approved 1988
ESMOLOL
CHEMBL768
Approved 1986
LEVOBUNOLOL
CHEMBL1201237
Approved 1985
BETAXOLOL HYDROCHLORIDE
CHEMBL1691
Approved 1985
BETAXOLOL
CHEMBL423
Approved 1985
ACEBUTOLOL
CHEMBL642
Approved 1984
LABETALOL
CHEMBL429
Approved 1984
PINDOLOL
CHEMBL500
Approved 1982
ALBUTEROL
CHEMBL714
Approved 1981
ATENOLOL
CHEMBL24
Approved 1981
TIMOLOL
CHEMBL499
Approved 1978
METOPROLOL
CHEMBL13
Approved 1978
PROPRANOLOL
CHEMBL27
Approved 1967
EPINEPHRINE
CHEMBL679
Approved 1965
ISOPROTERENOL HYDROCHLORIDE
CHEMBL1711
Approved 1956
ISOPROTERENOL
CHEMBL434
Approved 1956
Assay Landscape

Assay Landscape

664
Total Assays
973
Tested Compounds
3
Assay Types
Binding — 432 assays, 973 compounds
BAO Format Assays Compounds Avg pChEMBL
single protein format 315 255 6.7
cell-based format 106 621 6.1
assay format 5 32 7.7
cell membrane format 4 64 6.3
organism-based format 1 1 7.3
tissue-based format 1 0
Functional — 222 assays, 705 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 136 655 7.2
assay format 78 50 6.6
tissue-based format 4 0
organism-based format 3 0
single protein format 1 0
ADME — 10 assays, 40 compounds
BAO Format Assays Compounds Avg pChEMBL
cell-based format 6 40 7.5
single protein format 4 0

Confidence Score Distribution

Source · ChEMBL 36 via Core Engine