Dobutamine

drug
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Also known as COMPOUND 81929COMPOUND-81929Dl-dobutamineDobutaminaRacemic dobutamineSID26751752SID90341592SID104171143SID50104446SID144203677SID170465050Dobutamine (hydrochloride)

Summary

Dobutamine (CHEMBL926) is an approved small-molecule cardiotonic drug (ATC C01CA07) targeting ADRB1; indicated across 7 conditions including cardiovascular disorder and heart failure.

At a glance

  • Status: Approved (max clinical phase 4)
  • Modality: Small molecule
  • ATC class: C01CA07
  • Targets: 1 (ADRB1)
  • Indications: 7 conditions
  • Clinical trials: 55
  • Chemistry: 301.4 Da · C18H23NO3

Identifiers

Drug identity and classification

FieldValue
ChEMBL IDCHEMBL926
NameDobutamine
TypeSmall molecule
Max phase4
FDA approvedyes
PubChem CID36811
ChEBICHEBI:4670
ATCC01CA07
Molecular formulaC18H23NO3
Molecular weight301.4
InChIKeyJRWZLRBJNMZMFE-UHFFFAOYSA-N

SMILES: CC(CCC1=CC=C(C=C1)O)NCCC2=CC(=C(C=C2)O)O

IUPAC name: 4-[2-[4-(4-hydroxyphenyl)butan-2-ylamino]ethyl]benzene-1,2-diol

ChEBI definition: A catecholamine that is 4-(3-aminobutyl)phenol in which one of the hydrogens attached to the nitrogen is substituted by a 2-(3,4-dihydroxyphenyl)ethyl group. A β1-adrenergic receptor agonist that has cardiac stimulant action without evoking vasoconstriction or tachycardia, it is used as the hydrochloride to increase the contractility of the heart in the management of acute heart failure.

Pharmacological roles (ChEBI): cardiotonic drug, sympathomimetic agent, β-adrenergic agonist.

Also known as: COMPOUND 81929, COMPOUND-81929, Dl-dobutamine, Dobutamina, Dobutamine, Racemic dobutamine, SID26751752, SID90341592, dobutamine, SID104171143, SID50104446, DOBUTAMINE

Parent form; salt/anhydrous children: CHEMBL1200418, CHEMBL4297079

Patent coverage: 4,481 distinct patent families (17,095 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 17,091 (100%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.

Targets

Targets

Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).

GeneTargetActionpAffinityCancer dependencyUniProt
ADRB1β1-adrenoceptorPartial agonist6.80%P08588

Broader ChEMBL bioactivity targets: 46 (assay-derived). Sample: Prelamin-A/C, 4’-phosphopantetheinyl transferase ffp, Tyrosine-protein kinase Fyn, Alpha-2A adrenergic receptor, 5-hydroxytryptamine receptor 3A, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, Epidermal growth factor receptor, Carbonic anhydrase 2, D(1A) dopamine receptor.

Bioactivity

ChEMBL activities: 56 potent at pChembl ≥ 5 of 65 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):

TargetpChemblTypeValueUnitActivity ID
ADRA1A8.27AC505.4nMCHEMBL_ACT_25229731
P431407.35Ki45nMCHEMBL_ACT_7698724
ADRA1D7.25Ki56nMCHEMBL_ACT_7698728
ADRA1A7.15AC5070.4nMCHEMBL_ACT_25138401
P431406.96IC50110nMCHEMBL_ACT_7698723
ADRA1D6.94IC50114nMCHEMBL_ACT_7698727
SLC6A36.91Ki123nMCHEMBL_ACT_7700820
SLC6A36.81IC50155nMCHEMBL_ACT_7700819
P158236.73Ki186nMCHEMBL_ACT_7698726
ADRA1A6.59AC50255.1nMCHEMBL_ACT_25137875
P158236.47IC50336nMCHEMBL_ACT_7698725
SLC6A26.42IC50383nMCHEMBL_ACT_7700755
SLC6A26.42Ki380nMCHEMBL_ACT_7700756
Q99N236.41Ki390nMCHEMBL_ACT_3426932
CA26.32Ki480nMCHEMBL_ACT_3426855
P125306.22IC50599nMCHEMBL_ACT_7700863
DRD36.14AC50728nMCHEMBL_ACT_25193427
CA5A6.14Ki730nMCHEMBL_ACT_3426876
ADRA2C6.1AC50798.1nMCHEMBL_ACT_25147775
SLC6A36.05AC50897.2nMCHEMBL_ACT_25123852
CA5B6.05Ki890nMCHEMBL_ACT_3426883
SLC6A46Ki1006nMCHEMBL_ACT_7702975
ADRB25.98Ki1043nMCHEMBL_ACT_7700752
SIGMAR15.98Ki1058nMCHEMBL_ACT_7702977
ADRB15.95Ki1123nMCHEMBL_ACT_7700750
ADRA2B5.87Ki1354nMCHEMBL_ACT_7698732
ADRB25.82IC501517nMCHEMBL_ACT_7700751
OPRM15.77AC501700nMCHEMBL_ACT_25157384
DRD35.77Ki1693nMCHEMBL_ACT_7700816
SLC6A25.76AC501725nMCHEMBL_ACT_25144902

Target pathways

Aggregated over 1 target gene(s): ADRB1.

Top Reactome pathways

8 total, by targets touching each:

PathwayTargetsGenes
Signal Transduction1ADRB1
Signaling by GPCR1ADRB1
Class A/1 (Rhodopsin-like receptors)1ADRB1
Amine ligand-binding receptors1ADRB1
GPCR downstream signalling1ADRB1
Adrenoceptors1ADRB1
G alpha (s) signalling events1ADRB1
GPCR ligand binding1ADRB1

Dominant GO biological processes

GO termTargets
positive regulation of heart rate by epinephrine-norepinephrine1
positive regulation of the force of heart contraction by epinephrine-norepinephrine1
diet induced thermogenesis1
norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure1
adenylate cyclase-activating G protein-coupled receptor signaling pathway1
response to cold1
positive regulation of cardiac muscle cell apoptotic process1
heat generation1
negative regulation of multicellular organism growth1
fear response1
positive regulation of MAPK cascade1
regulation of circadian sleep/wake cycle, sleep1
brown fat cell differentiation1
adenylate cyclase-activating adrenergic receptor signaling pathway1
positive regulation of cold-induced thermogenesis1

Indications & clinical

Indications

7 indications (1 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).

IndicationTrial phaseMONDOEFO
cardiovascular disorder4MONDO:0004995EFO:0000319
heart failure3MONDO:0005252EFO:0003144
toxic shock syndrome2MONDO:0001881EFO:0006834
acute lung injury2MONDO:0015796EFO:0004610
brain injury2MONDO:0043510MONDO:0043510
burn0MONDO:0043519EFO:0009516

1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.

Clinical trials

Total trials: 55.

Phase distribution

PhaseTrials
Not specified21
PHASE412
PHASE28
PHASE34
PHASE1/PHASE24
EARLY_PHASE14
PHASE2/PHASE32

Top trials by phase / activity

NCTPhaseStatusTitle
NCT05267886PHASE4RECRUITINGCAPITAL DOREMI 2: Inotrope Versus Placebo Therapy for Cardiogenic Shock
NCT00484133PHASE4UNKNOWNMicrocirculation Guided Therapy Versus Standard Treatment of Severe Sepsis
NCT00549419PHASE4COMPLETEDArterial Pressure Based Cardiac Output for Goal-Directed Therapy in Abdominal Surgery
NCT01375335PHASE4SUSPENDEDThe Effects of Dobutamine on Postoperative Cardiac Function in Aortic Valve Replacement
NCT01418118PHASE4COMPLETEDAssessment of the Effects of Pressors on Graft Blood Flow After Free Tissue Transfer Surgery
NCT01427686PHASE4UNKNOWNDopamine Versus Dobutamine for Treatment of Arterial Hypotension in Term and Preterm Neonates
NCT01930734PHASE4UNKNOWNOutcome and Safety of Intermittent Dobutamine Infusion at a Day-Care Center in Advanced Heart Failure Patients
NCT01969071PHASE4COMPLETEDThe Effects of Levosimendan During Mitral Valve Surgery
NCT02012946PHASE4UNKNOWNLevosimendan Versus Dobutamine in Cardiopatic Patients Undergoing Major Non Cardiac Surgery
NCT02767024PHASE4WITHDRAWNIntravenous Vasodilator vs. Inotropic Therapy in Patients With Heart Failure
NCT03207165PHASE4COMPLETEDMilrinone Versus Dobutamine in Critically Ill Patients
NCT03846765PHASE4COMPLETEDInfluence of Continuous Administration of Phenylephrine Versus Dobutamine on Spinal Oxygen Saturation, Measured With Near-infrared Spectroscopy (NIRS).
NCT00001891PHASE3COMPLETEDMyocardial Contrast Echocardiography (MCE) to Check for Living and Working Heart Muscle
NCT00093301PHASE2/PHASE3UNKNOWNLevosimendan Versus Dobutamine in Shock Patients
NCT00148278PHASE2/PHASE3COMPLETEDNorepinephrine Plus Dobutamine Versus Epinephrine Alone for the Management of Septic Shock
NCT00348504PHASE3COMPLETEDSurvival of Patients With Acute Heart Failure in Need of Intravenous Inotropic Support: a Multicentre, Parallel-Group, Randomised, Double-Blind, Double-Dummy Study of Levosimendan Versus Dobutamine in Patients With Acute Heart Failure.
NCT02133105PHASE3COMPLETEDLevosimendan Versus Dobutamine for Renal Function in Heart Failure
NCT04166331PHASE3COMPLETEDAdjunctive DobutAmine in sePtic Cardiomyopathy With Tissue Hypoperfusion
NCT05350592PHASE2ACTIVE_NOT_RECRUITINGLow-Dose Dobutamine and Single-Dose Tocilizumab in Acute Myocardial Infarction With High Risk of Cardiogenic Shock
NCT06878742PHASE1/PHASE2RECRUITINGDose-finding for Dobutamine During Transitional Circulation in Very Preterm Infants
NCT07406477PHASE2NOT_YET_RECRUITINGThe PROTECT-HIE Pilot Trial
NCT00281255PHASE1/PHASE2WITHDRAWNIntravenous Allopurinol to Improve Heart Function in Individuals With Dilated Cardiomyopathy
NCT00624650PHASE2COMPLETEDHemodynamics and Extravascular Lung Water in Acute Lung Injury
NCT00800306PHASE2COMPLETEDEffects of Levosimendan on Microcirculation in Septic Shock
NCT01605279PHASE2COMPLETEDDobutamine Versus Placebo for Low Superior Vena Cava Flow in Newborns
NCT02019810PHASE2UNKNOWNImpact of Cardiac Blood Flow on Cerebral Blood Flow in Patients With Severe Traumatic Brain Injury
NCT02644057PHASE2WITHDRAWNDobutamaine Versus Milrinone in Cardiorenal Syndrome
NCT03311178PHASE1/PHASE2TERMINATEDDobutamine in the Treatment of Haemodynamic Insufficiency in the Immediate Postnatal Period
NCT04020172PHASE1/PHASE2COMPLETEDImproving Tissue Oxygenation in Breast Reconstruction Surgery
NCT05953142PHASE2UNKNOWNUse of Dobutamine in Patients With Sepsis and Maintained Hypoperfusion After Initial Volemic Resuscitation.
NCT00763035EARLY_PHASE1TERMINATEDComparison of Dobutamine and Regadenoson Stress Cardiac Magnetic Resonance (MR)
NCT04249258EARLY_PHASE1COMPLETEDDobutamine on the Cardiac Conduction System
NCT05241912EARLY_PHASE1UNKNOWNSupernormal Oxygen Delivery for Patients With Severe Burns
NCT06210217EARLY_PHASE1UNKNOWNEffect of TEE-guided Non-fluid Limited Combined With Dobutamine on Hepatic Venous Blood Flow Spectrum
NCT05944146Not specifiedRECRUITINGConsistency of Carotid Doppler Blood Flow and Thermodilution Technique
NCT00074724Not specifiedCOMPLETEDDobutamine Echocardiography In Patients With Ischemic Heart Failure Evaluated for Revascularization
NCT00250315Not specifiedCOMPLETEDDOCICAR: Cardiac Dysfunction in Cirrhosis
NCT00557934Not specifiedCOMPLETEDRight Ventricular Contractility Reserve Following Repair of Tetralogy of Fallot
NCT01271153Not specifiedCOMPLETEDEffects of Dobutamine on Microcirculation, Regional and Peripheral Perfusion in Septic Shock Patients
NCT01354613Not specifiedCOMPLETEDReduced Contractile Reserve: a Therapeutic Target in Heart Failure With Preserved Ejection Fraction(HFpEF)

Clinical evidence (CIViC)

No CIViC predictive evidence (expected for non-precision-medicine drugs).

Pharmacology

Pharmacogenomics

No CPIC/DPWG dosing guideline, but PharmGKB curates 2 clinical and 6 variant annotation(s) for this drug (gene-keyed; see PharmGKB).

Molecules sharing ≥1 of this drug’s curated primary targets, merged from two biobtree sources and ranked by shared-target count, then clinical phase: ChEMBL clinical-stage candidates (development phase ≥2) and PubChem drug-class bioactivity (approved / known drugs acting on the target). Deduplicated by drug name; the drug’s own salt forms are excluded. Note: for a drug with few primary targets a shared-target match can reflect off-target / promiscuous binding rather than the same therapeutic mechanism — the phase ordering surfaces bona-fide therapeutics first.

179 molecules share ≥1 primary target. Top 60 by shared-target count:

MoleculeSourceStatusShared targets
OLODATEROLChEMBL + PubChemPhase 4 (approved)ADRB1
TAMSULOSINChEMBL + PubChemPhase 4 (approved)ADRB1
ACEBUTOLOLChEMBLPhase 4 (approved)ADRB1
ALBUTEROLChEMBLPhase 4 (approved)ADRB1
AMIODARONEChEMBLPhase 4 (approved)ADRB1
AMITRIPTYLINEChEMBLPhase 4 (approved)ADRB1
ARFORMOTEROLChEMBLPhase 4 (approved)ADRB1
ARIPIPRAZOLEChEMBLPhase 4 (approved)ADRB1
ASTEMIZOLEChEMBLPhase 4 (approved)ADRB1
ATENOLOLChEMBLPhase 4 (approved)ADRB1
AZELASTINEChEMBLPhase 4 (approved)ADRB1
BENFLUOREXChEMBLPhase 4 (approved)ADRB1
BENPERIDOLChEMBLPhase 4 (approved)ADRB1
BENZBROMARONEChEMBLPhase 4 (approved)ADRB1
BEPRIDILChEMBLPhase 4 (approved)ADRB1
BETAXOLOLChEMBLPhase 4 (approved)ADRB1
BISOPROLOLChEMBLPhase 4 (approved)ADRB1
BREXPIPRAZOLEChEMBLPhase 4 (approved)ADRB1
BROMOCRIPTINEChEMBLPhase 4 (approved)ADRB1
CANDESARTAN CILEXETILChEMBLPhase 4 (approved)ADRB1
CARIPRAZINEChEMBLPhase 4 (approved)ADRB1
CARTEOLOLChEMBLPhase 4 (approved)ADRB1
CARVEDILOLChEMBLPhase 4 (approved)ADRB1
CELIPROLOLChEMBLPhase 4 (approved)ADRB1
CHLORHEXIDINEChEMBLPhase 4 (approved)ADRB1
CHLORPROTHIXENEChEMBLPhase 4 (approved)ADRB1
CINACALCETChEMBLPhase 4 (approved)ADRB1
CLEMASTINEChEMBLPhase 4 (approved)ADRB1
CLOMIPRAMINEChEMBLPhase 4 (approved)ADRB1
CLOTRIMAZOLEChEMBLPhase 4 (approved)ADRB1
CODEINEChEMBLPhase 4 (approved)ADRB1
DARIFENACINChEMBLPhase 4 (approved)ADRB1
DAUNORUBICINChEMBLPhase 4 (approved)ADRB1
DECITABINEChEMBLPhase 4 (approved)ADRB1
DIETHYLSTILBESTROLChEMBLPhase 4 (approved)ADRB1
DOMPERIDONEChEMBLPhase 4 (approved)ADRB1
DULOXETINEChEMBLPhase 4 (approved)ADRB1
EBASTINEChEMBLPhase 4 (approved)ADRB1
ECONAZOLEChEMBLPhase 4 (approved)ADRB1
EFAVIRENZChEMBLPhase 4 (approved)ADRB1
EPALRESTATChEMBLPhase 4 (approved)ADRB1
EPINEPHRINEChEMBLPhase 4 (approved)ADRB1
ERGOTAMINEChEMBLPhase 4 (approved)ADRB1
ESMOLOLChEMBLPhase 4 (approved)ADRB1
FENOTEROLChEMBLPhase 4 (approved)ADRB1
FLUSPIRILENEChEMBLPhase 4 (approved)ADRB1
FORMOTEROLChEMBLPhase 4 (approved)ADRB1
INDACATEROLChEMBLPhase 4 (approved)ADRB1
INDOCYANINE GREEN ACID FORMChEMBLPhase 4 (approved)ADRB1
ISOCONAZOLEChEMBLPhase 4 (approved)ADRB1
ISOPROTERENOLChEMBLPhase 4 (approved)ADRB1
LABETALOLChEMBLPhase 4 (approved)ADRB1
LASOFOXIFENEChEMBLPhase 4 (approved)ADRB1
LEVOBUNOLOLChEMBLPhase 4 (approved)ADRB1
LORCASERINChEMBLPhase 4 (approved)ADRB1
METARAMINOLChEMBLPhase 4 (approved)ADRB1
METHYLERGONOVINEChEMBLPhase 4 (approved)ADRB1
METOPROLOLChEMBLPhase 4 (approved)ADRB1
MICONAZOLEChEMBLPhase 4 (approved)ADRB1
MONTELUKASTChEMBLPhase 4 (approved)ADRB1