Albuterol
drug drugOn this page
Also known as AerolinAerolin 400Aerolin autoAiromirAirsalbAsmasal clickhalerAsmasal spacehalerAsmavenAsmaventCobutolinCombiventCombivent udvsDuonebEtinolineIpramol steri-nebKentamolLibetistMaxiventNSC-757417
Summary
Albuterol (CHEMBL714) is an approved small-molecule bronchodilator agent (ATC R03AC02) targeting ADRB2; indicated across 30 conditions including chronic obstructive pulmonary disease and obstructive lung disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: R03AC02 (+1 more)
- Targets: 1 (ADRB2)
- Indications: 30 conditions
- Clinical trials: 296
- Chemistry: 239.31 Da · C13H21NO3
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL714 |
| Name | Albuterol |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | yes |
| PubChem CID | 2083 |
| ChEBI | CHEBI:2549 |
| ATC | R03AC02, R03CC02 |
| Molecular formula | C13H21NO3 |
| Molecular weight | 239.31 |
| InChIKey | NDAUXUAQIAJITI-UHFFFAOYSA-N |
SMILES: CC(C)(C)NCC(C1=CC(=C(C=C1)O)CO)O
IUPAC name: 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(hydroxymethyl)phenol
ChEBI definition: A member of the class of phenylethanolamines that is 4-(2-amino-1-hydroxyethyl)-2-(hydroxymethyl)phenol having a tert-butyl group attached to the nirogen atom. It acts as a β-adrenergic agonist used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
Pharmacological roles (ChEBI): bronchodilator agent, β-adrenergic agonist.
Other ChEBI roles (chemical / environmental): environmental contaminant, xenobiotic.
Also known as: Aerolin, Aerolin 400, Aerolin auto, Airomir, Airsalb, Albuterol, Asmasal clickhaler, Asmasal spacehaler, Asmaven, Asmavent, Cobutolin, Combivent
Parent form; salt/anhydrous children: CHEMBL1201026, CHEMBL1437301, CHEMBL1441059
Patent coverage: 17,920 distinct patent families (67,291 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 66,920 (99%) 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).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| ADRB2 | β2-adrenoceptor | Partial agonist | 7.7 | 0.4% | P07550 |
Broader ChEMBL bioactivity targets: 4 (assay-derived). Sample: Beta-2 adrenergic receptor, Beta-1 adrenergic receptor, Beta-2 adrenergic receptor, Beta-2 adrenergic receptor.
Bioactivity
ChEMBL activities: 26 potent at pChembl ≥ 5 of 27 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| ADRB2 | 9.96 | EC50 | 0.11 | nM | CHEMBL_ACT_24911223 |
| Q8K4Z4 | 9.34 | EC50 | 0.45 | nM | CHEMBL_ACT_2688167 |
| ADRB1 | 8.81 | EC50 | 1.53 | nM | CHEMBL_ACT_24911244 |
| Q8K4Z4 | 8.04 | EC50 | 9.1 | nM | CHEMBL_ACT_2612963 |
| Q8K4Z4 | 7.77 | IC50 | 17 | nM | CHEMBL_ACT_3294072 |
| ADRB2 | 7.6 | EC50 | 25.12 | nM | CHEMBL_ACT_8007831 |
| ADRB2 | 7.17 | EC50 | 68 | nM | CHEMBL_ACT_3294074 |
| Q8K4Z4 | 6.96 | Kd | 109.7 | nM | CHEMBL_ACT_15153057 |
| ADRB2 | 6.7 | EC50 | 199.5 | nM | CHEMBL_ACT_6284209 |
| ADRB2 | 6.66 | Kd | 220 | nM | CHEMBL_ACT_19403986 |
| ADRB2 | 6.62 | AC50 | 240 | nM | CHEMBL_ACT_25233833 |
| Q8K4Z4 | 6.61 | Kd | 245.5 | nM | CHEMBL_ACT_15153054 |
| ADRB2 | 6.6 | EC50 | 251 | nM | CHEMBL_ACT_23194853 |
| Q8K4Z4 | 6.57 | EC50 | 268 | nM | CHEMBL_ACT_2688169 |
| ADRB2 | 6.29 | Ki | 510 | nM | CHEMBL_ACT_2612950 |
| Q28044 | 6.28 | Kd | 520 | nM | CHEMBL_ACT_473805 |
| ADRB2 | 6.25 | Ki | 557 | nM | CHEMBL_ACT_7826268 |
| Q28044 | 6.24 | Kd | 570 | nM | CHEMBL_ACT_876348 |
| ADRB2 | 6.09 | IC50 | 810.2 | nM | CHEMBL_ACT_7826267 |
| ADRB2 | 6.01 | IC50 | 980 | nM | CHEMBL_ACT_2612944 |
| Q8K4Z4 | 5.94 | Kd | 1160 | nM | CHEMBL_ACT_2688174 |
| ADRB1 | 5.93 | EC50 | 1170 | nM | CHEMBL_ACT_23194850 |
| ADRB2 | 5.85 | Kd | 1400 | nM | CHEMBL_ACT_19403975 |
| ADRB2 | 5.74 | Ki | 1828 | nM | CHEMBL_ACT_3294075 |
| ADRB2 | 5.7 | IC50 | 1995 | nM | CHEMBL_ACT_8007816 |
| ADRB2 | 5.31 | AC50 | 4891 | nM | CHEMBL_ACT_25123281 |
Target pathways
Aggregated over 1 target gene(s): ADRB2.
Top Reactome pathways
16 total, by targets touching each:
| Pathway | Targets | Genes |
|---|---|---|
| Signal Transduction | 1 | ADRB2 |
| Membrane Trafficking | 1 | ADRB2 |
| Signaling by GPCR | 1 | ADRB2 |
| Class A/1 (Rhodopsin-like receptors) | 1 | ADRB2 |
| Amine ligand-binding receptors | 1 | ADRB2 |
| GPCR downstream signalling | 1 | ADRB2 |
| Adrenoceptors | 1 | ADRB2 |
| Metabolism of proteins | 1 | ADRB2 |
| G alpha (s) signalling events | 1 | ADRB2 |
| GPCR ligand binding | 1 | ADRB2 |
| Vesicle-mediated transport | 1 | ADRB2 |
| Deubiquitination | 1 | ADRB2 |
| Ub-specific processing proteases | 1 | ADRB2 |
| Post-translational protein modification | 1 | ADRB2 |
| Cargo recognition for clathrin-mediated endocytosis | 1 | ADRB2 |
| Clathrin-mediated endocytosis | 1 | ADRB2 |
Dominant GO biological processes
| GO term | Targets |
|---|---|
| diet induced thermogenesis | 1 |
| norepinephrine-epinephrine-mediated vasodilation involved in regulation of systemic arterial blood pressure | 1 |
| regulation of sodium ion transport | 1 |
| transcription by RNA polymerase II | 1 |
| receptor-mediated endocytosis | 1 |
| smooth muscle contraction | 1 |
| cell surface receptor signaling pathway | 1 |
| adenylate cyclase-modulating G protein-coupled receptor signaling pathway | 1 |
| endosome to lysosome transport | 1 |
| response to cold | 1 |
| positive regulation of cardiac muscle cell apoptotic process | 1 |
| negative regulation of cardiac muscle cell apoptotic process | 1 |
| positive regulation of bone mineralization | 1 |
| heat generation | 1 |
| negative regulation of multicellular organism growth | 1 |
Indications & clinical
Indications
2 approved indications. FDA phase 4, plus an anticancer drug’s labelled cancer uses (which ChEMBL often logs at phase 3).
| Indication | Phase | MONDO | EFO |
|---|---|---|---|
| chronic obstructive pulmonary disease | 4 | MONDO:0005002 | EFO:0000341 |
| obstructive lung disease | 4 | MONDO:0002267 | HP:0006536 |
18 diseases in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| congestive heart failure | 3 | MONDO:0005009 | EFO:0000373 |
| Riley-Day syndrome | 3 | MONDO:0009131 | Orphanet:1764 |
| pulmonary arterial hypertension | 3 | MONDO:0015924 | EFO:0001361 |
| seasonal allergic rhinitis | 3 | MONDO:0005324 | EFO:0003956 |
| lung disorder | 3 | MONDO:0005275 | EFO:0003818 |
| pulmonary hypertension | 3 | MONDO:0005149 | MONDO:0005149 |
| heart failure | 3 | MONDO:0005252 | EFO:0003144 |
| pulmonary edema | 2 | MONDO:0006932 | EFO:1001134 |
| bronchiolitis | 2 | MONDO:0002465 | HP:0011950 |
| status asthmaticus | 2 | MONDO:0004766 | EFO:0008590 |
| respiratory failure | 2 | MONDO:0021113 | EFO:0009686 |
| allergic disease | 2 | MONDO:0005271 | MONDO:0005271 |
| spinal cord injury | 2 | MONDO:0043797 | MONDO:0043797 |
| congenital myasthenic syndrome | 1 | MONDO:0018940 | Orphanet:590 |
| idiopathic pulmonary fibrosis | 1 | MONDO:0800504 | EFO:0000768 |
| diabetes mellitus | 1 | MONDO:0005015 | EFO:0000400 |
| major depressive disorder | 1 | MONDO:0002009 | MONDO:0002009 |
| lymphangioleiomyomatosis | 1 | MONDO:0011705 | MONDO:0011705 |
9 further indication records had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 296.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE3 | 80 |
| PHASE4 | 74 |
| Not specified | 70 |
| PHASE2 | 36 |
| PHASE1 | 28 |
| EARLY_PHASE1 | 4 |
| PHASE2/PHASE3 | 2 |
| PHASE1/PHASE2 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT02797275 | PHASE4 | ACTIVE_NOT_RECRUITING | Secondhand Smoke Respiratory Health Study |
| NCT06152653 | PHASE4 | RECRUITING | The Effects of Positive Airway Pressure on the Mucolytic Effects of NAC (TEAM) |
| NCT06422689 | PHASE4 | ACTIVE_NOT_RECRUITING | Combination Short-Acting BroNchodilator and Inhaled Corticosteroid Rescue Therapy on Health Outcomes in Routine Care |
| NCT00070707 | PHASE4 | COMPLETED | Nasonex Compared With Placebo in Participants With Seasonal Allergic Rhinitis (SAR) and Concomitant Asthma (P03280) |
| NCT00272753 | PHASE4 | COMPLETED | Effect of Budesonide / Formoterol Combination in Repeated AMP Provocations |
| NCT00315744 | PHASE4 | COMPLETED | Viapaed Study In Children And Adolescents With Asthma |
| NCT00354354 | PHASE4 | COMPLETED | Bronchodilators and Oxygen Kinetics With Exercise in Chronic Obstructive Pulmonary Disease (COPD) Patients |
| NCT00363480 | PHASE4 | COMPLETED | Results Of Patient Rated Asthma Control Test In Comparison To Diary Card Data |
| NCT00385359 | PHASE4 | UNKNOWN | A Pilot Efficacy Study of Inhaled Albuterol Delivered With Akita Breath Control |
| NCT00388882 | PHASE4 | COMPLETED | Trial Comparing Treatment With Tiotropium Inhalation Capsules to Combivent® Inhalation Aerosol in COPD Patients. |
| NCT00393367 | PHASE4 | COMPLETED | Budesonide Inhalation Suspension for Acute Asthma in Children |
| NCT00440245 | PHASE4 | COMPLETED | Bronchoprotection of Salbutamol in Asthma and Chronic Obstructive Pulmonary Disease |
| NCT00487773 | PHASE4 | COMPLETED | Effect of Different Doses of Budesonide on Markers of Bone Metabolism in Children With Asthma |
| NCT00783250 | PHASE4 | TERMINATED | Bronchodilators and Respiratory Mechanics in Chronic Obstructive Pulmonary Disease (COPD) Patients |
| NCT00830882 | PHASE4 | WITHDRAWN | Peak Bronchoprotection Conferred by Levosalbutamol and Racemic Salbutamol |
| NCT00831376 | PHASE4 | COMPLETED | Trough Bronchoprotection Conferred by Levosalbutamol and Racemic Salbutamol |
| NCT00900874 | PHASE4 | UNKNOWN | Rapid Onset Action of Salbutamol Versus Formoterol |
| NCT00911651 | PHASE4 | COMPLETED | Study to Assess the Effect of Salbutamol and Ipratropium Bromide in Chronic Obstructive Pulmonary Disease (COPD) Patients |
| NCT00940927 | PHASE4 | COMPLETED | Dose-response of Albuterol in Asthmatics |
| NCT01091337 | PHASE4 | COMPLETED | Comparative Study on the Efficacy and Safety of Procaterol Versus Salbutamol Given Via Metered Dose Inhaler With Spacer in the Management of Acute Asthma Attack in the Emergency Room |
| NCT01151579 | PHASE4 | COMPLETED | Effect of Nebulized Bronchodilators on Heart Rate |
| NCT01253473 | PHASE4 | COMPLETED | Symbicort in Airway Predominant Chronic Obstructive Pulmonary Disease (COPD) |
| NCT01338311 | PHASE4 | COMPLETED | Salbutamol Tolerance Onset |
| NCT01471340 | PHASE4 | COMPLETED | A Serious Asthma Outcome Study With Mometasone Furoate/Formoterol Versus Mometasone Furoate in Asthmatics 12 Years and Over (P06241) |
| NCT01691482 | PHASE4 | COMPLETED | A Study to Look at Day to Day Changes in Lung Function in COPD Subjects Taking Albuterol/Salbutamol and Ipratropium |
| NCT01721291 | PHASE4 | COMPLETED | Inhaler Lung Deposition in Chronic Obstructive Pulmonary Disease (COPD) |
| NCT01903785 | PHASE4 | COMPLETED | Salbutamol, Pharmacogenetics and Breathing Mechanics |
| NCT01907334 | PHASE4 | COMPLETED | Dose-Response of Salmeterol in Children |
| NCT01922271 | PHASE4 | COMPLETED | Efficacy of NVA237 Compared to Tiotropium in Patients With Chronic Obstructive Pulmonary Disease (COPD) |
| NCT01951378 | PHASE4 | TERMINATED | Comparison of Nebulizers in ED in Pediatric Asthma Patients |
| NCT01978418 | PHASE4 | UNKNOWN | Inhaled Salbutamol in Elective Caesarean Section |
| NCT02103374 | PHASE4 | COMPLETED | Evaluation of Benefit of Nebulized Bronchodilators at Home in Severe Chronic Obstructive Pulmonary Disease and Very Severe Steady State |
| NCT02182713 | PHASE4 | COMPLETED | Combivent vs. Salbutamol in Patients With Metacholine Induced Bronchospasm |
| NCT02233803 | PHASE4 | COMPLETED | A Non-inferiority Study to Evaluate Efficacy, Safety and Tolerability of NEUMOTEROL® 400 and SYMBICORT® Forte in Adults With Asthma |
| NCT02235428 | PHASE4 | TERMINATED | Study to Assess the Efficacy of Ipratropium Bromide Associated With High Dose Salbutamol by Repeated Nebulisation Versus Repeat Nebulisation of Salbutamol Alone, in Acute Asthmatic Attacks in Young Children |
| NCT02257372 | PHASE4 | COMPLETED | A Study to Evaluate the Effect of Umeclidinium (UMEC) as Combination Therapy in Subjects With Chronic Obstructive Pulmonary Disease (COPD) |
| NCT02275052 | PHASE4 | COMPLETED | A Study to Evaluate the Effect of the Combination of Umeclidinium (UMEC) and Vilanterol (VI) on Exercise Endurance Time (EET) in Participants With Chronic Obstructive Pulmonary Disease (COPD) |
| NCT02319564 | PHASE4 | WITHDRAWN | Combined Glucocorticoid Adrenergic Therapy For Wheezy Preschool Children |
| NCT02371629 | PHASE4 | COMPLETED | A Study of the Efficacy and Safety of NVA237 in Patients With Moderate to Severe COPD |
| NCT02405598 | PHASE4 | COMPLETED | Evaluation of Salbutamol as an Adjuvant Therapy for Pompe Disease |
| NCT02584738 | PHASE4 | UNKNOWN | Nebulized Magnesium Sulfate as an Adjunct to Standard Therapy in Asthma Exacerbation |
| NCT02654145 | PHASE4 | COMPLETED | Omalizumab to Mepolizumab Switch Study in Severe Eosinophilic Asthma Patients |
| NCT02799784 | PHASE4 | COMPLETED | An Efficacy Study of Umeclidinium/Vilanterol With Tiotropium/Olodaterol in COPD Patients |
| NCT02877537 | PHASE4 | COMPLETED | Measurement of Respiratory Admittance for Pediatric Asthma Diagnosis |
| NCT02914652 | PHASE4 | COMPLETED | The Cardiopulmonary Effect of Inhaled Beta-2-agonists on Adult Patients Born With Ventricular Septum Defects. |
| NCT03044938 | PHASE4 | COMPLETED | Acute Effect of Salbutamol on Heart Rate and Blood Pressure During Exercise in Patients With Moderate or Severe Asthma and Healthy Subjects |
| NCT03199976 | PHASE4 | TERMINATED | Efficacy of Intermittent Tiotropium in Early Childhood Wheezing |
| NCT03333395 | PHASE4 | COMPLETED | Nebulized Heparin and Salbutamol in Mechanically Ventilated Patients With AECOPD |
| NCT03363191 | PHASE4 | WITHDRAWN | The Efficacy of Fluticasone Furoate/Vilanterol Versus (vs) Fluticasone Furoate on Asthma |
| NCT03380429 | PHASE4 | COMPLETED | A Clinical Study to Evaluate the Effect of the Connected Inhaler System (CIS) on Adherence to Maintenance Therapy in Poorly Controlled Asthmatic Subjects |
| NCT03405090 | PHASE4 | COMPLETED | Differential Mechanisms of Dyspnea Relief in Advanced COPD: Opiates vs. Bronchodilators |
| NCT03474081 | PHASE4 | COMPLETED | A Comparative Study Between Fluticasone Furoate/Umeclidinium/Vilanterol (FF/UMEC/VI) Single Inhaler Triple Therapy Versus Tiotropium Monotherapy in Subjects With Chronic Obstructive Pulmonary Disease (COPD) |
| NCT03478683 | PHASE4 | COMPLETED | A Randomized Study, Comparing Fluticasone Furoate/Umeclidinium/Vilanterol (FF/UMEC/VI) Single Inhaler Triple Therapy, Versus Multiple Inhaler Therapy (Budesonide/Formoterol Plus Tiotropium) in Subjects With Chronic Obstructive Pulmonary Disease (COPD) |
| NCT03478696 | PHASE4 | COMPLETED | A Randomized Study, Comparing Fluticasone Furoate/Umeclidinium/Vilanterol (FF/UMEC /VI) Single Inhaler Triple Therapy, Versus Multiple Inhaler Therapy (Budesonide/Formoterol Plus Tiotropium) in Subjects With Chronic Obstructive Pulmonary Disease (COPD) |
| NCT03493503 | PHASE4 | COMPLETED | Status Asthmaticus on the PICU; Intravenous Salbutamol |
| NCT03822637 | PHASE4 | TERMINATED | The Effect of NAC on Lung Function and CT Mucus Score |
| NCT03880903 | PHASE4 | UNKNOWN | Hypertonic Saline Inhalation in Acute Bronchiolitis |
| NCT03890666 | PHASE4 | COMPLETED | A 12-Week Treatment Study to Evaluate the Effectiveness of Albuterol Multidose Dry Powder Inhaler With Integrated Electronic Module Digital System (eMDPI DS) in Participants13 Years or Older With Asthma |
| NCT03924635 | PHASE4 | COMPLETED | An Exploratory Study to Characterise Changes in Airway Inflammation, Symptoms, Lung Function and Reliever Use in Adult Asthma Patients |
| NCT04012138 | PHASE4 | COMPLETED | Insulin Dextrose Infusion vs Nebulized Salbutamol vs Combination of Salbutamol and Insulin Dextrose in Acute Hyperkalemia |
| NCT04184609 | PHASE4 | WITHDRAWN | Mechanisms for Dyspnea on Exertion in Children With Obesity and Asthma: Distinct Physiological Phenotypes |
| NCT04207840 | PHASE4 | COMPLETED | Study of Drug Exposure in Systemic Circulation of Primatene Mist by Oral Inhalation, Versus Epinephrine Injection by Intramuscular Injection and ProAir by Oral Inhalation in Healthy Individuals |
| NCT04276233 | PHASE4 | COMPLETED | Efficacy and Safety Study of Mepolizumab 100 Milligram (mg) Subcutaneous (SC) in Indian Participants Aged Greater Than or Equal to (>=) 18 Years With Severe Eosinophilic Asthma |
| NCT04584034 | PHASE4 | WITHDRAWN | Bronchodilators for Wheeze in Young Children Presenting to Primary Care: a Randomised, Placebo-controlled, Multicentre, Parallel Group Trial |
| NCT04606394 | PHASE4 | COMPLETED | Peak Inspiratory Flow and Dry Powder Inhaler Performance in COPD |
| NCT04677959 | PHASE4 | COMPLETED | A 24-Week Treatment Study to Compare Standard of Care Versus the eMDPI DS in Participants 13 Years or Older With Asthma |
| NCT04750603 | PHASE4 | COMPLETED | Effect of Fluticasone Furoate/Vilanterol on EIA in Adolescents |
| NCT05087693 | PHASE4 | COMPLETED | Salbutamol Use in Ozone Air Pollution by People With Asthma and/or Exercise Induced Bronchoconstriction (EIB) |
| NCT05173584 | PHASE4 | UNKNOWN | Levalbuterol Compared to Albuterol Regarding Cardiac Side Effects and Potassium Lowering Effects. |
| NCT05667727 | PHASE4 | COMPLETED | The Effect of Nebulized Epinephrine in Asthma Exacerbation in Pediatric Age Group With the Standard Treatment Compared to Standard Treatment Using Improvement PRAM Score as a Primary Outcome |
| NCT06036823 | PHASE4 | COMPLETED | 5 Versus 10 Units of Insulin in Hyperkalemia Management |
| NCT06158893 | PHASE4 | UNKNOWN | Comparison of Preoperative Inhaled Budesonide With Salbutamol on the Respiratory Adverse Effects in Children Undergoing Tonsillectomy |
| NCT06563102 | PHASE4 | COMPLETED | Study to Investigate Changes in Airway Inflammation, Symptoms, and Rescue Therapy Utilization With AIRSUPRA Compared to Albuterol as Needed in Adults With Mild Asthma |
| NCT06918418 | PHASE4 | COMPLETED | A Comparative Study of Adding Ipratropium to Salbutamol for the Treatment of Asthma Attack in Children |
| NCT05527704 | PHASE3 | ACTIVE_NOT_RECRUITING | the Inhaled β2-adrenergic Receptor Agonist for Transient Tachypnoea of the Newborn (the REFSAL Trial) |
| NCT06471257 | PHASE3 | RECRUITING | A Study to Investigate Efficacy and Safety of PT027 Compared With PT007 in Symptomatic Chinese Adults With Asthma |
| NCT06473779 | PHASE3 | ACTIVE_NOT_RECRUITING | Open-label Study to Assess Reduction of Background Asthma Medication While Sustaining Asthma Control and Clinical Remission With Tezepelumab in Patients 12-80yrs With Severe Asthma. |
| NCT06618105 | PHASE3 | NOT_YET_RECRUITING | Bronchoprovocation Study to Demonstrate the Pharmacodynamic Bioequivalence of Albuterol Sulfate HFA Inhalation Aerosol (E.Q. 90 mcg of Albuterol Base/Inh) of Macleods Pharmaceuticals Ltd |
| NCT06946264 | PHASE3 | RECRUITING | Characterization of Bronchodilator Response in Children With Bronchiolitis Using Phenotypic and Genotypic Features |
| NCT00000577 | PHASE3 | WITHDRAWN | Asthma Clinical Research Network (ACRN) |
| NCT00064389 | PHASE3 | COMPLETED | Long Term Safety Study of Levalbuterol and Racemic Albuterol in Subjects Twelve Years of Age and Older With Asthma |
| NCT00144846 | PHASE3 | COMPLETED | Inhaled Albuterol Sulfate For Acute Wheezing Due To Obstructive Airways Disease In Children |
| NCT00308685 | PHASE3 | COMPLETED | Chronic-Dose Safety and Efficacy Study of Albuterol-HFA-BAI in Pediatric Asthmatics |
| NCT00382889 | PHASE3 | COMPLETED | As Needed Beclomethasone/Salbutamol Combination in Single Inhaler for Mild Persistent Asthma |
| NCT00384189 | PHASE3 | COMPLETED | A Comparative Study of Inhaled Ciclesonide Versus Placebo in Children (6-11 Years) With Asthma |
| NCT00497523 | PHASE3 | COMPLETED | Efficacy and Safety of Nebulised Beclomethasone Dipropionate Plus as Needed Salbutamol vs as Needed Salbutamol or as Needed Salbutamol/Beclomethasone Fixed Combination in Young Children With Asthma Symptoms |
| NCT00528723 | PHASE3 | COMPLETED | Efficacy and Tolerability of Beclomethasone Plus Salbutamol in HFA pMDI Fixed Combination vs Beclomethasone Plus Salbutamol in CFC pMDI Fixed Combination in a 12-week Treatment Period of Adult Patients With Uncontrolled Asthma |
| NCT00550550 | PHASE3 | COMPLETED | Efficacy and Safety of Grass Sublingual Tablet in Children and Adolescents (P05239 AM3)(COMPLETED) |
| NCT00562159 | PHASE3 | COMPLETED | Efficacy and Safety of Grass Sublingual Tablet in Adults (P05238 AM3)(COMPLETED) |
| NCT00577655 | PHASE3 | COMPLETED | Albuterol HFA MDI in Pediatric Participants With Asthma |
| NCT00588406 | PHASE3 | COMPLETED | Study of Budesonide as an Addition to Standard Therapy in Adult Asthmatics in the Emergency Room. |
| NCT00633919 | PHASE2/PHASE3 | COMPLETED | Efficacy of SLITone in House Dust Mite Allergic Patients |
| NCT00634517 | PHASE3 | TERMINATED | 4-Week Study of Efficacy, Safety and PK of Albuterol-HFA Versus Proventil-HFA in Pediatric Asthma |
| NCT00634829 | PHASE3 | TERMINATED | Single-Dose Cross-Over Study of the Effects of Albuterol-HFA in Exercise Induced Bronchoconstriction |
| NCT00646009 | PHASE3 | COMPLETED | Symbicort Onset of Action 2 |
| NCT00646620 | PHASE3 | COMPLETED | Symbicort Onset of Action 1 |
| NCT00669617 | PHASE3 | COMPLETED | Study to Determine the Onset of Action of Indacaterol in Patients With Moderate to Severe Chronic Obstructive Pulmonary Disease (COPD) |
| NCT00685126 | PHASE3 | COMPLETED | Study of Levalbuterol and Racemic Albuterol in Pediatric Subjects With Reactive Airways Disease (RAD) |
| NCT00685425 | PHASE3 | COMPLETED | Dose Response Study of Levalbuterol in the Prevention of Exercise Induced Bronchoconstriction Compared to Racemic Albuterol |
| NCT00861926 | PHASE3 | COMPLETED | Study on Foster Efficacy Maintenance and Reliever vs Foster Maintenance + Salbutamol Reliever in Asthmatics (MART2) |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline, but PharmGKB curates 21 clinical and 59 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
Related molecules
Related molecules
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.
188 molecules share ≥1 primary target. Top 100 by shared-target count:
| Molecule | Source | Status | Shared targets |
|---|---|---|---|
| DESLORATADINE | ChEMBL + PubChem | Phase 4 (approved) | ADRB2 |
| DIHYDROERGOTAMINE | ChEMBL + PubChem | Phase 4 (approved) | ADRB2 |
| OLODATEROL | ChEMBL + PubChem | Phase 4 (approved) | ADRB2 |
| PRAMIPEXOLE | ChEMBL + PubChem | Phase 4 (approved) | ADRB2 |
| ACEBUTOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| ADENOSINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| AMITRIPTYLINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| AMLODIPINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| AMOXAPINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| ARFORMOTEROL | ChEMBL | Phase 4 (approved) | ADRB2 |
| ARIPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRB2 |
| ATENOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| BENPERIDOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| BETAXOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| BISOPROLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| BREXPIPRAZOLE | ChEMBL | Phase 4 (approved) | ADRB2 |
| BROMOCRIPTINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| CANDESARTAN CILEXETIL | ChEMBL | Phase 4 (approved) | ADRB2 |
| CARTEOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| CARVEDILOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| CELIPROLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| CHLORHEXIDINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| CLEMASTINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| CLOMIPRAMINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| CLOTRIMAZOLE | ChEMBL | Phase 4 (approved) | ADRB2 |
| CLOZAPINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| DARIFENACIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| DEXAMETHASONE | ChEMBL | Phase 4 (approved) | ADRB2 |
| DIPIVEFRIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| DOBUTAMINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| DOMPERIDONE | ChEMBL | Phase 4 (approved) | ADRB2 |
| DOPAMINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| DOXAZOSIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| ELAGOLIX | ChEMBL | Phase 4 (approved) | ADRB2 |
| EPINEPHRINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| EPINEPHRINE BITARTRATE | ChEMBL | Phase 4 (approved) | ADRB2 |
| ERGOTAMINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| ESMOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| FENOTEROL | ChEMBL | Phase 4 (approved) | ADRB2 |
| FLUSPIRILENE | ChEMBL | Phase 4 (approved) | ADRB2 |
| FORMOTEROL | ChEMBL | Phase 4 (approved) | ADRB2 |
| HALOPERIDOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| INDACATEROL | ChEMBL | Phase 4 (approved) | ADRB2 |
| ISOETHARINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| ISOPROTERENOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| LABETALOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| LEVOBUNOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| LEVOSALBUTAMOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| LOFEPRAMINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| LOPERAMIDE | ChEMBL | Phase 4 (approved) | ADRB2 |
| LOXAPINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| MEBEVERINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| METAPROTERENOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| METOPROLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| MIFEPRISTONE | ChEMBL | Phase 4 (approved) | ADRB2 |
| MONTELUKAST | ChEMBL | Phase 4 (approved) | ADRB2 |
| NADOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| NEBIVOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| NITAZOXANIDE | ChEMBL | Phase 4 (approved) | ADRB2 |
| NOREPINEPHRINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| NORTRIPTYLINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| OLANZAPINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| OXPRENOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| PAROXETINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PERPHENAZINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PHENYLEPHRINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PIMAVANSERIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| PIMOZIDE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PINDOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| PIPERACETAZINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PRACTOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| PRENYLAMINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PRIMAQUINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PROMAZINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PROPAFENONE | ChEMBL | Phase 4 (approved) | ADRB2 |
| PROPRANOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| RANOLAZINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| REBOXETINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| RIBOFLAVIN 5’-PHOSPHATE | ChEMBL | Phase 4 (approved) | ADRB2 |
| RIFAMPIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| RIFAXIMIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| RIMEGEPANT | ChEMBL | Phase 4 (approved) | ADRB2 |
| RISPERIDONE | ChEMBL | Phase 4 (approved) | ADRB2 |
| RITODRINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| SALMETEROL | ChEMBL | Phase 4 (approved) | ADRB2 |
| SALMETEROL XINAFOATE | ChEMBL | Phase 4 (approved) | ADRB2 |
| SILODOSIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| SOTALOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| SUNITINIB | ChEMBL | Phase 4 (approved) | ADRB2 |
| TAMOXIFEN | ChEMBL | Phase 4 (approved) | ADRB2 |
| TAMSULOSIN | ChEMBL | Phase 4 (approved) | ADRB2 |
| TEGASEROD | ChEMBL | Phase 4 (approved) | ADRB2 |
| TERBUTALINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| THIORIDAZINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| TIMOLOL | ChEMBL | Phase 4 (approved) | ADRB2 |
| TIOCONAZOLE | ChEMBL | Phase 4 (approved) | ADRB2 |
| TOLTERODINE | ChEMBL | Phase 4 (approved) | ADRB2 |
| TOLVAPTAN | ChEMBL | Phase 4 (approved) | ADRB2 |
| VALDECOXIB | ChEMBL | Phase 4 (approved) | ADRB2 |
| VILANTEROL | ChEMBL | Phase 4 (approved) | ADRB2 |
Related Atlas pages
- Genes: ADRB2
- Indicated for: chronic obstructive pulmonary disease, obstructive lung disease
- In clinical trials for: congestive heart failure, Riley-Day syndrome, pulmonary arterial hypertension, seasonal allergic rhinitis, lung disorder, pulmonary hypertension, heart failure, pulmonary edema, bronchiolitis, status asthmaticus, respiratory failure, allergic disease, spinal cord injury
- Drugs: Desloratadine, Dihydroergotamine, Olodaterol, Pramipexole, Acebutolol, Adenosine, Amitriptyline, Amlodipine, Amoxapine, Arformoterol, Aripiprazole, Atenolol, Benperidol, Betaxolol, Bisoprolol, Brexpiprazole, Bromocriptine, Candesartan Cilexetil, Carteolol, Carvedilol, Celiprolol, Chlorhexidine, Clemastine, Clomipramine, Clotrimazole, Clozapine, Darifenacin, Dexamethasone, Dipivefrin, Dobutamine, Domperidone, Dopamine, Doxazosin, Elagolix, Epinephrine, Ergotamine, Esmolol, Fenoterol, Fluspirilene, Formoterol, Haloperidol, Indacaterol, Isoetharine, Isoproterenol, Labetalol, Levobunolol, Levosalbutamol, Lofepramine, Loperamide, Loxapine, Mebeverine, Metaproterenol, Metoprolol, Mifepristone, Montelukast, Nadolol, Nebivolol, Nitazoxanide, Norepinephrine, Nortriptyline, Olanzapine, Oxprenolol, Paroxetine, Perphenazine, Phenylephrine, Pimavanserin, Pimozide, Pindolol, Piperacetazine, Practolol, Prenylamine, Primaquine, Promazine, Propafenone, Propranolol, Ranolazine, Reboxetine, RIBOFLAVIN 5’-PHOSPHATE, Rifampin, Rifaximin, Rimegepant, Risperidone, Ritodrine, Salmeterol, Silodosin, Sotalol, Sunitinib, Tamoxifen, Tamsulosin, Tegaserod, Terbutaline, Thioridazine, Timolol, Tioconazole, Tolterodine, Tolvaptan, Valdecoxib, Vilanterol