bambuterol ๐Ÿถ Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | BioActivity |

Stem definitionDrug idCAS RN
bronchodilators, phenethylamine derivatives 285 81732-65-2

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • bambuterol
  • bambudil
  • terbutaline bisdimethylcarbamate
  • (+/-)-Bambuterol
  • bambuterol hydrochloride
  • bambuterol HCl
selective inhibitor of butyrylcholinesterase & acetylcholinesterase
  • Molecular weight: 367.45
  • Formula: C18H29N3O5
  • CLOGP: 0.74
  • LIPINSKI: 0
  • HAC: 8
  • HDO: 2
  • TPSA: 91.34
  • ALOGS: -2.89
  • ROTB: 8

Drug dosage:

DoseUnitRoute
20 mg O

ADMET properties:

PropertyValueReference
BDDCS (Biopharmaceutical Drug Disposition Classification System) 1 Benet LZ, Broccatelli F, Oprea TI
S (Water solubility) 33 mg/mL Benet LZ, Broccatelli F, Oprea TI
EoM (Fraction excreted unchanged in urine) 0 % Benet LZ, Broccatelli F, Oprea TI
MRTD (Maximum Recommended Therapeutic Daily Dose) 0.71 ยตM/kg/day Contrera JF, Matthews EJ, Kruhlak NL, Benz RD
BA (Bioavailability) 15 % Kim MT, Sedykh A, Chakravarti SK, Saiakhov RD, Zhu H
Vd (Volume of distribution) 1.60 L/kg Lombardo F, Berellini G, Obach RS
CL (Clearance) 18 mL/min/kg Lombardo F, Berellini G, Obach RS
t_half (Half-life) 2.60 hours Lombardo F, Berellini G, Obach RS

Approvals:

DateAgencyCompanyOrphan
Jan. 1, 1990 YEAR INTRODUCED

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

MedDRA adverse event termLikelihood ratioLikelihood ratio thresholdPatients taking drug having adverse eventPatients taking drug not having adverse eventPatients not taking drug having adverse eventPatients not taking drug not having adverse event
Acute kidney injury 71.68 58.01 36 274 519368 79224710

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC R03CC12 RESPIRATORY SYSTEM
DRUGS FOR OBSTRUCTIVE AIRWAY DISEASES
ADRENERGICS FOR SYSTEMIC USE
Selective beta-2-adrenoreceptor agonists
MeSH PA D018927 Anti-Asthmatic Agents
MeSH PA D001993 Bronchodilator Agents
MeSH PA D018373 Peripheral Nervous System Agents
MeSH PA D019141 Respiratory System Agents
CHEBI has role CHEBI:35522 beta-adrenergic agonists
CHEBI has role CHEBI:35523 bronchodilator
CHEBI has role CHEBI:35524 sympathomimetic
CHEBI has role CHEBI:38462 acetylcholinesterase inhibitors
CHEBI has role CHEBI:49167 anti-asthmatic drugs
CHEBI has role CHEBI:50266 Prodrugs
CHEBI has role CHEBI:66993 tocolytic drugs

Drug Use | Suggest Off label Use Form| |View source of the data|

None




๐Ÿถ Veterinary Drug Use

None

๐Ÿถ Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 13.12 acidic
pKa2 8.92 Basic

Orange Book patent data (new drug applications)

None

Orange Book exclusivity data (new drug applications)

None

Bioactivity Summary:

TargetClassPharosUniProtActionTypeActivity value
(-log[M])
Mechanism
action
Bioact sourceMoA source
Beta-2 adrenergic receptor GPCR WOMBAT-PK
Cytochrome P450 2D6 Enzyme IC50 5.70 DRUG MATRIX
Acetylcholinesterase Enzyme Ki 3.25 WOMBAT-PK
Cholinesterase Enzyme INHIBITOR IC50 8.50 IUPHAR
Butyrylcholinesterase; Protein Bche Enzyme IC50 8.52 CHEMBL
Acetylcholinesterase Enzyme IC50 4.52 CHEMBL
Cholinesterase Enzyme IC50 6.92 CHEMBL

External reference:

IDSource
D07377 KEGG_DRUG
18751 RXNORM
C0052944 UMLSCUI
CHEBI:553827 CHEBI
CHEMBL521589 ChEMBL_ID
DB01408 DRUGBANK_ID
C047766 MESH_SUPPLEMENTAL_RECORD_UI
54766 PUBCHEM_CID
6601 IUPHAR_LIGAND_ID
5304 INN_ID
81732-46-9 SECONDARY_CAS_RN
Y1850G1OVC UNII
349923005 SNOMEDCT_US
391812009 SNOMEDCT_US
396462008 SNOMEDCT_US
004156 NDDF
004157 NDDF

Pharmaceutical products:

None