bitolterol 🐶 Veterinary Use | Indications/Contra | FAERs-F | FAERs-M | Orange Bk | PK/Tox | Related Drugs | BioActivity |

Stem definitionDrug idCAS RN
bronchodilators, phenethylamine derivatives 384 30392-40-6

Description:

MoleculeDescription

Molfile Inchi Smiles

Synonyms:

  • bitolterol methanesulfonate
  • tornalate
  • bitolterol mesylate
  • bitolterol
  • bitolterol mesilate
a short-acting beta2 adrenergic receptor agonist used for the relief of bronchospasm in conditions such as asthma and COPD
  • Molecular weight: 461.56
  • Formula: C28H31NO5
  • CLOGP: 5.77
  • LIPINSKI: 1
  • HAC: 6
  • HDO: 2
  • TPSA: 84.86
  • ALOGS: -5.98
  • ROTB: 10

  • Status: OFM

  • Legend:
    OFP - off patent
    OFM - off market
    ONP - on patent

Drug dosage:

None

ADMET properties:

None

Predicted pharmacokinetic/toxicological properties (PK-AZ):

PropertyDescriptionValueUnitConfidenceSimilarity
azlogd74 LogD at pH 7.4 3.606 High 1
caco2-efflux Caco-2 efflux ratio (BA/AB) 2.360 High 1
caco2-intrinsic-papp Caco-2 intrinsic apparent permeability 5.546 10^-6 cm/s High 1
dh-clint Dog hepatocyte intrinsic clearance 51.286 uL/min/10^6 cells High 1
dppb Dog plasma protein binding (% unbound) 0.720 % High 1
fcs-ppb Fetal calf serum protein binding (% unbound) 2.260 % High 1
herg hERG pIC50 5.647 pIC50 High 1
hh-clint Human hepatocyte intrinsic clearance 299.226 uL/min/10^6 cells High 1
hlm-clint Human liver microsomal intrinsic clearance 189.234 uL/min/mg protein High 1
hppb Human plasma protein binding (% unbound) 0.920 % High 1
kinase-safety-class ACVR2B,AKT1,AKT2,AKT3,ALK,AURKA,AXL,BRAF,BTK,CAMK2B,CAMK2D,CDK5,CDK9,DDR1,DYRK1B,EGFR,EIF2AK3,EPHB4,ERBB2,FLT3,GRK2,ITK,JAK1,JAK2,JAK3,KIT,MAP2K6,MAP3K21,MAP3K7,MAPK10,MAPK12,MAPK7,MAPK9,MAPKAPK2,MARK4,MET,MTOR,NTRK2,PAK4,PDK1,PDK2,PDK4,PDPK1,PIK3CB,PIM2,PRKCD,PRKDC,SIK2,SIK3,STK33,SYK,TEK,TTK 53
kinase-selectivity-class ACVR2B,AXL,EIF2AK3,GRK2,PDK4 5
mdck-mdr1-efflux MDCK-MDR1 efflux ratio 7.295 High 1
mh-clint Mouse hepatocyte intrinsic clearance 368.978 High 1
mppb Mouse plasma protein binding (% unbound) 2.700 High 1
nih-mdck-mdr1-efflux NIH MDCK-MDR1 efflux ratio 17.783 High 1
pfas-class PFAS structural alert (1 = True, 0 = False) 0
pppb Pig plasma protein binding (% unbound) 6.810 % High 1
rh-clint Rat hepatocyte intrinsic clearance 283.139 uL/min/10^6 cells High 1
rh-fuinc Rat hepatocyte fraction unbound in incubation 11.180 % High 1
rppb Rat plasma protein binding (% unbound) 1.250 % High 1
solubility-dd Solubility at pH 7.4 in DMSO 22.751 uM High 1

Approvals:

DateAgencyCompanyOrphan
Dec. 28, 1984 FDA SANOFI AVENTIS US

FDA Adverse Event Reporting System (Female)

None

FDA Adverse Event Reporting System (Male)

None

FDA Adverse Event Reporting System (Geriatric)

None

FDA Adverse Event Reporting System (Pediatric)

None

Pharmacologic Action:

SourceCodeDescription
ATC R03AC17 RESPIRATORY SYSTEM
DRUGS FOR OBSTRUCTIVE AIRWAY DISEASES
ADRENERGICS, INHALANTS
Selective beta-2-adrenoreceptor agonists
CHEBI has role CHEBI:35522 β-adrenergic agonist
CHEBI has role CHEBI:35523 bronchodilator agent
CHEBI has role CHEBI:49167 anti-asthmatic drug
CHEBI has role CHEBI:50266 prodrug
MeSH PA D000318 Adrenergic beta-Agonists
MeSH PA D000322 Adrenergic Agonists
MeSH PA D001993 Bronchodilator Agents
MeSH PA D018373 Peripheral Nervous System Agents
MeSH PA D018377 Neurotransmitter Agents
MeSH PA D018663 Adrenergic Agents
MeSH PA D018927 Anti-Asthmatic Agents
MeSH PA D019141 Respiratory System Agents
MeSH PA D058666 Adrenergic beta-2 Receptor Agonists

Related Drugs by ATC class:

R03AC Selective beta-2-adrenoreceptor agonists 17 drugs

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

DiseaseRelationSNOMED_IDDOID
Bronchiectasis indication 12295008 DOID:9563
Bronchitis indication 32398004 DOID:6132
Pulmonary emphysema indication 87433001
Asthma indication 195967001 DOID:2841
Asthma management indication 406162001
Acute exacerbation of asthma indication 708038006
Bronchospasm Prevention indication




🐶 Veterinary Drug Use

None

🐶 Veterinary products

None

Acid dissociation constants calculated using MoKa v3.0.0

Dissociation levelDissociation constantType (acidic/basic)
pKa1 14.0 acidic
pKa2 9.19 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 AGONIST CHEMBL CHEMBL

External reference:

IDSource
4019101 VUID
N0000147359 NUI
D00684 KEGG_DRUG
30392-41-7 SECONDARY_CAS_RN
19499 RXNORM
C0053817 UMLSCUI
CHEBI:3133 CHEBI
CHEMBL1201295 ChEMBL_ID
CHEMBL1200405 ChEMBL_ID
DB00901 DRUGBANK_ID
C011685 MESH_SUPPLEMENTAL_RECORD_UI
3855 INN_ID
9KY0QXD6LI UNII
35330 PUBCHEM_CID
1209 MMSL
4292 MMSL
d00754 MMSL
387233000 SNOMEDCT_US
412217002 SNOMEDCT_US
41985001 SNOMEDCT_US
4019101 VANDF
4019636 VANDF
001816 NDDF
004733 NDDF
9KY0QXD6LI INXIGHT DRUGS

Pharmaceutical products:

None