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Details

Stereochemistry RACEMIC
Molecular Formula C28H31NO5.CH4O3S
Molecular Weight 557.655
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BITOLTEROL MESYLATE

SMILES

CS(O)(=O)=O.CC1=CC=C(C=C1)C(=O)OC2=C(OC(=O)C3=CC=C(C)C=C3)C=C(C=C2)C(O)CNC(C)(C)C

InChI

InChIKey=HODFCFXCOMKRCG-UHFFFAOYSA-N
InChI=1S/C28H31NO5.CH4O3S/c1-18-6-10-20(11-7-18)26(31)33-24-15-14-22(23(30)17-29-28(3,4)5)16-25(24)34-27(32)21-12-8-19(2)9-13-21;1-5(2,3)4/h6-16,23,29-30H,17H2,1-5H3;1H3,(H,2,3,4)

HIDE SMILES / InChI

Molecular Formula CH4O3S
Molecular Weight 96.106
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C28H31NO5
Molecular Weight 461.5494
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Bitolterol is a beta 2-adrenergic agonist. Since it in itself is biologically inactive, bitolterol is considered a pro-drug. When administered it is activated within the lung by esterase hydrolysis to the active compound colterol catecholamine N-t-butyl-arterenol. Bitolterol was marked under the name tornalate and was indicated to prevent and treat of reversible bronchospasm associated with asthma or chronic obstructive pulmonary diseases. But that drug was withdrawn from the market by Elan Pharmaceuticals in 2001.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
TORNALATE

Approved Use

Unknown

Launch Date

4.73039995E11
Primary
TORNALATE

Approved Use

Unknown

Launch Date

4.73039995E11
PubMed

PubMed

TitleDatePubMed
Bitolterol. A preliminary review of its pharmacological properties and therapeutic efficacy in reversible obstructive airways disease.
1988 Jan
Multicenter dose-ranging study of bitolterol mesylate solution for nebulization in children with asthma.
1994 Mar
Retrospective study of bitolterol mesylate in the treatment of conditions associated with reversible bronchospasm.
1995 May-Jun
Efficacy and safety of inhaled bitolterol mesylate via metered-dose inhaler in children with asthma.
1996 Jan
Accuracy of Veterans Affairs databases for diagnoses of chronic diseases.
2009 Oct
Patents

Patents

Sample Use Guides

Acute Bronchospasm: adults and children older than 12 yr of age: oral inhalation 2 inhalations at interval of 1 to 3 min, followed by third inhalation if necessary. Prevention of Bronchospasm: adults and children older than 12 yr of age: oral inhalation 2 inhalations every 8 h, not to exceed 3 inhalations every 6 h or 2 inhalations every 4 h.
Route of Administration: Other
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:23:27 UTC 2023
Edited
by admin
on Fri Dec 15 15:23:27 UTC 2023
Record UNII
4E53T3611U
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BITOLTEROL MESYLATE
ORANGE BOOK   USAN   VANDF  
USAN  
Official Name English
.ALPHA.((TERT-BUTYLAMINO)METHYL)-3,4-DIHYDROXYBENZYL ALCOHOL 3,4-DI-P-TOLUATE METHANESULFONATE (SALT)
Common Name English
ALPHA ((T-BUTYLAMINO)METHYL)-3,4-DIHYDROXYBENZYL ALCOHOL 3,4-DI(P-TOLUATE) METHANESULFONATE
Common Name English
BENZOIC ACID, 4-METHYL-, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-1,2-PHENYLENE ESTER METHANESULPHONATE (SALT)
Common Name English
4-(2-(TERT-BUTYLAMINO)-1-HYDROXYETHYL)-1,2-PHENYLENE BIS(4-METHYLBENZOATE) METHANESULPHONATE (SALT)
Common Name English
BITOLTEROL MESYLATE [VANDF]
Common Name English
BITOLTEROL MESILATE [JAN]
Common Name English
BENZOIC ACID, 4-METHYL-, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-1,2-PHENYLENE ESTER, METHANESULFONATE (1:1)
Common Name English
BITOLTEROL METHANESULFONATE [MI]
Common Name English
BITOLTEROL MESYLATE [USAN]
Common Name English
4-(2-(TERT-BUTYLAMINO)-1-HYDROXYETHYL)-O-PHENYLENE DI-P-TOLUATE METHANESULFONATE (SALT)
Common Name English
BENZOIC ACID, 4-METHYL-, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-1,2-PHENYLENE ESTER, METHANESULPHONATE (1:1)
Common Name English
BITOLTEROL MESYLATE [ORANGE BOOK]
Common Name English
BITOLTEROL MESILATE
JAN   MART.   WHO-DD  
Common Name English
4-(2-(TERT-BUTYLAMINO)-1-HYDROXYETHYL)-1,2-PHENYLENE BIS(4-METHYLBENZOATE) METHANESULFONATE (SALT)
Common Name English
BITOLTEROL METHANESULFONATE
MI  
Common Name English
BITOLTEROL MESILATE [MART.]
Common Name English
.ALPHA.((TERT-BUTYLAMINO)METHYL)-3,4-DIHYDROXYBENZYL ALCOHOL 3,4-DI-P-TOLUATE METHANESULPHONATE (SALT)
Common Name English
WIN 32,784
Code English
TORNALATE
Brand Name English
ALPHA ((T-BUTYLAMINO)METHYL)-3,4-DIHYDROXYBENZYL ALCOHOL 3,4-DI(P-TOLUATE) METHANESULPHONATE
Common Name English
4-(2-(TERT-BUTYLAMINO)-1-HYDROXYETHYL)-O-PHENYLENE DI-P-TOLUATE METHANESULPHONATE (SALT)
Common Name English
BENZOIC ACID, 4-METHYL-, 4-(2-((1,1-DIMETHYLETHYL)AMINO)-1-HYDROXYETHYL)-1,2-PHENYLENE ESTER METHANESULFONATE (SALT)
Common Name English
WIN-32784
Code English
Bitolterol mesilate [WHO-DD]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C319
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
NCI_THESAURUS C48149
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
Code System Code Type Description
PUBCHEM
35329
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
RXCUI
47187
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY RxNorm
NCI_THESAURUS
C65268
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
EVMPD
SUB00836MIG
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
ChEMBL
CHEMBL1201295
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
ECHA (EC/EINECS)
250-177-5
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
CAS
30392-41-7
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
DRUG BANK
DBSALT002788
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
EPA CompTox
DTXSID80952735
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
MERCK INDEX
m2578
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY Merck Index
SMS_ID
100000085139
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
FDA UNII
4E53T3611U
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
CHEBI
3134
Created by admin on Fri Dec 15 15:23:27 UTC 2023 , Edited by admin on Fri Dec 15 15:23:27 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY