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Details

Stereochemistry RACEMIC
Molecular Formula C16H22N2O3.ClH
Molecular Weight 326.818
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROCATEROL HYDROCHLORIDE

SMILES

Cl.CC[C@@H](NC(C)C)[C@@H](O)C1=CC=C(O)C2=C1C=CC(=O)N2

InChI

InChIKey=AEQDBKHAAWUCMT-KKJWGQAZSA-N
InChI=1S/C16H22N2O3.ClH/c1-4-12(17-9(2)3)16(21)11-5-7-13(19)15-10(11)6-8-14(20)18-15;/h5-9,12,16-17,19,21H,4H2,1-3H3,(H,18,20);1H/t12-,16+;/m1./s1

HIDE SMILES / InChI

Molecular Formula C16H22N2O3
Molecular Weight 290.3575
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/894683

Procaterol is a beta2-adrenoreceptor agonist. It is a bronchodilator that may be administered orally or by aerosol inhalation for the treatment of dyspnea caused by bronchial asthma, chronic bronchitis, and pulmonary emphysema. The drug is not approved in the USA, but is available in Japan, Indonesia, and other countries worldwide.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: P07550|||Q53GA6|||Q9UCZ3
Gene ID: 154.0
Gene Symbol: ADRB2
Target Organism: Homo sapiens (Human)
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Primary
MEPTIN

Approved Use

For the treatment of dyspnea caused by bronchial asthma, chronic bronchitis, and pulmonary emphysema
Primary
MEPTIN

Approved Use

For the treatment of dyspnea caused by bronchial asthma, chronic bronchitis, and pulmonary emphysema.
Primary
MEPTIN

Approved Use

For the treatment of dyspnea caused by bronchial asthma, chronic bronchitis, and pulmonary emphysema.
PubMed

PubMed

TitleDatePubMed
Procaterol and terbutaline in bronchial asthma. A double-blind, placebo-controlled, cross-over study.
1985 Oct
A comparison of oral procaterol and albuterol in reversible airflow obstruction.
1988 Dec
Beta 3-adrenergic receptor-mediated lipolysis and oxygen consumption in brown adipocytes from cynomolgus monkeys.
1997 Feb
Beta2-adrenoceptors on the glial cells mediate the induction of interleukin-1beta mRNA in the rat brain.
1997 Oct 3
Functional and molecular characterization of beta-adrenoceptors in the internal anal sphincter.
2003 May
The selectivity of beta-adrenoceptor agonists at human beta1-, beta2- and beta3-adrenoceptors.
2010 Jul
Interactions between theophylline and salbutamol on cytokine release in human monocytes.
2010 Jul
Patents

Sample Use Guides

Meptin tablets: the usual adult dose is 50 µg (one tablet) once before bed or twice daily (in the morning and before bed) by the oral route. Meptin air: in general, for adults, inhale 2 puffs (20 mcg of active ingredient) at a time, and for children, inhale 1 puff (10 mcg of active ingredient) at a time. The dosage may be adjusted according to your disease, age, or symptoms. Strictly follow the instructed dosing schedule. The maximum dosage is restricted to 4 times daily (8 puffs for adults and 4 puffs for children).
Route of Administration: Other
To study the beta2-blocking activity of procaterol, a guinea pig tracheal test was performed. The trachea was excised from male guinea pigs. A spiral section of the trachea was prepared and suspended in a 30-ml tissue bath. The condition of the tracheal muscle was monitored by isometric recordings using force transducers. Phentolamine was added to the bath fluid 15 min before induction of contraction with the test compound to block alpha-adrenergic receptors. ED50 for procaterol was 11 nM.
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:23:49 UTC 2023
Edited
by admin
on Fri Dec 15 15:23:49 UTC 2023
Record UNII
4VD1BRT7T8
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROCATEROL HYDROCHLORIDE
MART.   USAN   WHO-DD  
USAN  
Official Name English
PROCATEROL HYDROCHLORIDE [USAN]
Common Name English
PRO-AIR
Brand Name English
CI-888
Code English
2(1H)-QUINOLINONE, 8-HYDROXY-5-(1-HYDROXY-2-((1-METHYLETHYL)AMINO)BUTYL)-, MONOHYDROCHLORIDE, (R*,S*), (±)-
Common Name English
(±)-ERYTHRO-8-HYDROXY-5-(1-HYDROXY-2-(ISOPROPYLAMINO)BUTYL)CARBOSTYRIL MONOHYDROCHLORIDE
Common Name English
Procaterol hydrochloride [WHO-DD]
Common Name English
PROCATEROL HYDROCHLORIDE [MART.]
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID20975221
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
ChEMBL
CHEMBL160519
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
CAS
62929-91-3
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
FDA UNII
4VD1BRT7T8
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
NCI_THESAURUS
C166789
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
CAS
59828-07-8
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
PUBCHEM
16219912
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
SMS_ID
100000092636
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
RXCUI
58918
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY RxNorm
EVMPD
SUB04050MIG
Created by admin on Fri Dec 15 15:23:50 UTC 2023 , Edited by admin on Fri Dec 15 15:23:50 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> SALT/SOLVATE
SOLVATE->ANHYDROUS
Related Record Type Details
ACTIVE MOIETY