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Details

Stereochemistry ACHIRAL
Molecular Formula C16H23NO4
Molecular Weight 293.3581
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROMOLATE

SMILES

CC(C)(OC1=CC=CC=C1)C(=O)OCCN2CCOCC2

InChI

InChIKey=GMISKEUWHIRDNK-UHFFFAOYSA-N
InChI=1S/C16H23NO4/c1-16(2,21-14-6-4-3-5-7-14)15(18)20-13-10-17-8-11-19-12-9-17/h3-7H,8-13H2,1-2H3

HIDE SMILES / InChI
Promolate is an Isobutyric acid derivative with potent antitussive activity. In preclinical studies, Promolate shows low toxicity in experimental animals and an antitussive action like that of codeine, but without the side effects of the latter. Promolate displayed a dose-dependent antitussive effect in conscious guinea pigs with coughing induced by NH3 aerosol. The activity of Promolate did not diminish when it was administered orally to guinea pigs for 20 days. Promolate also displayed a dose-dependent antitussive effect in Na barbital anesthetized cats with coughing induced by stimulation of the superior laryngeal nerve. High doses of Promolate administered to rats for 125 days did not provoke side effects.

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacological activities of a new antitussive agent: morphethylbutyne (2-phenoxy-isobutyric acid, 2-morpholine-ethyl ester).
1969 Apr
Patents

Sample Use Guides

guinea pig: 400-​1400 mg​/kg orally or rectally
Route of Administration: Oral
Name Type Language
PROMOLATE
INN   MART.   WHO-DD  
INN  
Official Name English
PROMOLATE [MART.]
Common Name English
Promolate [WHO-DD]
Common Name English
ATUSIL
Brand Name English
promolate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
Code System Code Type Description
ChEMBL
CHEMBL2106992
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
PRIMARY
NCI_THESAURUS
C73178
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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ECHA (EC/EINECS)
222-797-6
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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EVMPD
SUB10090MIG
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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FDA UNII
5WGM277OKR
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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EPA CompTox
DTXSID80189721
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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INN
2607
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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MESH
C022055
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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CAS
3615-74-5
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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PUBCHEM
71133
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
PRIMARY
SMS_ID
100000081147
Created by admin on Fri Dec 15 16:36:01 GMT 2023 , Edited by admin on Fri Dec 15 16:36:01 GMT 2023
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