Details
Stereochemistry | RACEMIC |
Molecular Formula | C19H25N2OS |
Molecular Weight | 329.48 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 1 |
SHOW SMILES / InChI
SMILES
CC(CN1C2=C(SC3=C1C=CC=C3)C=CC=C2)[N+](C)(C)CCO
InChI
InChIKey=PDSVTRQOBUIQBQ-UHFFFAOYSA-N
InChI=1S/C19H25N2OS/c1-15(21(2,3)12-13-22)14-20-16-8-4-6-10-18(16)23-19-11-7-5-9-17(19)20/h4-11,15,22H,12-14H2,1-3H3/q+1
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/4386346
Sources: https://www.ncbi.nlm.nih.gov/pubmed/4386346
Promethazine hydroxyethyl quaternary derivative of promethazine with antihistamine and anticholinergic properties. The drug lacked the sedative properties of promethazine. It was used in the clinic under tradename Aprobit.
Approval Year
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Classification Tree | Code System | Code | ||
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WHO-ATC |
R06AD55
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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WHO-VATC |
QR06AD55
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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WHO-ATC |
R06AD05
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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Code System | Code | Type | Description | ||
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DTXSID30871861
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4571
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571559SLAJ
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16406
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DB13840
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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Hydroxyethylpromethazine
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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7647-63-4
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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CHEMBL3707371
Created by
admin on Sat Dec 16 10:44:09 GMT 2023 , Edited by admin on Sat Dec 16 10:44:09 GMT 2023
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PRIMARY |
ACTIVE MOIETY
SALT/SOLVATE (PARENT)