Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C19H25N2OS |
| Molecular Weight | 329.48 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Charge | 1 |
SHOW SMILES / InChI
SMILES
CC(CN1C2=CC=CC=C2SC3=CC=CC=C13)[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
| Molecular Formula | C19H24N2OS |
| Molecular Weight | 328.472 |
| Charge | 0 |
| Count |
|
| Stereochemistry | MIXED |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 2 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
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
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 23:24:37 GMT 2025
by
admin
on
Mon Mar 31 23:24:37 GMT 2025
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| Record UNII |
571559SLAJ
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| Record Status |
Validated (UNII)
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| Record Version |
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Preferred Name | English | ||
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Common Name | English | ||
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Systematic Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
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WHO-ATC |
R06AD55
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WHO-VATC |
QR06AD55
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WHO-ATC |
R06AD05
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admin on Mon Mar 31 23:24:37 GMT 2025 , Edited by admin on Mon Mar 31 23:24:37 GMT 2025
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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
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PRIMARY | |||
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Hydroxyethylpromethazine
Created by
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7647-63-4
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CHEMBL3707371
Created by
admin on Mon Mar 31 23:24:37 GMT 2025 , Edited by admin on Mon Mar 31 23:24:37 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |