Details
| Stereochemistry | RACEMIC |
| Molecular Formula | C20H26N2S |
| Molecular Weight | 326.499 |
| Optical Activity | ( + / - ) |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=CC=C2SC3=CC=CC=C3N(CC(C)CN(C)C)C2=C1
InChI
InChIKey=USKHCLAXJXCWMO-UHFFFAOYSA-N
InChI=1S/C20H26N2S/c1-5-16-10-11-20-18(12-16)22(14-15(2)13-21(3)4)17-8-6-7-9-19(17)23-20/h6-12,15H,5,13-14H2,1-4H3
| Molecular Formula | C20H26N2S |
| Molecular Weight | 326.499 |
| Charge | 0 |
| Count |
|
| Stereochemistry | RACEMIC |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 1 |
| E/Z Centers | 0 |
| Optical Activity | ( + / - ) |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| [DEMENTIA PRAECOX. CURE BY RP-6484]. | 1963-12 |
|
| [On the clinical use in neuropsychiatry of 3-ethyl-10-(2-methyl-3-dimethylaminopropyl)-phenothiazine HCl (RP-6484), new phenothiazine neuroleptic]. | 1962-06-02 |
|
| [Clinical study of a new phenothiazine derivative, RP-6484]. | 1960-06-11 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/5668177
Pigs: Ethyl isobutrazine (Etymemazine) and pethidine were each administered
at a dose rate of 5 mg/kg
Route of Administration:
Intramuscular
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:19:33 GMT 2025
by
admin
on
Mon Mar 31 19:19:33 GMT 2025
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| Record UNII |
861J4K81C7
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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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Official Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Common Name | English | ||
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Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
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NCI_THESAURUS |
C29756
Created by
admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
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CFR |
21 CFR 520.863
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admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
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NCI_THESAURUS |
C29578
Created by
admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
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CFR |
21 CFR 522.863
Created by
admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
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| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
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861J4K81C7
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3742
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100000082117
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SUB07349MIG
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1391
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523-54-6
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CHEMBL2008544
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DB11517
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71823
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C73062
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PRIMARY | |||
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DTXSID0046935
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m728
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admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
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PRIMARY | Merck Index | ||
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ETYMEMAZINE
Created by
admin on Mon Mar 31 19:19:33 GMT 2025 , Edited by admin on Mon Mar 31 19:19:33 GMT 2025
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PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ENANTIOMER -> RACEMATE | |||
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SALT/SOLVATE -> PARENT | |||
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ENANTIOMER -> RACEMATE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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ACTIVE MOIETY |