Details
Stereochemistry | RACEMIC |
Molecular Formula | C20H26N2S.ClH |
Molecular Weight | 362.96 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.CCC1=CC2=C(SC3=C(C=CC=C3)N2CC(C)CN(C)C)C=C1
InChI
InChIKey=ZVSKDFRXWJPINY-UHFFFAOYSA-N
InChI=1S/C20H26N2S.ClH/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;1H
Approval Year
PubMed
Title | Date | PubMed |
---|---|---|
[Clinical study of a new phenothiazine derivative, RP-6484]. | 1960 Jun 11 |
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[On the clinical use in neuropsychiatry of 3-ethyl-10-(2-methyl-3-dimethylaminopropyl)-phenothiazine HCl (RP-6484), new phenothiazine neuroleptic]. | 1962 Jun 2 |
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[DEMENTIA PRAECOX. CURE BY RP-6484]. | 1963 Dec |
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
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Classification Tree | Code System | Code | ||
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NCI_THESAURUS |
C29578
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169471
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CHEMBL2008544
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71822
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m728
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3737-33-5
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DTXSID1045110
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A7002E7T2Z
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DBSALT001681
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C81141
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223-111-8
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ACTIVE MOIETY
SUBSTANCE RECORD