Details
Stereochemistry | RACEMIC |
Molecular Formula | C10H15NS |
Molecular Weight | 181.298 |
Optical Activity | ( + / - ) |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CSC1=CC=C(CC(C)N)C=C1
InChI
InChIKey=OLEWMKVPSUCNLG-UHFFFAOYSA-N
InChI=1S/C10H15NS/c1-8(11)7-9-3-5-10(12-2)6-4-9/h3-6,8H,7,11H2,1-2H3
Molecular Formula | C10H15NS |
Molecular Weight | 181.298 |
Charge | 0 |
Count |
|
Stereochemistry | RACEMIC |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 1 |
E/Z Centers | 0 |
Optical Activity | ( + / - ) |
Approval Year
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:18:29 GMT 2023
by
admin
on
Sat Dec 16 08:18:29 GMT 2023
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Record UNII |
6JP2T8KXTR
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Record Status |
Validated (UNII)
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Record Version |
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-
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WIKIPEDIA |
Designer-drugs-4-MTA
Created by
admin on Sat Dec 16 08:18:29 GMT 2023 , Edited by admin on Sat Dec 16 08:18:29 GMT 2023
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Code System | Code | Type | Description | ||
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DTXSID90894854
Created by
admin on Sat Dec 16 08:18:29 GMT 2023 , Edited by admin on Sat Dec 16 08:18:29 GMT 2023
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PRIMARY | |||
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151900
Created by
admin on Sat Dec 16 08:18:29 GMT 2023 , Edited by admin on Sat Dec 16 08:18:29 GMT 2023
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PRIMARY | |||
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4-METHYLTHIOAMPHETAMINE
Created by
admin on Sat Dec 16 08:18:29 GMT 2023 , Edited by admin on Sat Dec 16 08:18:29 GMT 2023
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PRIMARY | 4-Methylthioamphetamine (4-MTA) is a designer drug developed in the 1990s by a team led by David E. Nichols at Purdue University. It acts as a non-neurotoxic highly selective serotonin releasing agent (SSRA) in animals. It is distantly related to several other SSRAs, including MMAI, MDAI, and MDMAI. | ||
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14116-06-4
Created by
admin on Sat Dec 16 08:18:29 GMT 2023 , Edited by admin on Sat Dec 16 08:18:29 GMT 2023
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PRIMARY | |||
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6JP2T8KXTR
Created by
admin on Sat Dec 16 08:18:29 GMT 2023 , Edited by admin on Sat Dec 16 08:18:29 GMT 2023
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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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Related Record | Type | Details | ||
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ACTIVE MOIETY |