Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C13H21NO2S |
| Molecular Weight | 255.376 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCCSC1=C(OC)C=C(CCN)C(OC)=C1
InChI
InChIKey=OLEVEPDJOFPJTF-UHFFFAOYSA-N
InChI=1S/C13H21NO2S/c1-4-7-17-13-9-11(15-2)10(5-6-14)8-12(13)16-3/h8-9H,4-7,14H2,1-3H3
| Molecular Formula | C13H21NO2S |
| Molecular Weight | 255.376 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Postmortem identification and quantitation of 2,5-dimethoxy-4-n-propylthiophenethylamine using GC-MSD and GC-NPD. | 2003 Oct |
|
| Schedules of controlled substances; placement of 2,5-dimethoxy-4-(n)-propylthiophenethylamine and N-benzylpiperazine into Schedule I of the Controlled Substances Act. Final rule. | 2004 Mar 18 |
|
| New designer drug, 2,5-dimethoxy-4-propylthio-beta-phenethylamine (2C-T-7): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. | 2005 Jan |
|
| New trends in the cyber and street market of recreational drugs? The case of 2C-T-7 ('Blue Mystic'). | 2005 Nov |
|
| New designer drug 2,5-dimethoxy-4-ethylthio-beta-phenethylamine (2C-T-2): studies on its metabolism and toxicological detection in rat urine using gas chromatography/mass spectrometry. | 2005 Sep |
|
| Hallucinogen-like actions of 2,5-dimethoxy-4-(n)-propylthiophenethylamine (2C-T-7) in mice and rats. | 2005 Sep |
|
| Optimization of the separation and on-line sample concentration of phenethylamine designer drugs with capillary electrophoresis-fluorescence detection. | 2006 Jan 6 |
|
| Studies on the metabolism and toxicological detection of the designer drug 4-ethyl-2,5-dimethoxy-beta-phenethylamine (2C-E) in rat urine using gas chromatographic-mass spectrometric techniques. | 2006 Oct 2 |
|
| [Analysis of the chemical drugs among structural isomer]. | 2006 Sep |
|
| Determination of four thiophenethylamine designer drugs (2C-T-series) in human plasma by capillary electrophoresis with mass spectrometry detection. | 2007 Aug 3 |
|
| In vivo metabolism of 2,5-dimethoxy-4-propylthiophenethylamine in rat. | 2007 Jun |
|
| Discriminative stimulus effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rhesus monkeys. | 2008 Feb |
|
| Discriminative stimulus effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rhesus monkeys: antagonism and apparent pA2 analyses. | 2009 Mar |
|
| Discriminative stimulus effects of psychostimulants and hallucinogens in S(+)-3,4-methylenedioxymethamphetamine (MDMA) and R(-)-MDMA trained mice. | 2009 Nov |
|
| Differential effects of serotonin 5-HT1A receptor agonists on the discriminative stimulus effects of the 5-HT2A receptor agonist 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane in rats and rhesus monkeys. | 2010 Apr |
|
| Metabolism of designer drugs of abuse: an updated review. | 2010 Jun 1 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Thu Jul 06 12:36:25 UTC 2023
by
admin
on
Thu Jul 06 12:36:25 UTC 2023
|
| Record UNII |
TJG366J9BA
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Common Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
WIKIPEDIA |
Designer-drugs-2C-T-7
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
||
|
DEA NO. |
7348
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
||
|
WIKIPEDIA |
PiHKAL
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
207740-26-9
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY | |||
|
7554
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY | |||
|
24728635
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY | |||
|
DTXSID90861566
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY | |||
|
2C-T-7
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY | 2C (2C-x) is a general name for the family of psychedelic phenethylamines containing methoxy groups on the 2 and 5 positions of a benzene ring. Most of these compounds also carry lipophilic substituents at the 4 position, usually resulting in more potent and more metabolically stable and longer acting compounds. Most of the currently known 2C compounds were first synthesized by Alexander Shulgin in the 1970s and 1980s, and published in his book, PiHKAL (Phenethylamines i Have Known And Loved). Dr. Shulgin also invented the term 2C, being an acronym for the 2 carbon atoms between the benzene ring and the amino group.[1] Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628. | ||
|
DB01458
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY | |||
|
TJG366J9BA
Created by
admin on Thu Jul 06 12:36:25 UTC 2023 , Edited by admin on Thu Jul 06 12:36:25 UTC 2023
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
SALT/SOLVATE -> PARENT |
|
||
|
TARGET -> AGONIST |
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |
|
