Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C10H14BrNO2.BrH |
| Molecular Weight | 341.04 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
Br.COC1=CC(CCN)=C(OC)C=C1Br
InChI
InChIKey=WGWOFNYIBCKZMV-UHFFFAOYSA-N
InChI=1S/C10H14BrNO2.BrH/c1-13-9-6-8(11)10(14-2)5-7(9)3-4-12;/h5-6H,3-4,12H2,1-2H3;1H
| Molecular Formula | C10H14BrNO2 |
| Molecular Weight | 260.128 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | BrH |
| Molecular Weight | 80.912 |
| 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 |
|---|---|---|
| WHO Expert Committee on Drug Dependence. Thirty-second report. | 2001 |
|
| [A case of acute psychotic episode after a single dose of ecstasy]. | 2001 Mar-Apr |
|
| Fluorometric determination of DL-fenfluramine, DL-norfenfluramine and phentermine in plasma by achiral and chiral high-performance liquid chromatography. | 2001 Nov 5 |
|
| Automated headspace solid-phase microextraction and in-matrix derivatization for the determination of amphetamine-related drugs in human urine by gas chromatography-mass spectrometry. | 2002 Jan |
|
| 4-Bromo-2,5-dimethoxyphenethylamine (2C-B) and structurally related phenylethylamines are potent 5-HT2A receptor antagonists in Xenopus laevis oocytes. | 2004 Apr |
|
| Metabolic pathways of 4-bromo-2,5-dimethoxyphenethylamine (2C-B): analysis of phase I metabolism with hepatocytes of six species including human. | 2005 Jan 5 |
|
| A study of the metabolism of methamphetamine and 4-bromo-2,5-dimethoxyphenethylamine (2C-B) in isolated rat hepatocytes. | 2005 Mar 10 |
|
| Comparative potencies of 3,4-methylenedioxymethamphetamine (MDMA) analogues as inhibitors of [3H]noradrenaline and [3H]5-HT transport in mammalian cell lines. | 2007 Dec |
|
| Disposition of 4-bromo-2,5-dimethoxyphenethylamine (2C-B) and its metabolite 4-bromo-2-hydroxy-5-methoxyphenethylamine in rats after subcutaneous administration. | 2008 Apr 21 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 18:39:04 GMT 2023
by
admin
on
Sat Dec 16 18:39:04 GMT 2023
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| Record UNII |
GE2MXV3PWY
|
| Record Status |
Validated (UNII)
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| Record Version |
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GE2MXV3PWY
Created by
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163203510
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2001061-73-8
Created by
admin on Sat Dec 16 18:39:04 GMT 2023 , Edited by admin on Sat Dec 16 18:39:04 GMT 2023
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ACTIVE MOIETY |
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