Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H16N2O |
Molecular Weight | 192.2575 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC=C(C=C1)N2CCNCC2
InChI
InChIKey=MRDGZSKYFPGAKP-UHFFFAOYSA-N
InChI=1S/C11H16N2O/c1-14-11-4-2-10(3-5-11)13-8-6-12-7-9-13/h2-5,12H,6-9H2,1H3
Molecular Formula | C11H16N2O |
Molecular Weight | 192.2575 |
Charge | 0 |
Count |
|
Stereochemistry | ACHIRAL |
Additional Stereochemistry | No |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Optical Activity | NONE |
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: CHEMBL213 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1347318 |
38000.0 nM [IC50] | ||
Target ID: CHEMBL287 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1662725 |
5850.0 nM [IC50] |
PubMed
Title | Date | PubMed |
---|---|---|
The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. | 2007 Mar 22 |
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4-(4-Methoxy-phen-yl)piperazin-1-ium chloride. | 2009 Feb 11 |
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Analysis of phenylpiperazine-like stimulants in human hair as trimethylsilyl derivatives by gas chromatography-mass spectrometry. | 2010 Oct 1 |
|
Structure-dependent inhibition of the human α1β2γ2 GABAA receptor by piperazine derivatives: A novel mode of action. | 2015 Dec |
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 11:10:45 GMT 2023
by
admin
on
Sat Dec 16 11:10:45 GMT 2023
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Record UNII |
P385M92GYG
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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-Methoxyphenylpiperazine
Created by
admin on Sat Dec 16 11:10:45 GMT 2023 , Edited by admin on Sat Dec 16 11:10:45 GMT 2023
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P385M92GYG
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PARA-METHOXYPHENYLPIPERAZINE
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DTXSID30191591
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253-829-7
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269722
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38212-30-5
Created by
admin on Sat Dec 16 11:10:45 GMT 2023 , Edited by admin on Sat Dec 16 11:10:45 GMT 2023
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Related Record | Type | Details | ||
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SALT/SOLVATE -> PARENT |
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Related Record | Type | Details | ||
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ACTIVE MOIETY |