Details
Stereochemistry | ACHIRAL |
Molecular Formula | C11H16N2O.ClH |
Molecular Weight | 228.718 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
Cl.COC1=CC=C(C=C1)N2CCNCC2
InChI
InChIKey=HFJDUYKRPHHPAX-UHFFFAOYSA-N
InChI=1S/C11H16N2O.ClH/c1-14-11-4-2-10(3-5-11)13-8-6-12-7-9-13;/h2-5,12H,6-9H2,1H3;1H
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 |
---|---|---|
Piperazine-like compounds: a new group of designer drugs-of-abuse on the European market. | 2001 Sep 15 |
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Screening for and validated quantification of amphetamines and of amphetamine- and piperazine-derived designer drugs in human blood plasma by gas chromatography/mass spectrometry. | 2003 Jun |
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In vivo metabolism of the new designer drug 1-(4-methoxyphenyl)piperazine (MeOPP) in rat and identification of the human cytochrome P450 enzymes responsible for the major metabolic step. | 2004 Feb |
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The effects of non-medically used psychoactive drugs on monoamine neurotransmission in rat brain. | 2007 Mar 22 |
|
4-(4-Methoxy-phen-yl)piperazin-1-ium chloride. | 2009 Feb 11 |
|
Structure-dependent inhibition of the human α1β2γ2 GABAA receptor by piperazine derivatives: A novel mode of action. | 2015 Dec |
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3019718
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ARJ7BR8SNG
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71661
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254-166-6
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38869-47-5
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admin on Sat Dec 16 11:08:35 GMT 2023 , Edited by admin on Sat Dec 16 11:08:35 GMT 2023
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ACTIVE MOIETY
SUBSTANCE RECORD