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Details

Stereochemistry ACHIRAL
Molecular Formula C8H12N4.2ClH
Molecular Weight 237.13
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1-(2-PYRIMIDINYL)PIPERAZINE DIHYDROCHLORIDE

SMILES

Cl.Cl.C1CN(CCN1)C2=NC=CC=N2

InChI

InChIKey=ZNZGJSLHXOMREP-UHFFFAOYSA-N
InChI=1S/C8H12N4.2ClH/c1-2-10-8(11-3-1)12-6-4-9-5-7-12;;/h1-3,9H,4-7H2;2*1H

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C8H12N4
Molecular Weight 164.2077
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Moving towards supraspinal TRPV1 receptors for chronic pain relief.
2010-10-11
Synthesis and biological activity of some novel trifluoromethyl-substituted 1,2,4-triazole and bis(1,2,4-triazole) Mannich bases containing piperazine rings.
2010-05-12
Piperazinyl pyrimidine derivatives as potent gamma-secretase modulators.
2010-02-01
A new strategy for antidepressant prescription.
2010
Two-injection workflow for a liquid chromatography/LTQ-Orbitrap system to complete in vivo biotransformation characterization: demonstration with buspirone metabolite identification.
2009-09
Carboxy group derivatization for enhanced electron-transfer dissociation mass spectrometric analysis of phosphopeptides.
2009-08
Group 11 metal chemistry of a tetradentate ligand, phenylene-1,4-diaminotetra(phosphonite), p-C6H4[N{P(OC6H4OMe-o)2}2]2.
2009-04-20
Cyndi: a multi-objective evolution algorithm based method for bioactive molecular conformational generation.
2009-03-31
Mass spectrometry analysis of phosphopeptides after peptide carboxy group derivatization.
2008-11-01
Pharmacokinetic interaction between tandospirone and fluvoxamine in the rat contextual conditioned fear stress model and its functional consequence: Involvement of cytochrome P450 3A4.
2008-10
TRPV1: a target for next generation analgesics.
2008-06
Pharmacokinetics of 6-hydroxybuspirone and its enantiomers administered individually or following buspirone administration in humans.
2007-10
A novel p38 alpha MAPK inhibitor suppresses brain proinflammatory cytokine up-regulation and attenuates synaptic dysfunction and behavioral deficits in an Alzheimer's disease mouse model.
2007-09-04
6-Hydroxybuspirone is a major active metabolite of buspirone: assessment of pharmacokinetics and 5-hydroxytryptamine1A receptor occupancy in rats.
2007-08
Novel vanilloid receptor-1 antagonists: 3. The identification of a second-generation clinical candidate with improved physicochemical and pharmacokinetic properties.
2007-07-26
Pharmacokinetics of buspirone in autistic children.
2006-05
Oral buspirone causes a shift in the dose-response curve between the elevated-plus maze and Vogel conflict tests in Long-Evans rats: relation of brain levels of buspirone and 1-PP to anxiolytic action.
2005-05
Inhibitory effects of the 5-HT(1A) receptor agonist buspirone on stress-induced hyperglycemia in mice: involvement of insulin and a buspirone metabolite, 1-(2-pyrimidinyl)piperazine (1-PP).
2005-04
Cytochrome P450 3A-mediated metabolism of buspirone in human liver microsomes.
2005-04
Cyp2D6 catalyzes 5-hydroxylation of 1-(2-pyrimidinyl)-piperazine, an active metabolite of several psychoactive drugs, in human liver microsomes.
2005-02
Combination benefit of a pyrimidylpiperazine derivative (Y-40138) and methotrexate in arthritic rats.
2004-08-30
The photocatalytic process as a tool to identify metabolitic products formed from dopant substances: the case of buspirone.
2004-04-01
1-(2-pyrimidinyl)-piperazine, a buspirone metabolite, modulates bladder function in the anesthetized rat.
2004
Effects of the serotonergic anxiolytic buspirone on plasma glucose and glucose-induced hyperglycemia in mice.
2003-12
Effect of the novel anxiolytic drug deramciclane on the pharmacokinetics and pharmacodynamics of the CYP3A4 probe drug buspirone.
2003-12
Pharmacokinetic evaluation of gepirone immediate-release capsules and gepirone extended-release tablets in healthy volunteers.
2003-09
Human cytochromes mediating gepirone biotransformation at low substrate concentrations.
2003-03
Science review: redox and oxygen-sensitive transcription factors in the regulation of oxidant-mediated lung injury: role for hypoxia-inducible factor-1alpha.
2003-02
In vivo comparison of two 5-HT1A receptors agonists alnespirone (S-20499) and buspirone on locus coeruleus neuronal activity.
2003-01-10
Pharmacokinetic-pharmacodynamic modeling of buspirone and its metabolite 1-(2-pyrimidinyl)-piperazine in rats.
2002-12
Pharmacological properties and SAR of new 1,4-disubstituted piperazine derivatives with hypnotic-sedative activity.
2002-05
Factors explaining variance in perceived pain in women with fibromyalgia.
2002-04-25
Oxygen-sensing mechanisms and the regulation of redox-responsive transcription factors in development and pathophysiology.
2002
Pharmacokinetics and tolerability of buspirone during oral administration to children and adolescents with anxiety disorder and normal healthy adults.
2001-12
Conformational analysis and pharmacophore design for selected 1-(2-pyrimidinyl)piperazine derivatives with sedative-hypnotic activity.
2001-08-15
A comparative multidose pharmacokinetic study of buspirone extended-release tablets with a reference immediate-release product.
2001-08
Pharmacokinetics of buspirone extended-release tablets: a single-dose study.
2001-07
The biphasic immunoregulation of pyrimidylpiperazine (Y-40138) is IL-10 sensitive and requires NF-kappa B targeting in the alveolar epithelium.
2001-05
Patents
Substance Class Chemical
Created
by admin
on Wed Apr 02 19:23:13 GMT 2025
Edited
by admin
on Wed Apr 02 19:23:13 GMT 2025
Record UNII
SLC2P2PLG8
Record Status Validated (UNII)
Record Version
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Name Type Language
1-(2-PYRIMIDINYL)PIPERAZINE DIHYDROCHLORIDE
Common Name English
2-PIPERAZINYLPYRIMIDINE DIHYDROCHLORIDE
Preferred Name English
1-PP dihydrochloride
Common Name English
Code System Code Type Description
CAS
94021-22-4
Created by admin on Wed Apr 02 19:23:13 GMT 2025 , Edited by admin on Wed Apr 02 19:23:13 GMT 2025
PRIMARY
PUBCHEM
11680272
Created by admin on Wed Apr 02 19:23:13 GMT 2025 , Edited by admin on Wed Apr 02 19:23:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
301-415-2
Created by admin on Wed Apr 02 19:23:13 GMT 2025 , Edited by admin on Wed Apr 02 19:23:13 GMT 2025
PRIMARY
FDA UNII
SLC2P2PLG8
Created by admin on Wed Apr 02 19:23:13 GMT 2025 , Edited by admin on Wed Apr 02 19:23:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID70240234
Created by admin on Wed Apr 02 19:23:13 GMT 2025 , Edited by admin on Wed Apr 02 19:23:13 GMT 2025
PRIMARY
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