Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C8H12N4 |
| Molecular Weight | 164.2077 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
C1CN(CCN1)C2=NC=CC=N2
InChI
InChIKey=MRBFGEHILMYPTF-UHFFFAOYSA-N
InChI=1S/C8H12N4/c1-2-10-8(11-3-1)12-6-4-9-5-7-12/h1-3,9H,4-7H2
| 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
| Title | Date | PubMed |
|---|---|---|
| The biphasic immunoregulation of pyrimidylpiperazine (Y-40138) is IL-10 sensitive and requires NF-kappa B targeting in the alveolar epithelium. | 2001 May |
|
| Pharmacological properties and SAR of new 1,4-disubstituted piperazine derivatives with hypnotic-sedative activity. | 2002 May |
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| Effects of the serotonergic anxiolytic buspirone on plasma glucose and glucose-induced hyperglycemia in mice. | 2003 Dec |
|
| Effect of the novel anxiolytic drug deramciclane on the pharmacokinetics and pharmacodynamics of the CYP3A4 probe drug buspirone. | 2003 Dec |
|
| Science review: redox and oxygen-sensitive transcription factors in the regulation of oxidant-mediated lung injury: role for hypoxia-inducible factor-1alpha. | 2003 Feb |
|
| Human cytochromes mediating gepirone biotransformation at low substrate concentrations. | 2003 Mar |
|
| Pharmacokinetic evaluation of gepirone immediate-release capsules and gepirone extended-release tablets in healthy volunteers. | 2003 Sep |
|
| 1-(2-pyrimidinyl)-piperazine, a buspirone metabolite, modulates bladder function in the anesthetized rat. | 2004 |
|
| The photocatalytic process as a tool to identify metabolitic products formed from dopant substances: the case of buspirone. | 2004 Apr 1 |
|
| 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 Apr |
|
| Cytochrome P450 3A-mediated metabolism of buspirone in human liver microsomes. | 2005 Apr |
|
| Cyp2D6 catalyzes 5-hydroxylation of 1-(2-pyrimidinyl)-piperazine, an active metabolite of several psychoactive drugs, in human liver microsomes. | 2005 Feb |
|
| Pharmacokinetics of buspirone in autistic children. | 2006 May |
|
| 6-Hydroxybuspirone is a major active metabolite of buspirone: assessment of pharmacokinetics and 5-hydroxytryptamine1A receptor occupancy in rats. | 2007 Aug |
|
| Mass spectrometry analysis of phosphopeptides after peptide carboxy group derivatization. | 2008 Nov 1 |
|
| Carboxy group derivatization for enhanced electron-transfer dissociation mass spectrometric analysis of phosphopeptides. | 2009 Aug |
|
| Cyndi: a multi-objective evolution algorithm based method for bioactive molecular conformational generation. | 2009 Mar 31 |
|
| Two-injection workflow for a liquid chromatography/LTQ-Orbitrap system to complete in vivo biotransformation characterization: demonstration with buspirone metabolite identification. | 2009 Sep |
|
| A new strategy for antidepressant prescription. | 2010 |
|
| Piperazinyl pyrimidine derivatives as potent gamma-secretase modulators. | 2010 Feb 1 |
|
| 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 May 12 |
|
| Moving towards supraspinal TRPV1 receptors for chronic pain relief. | 2010 Oct 11 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 15:32:16 GMT 2023
by
admin
on
Fri Dec 15 15:32:16 GMT 2023
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| Record UNII |
H3B5B38F56
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| Record Status |
Validated (UNII)
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| Record Version |
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244-135-5
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1078573
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Pyrimidinylpiperazine
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88747
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H3B5B38F56
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20980-22-7
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DTXSID00864967
Created by
admin on Fri Dec 15 15:32:16 GMT 2023 , Edited by admin on Fri Dec 15 15:32:16 GMT 2023
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| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> METABOLITE ACTIVE |
| Related Record | Type | Details | ||
|---|---|---|---|---|
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PARENT -> IMPURITY |
impurity detected at UV 240 nm
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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