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Details

Stereochemistry ACHIRAL
Molecular Formula C5H10N2O
Molecular Weight 114.1457
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of N-NITROSOPIPERIDINE

SMILES

O=NN1CCCCC1

InChI

InChIKey=UWSDONTXWQOZFN-UHFFFAOYSA-N
InChI=1S/C5H10N2O/c8-6-7-4-2-1-3-5-7/h1-5H2

HIDE SMILES / InChI

Molecular Formula C5H10N2O
Molecular Weight 114.1457
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
New short term prediction method for chemical carcinogenicity by hepatic transcript profiling following 28-day toxicity tests in rats.
2011
Determination of volatile nitrosamines in various meat products using comprehensive gas chromatography-nitrogen chemiluminescence detection.
2010-11
UVA activation of N-dialkylnitrosamines releasing nitric oxide, producing strand breaks as well as oxidative damages in DNA, and inducing mutations in the Ames test.
2010-09-10
Bronchogenic and alveologenic tumors in mice induced by N-nitrosopiperidine.
2010-08
Radical mechanisms in nitrosamine- and nitrosamide-induced whole-genome gene expression modulations in Caco-2 cells.
2010-07
Development of an in vitro system combining aqueous and lipid phases as a tool to understand gastric nitrosation.
2010-03-15
Screening of N-nitrosamines in tap and swimming pool waters using fast gas chromatography.
2010-03
N-Nitrosopiperidine and N-Nitrosodibutylamine induce apoptosis in HepG2 cells via the caspase dependent pathway.
2009-12
Myricetin, quercetin, (+)-catechin and (-)-epicatechin protect against N-nitrosamines-induced DNA damage in human hepatoma cells.
2009-10
Antiapoptotic effects of dietary antioxidants towards N-nitrosopiperidine and N-nitrosodibutylamine-induced apoptosis in HL-60 and HepG2 cells.
2009-07
Biogenic amines in fish: roles in intoxication, spoilage, and nitrosamine formation--a review.
2009-04
Molecular signatures of N-nitroso compounds in Caco-2 cells: implications for colon carcinogenesis.
2009-04
Identification of N-nitrosamines in treated drinking water using nanoelectrospray ionization high-field asymmetric waveform ion mobility spectrometry with quadrupole time-of-flight mass spectrometry.
2009-01
Synthesis of new 4-[2-(4-methyl(amino)sulfonylphenyl)-5-trifluoromethyl-2H-pyrazol-3-yl]-1,2,3,6-tetrahydropyridines: a search for novel nitric oxide donor anti-inflammatory agents.
2008-10-01
A cell-microelectronic sensing technique for profiling cytotoxicity of chemicals.
2008-05-12
Organosulfur compounds alone or in combination with vitamin C protect towards N-nitrosopiperidine- and N-nitrosodibutylamine-induced oxidative DNA damage in HepG2 cells.
2008-05-09
Induction of apoptosis and reactive oxygen species production by N-nitrosopiperidine and N-nitrosodibutylamine in human leukemia cells.
2008-05
Protective effects of isothiocyanates alone or in combination with vitamin C towards N-nitrosodibutylamine or N-nitrosopiperidine-induced oxidative DNA damage in the single-cell gel electrophoresis (SCGE)/HepG2 assay.
2008-03
Nitrosamine carcinogens also swim in chlorinated pools.
2008-02-15
N-nitrosodimethylamine (NDMA) removal by reverse osmosis and UV treatment and analysis via LC-MS/MS.
2008-01
Fat transforms ascorbic acid from inhibiting to promoting acid-catalysed N-nitrosation.
2007-12
Protective effect of vitamin C towards N-nitrosamine-induced DNA damage in the single-cell gel electrophoresis (SCGE)/HepG2 assay.
2007-10
Photochemical attenuation of N-nitrosodimethylamine (NDMA) and other nitrosamines in surface water.
2007-09-01
Evaluating the impacts of membrane type, coating, fouling, chemical properties and water chemistry on reverse osmosis rejection of seven nitrosoalklyamines, including NDMA.
2007-09
Analysis of nitrosamines by capillary electrospray-high-field asymmetric waveform ion mobility spectrometry-MS with programmed compensation voltage.
2007-05
Characterization of new nitrosamines in drinking water using liquid chromatography tandem mass spectrometry.
2006-12-15
Fate and transport of N-nitrosamines under conditions simulating full-scale groundwater recharge operations.
2006-12
[The promotive effects of N-nitrosopiperidine on the malignant transformation of the immortalized esophageal epithelium induced by human papillomavirus].
2006-06
Occurrence of N-nitrosodimethylamine in South Korean and imported alcoholic beverages.
2005-11
Automated solid-phase extraction and high-performance liquid chromatographic determination of nitrosamines using post-column photolysis and tris(2,2'-bipyridyl) ruthenium(III) chemiluminescence.
2005-06-03
Cytochrome P450 2A-catalyzed metabolic activation of structurally similar carcinogenic nitrosamines: N'-nitrosonornicotine enantiomers, N-nitrosopiperidine, and N-nitrosopyrrolidine.
2005-01
DNA damage and cytotoxicity in pancreatic beta-cells expressing human CYP2E1.
2004-08-01
Stereochemical effects in the metabolic activation of nitrosopiperidines: correlations with genotoxicity.
2004-03-14
N-Nitrosopiperidine.
2004
Preferential metabolic activation of N-nitrosopiperidine as compared to its structural homologue N-nitrosopyrrolidine by rat nasal mucosal microsomes.
2003-10
Extended-term cultures of human T-lymphocytes and the comet assay: a useful combination when testing for genotoxicity in vitro?
2003-09-09
Development of a new method for the determination of nitrosamines by micellar electrokinetic capillary chromatography.
2003-09
Comparative metabolism of N-nitrosopiperidine and N-nitrosopyrrolidine by rat liver and esophageal microsomes and cytochrome P450 2A3.
2003-02
Intake of volatile N-nitrosamines and their ability to exogenously synthesize in the diet of inhabitants from high-risk area of esophageal cancer in southern China.
2002-12
Dietary exposure and urinary excretion of total N-nitroso compounds, nitrosamino acids and volatile nitrosamine in inhabitants of high- and low-risk areas for esophageal cancer in southern China.
2002-11-20
Role of human cytochrome P450 (CYP) in the metabolic activation of nitrosamine derivatives: application of genetically engineered Salmonella expressing human CYP.
2002-08
Fast microwave-assisted dansylation of N-nitrosamines. Analysis by high-performance liquid chromatography with fluorescence detection.
2002-02-08
N-Nitrosopiperidine.
2002
Predicting the mutagenicity of tobacco-related N-nitrosamines in humans using 11 strains of Salmonella typhimurium YG7108, each coexpressing a form of human cytochrome P450 along with NADPH-cytochrome P450 reductase.
2001
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:19 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:19 GMT 2025
Record UNII
6N066XUL4L
Record Status Validated (UNII)
Record Version
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Name Type Language
N-NITROSOPIPERIDINE
HSDB  
Systematic Name English
NSC-138
Preferred Name English
NPI
Common Name English
NITROSOPIPERIDINE, N-
Systematic Name English
1-NITROSOPIPERIDINE
Systematic Name English
N-NITROSOPIPERIDINE [IARC]
Common Name English
NPIP
Common Name English
N-NITROSOPIPERIDINE [HSDB]
Common Name English
PIPERIDINE, 1-NITROSO-
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C45402
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
Code System Code Type Description
FDA UNII
6N066XUL4L
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
MESH
C002743
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
NSC
138
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
HSDB
5115
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
PUBCHEM
7526
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
CHEBI
76324
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
CAS
100-75-4
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
NCI_THESAURUS
C44423
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-886-6
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY
EPA CompTox
DTXSID8021060
Created by admin on Mon Mar 31 19:15:19 GMT 2025 , Edited by admin on Mon Mar 31 19:15:19 GMT 2025
PRIMARY