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
SMILES
O=NN1CCCCC1
InChI
InChIKey=UWSDONTXWQOZFN-UHFFFAOYSA-N
InChI=1S/C5H10N2O/c8-6-7-4-2-1-3-5-7/h1-5H2
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
Title | Date | PubMed |
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Cytochrome P450 2A-catalyzed metabolic activation of structurally similar carcinogenic nitrosamines: N'-nitrosonornicotine enantiomers, N-nitrosopiperidine, and N-nitrosopyrrolidine. | 2005 Jan |
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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 Jun 3 |
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Protective effect of vitamin C towards N-nitrosamine-induced DNA damage in the single-cell gel electrophoresis (SCGE)/HepG2 assay. | 2007 Oct |
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Evaluating the impacts of membrane type, coating, fouling, chemical properties and water chemistry on reverse osmosis rejection of seven nitrosoalklyamines, including NDMA. | 2007 Sep |
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Induction of apoptosis and reactive oxygen species production by N-nitrosopiperidine and N-nitrosodibutylamine in human leukemia cells. | 2008 May |
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Molecular signatures of N-nitroso compounds in Caco-2 cells: implications for colon carcinogenesis. | 2009 Apr |
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Antiapoptotic effects of dietary antioxidants towards N-nitrosopiperidine and N-nitrosodibutylamine-induced apoptosis in HL-60 and HepG2 cells. | 2009 Jul |
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Bronchogenic and alveologenic tumors in mice induced by N-nitrosopiperidine. | 2010 Aug |
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Determination of volatile nitrosamines in various meat products using comprehensive gas chromatography-nitrogen chemiluminescence detection. | 2010 Nov |
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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 Sep 10 |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:33:09 GMT 2023
by
admin
on
Fri Dec 15 18:33:09 GMT 2023
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Record UNII |
6N066XUL4L
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Record Status |
Validated (UNII)
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Record Version |
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NCI_THESAURUS |
C45402
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6N066XUL4L
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C002743
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138
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76324
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100-75-4
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C44423
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202-886-6
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DTXSID8021060
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