Page last updated: 2024-12-06

1-nitrosopiperazine

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

1-Nitrosopiperazine, also known as **N-nitrosopiperazine**, is a **potent nitrosamine**. Nitrosamines are a class of chemical compounds that are generally considered **carcinogenic** (cancer-causing).

Here's why it's important for research:

**1. Understanding Carcinogenesis:**

* 1-Nitrosopiperazine has been found in various food products, drinking water, and even tobacco smoke.
* Research on this compound helps scientists understand the mechanisms of nitrosamine-induced carcinogenesis. This knowledge is crucial for developing strategies to prevent or mitigate the risk of cancer.

**2. Toxicology Studies:**

* Researchers use 1-Nitrosopiperazine as a model compound to study the toxic effects of nitrosamines.
* This research helps evaluate the risk posed by these compounds and identify potential biomarkers for exposure.

**3. Environmental Monitoring:**

* Monitoring for 1-Nitrosopiperazine and other nitrosamines in environmental samples (like water, soil, and air) provides information about potential contamination sources and helps assess public health risks.

**4. Food Safety:**

* Research on 1-Nitrosopiperazine is crucial for developing safer food processing techniques and minimizing the formation of nitrosamines in food products.

**5. Drug Development:**

* Understanding the mechanisms of action of 1-Nitrosopiperazine can aid in the development of drugs that target specific pathways involved in carcinogenesis.

**Safety Concerns:**

* 1-Nitrosopiperazine is a **potent carcinogen** and should be handled with extreme caution in research settings.
* Strict safety protocols are essential to minimize exposure and prevent health risks.

**In summary**, 1-Nitrosopiperazine is an important research compound due to its role in understanding carcinogenesis, toxicology, environmental monitoring, food safety, and drug development. However, its carcinogenic nature requires researchers to prioritize safety and handle it with extreme care.

Cross-References

ID SourceID
PubMed CID21845
CHEMBL ID1333
CHEBI ID179298
SCHEMBL ID1678714
MeSH IDM0063458

Synonyms (37)

Synonym
nsc-50269
AKOS002337536
n-mononitrosopiperazine
CHEBI:179298
nsc 525340
ccris 6928
brn 0112147
nsc525340
5632-47-3
wln: t6m dntj dno
mononitrosopiperazine
n-nitrosopiperazine
nsc-525340
piperazine, 1-nitroso-
1-nitrosopiperazine
CHEMBL1333
nitrosopiperazine
dtxcid201059
tox21_202786
cas-5632-47-3
dtxsid9021059 ,
NCGC00260332-01
ruf459i8ks ,
unii-ruf459i8ks
FT-0672986
FT-0672987
n-nitroso piperazine
n-nitroso-piperazine
SCHEMBL1678714
nitrosopiperazine, 1-
1-nitrosopiperazine-
n-nitrosopiperazine (npaz)
CS-0106309
Q27888779
D76638
EN300-179415
Z1198149478
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
phytanoyl-CoAs
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Protein Targets (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency32.15240.006038.004119,952.5996AID1159521; AID1159523
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency76.11920.003041.611522,387.1992AID1159552; AID1159555
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency17.55320.001530.607315,848.9004AID1224841; AID1259401
activating transcription factor 6Homo sapiens (human)Potency68.43220.143427.612159.8106AID1159516
heat shock protein beta-1Homo sapiens (human)Potency24.28070.042027.378961.6448AID743210; AID743228
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID226733Carcinogenic potency modelled in silico, (- = non-carcinogen)1982Journal of medicinal chemistry, Jul, Volume: 25, Issue:7
Computer-assisted studies of structure-activity relationships of N-nitroso compounds using pattern recognition.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (16)

TimeframeStudies, This Drug (%)All Drugs %
pre-199010 (62.50)18.7374
1990's4 (25.00)18.2507
2000's0 (0.00)29.6817
2010's1 (6.25)24.3611
2020's1 (6.25)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 32.09

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index32.09 (24.57)
Research Supply Index2.83 (2.92)
Research Growth Index4.57 (4.65)
Search Engine Demand Index37.47 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (32.09)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (6.25%)4.05%
Observational0 (0.00%)0.25%
Other15 (93.75%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]