Page last updated: 2024-11-06

n-nitrosothiazolidine

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

Description

N-nitrosothiazolidine is a heterocyclic compound that has been studied for its potential carcinogenic properties. It is formed as a byproduct of the reaction of thiazolidine with nitrous acid, which can occur under conditions of high nitrite concentration. The compound has been detected in various food products, such as cured meats, smoked fish, and beer, and has been shown to be mutagenic in bacterial assays. Research on N-nitrosothiazolidine focuses on understanding its formation pathways, its toxicity and potential carcinogenicity, and methods for reducing its levels in food. The compound's importance lies in its potential health risks and the need to develop strategies for minimizing human exposure.'

N-nitrosothiazolidine: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID52687
CHEBI ID7329
MeSH IDM0124711

Synonyms (15)

Synonym
73870-33-4
n-nitroso-1,3-thiazolidine
3-nitrosothiazolidine
ccris 5493
n-nitrosothiazolidine
thiazolidine, 3-nitroso-
3-nitroso-1,3-thiazolidine
AKOS006272878
DTXSID70224458
CHEBI:7329
PROHBUGJUQHONA-UHFFFAOYSA-N
3-nitroso-1,3-thiazolidine #
ag-g-92849
n-nitrosothiazolidin
Q27107476
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
nitrosamineN-Nitroso amines, compounds of the structure R2NNO. Compounds RNHNO are not ordinarily isolable, but they, too, are nitrosamines. The name is a contraction of N-nitrosoamine and, as such, does not require the N locant.
thiazolidines
[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]

Research

Studies (12)

TimeframeStudies, This Drug (%)All Drugs %
pre-19909 (75.00)18.7374
1990's2 (16.67)18.2507
2000's0 (0.00)29.6817
2010's1 (8.33)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.38

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index11.38 (24.57)
Research Supply Index2.77 (2.92)
Research Growth Index4.15 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.38)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other15 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]