Page last updated: 2024-12-06

1-nitrosoindole-3-acetonitrile

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

Description

1-Nitrosoindole-3-acetonitrile is a chemical compound that belongs to the indole family. It has the following chemical formula:

**C9H6N2O**

Here's a breakdown of its features and importance:

**Structure:**

* **Indole core:** The molecule contains the indole ring system, which is a fundamental building block in many natural products and pharmaceuticals.
* **Nitroso group:** The nitrogen atom in the nitroso group (-NO) is directly attached to the indole ring.
* **Acetonitrile group:** This is a functional group with the formula -CH2CN.

**Importance in Research:**

1-Nitrosoindole-3-acetonitrile has gained attention in research due to its diverse potential applications. It exhibits:

* **Antibacterial activity:** Studies have shown that this compound can inhibit the growth of certain bacteria, including **Mycobacterium tuberculosis**, which is the causative agent of tuberculosis.
* **Antioxidant properties:** It can scavenge free radicals, protecting cells from damage caused by oxidative stress.
* **Potential for drug development:** The compound's biological activities make it a promising candidate for the development of new drugs against various diseases, including bacterial infections and neurodegenerative disorders.
* **Synthetic versatility:** The nitroso group can be readily transformed into other functional groups, making it a valuable synthetic intermediate for organic chemistry research.

**Research areas of focus:**

* **Tuberculosis research:** Its antibacterial activity against Mycobacterium tuberculosis makes it a valuable tool for studying the disease and potentially developing new treatment strategies.
* **Neuroprotective effects:** Investigations are ongoing to understand the mechanism by which this compound might protect brain cells from damage.
* **Organic synthesis:** Chemists are exploring various chemical reactions involving 1-nitrosoindole-3-acetonitrile to synthesize new and useful molecules.

**Important note:** While 1-nitrosoindole-3-acetonitrile shows promising potential in research, it's crucial to remember that it's still in the early stages of investigation. More research is required to fully understand its properties, safety, and potential clinical applications.

In conclusion, 1-nitrosoindole-3-acetonitrile is an intriguing compound with a unique combination of structural features and biological activities. It is attracting the attention of researchers for its potential in fighting bacterial infections, combating oxidative stress, and potentially developing new drug therapies.

1-nitrosoindole-3-acetonitrile: induces ornithine decarboxylase activity in rats [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID57273
MeSH IDM0150431

Synonyms (13)

Synonym
1-nitrosoindole-3-acetonitrile
nitrosated indole-3-acetonitrile
ccris 7732
1h-indole-3-acetonitrile, 1-nitroso-
2-(1-nitrosoindol-3-yl)acetonitrile
AKOS006277373
unii-0s8432ks6r
0s8432ks6r ,
97672-08-7
1-nitroso-1h-indole-3-acetonitrile
J533.292C ,
DTXSID50243122
Q27237181

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The former pathway was clearly the most important, and all reaction products exhibited a dose-response relationship."( Characterization of DNA damage at purine residues in oligonucleotides and calf thymus DNA induced by the mutagen 1-nitrosoindole-3-acetonitrile.
Gatehouse, D; Jones, GD; Lucas, LT; Shuker, DE, 2001
)
0.52
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (8)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (37.50)18.7374
1990's2 (25.00)18.2507
2000's1 (12.50)29.6817
2010's1 (12.50)24.3611
2020's1 (12.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.49

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 Index12.49 (24.57)
Research Supply Index2.20 (2.92)
Research Growth Index4.69 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.49)

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%
Other8 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]