Page last updated: 2024-12-05

1,8-pyrenequinone

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

Description

1,8-pyrenequinone (also known as 1,8-PQ) is a **quinone derivative of pyrene**, a polycyclic aromatic hydrocarbon (PAH). It's a **highly reactive and cytotoxic compound** with a significant role in various research fields, including:

**1. Chemical Biology & Drug Discovery:**

* **Anti-cancer activity:** 1,8-PQ has demonstrated **anti-proliferative effects** against several cancer cell lines, making it a potential lead compound for developing new cancer therapies. Its mechanism of action involves **inducing apoptosis (programmed cell death)** and inhibiting cell growth.
* **Antioxidant and Anti-inflammatory properties:** 1,8-PQ exhibits **radical scavenging activity**, suggesting potential applications as an antioxidant in various biological systems. It can also **inhibit inflammation** by modulating signaling pathways involved in inflammatory responses.
* **Targeting specific biological processes:** 1,8-PQ can **interact with specific proteins and enzymes** involved in key biological processes like cell signaling and DNA replication. This property is being explored for designing drugs that target these specific pathways.

**2. Environmental Science and Toxicology:**

* **Environmental pollutants:** 1,8-PQ is a **product of pyrene oxidation**, which occurs during combustion processes and environmental degradation of PAHs. Studying its formation and environmental fate is crucial for understanding the impact of PAHs on human health and the environment.
* **Bioremediation:** 1,8-PQ is a **substrate for certain bacterial enzymes**, which can be utilized in **bioremediation strategies** to degrade and remove pyrene and other PAHs from contaminated environments.
* **Toxicity assessment:** Research on 1,8-PQ helps understand the **toxicological effects of PAHs**, including its potential to induce oxidative stress and genotoxicity.

**3. Materials Science and Nanotechnology:**

* **Organic semiconductors:** 1,8-PQ is a **potential component of organic semiconductors** due to its unique electronic properties. It can act as an electron acceptor, contributing to the charge transport in these materials.
* **Organic light-emitting diodes (OLEDs):** 1,8-PQ is explored for its potential to **enhance the performance of OLEDs** by improving charge injection and carrier transport.
* **Sensors and imaging:** The strong fluorescence properties of 1,8-PQ can be harnessed for **developing fluorescent probes and sensors** for various applications, including detecting specific analytes and imaging biological processes.

**In summary, 1,8-pyrenequinone is a versatile molecule with potential applications in various fields.** Its unique properties, including its reactivity, cytotoxicity, and fluorescence, make it a valuable subject for research aimed at developing new drugs, understanding environmental hazards, and advancing materials science.

1,8-pyrenequinone: RN given refers to cpd with locants for oxo moiety in positions 1 & 8 [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID16820
CHEBI ID81609
SCHEMBL ID236503
MeSH IDM0098143

Synonyms (20)

Synonym
pyrene-1,8-dione
1,8-pyrenequinone
1,8-pyrenedione
3,10-pyrenequinone
ccris 5486
3,10-pyrenedione
einecs 218-966-9
brn 1963134
2304-85-0
C18258
n55g3tlc7d ,
unii-n55g3tlc7d
3,6-pyrenequinone
3,6-pyrenedione
SCHEMBL236503
CHEBI:81609
DTXSID8062317
1,8-pyrene quinone
Q27155496
1,8-dihydropyrene-1,8-dione
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
pyrenes
[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 (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (20.00)18.7374
1990's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)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: 12.80

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 Index12.80 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.59 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.80)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]