Page last updated: 2024-12-11

1,3'-diethyl-4,2'-quinolylthiacyanine iodide

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

Description

1,3'-diethyl-4,2'-quinolylthiacyanine iodide, often abbreviated as **DQTI**, is a **cyanine dye** used in various research applications. Let's break down its significance:

**What is it?**

* **Cyanine Dyes:** These are organic compounds characterized by a polymethine bridge (a chain of carbon atoms with alternating single and double bonds) linking two nitrogen-containing heterocycles. They exhibit strong absorption and fluorescence properties, making them useful in various fields.
* **DQTI Structure:** DQTI is a specific cyanine dye with two quinoline rings connected by a sulfur atom and a polymethine chain. The diethyl part refers to two ethyl groups attached to the quinoline rings, which modify its properties.

**Why is it Important in Research?**

DQTI's importance stems from its unique characteristics and applications:

1. **Fluorescence Properties:** DQTI exhibits strong fluorescence, making it valuable for:
* **Fluorescence Microscopy:** It can be used as a fluorescent probe to visualize and study biological structures and processes.
* **Fluorescence Spectroscopy:** Its fluorescence properties are used to measure and analyze various biochemical and physical phenomena.

2. **Antimicrobial Activity:** DQTI has shown antimicrobial activity against certain bacteria and fungi. Research explores its potential as a new antibiotic or antifungal agent.

3. **Photodynamic Therapy (PDT):** This involves using light to activate a photosensitizer, like DQTI, to generate reactive oxygen species that kill cancer cells. Its photophysical properties make it a potential candidate for PDT.

4. **Optical Materials:** DQTI's optical properties, including its ability to absorb and emit light, make it potentially useful in:
* **Solar cells:** As a sensitizer to improve the efficiency of solar energy conversion.
* **Lasers:** As a gain medium for dye lasers.

**Research Areas:**

* **Biological and Biomedical Research:** To study cell processes, develop new diagnostic tools, and explore potential therapies.
* **Material Science:** To create new materials with improved optical and electronic properties.
* **Pharmacology:** To develop novel antimicrobial and anticancer agents.

**Overall, 1,3'-diethyl-4,2'-quinolylthiacyanine iodide is a versatile compound with applications in a variety of research fields. Its fluorescence, antimicrobial activity, and photodynamic properties make it a valuable tool for scientists across disciplines.**

cyanine dye 7: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID6440951
SCHEMBL ID1807089
MeSH IDM0057313

Synonyms (15)

Synonym
cyanine dye 7
einecs 240-075-9
l-lysine, n2-(n2-(n2-l-lysyl-l-lysyl)-l-lysyl)-, hydrochloride
1-ethyl-4-((3-ethyl-2(3h)-benzothiazolylidene)methyl)quinolinium iodide
1,3'-diethyl-4,2'-quinolylthiacyanine iodide
1-ethyl-4-((3-ethyl-3h-benzothiazol-2-ylidene)methyl)quinolinium iodide
15941-82-9
AKOS015911912
SCHEMBL1807089
(2z)-3-ethyl-2-[(1-ethylquinolin-1-ium-4-yl)methylidene]-1,3-benzothiazole;iodide
DTXSID40936096
3-ethyl-2-[(1-ethylquinolin-4(1h)-ylidene)methyl]-1,3-benzothiazol-3-ium iodide
1-ethyl-4-((3-ethylbenzo[d]thiazol-2(3h)-ylidene)methyl)quinolin-1-iumiodide
1-ethyl-4-((3-ethylbenzo[d]thiazol-2(3h)-ylidene)methyl)quinolin-1-ium iodide
1,3-diethyl-4,2-quinolylthiacyanineiodide

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
"4 kDa) moiety in order to increase its solubility and bioavailability to circulating neutrophils."( Synthesis of the Cyanine 7 labeled neutrophil-specific agents for noninvasive near infrared fluorescence imaging.
Liu, Z; Pan, D; Pu, L; Xiao, L; Yang, M; Zhang, Y, 2010
)
0.36
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (26)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (3.85)18.7374
1990's3 (11.54)18.2507
2000's2 (7.69)29.6817
2010's14 (53.85)24.3611
2020's6 (23.08)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.09

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

MetricThis Compound (vs All)
Research Demand Index12.09 (24.57)
Research Supply Index3.33 (2.92)
Research Growth Index5.43 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.09)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (3.70%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other26 (96.30%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]