Page last updated: 2024-11-07

indolo(3,2-b)carbazole

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

Description

Indolo(3,2-b)carbazole is a polycyclic aromatic hydrocarbon with a fused indole and carbazole ring system. It exhibits strong fluorescence and has been investigated for its potential applications in organic electronics, optoelectronics, and materials science. Notably, it serves as a core structure for various functional materials, including organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs). The compound's synthesis often involves the condensation of indole derivatives, leading to the formation of the fused ring structure. Research efforts focus on exploring the effects of structural modifications and functionalization on its electronic and optical properties. Its unique structure and promising applications have made indolo(3,2-b)carbazole a subject of ongoing investigation in various fields.'

indolo(3,2-b)carbazole: potent inducer of cytochrome P-4501A1-dependent monooxygenase [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID114764
SCHEMBL ID550600
MeSH IDM0204427

Synonyms (12)

Synonym
AKOS015840848
icz-carbazole
indolo(3,2-b)carbazole
241-55-4
indolo[3,2-b]carbazole
HLVSZSQYBQCBQG-UHFFFAOYSA-N
SCHEMBL550600
DTXSID70178826
gtpl10046
OL10030
OL10032
A878005

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
"5, 127 or 508 microg/kg) or with repeated sc dosing (508 microg/kg for 5 days) failed to reproduce any toxic impacts of TCDD."( Comparison of acute toxicities of indolo[3,2-b]carbazole (ICZ) and 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in TCDD-sensitive rats.
Bergman, J; Juvonen, R; Korkalainen, M; McGuire, J; Poellinger, L; Pohjanvirta, R; Simanainen, U; Tuomisto, J; Tuomisto, JT; Unkila, M; Viluksela, M, 2002
)
0.31
" Moreover, the ICZ-induced QR activity showed a higher response and expressed a more-significant dose-response in Hepa-1 cells."( Differential effects of vegetable-derived indoles on the induction of quinone reductase in hepatoma cells.
Chen, YH; Yang, D, 2002
)
0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (28)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's8 (28.57)18.2507
2000's12 (42.86)29.6817
2010's8 (28.57)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: 18.69

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 Index18.69 (24.57)
Research Supply Index3.43 (2.92)
Research Growth Index4.50 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (18.69)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (3.33%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other29 (96.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]