Page last updated: 2024-11-05

phenalen-1-one

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

Description

Phenalen-1-one is a polycyclic aromatic ketone with a unique structure. It is a highly conjugated system with a fused three-ring structure. Phenalen-1-one has been investigated for its potential applications in organic electronics, fluorescence sensing, and as a building block for the synthesis of other complex molecules. The compound exhibits interesting photophysical properties, including strong fluorescence and a large Stokes shift. Research on phenalen-1-one has focused on exploring its synthesis, characterization, and potential applications in various fields. Its synthesis often involves the use of cyclization reactions, such as the Diels-Alder reaction. The compound's properties, including its fluorescence and electronic structure, make it a promising candidate for applications in organic light-emitting diodes (OLEDs), sensors, and other optoelectronic devices.'

phenalen-1-one: fossil fuel combustion product [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID11050
CHEMBL ID227511
SCHEMBL ID188491
MeSH IDM0114701

Synonyms (34)

Synonym
evu6ex9g8h ,
unii-evu6ex9g8h
einecs 208-945-2
nsc 150161
ccris 4923
phenalen-1-one
nsc-150161
1h-phenalen-1-one
548-39-0
7-perinaphthenone
nsc150161
perinaphthenone
phenalenone
perinaphthenone, 97%
CHEMBL227511
phenalenone-1-one
wwbgwphhlrstfi-uhfffaoysa-
inchi=1/c13h8o/c14-12-8-7-10-4-1-3-9-5-2-6-11(12)13(9)10/h1-8h
AKOS004902220
AE-562/43459279
FT-0632364
SCHEMBL188491
J-504714
WWBGWPHHLRSTFI-UHFFFAOYSA-N
DTXSID20203278
perinaphthenon
ccris-4923
1h-benzonaphthen-1-one
mfcd00004143
D79953
STARBLD0009638
AB92503
CS-0331802
AS-82921

Research Excerpts

Bioavailability

ExcerptReferenceRelevance
" UVB is well absorbed in proteins and DNA leading to products such as cyclobutane pyrimidine dimers."( Fatty acids and vitamins generate singlet oxygen under UVB irradiation.
Bäumler, W; Knak, A; Landthaler, M; Maisch, T; Regensburger, J, 2012
)
0.38
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (12)

Assay IDTitleYearJournalArticle
AID1777619Induction of singlet oxygen generation in PBS assessed as singlet oxygen quantum yield at pH 7.4 irradiated with 415 nm LED light by ABDA sensor based UV-Vis spectrometer analysis2021ACS medicinal chemistry letters, Aug-12, Volume: 12, Issue:8
A Green-Absorbing, Red-Fluorescent Phenalenone-Based Photosensitizer as a Theranostic Agent for Photodynamic Therapy.
AID1493778Antileishmanial activity against Leishmania amazonensis MHOM/BR/77/LTB0016 promastigotes after 72 hrs by Alamarblue assay2018European journal of medicinal chemistry, Jan-01, Volume: 143Design, synthesis and evaluation of amino-substituted 1H-phenalen-1-ones as anti-leishmanial agents.
AID1493777Antileishmanial activity against Leishmania donovani MHOM/IN/90/GE1F8R promastigotes after 72 hrs by Alamarblue assay2018European journal of medicinal chemistry, Jan-01, Volume: 143Design, synthesis and evaluation of amino-substituted 1H-phenalen-1-ones as anti-leishmanial agents.
AID286605Inhibition of Mycosphaerella fijiensis spore germination2007Journal of natural products, May, Volume: 70, Issue:5
Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijiensis.
AID488604Cytotoxicity against human MCF7 cells assessed as growth inhibition at 10 uM after 72 hrs by MTT assay2010Bioorganic & medicinal chemistry, Jun-15, Volume: 18, Issue:12
Synthesis and in vitro antiprotozoal evaluation of substituted phenalenone analogues.
AID488603Antiprotozoal activity against epimastigotes of Trypanosoma cruzi Y by alamar blue assay2010Bioorganic & medicinal chemistry, Jun-15, Volume: 18, Issue:12
Synthesis and in vitro antiprotozoal evaluation of substituted phenalenone analogues.
AID286609Inhibition of Mycosphaerella fijiensis mycelial growth2007Journal of natural products, May, Volume: 70, Issue:5
Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijiensis.
AID488601Antiprotozoal activity against promastigotes of Leishmania amazonensis MHOM/ BR/77/LTB0016 after 72 hrs by alamar blue assay2010Bioorganic & medicinal chemistry, Jun-15, Volume: 18, Issue:12
Synthesis and in vitro antiprotozoal evaluation of substituted phenalenone analogues.
AID1777617Absorption property of the compound in PBS assessed as molar extinction coefficient by absorbance based analysis2021ACS medicinal chemistry letters, Aug-12, Volume: 12, Issue:8
A Green-Absorbing, Red-Fluorescent Phenalenone-Based Photosensitizer as a Theranostic Agent for Photodynamic Therapy.
AID1091773Antifungal activity against Pseudocercospora fijiensis assessed as inhibition of mycelial growth under 12 hr photoperiod measured after 8 days2009Journal of agricultural and food chemistry, Aug-26, Volume: 57, Issue:16
Structure-activity relationship in the interaction of substituted perinaphthenones with Mycosphaerella fijiensis.
AID488602Antiprotozoal activity against promastigotes of Leishmania donovani MHOM/IN/90/GE1F8R after 72 hrs by alamar blue assay2010Bioorganic & medicinal chemistry, Jun-15, Volume: 18, Issue:12
Synthesis and in vitro antiprotozoal evaluation of substituted phenalenone analogues.
AID286606Inhibition of Mycosphaerella fijiensis mycelial growth at 50 to 100 ppm after 15 days2007Journal of natural products, May, Volume: 70, Issue:5
Phenalenone-type compounds from Musa acuminata var. "Yangambi km 5" (AAA) and their activity against Mycosphaerella fijiensis.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (79)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (2.53)18.7374
1990's2 (2.53)18.2507
2000's18 (22.78)29.6817
2010's41 (51.90)24.3611
2020's16 (20.25)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.88

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 Index10.88 (24.57)
Research Supply Index4.42 (2.92)
Research Growth Index5.30 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.88)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews3 (3.66%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other79 (96.34%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]