Page last updated: 2024-11-06

phellodendrine

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

Description

Phellodendrine is a quaternary ammonium alkaloid found in the bark of the Amur cork tree (Phellodendron amurense). It is a bioactive compound with a variety of pharmacological effects, including anti-inflammatory, antibacterial, and antiviral activities. Phellodendrine is thought to exert its effects by inhibiting the activity of various enzymes, such as cyclooxygenase and phospholipase A2. Its anti-inflammatory properties have been studied in various models, including rodent models of arthritis and inflammation. Additionally, phellodendrine has shown potential for treating viral infections, such as influenza. The compound is also being investigated for its potential in treating cancer. Research into phellodendrine continues to explore its mechanisms of action and its potential therapeutic applications.'

phellodendrine: structure given in first source; isolated from Phellodendron amurense, used in Japanese herbal medicines; exerts antinephritic effects [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
PhellodendrongenusA plant genus of the family RUTACEAE. Members contain BERBERINE, indolopyridoquinazoline and other ALKALOIDS and limonoids.[MeSH]RutaceaeA plant family in the order Sapindales that grows in warmer regions and has conspicuous flowers.[MeSH]
Phellodendron amurensespecies[no description available]RutaceaeA plant family in the order Sapindales that grows in warmer regions and has conspicuous flowers.[MeSH]

Cross-References

ID SourceID
PubMed CID59819
MeSH IDM0212593

Synonyms (5)

Synonym
phellodendrine
(13as)-3,10-dimethoxy-7-methyl-6,8,13,13a-tetrahydro-5h-isoquinolino[2,1-b]isoquinolin-7-ium-2,11-diol
6873-13-8
S9172
CCG-267948

Research Excerpts

Overview

Phellodendrine was expected to be a valuable new type of immunosuppressor against the cellular immune response.

ExcerptReferenceRelevance
"Phellodendrine was expected to be a valuable new type of immunosuppressor against the cellular immune response."( Principle of the bark of Phellodendron amurense to suppress the cellular immune response: effect of phellodendrine on cellular and humoral immune responses.
Fuchigami, M; Inoue, N; Koda, A; Meguro, K; Mori, H; Nagai, H; Nishioka, I, 1995
)
1.23

Pharmacokinetics

ExcerptReferenceRelevance
" However, few investigations have been conducted for the pharmacokinetic study of phellodendrine."( Pharmacokinetic studies of phellodendrine in rat plasma and tissues after intravenous administration using ultra-high performance liquid chromatography-tandem mass spectrometry.
Dong, X; Gao, W; Li, P; Li, Y; Liu, XG; Wang, HY; Xu, XJ; Yang, H, 2016
)
0.96
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (14)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (7.14)18.7374
1990's2 (14.29)18.2507
2000's0 (0.00)29.6817
2010's6 (42.86)24.3611
2020's5 (35.71)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 51.68

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 very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index51.68 (24.57)
Research Supply Index2.71 (2.92)
Research Growth Index4.63 (4.65)
Search Engine Demand Index79.51 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (51.68)

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%
Other14 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]