Page last updated: 2024-12-08

lusianthridin

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

Description

lusianthridin: from rhizome of Arundina graminifolia [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

FloraRankFlora DefinitionFamilyFamily Definition
Arundinagenus[no description available]OrchidaceaeA plant family of the order Asparagales. All members of the orchid family have the same bilaterally symmetrical flower structure, with three sepals, but the flowers vary greatly in color and shape.[MeSH]
Arundina graminifoliaspecies[no description available]OrchidaceaeA plant family of the order Asparagales. All members of the orchid family have the same bilaterally symmetrical flower structure, with three sepals, but the flowers vary greatly in color and shape.[MeSH]

Cross-References

ID SourceID
PubMed CID442702
CHEMBL ID254187
CHEBI ID28678
SCHEMBL ID4743850
MeSH IDM0491517

Synonyms (16)

Synonym
CHEBI:28678 ,
7-methoxy-9,10-dihydrophenanthrene-2,5-diol
87530-30-1
4,7-dihydroxy-2-methoxy-9,10-dihydrophenanthrene
lusianthridin
CHEMBL254187
SCHEMBL4743850
DTXSID50331917
2,5-dihydroxy-7-methoxy-9,10-dihydrophenanthrene (14)
bdbm246496
Q27103833
HY-121418
CS-0081991
D85190
AKOS040760533
FS-7984

Research Excerpts

Overview

Lusianthridin is a phenanthrene derivative.

ExcerptReferenceRelevance
"Lusianthridin is a phenanthrene derivative isolated from "( Inhibitory Mechanisms of Lusianthridin on Human Platelet Aggregation.
Luechapudiporn, R; Rojnuckarin, P; Sritularak, B; Swe, HN, 2021
)
2.37

Pharmacokinetics

ExcerptReferenceRelevance
" The validated method was applied to the pre-clinical pharmacokinetic study of lusianthridin in rats."( Pharmacokinetic, bioavailability, and metabolism studies of lusianthridin, a dihydrophenanthrene compound, in rats by liquid chromatography/electrospray ionization tandem mass spectrometry.
Guan, H; Ju, Z; Liao, Q; Tang, X; Wang, Z; Yang, L, 2021
)
1.09

Compound-Compound Interactions

ExcerptReferenceRelevance
" The incubation samples were analyzed by liquid chromatography combined with electrospray ionization high-resolution mass spectrometry."( Identification of lusianthridin metabolites in rat liver microsomes by liquid chromatography combined with electrospray ionization time-of-flight mass spectrometry.
Guan, H; Ju, Z; Liao, Q; Ma, C; Tang, X; Wang, Z; Yang, L; Yang, Y, 2021
)
0.96

Bioavailability

ExcerptReferenceRelevance
"47 min and the oral absolute bioavailability was calculated as 30."( Pharmacokinetic, bioavailability, and metabolism studies of lusianthridin, a dihydrophenanthrene compound, in rats by liquid chromatography/electrospray ionization tandem mass spectrometry.
Guan, H; Ju, Z; Liao, Q; Tang, X; Wang, Z; Yang, L, 2021
)
0.86
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
dihydrophenanthreneAny member of the class of phenanthrenes that is the dihydrogenated derivative of phenanthrene and its substituted derivatives.
[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]

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Pancreatic triacylglycerol lipaseSus scrofa (pig)Ki4.96000.26005.09149.8000AID1803387
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (22)

Assay IDTitleYearJournalArticle
AID414771Inhibition of ovine COX1 by colorimetric assay2009Bioorganic & medicinal chemistry, Apr-01, Volume: 17, Issue:7
Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita.
AID414769Antioxidant activity assessed as DPPH radical scavenging activity after 30 mins by microplate reader assay2009Bioorganic & medicinal chemistry, Apr-01, Volume: 17, Issue:7
Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita.
AID312043Antiproliferative activity against rat HSC-T6 cells after 48 hrs by MTT assay2007Journal of natural products, Dec, Volume: 70, Issue:12
Antifibrotic phenanthrenes of Dendrobium nobile stems.
AID399545Spasmolytic activity in guinea pig ileum assessed as inhibition of spontaneous contraction2004Journal of natural products, Feb, Volume: 67, Issue:2
Spasmolytic effects, mode of action, and structure-activity relationships of stilbenoids from Nidema boothii.
AID484514Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced NO production2010Bioorganic & medicinal chemistry letters, Jun-15, Volume: 20, Issue:12
Phenanthrenes from Dendrobium nobile and their inhibition of the LPS-induced production of nitric oxide in macrophage RAW 264.7 cells.
AID312044Cytotoxicity against rat hepatocytes at 10 to 100 uM2007Journal of natural products, Dec, Volume: 70, Issue:12
Antifibrotic phenanthrenes of Dendrobium nobile stems.
AID414770Antioxidant activity assessed as superoxide radical scavenging activity after 20 mins by NBT reduction assay2009Bioorganic & medicinal chemistry, Apr-01, Volume: 17, Issue:7
Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita.
AID1320953Cytotoxicity against human A549 cells assessed as decrease in cell viability after 6 days by MTT assay2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320959Antifungal activity against Exserohilum turcicum after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320961Antifungal activity against Alternaria citri after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320960Antifungal activity against Pestallozzia theae after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320952Cytotoxicity against human MCF7 cells assessed as decrease in cell viability after 6 days by MTT assay2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320954Antifungal activity against Phytophthora parasitica var. nicotianae after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320957Antifungal activity against Diaporthe medusaea nitschke after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320950Antifungal activity against Alternaria brassicicola after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320951Cytotoxicity against human HeLa cells assessed as decrease in cell viability after 6 days by MTT assay2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320958Antifungal activity against Ceratocystis paradoxa moreau after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320955Antifungal activity against Colletotrichum capsici after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID1320956Antifungal activity against Bipolaris oryzae after 4 to 14 days by serial dilution method2016Journal of natural products, 07-22, Volume: 79, Issue:7
Bioactive Phenanthrene and Bibenzyl Derivatives from the Stems of Dendrobium nobile.
AID414773Selectivity ratio of IC50 for ovine COX1 to IC50 for ovine COX22009Bioorganic & medicinal chemistry, Apr-01, Volume: 17, Issue:7
Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita.
AID414772Inhibition of ovine COX2 by colorimetric assay2009Bioorganic & medicinal chemistry, Apr-01, Volume: 17, Issue:7
Phenolic compounds with radical scavenging and cyclooxygenase-2 (COX-2) inhibitory activities from Dioscorea opposita.
AID1803387In Vitro Pancreatic Lipase Assay from Article 10.3109/14756366.2012.742517: \\Phenolic compounds with pancreatic lipase inhibitory activity from Korean yam (Dioscorea opposita).\\2014Journal of enzyme inhibition and medicinal chemistry, Feb, Volume: 29, Issue:1
Phenolic compounds with pancreatic lipase inhibitory activity from Korean yam (Dioscorea opposita).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (18)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's4 (22.22)29.6817
2010's7 (38.89)24.3611
2020's7 (38.89)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 21.17

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 Index21.17 (24.57)
Research Supply Index2.94 (2.92)
Research Growth Index4.82 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (21.17)

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%
Other18 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]