Page last updated: 2024-11-07

matairesinol

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

Description

Matairesinol is a lignan found in a variety of plants, including flaxseed, sesame seeds, and Norway spruce. It has been studied for its potential health benefits, including antioxidant, anti-inflammatory, and anticancer properties. Matairesinol is thought to exert its biological effects by modulating various signaling pathways, such as the NF-κB pathway and the MAPK pathway. It has also been shown to inhibit the growth of cancer cells in vitro and in vivo. The synthesis of matairesinol can be achieved through different methods, including extraction from natural sources, chemical synthesis, and biotransformation. Further research is ongoing to investigate the potential therapeutic applications of matairesinol in human health.'

matairesinol: lignan that is a central precursor in plants in the biosynthesis of numerous lignans (coordinate with specific); RN refers to (3R-trans)-isomer [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

(-)-matairesinol : A lignan that is gamma-butyrolactone in which the 3 and 4 positions are substituted by 4-hydroxy-3-methoxybenzyl groups (the 3R,4R-diastereomer). [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]

Cross-References

ID SourceID
PubMed CID119205
CHEMBL ID425148
CHEBI ID6698
SCHEMBL ID120499
MeSH IDM0188330

Synonyms (52)

Synonym
ACON1_001075
MAX ,
(-)-matairesinol
matairesinol
580-72-3
(3r,4r)-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one
(3r,4r)-3,4-bis[(4-hydroxy-3-methoxy-phenyl)methyl]tetrahydrofuran-2-one
2(3h)-furanone, dihydro-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]-
artigenin congener
DB04200
3r,4r-bis((4-hydroxy-3-methoxyphenyl)methyl)dihydro-2(3h)-furanone
2(3h)-furanone, dihydro-3,4-bis((4-hydroxy-3-methoxyphenyl)methyl)-, (3r-trans)-
MEGXP0_001689
NCGC00169701-01
bdbm50240921
(3r,4r)-3,4-bis-(4-hydroxy-3-methoxy-benzyl)-dihydro-furan-2-one
(3r,4r)-3,4-bis(4-hydroxy-3-methoxybenzyl)dihydrofuran-2(3h)-one
(2r,3r)-2,3-bis(4-hydroxy-3-methoxybenzyl)-4-butanolide
BRD-K66216249-001-01-7
rac matairesinol
chebi:6698 ,
CHEMBL425148 ,
A831721
xlw63p8wua ,
unii-xlw63p8wua
matai-resinol
SCHEMBL120499
2(3h)-furanone, dihydro-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]-, (3r-trans)-
3,4-bis(4-hydroxy-3-methoxybenzyl)dihydro-2(3h)-furanone #
2(3h)-furanone, dihydro-3,4-divanillyl-
HMS3649D06
matairesinol, >=85% (hplc)
matairesinol, analytical standard
dihydro-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]-(3r,4r)-2(3h)-furanone
(8r,8'r)-(-)-matairesinol
dihydro-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]-(3r-trans)-2(3h)-furanone
NCGC00169701-03
artigenin congener; dibenzylbutyrolactone lignanolide
DTXSID40920490 ,
Q4284467
sr-01000946700
SR-01000946700-1
2(3h)-furanone, dihydro-3,4-bis((4-hydroxy-3-methoxyphenyl)methyl)-, (3r,4r)-
fema no. 4762
(3r,4r)-dihydro-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]-2(3h)-furanone; (-)-matairesinol; (8r,8'r)-(-)-matairesinol
MS-25629
2(3h)-furanone, dihydro-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]-,(3r,4r)-
CS-0023873
HY-N3312
dtxcid301349397
(3r,4r)-3,4-bis((4-hydroxy-3-methoxyphenyl)methyl)oxolan-2-one
AKOS040760547

Research Excerpts

Overview

Matairesinol is a plant lignan present in a wide variety of foodstuffs such as seeds, vegetables and fruits.

ExcerptReferenceRelevance
"Matairesinol is a plant lignan present in a wide variety of foodstuffs such as seeds, vegetables and fruits. "( Anti-osteoclastogenic activity of matairesinol via suppression of p38/ERK-NFATc1 signaling axis.
Choi, SW; Kim, KJ; Kim, SH; Park, KI; Ryu, BJ; Yeon, JT, 2014
)
2.12

Effects

ExcerptReferenceRelevance
"Matairesinol, which has the basic structure of the other lignans, showed the weakest inhibition."( Inhibitory effects of lignans on the activity of human matrix metalloproteinase 7 (matrilysin).
Inouye, K; Muta, Y; Oyama, S; Shimada, M; Umezawa, T, 2004
)
1.04

Actions

ExcerptReferenceRelevance
"Matairesinol from safflower fruit was determined as (-)-enantiomer."( Chiral separation of the plant lignan matairesinol by capillary electrophoresis.
Dräger, B; Mrestani, Y; Müller, U; Neubert, R, 2008
)
1.34

Toxicity

ExcerptReferenceRelevance
"Radix Wikstroemia indica (RWI), named "Liao Ge Wang" in Chinese, is a kind of toxic Chinese herbal medicine (CHM) commonly used in Miao nationality of South China."( Exploring the Q-marker of "sweat soaking method" processed radix Wikstroemia indica: Based on the "effect-toxicity-chemicals" study.
Chen, YL; Feng, G; Hai, Y; He, X; Li, LL; Li, W; Liu, CX; Wu, ZG; Wu, ZJ; Zhang, SC; Zheng, CQ, 2018
)
0.48

Bioavailability

ExcerptReferenceRelevance
" Information concerning their dietary sources and bioavailability is scarce."( Intake of lignans is associated with serum enterolactone concentration in Finnish men and women.
Adlercreutz, H; Kilkkinen, A; Pietinen, P; Stumpf, K; Valsta, LM; Virtamo, J, 2003
)
0.32
" Methyl pinosylvin, pinosylvin, matairesinol, nortrachelogenin, as well as resveratrol, a metabolite of pinosylvin, were detected in serum at total concentration of 7-73 μM, confirming the bioavailability of pine knot extract derived lignans and stilbenoids."( Novel Lignan and stilbenoid mixture shows anticarcinogenic efficacy in preclinical PC-3M-luc2 prostate cancer model.
Aittokallio, T; Eckerman, C; Holmbom, B; Laajala, TD; Mäkelä, SI; Polari, L; Saarinen, NM; Smeds, A; Yatkin, E, 2014
)
0.69
"The ATP-binding cassette transporter P-glycoprotein (P-gp) is known to limit both brain penetration and oral bioavailability of many chemotherapy drugs."( A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
Ambudkar, SV; Brimacombe, KR; Chen, L; Gottesman, MM; Guha, R; Hall, MD; Klumpp-Thomas, C; Lee, OW; Lee, TD; Lusvarghi, S; Robey, RW; Shen, M; Tebase, BG, 2019
)
0.51

Dosage Studied

ExcerptRelevanceReference
" However, from preliminary experiments with rats dosed orally with secoisolariciresinol and matairesinol, it appears that the intestinal absorption and subsequent oxidative metabolism of these plant lignans occur only to a very small extent due to the highly efficient conversion of secoisolariciresinol and matairesinol to the mammalian lignans enterodiol and enterolactone by the gut microflora."( Studies on the metabolism of the plant lignans secoisolariciresinol and matairesinol.
Honig, DM; Kulling, SE; Metzler, M; Niemeyer, HB, 2003
)
0.77
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (4)

RoleDescription
angiogenesis inhibitorAn agent and endogenous substances that antagonize or inhibit the development of new blood vessels.
anti-asthmatic agentAny compound that has anti-asthmatic effects.
phytoestrogenAny compound produced by a plant that happens to have estrogenic activity.
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[role 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]

Drug Classes (3)

ClassDescription
lignanAny phenylpropanoid derived from phenylalanine via dimerization of substituted cinnamic alcohols, known as monolignols, to a dibenzylbutane skeleton. Note that while individual members of the class have names ending ...lignane, ...lignene, ...lignadiene, etc., the class names lignan, neolignan, etc., do not end with an "e".
gamma-lactoneA lactone having a five-membered lactone ring.
polyphenolMembers of the class of phenols that contain 2 or more benzene rings each of which is substituted by at least one hydroxy group.
[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]

Pathways (6)

PathwayProteinsCompounds
hinokinin biosynthesis08
yatein biosynthesis II19
matairesinol biosynthesis019
yatein biosynthesis I010
justicidin B biosynthesis116
arctigenin and isoarctigenin biosynthesis36
hinokinin biosynthesis28
matairesinol biosynthesis220
justicidin B biosynthesis118
yatein biosynthesis II112
yatein biosynthesis I110

Protein Targets (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Sex hormone-binding globulinHomo sapiens (human)IC50 (µMol)52.00000.00380.00380.0038AID399375
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Sex hormone-binding globulinHomo sapiens (human)Kd0.30900.00020.34964.7863AID318680
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Molecular Functions (3)

Processvia Protein(s)Taxonomy
androgen bindingSex hormone-binding globulinHomo sapiens (human)
protein bindingSex hormone-binding globulinHomo sapiens (human)
steroid bindingSex hormone-binding globulinHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (2)

Processvia Protein(s)Taxonomy
extracellular regionSex hormone-binding globulinHomo sapiens (human)
extracellular exosomeSex hormone-binding globulinHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (47)

Assay IDTitleYearJournalArticle
AID1346987P-glycoprotein substrates identified in KB-8-5-11 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347159Primary screen GU Rhodamine qHTS for Zika virus inhibitors: Unlinked NS2B-NS3 protease assay2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID1296008Cytotoxic Profiling of Annotated Libraries Using Quantitative High-Throughput Screening2020SLAS discovery : advancing life sciences R & D, 01, Volume: 25, Issue:1
Cytotoxic Profiling of Annotated and Diverse Chemical Libraries Using Quantitative High-Throughput Screening.
AID1346986P-glycoprotein substrates identified in KB-3-1 adenocarcinoma cell line, qHTS therapeutic library screen2019Molecular pharmacology, 11, Volume: 96, Issue:5
A High-Throughput Screen of a Library of Therapeutics Identifies Cytotoxic Substrates of P-glycoprotein.
AID1347160Primary screen NINDS Rhodamine qHTS for Zika virus inhibitors2020Proceedings of the National Academy of Sciences of the United States of America, 12-08, Volume: 117, Issue:49
Therapeutic candidates for the Zika virus identified by a high-throughput screen for Zika protease inhibitors.
AID436320Antiinflammatory activity in mouse RAW264.7 cells assessed as inhibition of LPS-induced nitric oxide production after 24 hrs2008Journal of natural products, Nov, Volume: 71, Issue:11
Phenylpropanoids from Daphne feddei and their inhibitory activities against NO production.
AID1489043Cytotoxicity against human HeLa cells assessed as reduction in cell viability after 48 hrs by WST-8 assay2017Bioorganic & medicinal chemistry letters, 09-01, Volume: 27, Issue:17
Syntheses of cytotoxic novel arctigenin derivatives bearing halogen and alkyl groups on aromatic rings.
AID357032Cytotoxicity against human H9 cells2001Journal of natural products, Jul, Volume: 64, Issue:7
Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives.
AID1371012Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation by measuring superoxide dismutase SOD-inhibitable ferricytochrome c reduction at 10 ug/ml incubated for 5 mins before fMLP/CB stimulation2017Journal of natural products, 04-28, Volume: 80, Issue:4
Chemical Constituents and Anti-inflammatory Principles from the Fruits of Forsythia suspensa.
AID1371027Cytotoxicity against human HeLa cells assessed as reduction in cell viability incubated for 72 hrs by WST-8 dye based assay2017Journal of natural products, 04-28, Volume: 80, Issue:4
α-Glucosidase Inhibitory and Cytotoxic Taxane Diterpenoids from the Stem Bark of Taxus wallichiana.
AID426072Antioxidant activity in human E2R cells assessed as intracellular peroxide level at 25 to 100 uM after 1 hr by flow cytometry in presence of DCFH-DA2009Bioorganic & medicinal chemistry, Aug-01, Volume: 17, Issue:15
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activity.
AID1657513Anti-inflammatory activity against human neutrophils assessed as inhibition of fMLF/CB-induced superoxide anion generation at 10 uM preincubated for 5 mins followed by fMLF addition after priming with CB for 3 mins and measured after 10 mins by spectropho2020Bioorganic & medicinal chemistry letters, 05-15, Volume: 30, Issue:10
AID332524Antiviral activity against HSV1 at 40 ug/ml1994Journal of natural products, Jun, Volume: 57, Issue:6
Lignans from the wood of Abies pinsapo.
AID1169294Inhibition of TTR V30M mutant (unknown origin) expressed in Escherichia coli assessed as inhibition of amyloid fibril formation at 20 uM by fluorescence assay2014Journal of medicinal chemistry, Nov-13, Volume: 57, Issue:21
Inhibitory activities of propolis and its promising component, caffeic acid phenethyl ester, against amyloidogenesis of human transthyretin.
AID591310Anticancer activity against human XF498 cells by SRB assay2011Bioorganic & medicinal chemistry letters, Apr-15, Volume: 21, Issue:8
Biological evaluation of phenolic constituents from the trunk of Berberis koreana.
AID333835Antioxidant activity assessed as AAPH radical scavenging activity after 3 hrs2005Journal of natural products, Oct, Volume: 68, Issue:10
Effect of benzylic oxygen on the antioxidant activity of phenolic lignans.
AID1657514Anti-inflammatory activity against human neutrophils assessed as inhibition of fMLF/CB-induced elastase release preincubated for 5 mins followed by fMLF addition after priming with CB for 3 mins and measured after 10 mins by spectrophotometric analysis2020Bioorganic & medicinal chemistry letters, 05-15, Volume: 30, Issue:10
AID91560Inhibitory activity against strand transfer by HIV-1 Integrase at 100 uM1996Journal of medicinal chemistry, Jan-05, Volume: 39, Issue:1
(-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase.
AID332523Antifungal ativity against Penicillium1994Journal of natural products, Jun, Volume: 57, Issue:6
Lignans from the wood of Abies pinsapo.
AID332522Antifungal ativity against Aspergillus niger CECT 20891994Journal of natural products, Jun, Volume: 57, Issue:6
Lignans from the wood of Abies pinsapo.
AID332525Antiviral activity against VSV at 40 ug/ml1994Journal of natural products, Jun, Volume: 57, Issue:6
Lignans from the wood of Abies pinsapo.
AID1657515Anti-inflammatory activity against human neutrophils assessed as inhibition in fMLF/CB-induced elastase release at 10 uM preincubated for 5 mins followed by fMLF addition after priming with CB for 3 mins and measured after 10 mins by spectrophotometric an2020Bioorganic & medicinal chemistry letters, 05-15, Volume: 30, Issue:10
AID1657512Anti-inflammatory activity against human neutrophils assessed as inhibition of fMLF/CB-induced superoxide anion generation preincubated for 5 mins followed by fMLF addition after priming with CB for 3 mins and measured after 10 mins by spectrophotometric 2020Bioorganic & medicinal chemistry letters, 05-15, Volume: 30, Issue:10
AID1377003Inhibition of Saccharomyces cerevisiae alpha-glucosidase using p-nitrophenyl-alpha-D-glucopyranoside as substrate after 30 mins2017Journal of natural products, 06-23, Volume: 80, Issue:6
Lignans from the Roots of Taxus wallichiana and Their α-Glucosidase Inhibitory Activities.
AID1537190Cytotoxicity against human HeLa cells assessed as growth inhibition after 2 days by SRB assay2019Journal of natural products, 02-22, Volume: 82, Issue:2
Lignan Dimers from Forsythia viridissima Roots and Their Antiviral Effects.
AID1666597Induction of DNA damage in human SU8686 cells assessed as increase in gammaH2AX phosphorylation at ser193 at cytotoxic IC50 in presence of 0.3 uM doxorubicin by fluorometry method2020Bioorganic & medicinal chemistry, 02-15, Volume: 28, Issue:4
Targeting the DNA damage response (DDR) by natural compounds.
AID1537189Antiviral activity against Human rhinovirus 1B infected in human HeLa cells assessed as reduction in virus-induced cytopathic effect after 2 days by SRB staining based microscopic method2019Journal of natural products, 02-22, Volume: 82, Issue:2
Lignan Dimers from Forsythia viridissima Roots and Their Antiviral Effects.
AID1371010Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced superoxide anion generation by measuring superoxide dismutase SOD-inhibitable ferricytochrome c reduction incubated for 5 mins before fMLP/CB stimulation for 3 mins 2017Journal of natural products, 04-28, Volume: 80, Issue:4
Chemical Constituents and Anti-inflammatory Principles from the Fruits of Forsythia suspensa.
AID1489042Cytotoxicity against human HL60 cells assessed as reduction in cell viability after 48 hrs by WST-8 assay2017Bioorganic & medicinal chemistry letters, 09-01, Volume: 27, Issue:17
Syntheses of cytotoxic novel arctigenin derivatives bearing halogen and alkyl groups on aromatic rings.
AID426070Induction of apoptosis in human EBV deficient BL41 cells assessed as condensed and fragmented nuclei at 25 to 100 uM after 18 hrs by epifluorescent microscopy2009Bioorganic & medicinal chemistry, Aug-01, Volume: 17, Issue:15
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activity.
AID1062030Inhibition of Streptococcus mutans OMZ65 recombinant sortase A delta-40 mutant using Dabcyl-QALPETGEE-Edans as substrate after 1 hr by fluorescence spectrophotometry2014Bioorganic & medicinal chemistry letters, Jan-01, Volume: 24, Issue:1
Sortase A inhibitory metabolites from the roots of Pulsatilla koreana.
AID357033Antiviral activity against HIV1 in human H9 cells assessed as inhibition of viral replication2001Journal of natural products, Jul, Volume: 64, Issue:7
Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives.
AID591307Anticancer activity against human SKOV3 cells by SRB assay2011Bioorganic & medicinal chemistry letters, Apr-15, Volume: 21, Issue:8
Biological evaluation of phenolic constituents from the trunk of Berberis koreana.
AID318680Displacement of [3H]5alpha dihydrotestosterone from human sex hormone binding globulin2008Journal of medicinal chemistry, Apr-10, Volume: 51, Issue:7
An updated steroid benchmark set and its application in the discovery of novel nanomolar ligands of sex hormone-binding globulin.
AID1371011Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release pre-incubated for 5 mins before fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-pnitroanilide as substrate2017Journal of natural products, 04-28, Volume: 80, Issue:4
Chemical Constituents and Anti-inflammatory Principles from the Fruits of Forsythia suspensa.
AID591309Anticancer activity against human SK-MEL-2 cells by SRB assay2011Bioorganic & medicinal chemistry letters, Apr-15, Volume: 21, Issue:8
Biological evaluation of phenolic constituents from the trunk of Berberis koreana.
AID591308Anticancer activity against human A549 cells by SRB assay2011Bioorganic & medicinal chemistry letters, Apr-15, Volume: 21, Issue:8
Biological evaluation of phenolic constituents from the trunk of Berberis koreana.
AID1371013Anti-inflammatory activity in human neutrophils assessed as inhibition of fMLP/CB-induced elastase release at 10 ug/ml pre-incubated for 5 mins before fMLP/CB stimulation using MeO-Suc-Ala-Ala-Pro-Val-pnitroanilide as substrate2017Journal of natural products, 04-28, Volume: 80, Issue:4
Chemical Constituents and Anti-inflammatory Principles from the Fruits of Forsythia suspensa.
AID1537191Selectivity index, ratio of CC50 for human HeLa cells to IC50 for Human rhinovirus 1B infected in human HeLa cells2019Journal of natural products, 02-22, Volume: 82, Issue:2
Lignan Dimers from Forsythia viridissima Roots and Their Antiviral Effects.
AID1371026Inhibition of Saccharomyces cerevisiae alpha-glucosidase using p-nitrophenyl-alpha-D-glucopyranoside substrate incubated for 30 mins2017Journal of natural products, 04-28, Volume: 80, Issue:4
α-Glucosidase Inhibitory and Cytotoxic Taxane Diterpenoids from the Stem Bark of Taxus wallichiana.
AID91438Inhibitory activity against 3'-processing by HIV-1 Integrase at 100 uM1996Journal of medicinal chemistry, Jan-05, Volume: 39, Issue:1
(-)-Arctigenin as a lead structure for inhibitors of human immunodeficiency virus type-1 integrase.
AID399375Displacement of [3H]DHT from human serum SHBG1998Journal of natural products, Jan, Volume: 61, Issue:1
Lignans interfering with 5 alpha-dihydrotestosterone binding to human sex hormone-binding globulin.
AID333834Antioxidant activity assessed as DPPH radical scavenging activity2005Journal of natural products, Oct, Volume: 68, Issue:10
Effect of benzylic oxygen on the antioxidant activity of phenolic lignans.
AID357034Therapeutic index, ratio of IC50 for human H9 cells to EC50 for HIV12001Journal of natural products, Jul, Volume: 64, Issue:7
Anti-AIDS agents. 46. Anti-HIV activity of harman, an anti-HIV principle from Symplocos setchuensis, and its derivatives.
AID426071Induction of apoptosis in human E2R cells expressing EBV assessed as condensed and fragmented nuclei at 25 to 100 uM after 18 hrs by epifluorescent microscopy2009Bioorganic & medicinal chemistry, Aug-01, Volume: 17, Issue:15
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activity.
AID1657509Antiproliferative activity against human HepG2 cells assessed as inhibition of cell viability by MTT assay2020Bioorganic & medicinal chemistry letters, 05-15, Volume: 30, Issue:10
AID591311Antiinflammatory activity in mouse BV2 cells assessed as inhibition of lipopolysaccharide induced NO production2011Bioorganic & medicinal chemistry letters, Apr-15, Volume: 21, Issue:8
Biological evaluation of phenolic constituents from the trunk of Berberis koreana.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (102)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's9 (8.82)18.2507
2000's39 (38.24)29.6817
2010's40 (39.22)24.3611
2020's14 (13.73)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.26

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 Index31.26 (24.57)
Research Supply Index4.67 (2.92)
Research Growth Index4.89 (4.65)
Search Engine Demand Index42.09 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.26)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (0.95%)5.53%
Reviews2 (1.90%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other102 (97.14%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]