Page last updated: 2024-11-05

tryptophol

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

Description

Tryptophol, also known as 3-indolylethanol, is a naturally occurring indole derivative found in various organisms, including plants, animals, and fungi. It is a colorless liquid with a characteristic floral aroma.

**Synthesis:** Tryptophol is biosynthesized from the amino acid tryptophan through a series of enzymatic reactions. It can also be synthesized in the laboratory through various chemical methods.

**Effects:** Tryptophol has been shown to exhibit a wide range of pharmacological effects, including anxiolytic, hypnotic, and anticonvulsant activities. It has also been reported to have antioxidant and neuroprotective properties.

**Importance:** Tryptophol is of interest to researchers for its potential therapeutic applications. Its anxiolytic and hypnotic effects have led to its investigation as a potential treatment for anxiety disorders and insomnia. Its antioxidant and neuroprotective properties have raised interest in its potential to protect against neurodegenerative diseases.

**Why it is studied:** Tryptophol is studied because of its potential therapeutic applications, its role in various biological processes, and its unique chemical structure. Research aims to further understand its mechanisms of action, its potential side effects, and its efficacy in treating various conditions.

**Other interesting points:**
* Tryptophol is found in some fermented foods, such as wine and cheese.
* It is a component of the aroma of some flowers and fruits.
* It has been suggested to play a role in plant defense mechanisms.
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tryptophol : An indolyl alcohol that is ethanol substituted by a 1H-indol-3-yl group at position 2. [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 CID10685
CHEMBL ID226545
CHEBI ID17890
SCHEMBL ID196126
MeSH IDM0047834

Synonyms (95)

Synonym
AC-3286
5-21-03-00061 (beilstein handbook reference)
5809lz7g1u ,
unii-5809lz7g1u
1h-indole-3-ethanol
3-indoleethanol
nsc3884
3-(2-hydroxyethyl)indole
IEA ,
3-indolylethanol
ethanol, 2-indol-3-yl-
indole ethanol
3-(.beta.-hydroxyethyl)indole
indoleethanol
2-(3-indolyl)ethanol
wln: t56 bmj d2q
nsc-3884
.beta.-(3-indole)ethanol
ethanol, 3-indolyl-
2-(indol-3-yl)ethanol
2-(1h-indol-3-yl)ethanol
CHEBI:17890 ,
1h-indolyl-3-ethanol
DIVK1C_001174
smr000686021
MLS001250154
brn 0125553
3-(beta-hydroxyethyl)indole
beta-indol-3-ylethanol
einecs 208-393-2
nsc 3884
CDS1_000134
ISUPSL100239
indole-3-ethanol
C00955
tryptophol
526-55-6
3-(2-hydroxyethyl)indole, 97%
MAYBRIDGE1_002422 ,
T-8495
T-8500
(indol-3-yl)ethanol
3-(2-hydroxyethyl) indole
08DD2DF3-02E7-44DC-9714-864651873577
mbbomcvgycrmea-uhfffaoysa-
inchi=1/c10h11no/c12-6-5-8-7-11-10-4-2-1-3-9(8)10/h1-4,7,11-12h,5-6h2
CHEMBL226545
HMS548G02
BMSE000473
I0030
AKOS002666320
NCGC00247328-01
EN300-70080
2-(1h-indol-3-yl)ethan-1-ol
2-(1h-indol-3-yl)ethanol;tryptophol
A829187
2-(1h-indol-3-yl)-ethanol
HMS2270O23
bdbm92686
tryptaphol, 6
FT-0600657
STL382051
AM1052
S4858
BBL027534
SCHEMBL196126
2-indolyl(3)-ethanol
3-.omega.-hydroxyethylindole
3-.beta.-hydroxyethylindole
2-(3-indolyl)ethyl alcohol
.beta.-indolylethyl alcohol
tryptophol [mi]
2-(indol-3-yl)-ethanol
3-(2-hydroxy-ethyl)-1h-indole
3-indolethanol
DTXSID2060173
AE-508/40182784
2-(1h-indol-3-yl)ethanol #
2-(3-indole)ethanol
mfcd00005659
b-(3-indole)ethanol
2-(3-indolylethanol
3-(b-hydroxyethyl)indole
3-(2-hydroxyethyl)indole, vetec(tm) reagent grade, 97%
zcw ,
BCP15412
HY-W010155
Q5479351
SY004666
beta-(3-indole)ethanol
AS-15780
SB14961
CCG-266289
CS-W010871
Z1123806416

Research Excerpts

Overview

Tryptophol (TOL) is a metabolic derivative of tryptophan (Trp) and shows pleiotropic effects in humans, plants and microbes. It is an aromatic alcohol and secondary metabolite of the opportunistic fungus Candida albicans.

ExcerptReferenceRelevance
"Tryptophol (TOL) is a metabolic derivative of tryptophan (Trp) and shows pleiotropic effects in humans, plants and microbes. "( Effects of tryptophan and phenylalanine on tryptophol production in Saccharomyces cerevisiae revealed by transcriptomic and metabolomic analyses.
Dao, Y; Gong, X; Han, Y; Hong, L; Luo, H; Luo, Y; Song, C; Wu, H; Wu, J; Zhang, X; Zhao, W; Zhu, D, 2022
)
2.43
"Tryptophol is an aromatic alcohol and secondary metabolite of the opportunistic fungus Candida albicans. "( Assessment of tryptophol genotoxicity in four cell lines in vitro: a pilot study with alkaline comet assay.
Antolović, R; Jelić, D; Kopjar, N; Kosalec, I; Pepeljnjak, S; Ramić, S, 2011
)
2.17
"Tryptophol is a natural component isolated from vinegar produced from the boiled extract of black soybean. "( Tryptophol induces death receptor (DR) 5-mediated apoptosis in U937 cells.
Akutagawa, H; Inagaki, S; Kida, K; Morimura, S; Tang, Y, 2007
)
3.23

Actions

ExcerptReferenceRelevance
"Tryptophol could inhibit the infection/replication of GVE2 by interacting with the host's Clp protease."( The effect of tryptophol on the bacteriophage infection in high-temperature environment.
Jin, M; Xu, C; Zhang, X, 2015
)
1.5

Treatment

ExcerptReferenceRelevance
"Mice treated with tryptophol plus ethanol became highly susceptible to convulsion."( Changes in seizure susceptibility after successive treatments of mice with tryptophol and ethanol.
Fukumori, R; Kitagawa, H; Minegishi, A; Satoh, T, 1981
)
0.82

Toxicity

ExcerptReferenceRelevance
" Future studies with tryptophol should look further into mechanisms involved in its toxic action and should focus on other cell types prone to infection with Candida spp."( Assessment of tryptophol genotoxicity in four cell lines in vitro: a pilot study with alkaline comet assay.
Antolović, R; Jelić, D; Kopjar, N; Kosalec, I; Pepeljnjak, S; Ramić, S, 2011
)
1.05
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
Saccharomyces cerevisiae metaboliteAny fungal metabolite produced during a metabolic reaction in Baker's yeast (Saccharomyces cerevisiae).
auxinAny of a group of compounds, both naturally occurring and synthetic, that induce cell elongation in plant stems (from Greek alphaupsilonxialphanuomega, "to grow").
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 (1)

ClassDescription
indolyl alcohol
[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 (10)

PathwayProteinsCompounds
alpha-Linolenic Acid Metabolism1020
tryptophan degradation via tryptamine416
superpathway of tryptophan utilization4292
L-tryptophan degradation V (side chain pathway)020
L-tryptophan degradation X (mammalian, via tryptamine)519
L-tryptophan degradation VIII (to tryptophol)1213
tryptophan degradation VIII (to tryptophol)1213
tryptophan degradation X (mammalian, via tryptamine)015
Tryptophan degradation07
Tryptophan metabolism2342

Protein Targets (4)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
glp-1 receptor, partialHomo sapiens (human)Potency31.62280.01846.806014.1254AID624417
BRCA1Homo sapiens (human)Potency0.31620.89137.722525.1189AID624202
67.9K proteinVaccinia virusPotency4.46680.00018.4406100.0000AID720580
[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)
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (2)

Processvia Protein(s)Taxonomy
regulation of DNA-templated transcriptionTrp operon repressorEscherichia coli K-12
regulation of DNA-templated transcriptionTrp operon repressorEscherichia coli K-12
negative regulation of DNA-templated transcriptionTrp operon repressorEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (3)

Processvia Protein(s)Taxonomy
DNA bindingTrp operon repressorEscherichia coli K-12
DNA-binding transcription factor activityTrp operon repressorEscherichia coli K-12
sequence-specific DNA bindingTrp operon repressorEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
cytoplasmTrp operon repressorEscherichia coli K-12
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (45)

Assay IDTitleYearJournalArticle
AID1879485Antiinflammatory activity against human HaCaT cells assessed as inhibition of UVB irradiation-induced PGE2 production measured after 2 hrs by ELISA2022Journal of natural products, 03-25, Volume: 85, Issue:3
Adiponectin-Secretion-Promoting Cyclic Peptide-Polyketide Hybrids from a Halophyte-Associated Fungus,
AID470187Antioxidant activity assessed as DPPH radical scavenging activity at 300 uM after 48 hrs by spectrophotometry2009Journal of natural products, Nov, Volume: 72, Issue:11
Indole derivatives from a marine sponge-derived yeast as DPPH radical scavengers.
AID1439694Cytotoxicity against human U251 cells assessed as decrease in cell proliferation after 72 hrs by SRB assay2017Bioorganic & medicinal chemistry letters, 04-01, Volume: 27, Issue:7
Preliminary SAR on indole-3-carbinol and related fragments reveals a novel anticancer lead compound against resistant glioblastoma cells.
AID1082988Antifungal activity against Leptosphaeria maculans isolate BJ-125/UAMH-9410 assessed as mycelial growth inhibition at 0.1 mM incubated under constant light for 5 days by mycelial radial growth bioassay2012Journal of agricultural and food chemistry, Aug-15, Volume: 60, Issue:32
Metabolism and metabolites of dithiocarbamates in the plant pathogenic fungus Leptosphaeria maculans.
AID1439693Cytotoxicity against human U87 cells assessed as decrease in cell proliferation after 72 hrs by SRB assay2017Bioorganic & medicinal chemistry letters, 04-01, Volume: 27, Issue:7
Preliminary SAR on indole-3-carbinol and related fragments reveals a novel anticancer lead compound against resistant glioblastoma cells.
AID288184Permeability coefficient through artificial membrane in presence of unstirred water layer by PAMPA2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1101157Fungicidal activity against Magnaporthe poae assessed as inhibition of fungal growth at 10 to 1000 mg/L2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1879486Induction of adiponectin secretion in human differentiated BMMSC cells assessed as increase in lipid droplet accumulation at 300 uM in the presence of IDX induction medium by Oil red O staining based inverted phase contrast microscope analysis2022Journal of natural products, 03-25, Volume: 85, Issue:3
Adiponectin-Secretion-Promoting Cyclic Peptide-Polyketide Hybrids from a Halophyte-Associated Fungus,
AID470189Antioxidant activity assessed as ABTS radical scavenging activity2009Journal of natural products, Nov, Volume: 72, Issue:11
Indole derivatives from a marine sponge-derived yeast as DPPH radical scavengers.
AID1439696Cytotoxicity against human IN1528 cells assessed as decrease in cell proliferation after 72 hrs by SRB assay2017Bioorganic & medicinal chemistry letters, 04-01, Volume: 27, Issue:7
Preliminary SAR on indole-3-carbinol and related fragments reveals a novel anticancer lead compound against resistant glioblastoma cells.
AID1082989Antifungal activity against Leptosphaeria maculans isolate BJ-125/UAMH-9410 assessed as mycelial growth inhibition at 0.2 mM incubated under constant light for 5 days by mycelial radial growth bioassay2012Journal of agricultural and food chemistry, Aug-15, Volume: 60, Issue:32
Metabolism and metabolites of dithiocarbamates in the plant pathogenic fungus Leptosphaeria maculans.
AID1101159Fungicidal activity against Cryphonectria parasitica assessed as inhibition of fungal growth at 12.5 ug after 7 days2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1694894Induction of TrkB activation in human SH-SY5Y cells assessed as increase in ERK1/2 phosphorylation at 10 uM after 4 hrs by Western blot analysis2020RSC medicinal chemistry, Jan-01, Volume: 11, Issue:1
Conversion of amino acids to aryl/heteroaryl ethanol metabolites using human CYP2D6-expressing live baker's yeast.
AID288192Partition coefficient, log P of the compound2007Bioorganic & medicinal chemistry, Jun-01, Volume: 15, Issue:11
QSAR study on permeability of hydrophobic compounds with artificial membranes.
AID1439697Cytotoxicity against human IN1760 cells assessed as decrease in cell proliferation after 72 hrs by SRB assay2017Bioorganic & medicinal chemistry letters, 04-01, Volume: 27, Issue:7
Preliminary SAR on indole-3-carbinol and related fragments reveals a novel anticancer lead compound against resistant glioblastoma cells.
AID1101156Fungicidal activity against Laetisaria fuciformis assessed as inhibition of fungal growth at 10 to 1000 mg/L2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1694888Neuroprotective activity against corticosterone-induced neurotoxicity in mouse N2a cells assessed as increase in cell viability at 10 uM preincubated for 24 hrs followed by corticosterone addition and measured after 24 hrs2020RSC medicinal chemistry, Jan-01, Volume: 11, Issue:1
Conversion of amino acids to aryl/heteroaryl ethanol metabolites using human CYP2D6-expressing live baker's yeast.
AID1694893Induction of TrkB activation in human SH-SY5Y cells assessed as increase in Akt phosphorylation at 10 uM after 4 hrs by Western blot analysis2020RSC medicinal chemistry, Jan-01, Volume: 11, Issue:1
Conversion of amino acids to aryl/heteroaryl ethanol metabolites using human CYP2D6-expressing live baker's yeast.
AID1101162Fungicidal activity against Cryphonectria parasitica assessed as inhibition of fungal growth at 100 ug after 7 days2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1101158Fungicidal activity against Rhizoctonia solani assessed as inhibition of fungal growth at 10 to 1000 mg/L2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1101160Fungicidal activity against Cryphonectria parasitica assessed as inhibition of fungal growth at 25 ug after 7 days2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1694887Induction of TrkB activation in human SH-SY5Y cells assessed as increase in phosphorylated TrkB level at 10 uM after 4 hrs by Western blot analysis2020RSC medicinal chemistry, Jan-01, Volume: 11, Issue:1
Conversion of amino acids to aryl/heteroaryl ethanol metabolites using human CYP2D6-expressing live baker's yeast.
AID1879484Antiinflammatory activity against human HaCaT cells assessed as inhibition of UVB irradiation-induced PGE2 production at 10 uM measured after 2 hrs by ELISA2022Journal of natural products, 03-25, Volume: 85, Issue:3
Adiponectin-Secretion-Promoting Cyclic Peptide-Polyketide Hybrids from a Halophyte-Associated Fungus,
AID1082990Antifungal activity against Leptosphaeria maculans isolate BJ-125/UAMH-9410 assessed as mycelial growth inhibition at 0.5 mM incubated under constant light for 5 days by mycelial radial growth bioassay2012Journal of agricultural and food chemistry, Aug-15, Volume: 60, Issue:32
Metabolism and metabolites of dithiocarbamates in the plant pathogenic fungus Leptosphaeria maculans.
AID1694889Neuroprotective activity against corticosterone-induced neurotoxicity in human SH-SY5Y cells assessed as induction of BDNF neurotropic response at 10 uM preincubated for 2 hrs followed by corticosterone addition and measured after 4 hrs by ELISA2020RSC medicinal chemistry, Jan-01, Volume: 11, Issue:1
Conversion of amino acids to aryl/heteroaryl ethanol metabolites using human CYP2D6-expressing live baker's yeast.
AID1439695Cytotoxicity against human IN1472 cells assessed as decrease in cell proliferation after 72 hrs by SRB assay2017Bioorganic & medicinal chemistry letters, 04-01, Volume: 27, Issue:7
Preliminary SAR on indole-3-carbinol and related fragments reveals a novel anticancer lead compound against resistant glioblastoma cells.
AID1101161Fungicidal activity against Cryphonectria parasitica assessed as inhibition of fungal growth at 50 ug after 7 days2000Journal of agricultural and food chemistry, Oct, Volume: 48, Issue:10
Isolation and characterization of fungal inhibitors from Epichloë festucae.
AID1879483Induction of adiponectin secretion in human differentiated BMMSC cells measured at 5 day in the presence of IDX induction medium by ELISA2022Journal of natural products, 03-25, Volume: 85, Issue:3
Adiponectin-Secretion-Promoting Cyclic Peptide-Polyketide Hybrids from a Halophyte-Associated Fungus,
AID504812Inverse Agonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID651635Viability Counterscreen for Primary qHTS for Inhibitors of ATXN expression
AID1347086qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lymphocytic Choriomeningitis Arenaviruses (LCMV): LCMV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID504810Antagonists of the Thyroid Stimulating Hormone Receptor: HTS campaign2010Endocrinology, Jul, Volume: 151, Issue:7
A small molecule inverse agonist for the human thyroid-stimulating hormone receptor.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588497High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain F protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588501High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Lethal Factor Protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Current protocols in cytometry, Oct, Volume: Chapter 13Microsphere-based flow cytometry protease assays for use in protease activity detection and high-throughput screening.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2006Cytometry. Part A : the journal of the International Society for Analytical Cytology, May, Volume: 69, Issue:5
Microsphere-based protease assays and screening application for lethal factor and factor Xa.
AID588499High-throughput multiplex microsphere screening for inhibitors of toxin protease, specifically Botulinum neurotoxin light chain A protease, MLPCN compound set2010Assay and drug development technologies, Feb, Volume: 8, Issue:1
High-throughput multiplex flow cytometry screening for botulinum neurotoxin type a light chain protease inhibitors.
AID1347082qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: LASV Primary Screen - GLuc reporter signal2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1347083qHTS for Inhibitors of the Functional Ribonucleoprotein Complex (vRNP) of Lassa (LASV) Arenavirus: Viability assay - alamar blue signal for LASV Primary Screen2020Antiviral research, 01, Volume: 173A cell-based, infectious-free, platform to identify inhibitors of lassa virus ribonucleoprotein (vRNP) activity.
AID1745845Primary qHTS for Inhibitors of ATXN expression
AID1799822Binding Assay from Article : \\The structural basis for the interaction between L-tryptophan and the Escherichia coli trp aporepressor.\\1987The Journal of biological chemistry, Apr-05, Volume: 262, Issue:10
The structural basis for the interaction between L-tryptophan and the Escherichia coli trp aporepressor.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (85)

TimeframeStudies, This Drug (%)All Drugs %
pre-199018 (21.18)18.7374
1990's3 (3.53)18.2507
2000's20 (23.53)29.6817
2010's29 (34.12)24.3611
2020's15 (17.65)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 39.76

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

MetricThis Compound (vs All)
Research Demand Index39.76 (24.57)
Research Supply Index4.48 (2.92)
Research Growth Index5.13 (4.65)
Search Engine Demand Index54.90 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (39.76)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews6 (6.90%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other81 (93.10%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]