Page last updated: 2024-12-06

pendimethalin

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

Description

Pendimethalin is a pre-emergent herbicide used to control a wide range of weeds in various crops. It is a dinitroaniline derivative, synthesized through a multi-step process involving reactions of aromatic amines, nitro compounds, and halogenated alkanes. Pendimethalin inhibits root growth by interfering with microtubule assembly in plant cells, thereby preventing cell division and elongation. Its effectiveness against weeds stems from its ability to be absorbed through the roots and transported to the growing points. Pendimethalin's importance lies in its widespread use for weed control, leading to increased crop yields and reduced herbicide application rates compared to older formulations. Research on pendimethalin focuses on understanding its mode of action, optimizing its application for different crops and weed species, and exploring potential environmental impacts and mitigation strategies.'

pendimethalin : A member of the class of substituted anilines that is N-(pentan-3-yl)aniline bearing two additional nitro substituents at positions 2 and 6 as well as two methyl substituents at positions 3 and 4. A herbicide used to control most annual grasses and many annual broad-leaved weeds. [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 CID38479
CHEMBL ID1256630
CHEBI ID83569
SCHEMBL ID21821
MeSH IDM0097354

Synonyms (95)

Synonym
BIDD:ER0107
caswell no. 454bb
3,4-dimethyl-2,6-dinitro-n-(1-ethylpropyl)aniline
penoxalin
n-(1-aethylpropyl)-3,4-dimethyl-2,6-dinitroanilin [german]
pendimethaline
benzenamine, 3,4-dimethyl-2,6-dinitro-n-(1-ethylpropyl)-
epa pesticide chemical code 108501
go-go-san
prowl
n-(1-ethylpropyl)-2,6-dinitro-3,4-xylidine
accotab
wayup
3,4-xylidine, 2,6-dinitro-n-(1-ethylpropyl)-
herbadox
n-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitrobenzenamine
way up
sipaxol
tendimethalin
ac 92553
einecs 254-938-2
stomp
phenoxalin
LS-14236
pendimethaline [iso-french]
swgc
southern weed grass control
stomp 330d
brn 2157711
hsdb 6721
penoxyn
n-(1-aethylpropyl)-2,6-dinitro-3,4-xylidin [german]
n-(3-pentyl)-3,4-dimethyl-2,6-dinitroaniline
stomp 330e
pendimethalin [ansi:bsi:iso]
penoxaline
aniline, 3,4-dimethyl-2,6-dinitro-n-(1-ethylpropyl)-
pendimethalin
40487-42-1
benzenamine, n-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitro-
n-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitro-aniline
NCGC00163941-01
OPREA1_039175
n-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitroaniline
NCGC00163941-02
3,4-dimethyl-2,6-dinitro-n-pentan-3-ylaniline
AKOS001705353
NCGC00163941-03
NCGC00163941-04
chebi:83569 ,
CHEMBL1256630
dtxsid7024245 ,
NCGC00259445-01
tox21_300867
NCGC00254771-01
cas-40487-42-1
dtxcid004245
tox21_201896
3,4-dimethyl-2,6-dinitro-n-(3-pentyl)aniline
P1964
FT-0673556
vl6l14c06u ,
n-(1-aethylpropyl)-2,6-dinitro-3,4-xylidin
unii-vl6l14c06u
n-(1-aethylpropyl)-3,4-dimethyl-2,6-dinitroanilin
FT-0630611
3,4-dimethyl-2,6-dinitro-n-(pentan-3-yl)aniline
SCHEMBL21821
pendimethalin [hsdb]
pendimethalin [iso]
pendimethalin [mi]
3,4-dimethyl-2,6 -dinitro-n-3-pentylaniline
2,6-dinitro-n-(1-ethylpropyl)-3,4-dimethylaniline
n-(1-ethylpropyl)-2,6-dinitro-3,4-dimethyl-benzenamine
prowl 4e
prowl 3.3
herbodox
pre-m 60dg
n-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitroaniline #
pendimethalin d5
pendimethalin, pestanal(r), analytical standard
prowl(r) (pendimethaline), analytical standard
pendimethalin 10 microg/ml in acetonitrile
pendimethalin 100 microg/ml in cyclohexane
prowl(tm)
Q423895
mfcd00055332
pendimethalin 1000 microg/ml in acetone
D92175
pendimethalin 1000 microg/ml in toluene
CS-0012876
HY-B0862
AKOS040758114
EN300-7409229
Z3221533686

Research Excerpts

Overview

Pendimethalin (PND) is a dinitroaniline preemergent herbicide widely used to control grasses and weeds. Pendimethaline (PDM) is an herbicide that is widely used in many countries to control annual grasses. Pendamethalin is a herbicide active substance commonly used in terrestrial agricultural systems and is thus detected at high concentrations in the surface water of several European countries.

ExcerptReferenceRelevance
"Pendimethalin is a dinitroaniline herbicide used to control broadleaf weeds by inhibiting the formation of microtubules during cell division. "( Assessing sub-lethal effects of the dinitroaniline herbicide pendimethalin in zebrafish embryos/larvae (Danio rerio).
El Ahmadie, N; Ganter, J; Lopez, S; Martyniuk, CJ; Souders, CL; Wang, S; Wengrovitz, AS; Zhao, YH,
)
1.82
"Pendimethalin (PND) is a dinitroaniline preemergent herbicide widely used to control grasses and weeds. "( Dinitroaniline herbicide pendimethalin affects development and induces biochemical and histological alterations in zebrafish early-life stages.
Amorena, M; Crescenzo, G; Fabrello, J; Faggio, C; Iannetta, A; Matozzo, V; Merola, C; Perugini, M; Tinelli, A, 2022
)
2.47
"Pendimethalin (PDM) is an herbicide that is widely used in many countries to control annual grasses."( Pendimethalin exposure induces bovine mammary epithelial cell death through excessive ROS production and alterations in the PI3K and MAPK signaling pathways.
An, G; Lee, H; Lim, W; Song, G, 2022
)
2.89
"Pendimethalin (PND) is a widely used herbicide in modern means of agricultural practices. "( Studies on conformational changes induced by binding of pendimethalin with human serum albumin.
Ahmad, M; Ahmad, MI; Javed, M; Potshangbam, AM, 2020
)
2.25
"Pendimethalin (PM) is a selective herbicide, widely present in aquatic environment. "( Impacts of herbicide pendimethalin on sex steroid level, plasma vitellogenin concentration and aromatase activity in teleost Clarias batrachus (Linnaeus).
Gupta, P; Verma, SK, 2020
)
2.32
"Pendimethalin (PDM) is a dinitroaniline crop pesticide that is extensively utilized worldwide. "( Pendimethalin induces apoptosis in testicular cells via hampering ER-mitochondrial function and autophagy.
Ham, J; Lim, W; Song, G, 2021
)
3.51
"Pendimethalin is a herbicide active substance commonly used in terrestrial agricultural systems and is thus detected at high concentrations in the surface water of several European countries. "( Transchem project - Part I: Impact of long-term exposure to pendimethalin on the health status of rainbow trout (Oncorhynchus mykiss L.) genitors.
Danion, M; Le Floch, S; Morin, T; Pannetier, P; Van Arkel, K, 2018
)
2.17
"Pendimethalin (PND) is a systemic herbicide widely used on rice, cotton, peas, wheat, potatoes, fruits, nuts and other residential and non-residential crops; however, it concurrently exerts toxic effects on beneficial organisms like earthworms, aquatic invertebrates and other non-targeted animals including humans. "( Binding properties of pendimethalin herbicide to DNA: multispectroscopic and molecular docking approaches.
Ahmad, A; Ahmad, I; Ahmad, M, 2016
)
2.19

Effects

Pendimethalin (PDM) has been increasingly used as a herbicide for approximately 30 years. It has a geometric mean (GM) half-life of 76-98 d in agriculturally relevant soils.

ExcerptReferenceRelevance
"Pendimethalin has a geometric mean (GM) half-life of 76-98 d in agriculturally relevant soils under aerobic conditions in the lab."( Critical assessment of pendimethalin in terms of persistence, bioaccumulation, toxicity, and potential for long-range transport.
Matthies, M; Solomon, KR; Vighi, M, 2017
)
1.49
"Pendimethalin (PDM) has been increasingly used as a herbicide for approximately 30 years."( Pendimethalin exposure disrupts mitochondrial function and impairs processes related to implantation.
An, G; Kim, M; Lim, W; Park, J; Song, G, 2023
)
3.07
"Pendimethalin has a geometric mean (GM) half-life of 76-98 d in agriculturally relevant soils under aerobic conditions in the lab."( Critical assessment of pendimethalin in terms of persistence, bioaccumulation, toxicity, and potential for long-range transport.
Matthies, M; Solomon, KR; Vighi, M, 2017
)
1.49

Treatment

ExcerptReferenceRelevance
"Pendimethalin treatment also activated ER stress and autophagy, leading to loss of mitochondrial membrane potential."( Pendimethalin induces apoptotic cell death through activating ER stress-mediated mitochondrial dysfunction in human umbilical vein endothelial cells.
Amarakoon, D; Lee, HS; Lee, SH; Park, Y; Smolensky, D; Tamia, G, 2022
)
2.89

Toxicity

The toxic effects of a widely used herbicide (Stomp 330 containing 33% pendimethalin as active ingredient) applied alone or in combination with three heavy elements were studied.

ExcerptReferenceRelevance
"The benthic macroinvertebrates Lumbriculus variegatus and Chironomus riparius were used in toxicity and bioaccumulation tests to determine the toxic concentrations and accumulation potential of sediment associated herbicides."( Bioaccumulation and toxicity of sediment associated herbicides (ioxynil, pendimethalin, and bentazone) in Lumbriculus variegatus (Oligochaeta) and Chironomus riparius (Insecta).
Kukkonen, JV; Mäenpää, KA; Sormunen, AJ, 2003
)
0.55
"The toxic effects of a widely used herbicide (Stomp 330 containing 33% pendimethalin as active ingredient) applied alone or in combination with three heavy elements (copper sulphate, cadmium sulphate and lead acetate) modelling the heavy metal load of the environment were studied on chicken embryos with injection treatment."( Toxicity of a pendimethalin containing herbicide formulation and three heavy metals in chicken embryos.
Budai, P; Juhász, E; Keserü, M; Szabó, R; Várnagy, L, 2006
)
0.93
"The indiscriminate use of pesticides and herbicides to increase crop productivity has aroused a great concern among the environmental and health scientists due to their adverse effects in both target as well as non-target species."( In vitro induction of cytotoxicity and DNA strand breaks in CHO cells exposed to cypermethrin, pendimethalin and dichlorvos.
Bajpayee, M; Dhawan, A; Pandey, AK; Parmar, D; Patel, S, 2007
)
0.56
"The aim of this study was to determine the individual and combined toxic effects of STOMP 330 EC herbicide (33% pendimethalin) and copper sulphate on the development of chicken embryos."( Toxicity of pendimethalin containing formulation and copper sulphate to chicken embryos.
Budai, P; Lehel, J; Marczali, Z; Szabó, R, 2013
)
0.98
" Biological markers used for the evaluation of toxic effects of pesticides have increased these days."( Morphotoxicity and cytogenotoxicity of pendimethalin in the test plant Allium cepa L. - A biomarker based study.
Srivastava, A; Verma, S, 2018
)
0.75
"Pesticides have adverse effects on the cellular functionality, which may trigger myriad of health consequences."( Cytotoxicity and genotoxicity of methomyl, carbaryl, metalaxyl, and pendimethalin in human umbilical vein endothelial cells.
Al-Khedhairy, AA; Alwathnani, HA; Ansari, SM; Musarrat, J; Saquib, Q; Siddiqui, MA, 2021
)
0.86
" It has been found to be especially toxic to aquatic life."( Assessment of the in vivo genotoxicity of pendimethalin via mitochondrial bioenergetics and transcriptional profiles during embryogenesis in zebrafish: Implication of electron transport chain activity and developmental defects.
Lee, JY; Lim, W; Park, H; Song, G, 2021
)
0.89

Bioavailability

ExcerptReferenceRelevance
" Bioavailability of residues to sensitive plant species was also determined."( Degradation of atrazine, metolachlor, and pendimethalin in pesticide-contaminated soils: effects of aged residues on soil respiration and plant survival.
Anderson, TA; Anhalt, JC; Arthur, EL; Coats, JR, 2000
)
0.57

Dosage Studied

ExcerptRelevanceReference
" He was successfully treated by increasing his dosage of omeprazol (20 mg/day) for two weeks."( Acute gastroduodenal injury after ingestion of diluted herbicide pendimethalin.
Azuhata, H; Katoh, H; Kuwano, H; Tsukada, K, 2009
)
0.59
" The aim of this paper is to assess selectivity of various herbicides in grass seed crops by using dose-response curves."( Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
Jensen, JE; Mathiesen, TJ; Ritz, C; Streibig, JC; Tind, T, 2009
)
0.35
" The two pesticides were applied in equal dosage to a structured, tile-drained soil, and the concentration of the pesticides was then measured in drainage water sampled flow-proportionally."( Transport modes and pathways of the strongly sorbing pesticides glyphosate and pendimethalin through structured drained soils.
de Jonge, LW; Ernsten, V; Hansen, N; Jacobsen, OH; Kjær, J; Olsen, P, 2011
)
0.6
"67%)) in a dose-response study."( Toxicity and tissue accumulation characteristics of the herbicide pendimethalin under silicon application in ginger (Zingiber officinale Roscoe).
Kong, Y; Li, Y; Lv, Y; Wang, K; Xu, K, 2022
)
0.96
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
herbicideA substance used to destroy plant pests.
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
[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
C-nitro compoundA nitro compound having the nitro group (-NO2) attached to a carbon atom.
substituted aniline
secondary amino compoundA compound formally derived from ammonia by replacing two hydrogen atoms by organyl groups.
[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 (16)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
pregnane X receptorRattus norvegicus (Norway rat)Potency39.81070.025127.9203501.1870AID651751
GLI family zinc finger 3Homo sapiens (human)Potency7.42800.000714.592883.7951AID1259369
AR proteinHomo sapiens (human)Potency15.09870.000221.22318,912.5098AID1259243; AID1259247
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency12.35860.000657.913322,387.1992AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency22.71970.001022.650876.6163AID1224838; AID1224839; AID1224893
progesterone receptorHomo sapiens (human)Potency18.54750.000417.946075.1148AID1346795
retinoid X nuclear receptor alphaHomo sapiens (human)Potency40.40210.000817.505159.3239AID1159531; AID588546
farnesoid X nuclear receptorHomo sapiens (human)Potency24.82210.375827.485161.6524AID588527; AID743217
pregnane X nuclear receptorHomo sapiens (human)Potency50.87520.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency14.60840.000229.305416,493.5996AID743075; AID743079
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency2.21750.023723.228263.5986AID743223
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency69.00860.001723.839378.1014AID743083
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency21.94530.057821.109761.2679AID1159526; AID1159528
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency69.00860.000323.4451159.6830AID743065; AID743067
heat shock protein beta-1Homo sapiens (human)Potency62.49810.042027.378961.6448AID743210
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency50.39510.000627.21521,122.0200AID651741; AID743202; AID743219
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (20)

Assay IDTitleYearJournalArticle
AID1104245Herbicidal activity against Poa pratensis subsp. pratensis applied using logarithmic sprayer2009Pest management science, Nov, Volume: 65, Issue:11
Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
AID1102468Effect on root elongation in Lactuca sativa (lettuce) at 10'-4 to 10'-9 M after 5 days relative to control2003Journal of agricultural and food chemistry, Oct-08, Volume: 51, Issue:21
Lignans and neolignans from Brassica fruticulosa: effects on seed germination and plant growth.
AID522811Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin I235L mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522809Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin H28Q mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1110716Pre-emergence herbicidal activity against Amaranthus viridis assessed as reduction of seed germination at 1 ppm after 7 to 21 days by pot test2000Farmaco (Societa chimica italiana : 1989), May, Volume: 55, Issue:5
Studies on arylfuran derivatives. Part XI. Synthesis, characterisation and biological studies on some Mannich bases carrying 2,4-dichlorophenylfurfural moiety.
AID522813Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin I235V mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522819Antimicrobial activity against Cryptosporidium parvum by short-term in vitro culture assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522806Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin V4L mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522810Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin L136F mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522812Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin I235T mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522815Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin R243C mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522807Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin S6I mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522814Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin T239I mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522816Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin R243S mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID522805Antimicrobial activity against Toxoplasma gondii RH infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1102464Stimulation of shoot elongation in Lactuca sativa (lettuce) at 10'-4 to 10'-9 M after 5 days relative to control2003Journal of agricultural and food chemistry, Oct-08, Volume: 51, Issue:21
Lignans and neolignans from Brassica fruticulosa: effects on seed germination and plant growth.
AID1102472Inhibition of seed germination in Lactuca sativa (lettuce) at 10'-4 to 10'-9 M after 5 days relative to control2003Journal of agricultural and food chemistry, Oct-08, Volume: 51, Issue:21
Lignans and neolignans from Brassica fruticulosa: effects on seed germination and plant growth.
AID522808Antimicrobial activity against Toxoplasma gondii RH containing alpha1-tubulin F24H mutation infected in HFF cells by plaque assay2010Antimicrobial agents and chemotherapy, Apr, Volume: 54, Issue:4
Dinitroaniline activity in Toxoplasma gondii expressing wild-type or mutant alpha-tubulin.
AID1110719Pre-emergence herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as reduction of seed germination at 1 ppm after 7 to 21 days by pot test2000Farmaco (Societa chimica italiana : 1989), May, Volume: 55, Issue:5
Studies on arylfuran derivatives. Part XI. Synthesis, characterisation and biological studies on some Mannich bases carrying 2,4-dichlorophenylfurfural moiety.
AID1104243Toxicity against Festuca rubra applied using logarithmic sprayer2009Pest management science, Nov, Volume: 65, Issue:11
Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (164)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (1.83)18.7374
1990's11 (6.71)18.2507
2000's47 (28.66)29.6817
2010's73 (44.51)24.3611
2020's30 (18.29)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 42.12

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 Index42.12 (24.57)
Research Supply Index5.17 (2.92)
Research Growth Index5.34 (4.65)
Search Engine Demand Index114.37 (26.88)
Search Engine Supply Index3.65 (0.95)

This Compound (42.12)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials2 (1.16%)5.53%
Reviews1 (0.58%)6.00%
Case Studies2 (1.16%)4.05%
Observational1 (0.58%)0.25%
Other167 (96.53%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]