Page last updated: 2024-11-06

fenarimol

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

Description

Fenarimol is a fungicide that inhibits the biosynthesis of ergosterol, a key component of fungal cell membranes. It is used to control a wide range of fungal diseases, including powdery mildew, rust, and leaf spot. Fenarimol was first synthesized in the 1970s and has been widely used in agriculture since then. It is a systemic fungicide, meaning that it is absorbed by the plant and translocated throughout the plant tissue. This makes it effective against both foliar and soilborne diseases. Fenarimol has been shown to be effective at low application rates, making it a cost-effective option for farmers. However, there is concern about the potential environmental impact of fenarimol, as it can persist in the soil and water. Research on fenarimol continues to focus on understanding its environmental fate, optimizing its use, and developing new, more environmentally friendly fungicides.'

fenarimol : A racemate comprising equimolar amounts of (R)- and (S)-fenarimol. A sterol demethylation inhibitor, it is used as a fungicide for the treatment of blackspot, mildew and rust in tomatoes, peppers and melons, but is not approved for use within the European Union. [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]

(2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol : A member of the class of pyrimidines that is pyrimidin-5-ylmethanol in which one of the hydrogens attached to the carbon bearing the hydroxy group is replaced by a 2-chlorophenyl group while the other is replaced by a 4-chlorophenyl group. [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 CID43226
CHEMBL ID28971
CHEBI ID83686
SCHEMBL ID42209
MeSH IDM0104612

Synonyms (62)

Synonym
epa pesticide chemical code 206600
einecs 262-095-7
alpha-(2-chlorophenyl)-alpha-4-(chlorophenyl)-5-pyrimidinemethanol
alpha-(2-chlorophenyl)-alpha-(4-chlorophenyl)-5-pyrimidinemethanol
caswell no. 207aa
bloc
5-pyrimidinemethanol, alpha-(2-chlorophenyl)-alpha-(4-chlorophenyl)-
el 222
(+-)-2,4'-dichloro-alpha-(pyrimidin-5-yl)benzhydryl alcohol
compound 56722
2,4'-dichloro-alpha(pyrimidin-5-yl)benzhydryl alcohol
rubigan
brn 5972869
rimidin
fenarimol [ansi:bsi:iso]
.alpha.-(2-chlorophenyl)-.alpha.-(4-chlorophenyl)-5-pyrimidinemethanol
5-pyrimidinemethanol, .alpha.-(2-chlorophenyl)-.alpha.-(4-chlorophenyl)-
60168-88-9
fenarimol
NCGC00163917-02
NCGC00163917-01
(2-chlorophenyl)(4-chlorophenyl)pyrimidin-5-ylmethanol
NCGC00163917-03
CHEMBL28971 ,
dndi1246778
chebi:83686 ,
(2-chlorophenyl)-(4-chlorophenyl)-pyrimidin-5-ylmethanol
bdbm50024511
(4-chloro-phenyl)-(2-chloro-phenyl)-pyrimidin-5-yl-methanol
NCGC00163917-05
NCGC00163917-04
NCGC00254558-01
tox21_300650
dtxsid2032390 ,
tox21_201631
cas-60168-88-9
dtxcid0012390
NCGC00259180-01
unii-o088gu930q
o088gu930q ,
FT-0630719
AKOS015895790
2,4'-dichloro-.alpha.(pyrimidin-5-yl)benzhydryl alcohol
fenari
fenarimol [mi]
(+-)-2,4'-dichloro-.alpha.-(pyrimidin-5-yl)benzhydryl alcohol
fenarimol [iso]
(+/-)-fenarimol
SCHEMBL42209
(2-chlorophenyl)(4-chlorophenyl)5-pyrimidinylmethanol #
(2-chlorophenyl)-.alpha.-(4-chlorophenyl)-5-pyrimidinemethanol
(2-chlorophenyl)(4-chlorophenyl)(pyrimidin-5-yl)methanol
2,4'-dichloro-(pyrimidin-5-yl)benzhydryl alcohol
W-111179
fenarimol, pestanal(r), analytical standard
fenarimol 10 microg/ml in cyclohexane
fenarimol 100 microg/ml in cyclohexane
fenarimol 10 microg/ml in ethyl acetate
fenarimol 1000 microg/ml in acetone
Q906987
el 222;rubigan
spiro[furo[3,4-c]pyridine-1(3h),4-piperidin]-3-one

Research Excerpts

Overview

Fenarimol (Rubigan) is a pyrimidine ergosterol biosynthesis inhibitor used as a systemic fungicide. It can affect estrogen/androgen levels in vivo in rodents.

ExcerptReferenceRelevance
"Fenarimol (Rubigan) is a pyrimidine ergosterol biosynthesis inhibitor used as a systemic fungicide. "( A fatal forensic intoxication with fenarimol: analysis by HPLC/DAD/MSD.
Avila, S; Barroso, M; Castanheira, F; Pinho Marques, E; Proença, P; Teixeira, H; Vieira, DN, 2003
)
2.04
"Fenarimol is an aromatase inhibitor and therefore can affect estrogen/androgen levels in vivo in rodents."( Neurodevelopmental effects of perinatal fenarimol exposure on rats.
de Castro, VL; de Mello, MA; Diniz, C; Morita, L; Poli, P; Zucchi, T, 2007
)
1.33

Actions

ExcerptReferenceRelevance
"Fenarimol did not increase the number of chromosome aberrations significantly, but it reduced the mitotic index at the higher doses (P < 0.05)."( The investigation of the genotoxic effects of fenarimol and propamocarb in mouse bone marrow in vivo.
Aydemir, N; Bilaloğlu, R, 2004
)
1.3

Toxicity

ExcerptReferenceRelevance
"The identification of environmental compounds that have adverse effects on reproductive health and animal development is particularly challenging."( Prenatal and perinatal fenarimol-induced genotoxicity in leukocytes of in vivo treated rats.
de Castro, VL; de Mello, MA; Poli, P; Zucchi, TM, 2005
)
0.64

Dosage Studied

The MCF-7 cell proliferation assay was used to investigate further the dose-response curves for the estrogenic, antiestrogenic, and aromatase inhibiting properties of fenarimol in vitro. The IC(50)s of prochloraz, imazalil, propioconazole fenrimol, triadimenol, and triadimefon were calculated to be 0.

ExcerptRelevanceReference
" The MCF-7 cell proliferation assay was used to investigate further the dose-response curves for the estrogenic, antiestrogenic, and aromatase inhibiting properties of fenarimol in vitro."( Estrogenic effects in vitro and in vivo of the fungicide fenarimol.
Andersen, HR; Bonefeld-Jørgensen, EC; Jarfeldt, K; Jayatissa, MN; Nielsen, F; Vinggaard, AM, 2006
)
0.77
" The MN response depended on the sampling time and the concentration used, which showed a significant dose-response correlation (r=0."( Genotoxic effects of the pesticides Rubigan, Omite and Rovral in root-meristem cells of Crepis capillaris L.
Dimitrov, B; Gadeva, P, 2008
)
0.35
" cruzi infection after once daily oral dosing at 20, 50 and 100 mg/kg for 5 days."( Design, structure-activity relationship and in vivo efficacy of piperazine analogues of fenarimol as inhibitors of Trypanosoma cruzi.
Alexander, PW; Best, WM; Charman, SA; Chatelain, E; Diao, H; Gregg, AD; Keenan, M; Kerfoot, M; Khong, A; Ryan, E; Scandale, I; Shackleford, DM; Thompson, RC; von Geldern, TW; White, KL, 2013
)
0.61
" cruzi infection after once daily oral dosing for 20 days at 20 mg/kg 6 and 10 mg/kg (S)-7."( Two analogues of fenarimol show curative activity in an experimental model of Chagas disease.
Abbott, MJ; Alexander, PW; Best, WM; Botero, A; Campbell, M; Chaplin, JH; Charman, SA; Chatelain, E; Chiu, FC; Cornwall, S; Keenan, M; Khong, A; Koltun, M; Morizzi, J; Perez, C; Ryan, E; Scandale, I; Shackleford, DM; Thompson, RA; von Geldern, TW; White, KL, 2013
)
0.73
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (3)

ClassDescription
tertiary alcoholA tertiary alcohol is a compound in which a hydroxy group, -OH, is attached to a saturated carbon atom which has three other carbon atoms attached to it.
monochlorobenzenesAny member of the class of chlorobenzenes containing a mono- or poly-substituted benzene ring in which only one substituent is chlorine.
pyrimidinesAny compound having a pyrimidine as part of its structure.
[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 (31)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency81.07220.007215.758889.3584AID1224835
pregnane X receptorRattus norvegicus (Norway rat)Potency44.66840.025127.9203501.1870AID651751
hypoxia-inducible factor 1 alpha subunitHomo sapiens (human)Potency19.83543.189029.884159.4836AID1224846
RAR-related orphan receptor gammaMus musculus (house mouse)Potency29.35010.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency19.73480.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency40.62610.000221.22318,912.5098AID1259243; AID1259247; AID1259381; AID743035; AID743042; AID743054; AID743063
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency49.57140.000657.913322,387.1992AID1259377; AID1259378
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency65.51290.001022.650876.6163AID1224838; AID1224839; AID1224893
progesterone receptorHomo sapiens (human)Potency19.22170.000417.946075.1148AID1346795
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency48.96620.000214.376460.0339AID720692
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency43.59980.003041.611522,387.1992AID1159552; AID1159553; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency30.79340.000817.505159.3239AID1159527; AID1159531; AID588544
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency32.73320.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259403
farnesoid X nuclear receptorHomo sapiens (human)Potency39.00240.375827.485161.6524AID588526; AID743217
pregnane X nuclear receptorHomo sapiens (human)Potency24.79850.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency46.43620.000229.305416,493.5996AID1259244; AID1259248; AID743069; AID743075; AID743077; AID743078; AID743079; AID743080
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency47.88360.001019.414170.9645AID588536; AID743140; AID743191
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency50.11870.023723.228263.5986AID588541
aryl hydrocarbon receptorHomo sapiens (human)Potency27.77880.000723.06741,258.9301AID743085
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency26.42910.001723.839378.1014AID743083
thyroid stimulating hormone receptorHomo sapiens (human)Potency25.84420.001628.015177.1139AID1224843; AID1224895
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1 (p105), isoform CRA_aHomo sapiens (human)Potency48.966219.739145.978464.9432AID1159509
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency12.51530.057821.109761.2679AID1159526
Histone H2A.xCricetulus griseus (Chinese hamster)Potency91.35130.039147.5451146.8240AID1224845
vitamin D3 receptor isoform VDRAHomo sapiens (human)Potency89.12510.354828.065989.1251AID504847
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency54.10450.000323.4451159.6830AID743065; AID743067
heat shock protein beta-1Homo sapiens (human)Potency54.94100.042027.378961.6448AID743210
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency25.85070.000627.21521,122.0200AID743202; AID743219
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency69.18330.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency69.18330.001551.739315,848.9004AID1259244
[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)
AromataseRattus norvegicus (Norway rat)EC50 (µMol)4.10000.05500.83504.1000AID54068
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (35)

Assay IDTitleYearJournalArticle
AID1112263Fungicidal activity against Diplodia mutila Q assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112229Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as non-lesion areas compound applied 24 hr prior inoculation to pruning wound measured after 1 year2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112268Fungicidal activity against Neofusicoccum luteum G(s)-1 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673491Antitrypanosomal activity against trypomastigotes of Trypanosoma cruzi Tulahuen infected in Swiss mouse model of chagas disease assessed as decrease in parasite level in blood at 100 mg/kg, ip administered 8 days after post infection qd for 5 days2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112257Fungicidal activity against Neofusicoccum luteum N(12)2 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673466Plasma concentration in Swiss mouse at 20 mg/kg, po after 1 hr2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112271Fungicidal activity against Neofusicoccum australe Kat-1 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112261Fungicidal activity against Neofusicoccum australe Mel-2 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID54068In vitro inhibition of cytochrome P450 19A1 by rat ovarian microsomes incubated with [3H]androstenedione and NADPH-generating system.1987Journal of medicinal chemistry, Aug, Volume: 30, Issue:8
Aromatase inhibition by 5-substituted pyrimidines and dihydropyrimidines.
AID1112227Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as pathogen incidence at area beyond node compound applied 24 hr prior inoculation to pruning wound measured after 1 year2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673463Inhibition of CYP3A4/6 in human liver microsomes at 20 uM2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112228Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as pathogen incidence at closest side shoot compound applied 24 hr prior inoculation to pruning wound measured after 6 months2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673467Plasma concentration in Swiss mouse at 20 mg/kg, po after 8 hrs2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112231Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as pathogen incidence at dieback sites compound applied 24 hr prior inoculation to pruning wound measured after 1 year2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673460Cytotoxicity against rat L6 cells after 72 hrs by Alamar Blue assay2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112234Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as pathogen incidence at 2.5 g AI /100 L applied 24 hr prior inoculation to pruning wound measured after 3 months2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673459Antitrypanosomal activity against trypomastigotes of Trypanosoma cruzi Tulahuen expressing the beta- galactosidase gene infected rat L6 cells after 96 hrs2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112259Fungicidal activity against Neofusicoccum luteum G(s)-1 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673461Kinetic solubility of the compound at pH 6.5 by nephelometric analysis2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112255Fungicidal activity against Diplodia mutila F (12)2 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID673488Antitrypanosomal activity against trypomastigotes of Trypanosoma cruzi Tulahuen infected in Swiss mouse model of chagas disease assessed as increase of host survival at 100 mg/kg, ip administered 8 days after post infection qd for 5 days2012Journal of medicinal chemistry, May-10, Volume: 55, Issue:9
Analogues of fenarimol are potent inhibitors of Trypanosoma cruzi and are efficacious in a murine model of Chagas disease.
AID1112260Fungicidal activity against Neofusicoccum australe J-3 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112245Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as dieback lesion length at 2.5 g AI /100 L applied 24 hr prior inoculation to pruning wound measured after 3 months2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112269Fungicidal activity against Neofusicoccum australe J-3 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112264Fungicidal activity against Diplodia mutila Iso-2 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112230Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as pathogen incidence at dieback edges compound applied 24 hr prior inoculation to pruning wound measured after 1 year2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112226Fungicidal activity against Neofusicoccum luteum infected Pinot noir grapevine assessed as mean pathogen compound applied 24 hr prior inoculation to pruning wound measured after 1 year2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112262Fungicidal activity against Neofusicoccum australe Kat-1 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112267Fungicidal activity against Neofusicoccum luteum N(12)2 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112254Fungicidal activity against Diplodia mutila Q assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112256Fungicidal activity against Diplodia mutila Iso-2 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112265Fungicidal activity against Diplodia mutila F (12)2 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112258Fungicidal activity against Neofusicoccum luteum M (13)8 assessed as conidial germination inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112266Fungicidal activity against Neofusicoccum luteum M (13)8 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
AID1112270Fungicidal activity against Neofusicoccum australe Mel-2 assessed as mycelial growth inhibition after 48 hr2012Pest management science, May, Volume: 68, Issue:5
Evaluation of fungicides for the management of Botryosphaeria dieback diseases of grapevines.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (71)

TimeframeStudies, This Drug (%)All Drugs %
pre-19905 (7.04)18.7374
1990's22 (30.99)18.2507
2000's30 (42.25)29.6817
2010's14 (19.72)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 24.55

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 Index24.55 (24.57)
Research Supply Index4.30 (2.92)
Research Growth Index4.95 (4.65)
Search Engine Demand Index49.81 (26.88)
Search Engine Supply Index3.98 (0.95)

This Compound (24.55)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.37%)6.00%
Case Studies2 (2.74%)4.05%
Observational0 (0.00%)0.25%
Other70 (95.89%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]