Page last updated: 2024-12-04

bentazone

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

Description

bentazone: RN given refers to parent cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

bentazone : A benzothiadiazine that is 1H-2,1,3-benzothiadiazin-4(3H)-one 2,2-dioxide substituted by an isopropyl group at position 3. [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 CID2328
CHEMBL ID1567045
CHEBI ID3018
SCHEMBL ID53939
MeSH IDM0042455

Synonyms (119)

Synonym
BRD-K33986892-001-02-3
1h-2,1,3-benzothiadiazin-4(3h)-one, 3-isopropyl-, 2,2-dioxide
1h-2,1,3-benzothiadiazin-4(3h)-one, 3-(1-methylethyl)-, 2,2-dioxide
DIVK1C_006558
KBIO1_001502
laddok
bentazon [ansi]
basagran 480
bas 3512h
3-isopropyl-4h-2,1,3-benzothiadiazin-4-one 2,2-dioxide
einecs 246-585-8
bas 3510h
graminon-plus
bentazone [bsi:iso]
bas 3517h
bendioxide
basagran-plus
caswell no. 509c
bas 351-h
pentazone
pledge
3-isopropyl-2,1,3-benzothiadiazinon-(4)-2,2-dioxid [german]
bas 351-07h
3-isopropyl-1h-benzo-2,1,3-thiadiazin-4-one 2,2-dioxide
bas 351h
hsdb 3430
3-(1-methylethyl)-(1h)-2,1,3-benzothiadiazin-4(3h)-one-2,2-dioxide
leader
ccris 6977
epa pesticide chemical code 275200
3-isopropyl-1h-2,1,3-benzothiadiazin-4(3h)-one-2,2-dioxide
brn 0530220
bas 3510
1h-2,1,3-benzothiadiazin-4(3h)-one-2,2-dioxide, 3-isopropyl-
basagran kv
SPECTRUM_001851
BSPBIO_002381
OPREA1_558180
25057-89-0
bentazone
NCGC00094531-03
NCGC00094531-01
NCGC00094531-02
KBIO2_004932
KBIO3_001881
KBIO2_007500
KBIO2_002364
KBIOSS_002368
KBIOGR_001101
SPECTRUM2_001889
SPECTRUM4_000671
SPECTRUM3_000831
SPECPLUS_000462
SPBIO_001798
SPECTRUM330039
bentazon
3-isopropyl-1h-2,1,3-benzothiadiazin-4(3h)-one 2,2-dioxide
basagran
OPREA1_729468
SPECTRUM5_001976
NCGC00094531-04
NCGC00094531-05
inchi=1/c10h12n2o3s/c1-7(2)12-10(13)8-5-3-4-6-9(8)11-16(12,14)15/h3-7,11h,1-2h3
zomsmjklgfbrbs-uhfffaoysa-
2,2-dioxo-3-propan-2-yl-1h-benzo[d][1,2,6]thiadiazin-4-one
NCGC00094531-07
NCGC00094531-06
tox21_201951
dtxsid0023901 ,
NCGC00259500-01
dtxcid503901
cas-25057-89-0
tox21_300742
NCGC00254648-01
A817619
2,2-dioxo-3-propan-2-yl-1h-2$l^{6},1,3-benzothiadiazin-4-one
2,2-bis(oxidanylidene)-3-propan-2-yl-1h-2$l^{6},1,3-benzothiadiazin-4-one
CCG-15052
3-(1-methylethyl)-1h-2,1,3-benzothiadiazin-4(3h)-one 2,2-dioxide
3-isopropyl-2,1,3-benzothiadiazinon-(4)-2,2-dioxid
unii-r4s7zgz9ct
r4s7zgz9ct ,
FT-0638490
JC10172
AKOS015897484
CHEMBL1567045
chebi:3018 ,
SCHEMBL53939
bentazone [iso]
bentazon [mi]
bentazone [hsdb]
3-isopropyl-2,2-dioxo-1h-2$l^{6},1,3-benzothiadiazin-4-one
3-(1-methylethyl)-1h-2,1,3-benzothiadiazin-4(3h)-one-2,2-dioxide
3-(1-methylethyl)-1h-2,1,3-benzothiadiazin- -4 (3h)-one-2,2-dioxide
3-isopropyl-2,1,3-benzothiadiazin-4-one-2,2-dioxide
3-(1-methylethyl)-1h-2,1,3-benzothiadiazin-4(3h)-one- -2,2-dioxide
3-(propan-2-yl)-1h-2,1,3-benzothiadiazin-4(3h)-one 2,2-dioxide
adagio
3-(1-methylethyl)-1h-2,1,3-benzothia-diazin-4(3h)-one 2,2-dioxide
3-isopropyl-4-oxo-2,1,3-benzothiadiazine 2,2-dioxide
SR-01000388483-1
sr-01000388483
bentazon, pestanal(r), analytical standard
bentazon, analytical standard
bentazone 10 microg/ml in acetonitrile
bentazone 100 microg/ml in acetonitrile
B3825
3-(1-methylethyl)-1h-2,1,3-benzothiadiazin-4(3h)-ol
BCP27977
Q148937
CS-0014134
3-isopropyl-d7-1h-2,1,3-benzothiadiazin-4(3h)-one 2,2-dioxide
3-isopropyl-1h-benzo[c][1,2,6]thiadiazin-4(3h)-one 2,2-dioxide
HY-B2039
2,2-dioxo-3-propan-2-yl-1h-2lambda6,1,3-benzothiadiazin-4-one
3-(propan-2-yl)-3,4-dihydro-1h-2lambda6,1,3-benzothiadiazine-2,2,4-trione
EN300-11686574
F88281
Z56755983

Research Excerpts

Overview

Bentazone (BNTZ) is a selective and efficient herbicide used in crop production worldwide. Bentazone is a hydrophobic ionizable organic compound.

ExcerptReferenceRelevance
"Bentazone is a widely used post-emergence herbicide, while no data was available on its concentrations in tap water from China and in urine among the general population. "( Bentazone in water and human urine in Wuhan, central China: exposure assessment.
Cao, M; Liu, J; Pan, F; Wan, Y; Wang, H; Wang, P; Xia, W, 2022
)
3.61
"Bentazone (BNTZ) is a selective and efficient herbicide used in crop production worldwide. "( Multiple Metabolism Pathways of Bentazone Potentially Regulated by Metabolic Enzymes in Rice.
Chen, ZJ; Liu, J; Lv, Y; Qiao, Y; Yang, H; Zhang, N, 2023
)
2.64
"Bentazone is a hydrophobic ionizable organic compound, and both ionic charge and hydrophobic aromatic structure governed the sorption characteristics on MIEX resin."( Removal of bentazone from micro-polluted water using MIEX resin: kinetics, equilibrium, and mechanism.
Drikas, M; Liu, Z; Qu, J; Wang, D; Yan, X; Yang, M; Zhou, D, 2011
)
1.48
"Bentazone is a herbicide widely used in the agrochemical field and acts by interference in photosynthesis in plants. "( Acute renal failure induced by bentazone: 2 case reports and a comprehensive review.
Lin, JL; Wu, IW; Wu, MS,
)
1.86

Toxicity

ExcerptReferenceRelevance
"Adult rabbits of the New Zealand White breed and pheasants were used to determine the rate of acute oral toxicity (LD50), clinical symptomatology of poisoning of organisms loaded with lethal doses, and the recovery of intoxicated individuals from the toxic effects of bentazon, Czechoslovak developmental herbicide (Research Institute of Chemical Technology, Bratislava), administered at sublethal doses within the framework of obligatory toxicological testing of this herbicide."( [Acute oral toxicity of bentazon, an herbicide developed in Czechoslovakia, in pheasants and rabbits and the clinical symptoms of poisoning].
Kacmár, P; Neuschl, J, 1993
)
0.29
"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
)
0.54
" Results showed that toxic concentrations (0."( Comparative toxicity of bentazon and molinate on growth, photosynthetic pigments, photosynthesis, and respiration of the Portuguese ricefield cyanobacterium Nostoc muscorum.
Fernández-Valiente, E; Galhano, V; Gomes-Laranjo, J; Peixoto, F, 2010
)
0.36
" However, no TG can answer the realistic exposure effect hypotheses of academics; therefore, crucially in pre-market RA, tens of thousands of published experimental findings (increasingly at low dose) are ignored to determine the safe dose."( The inadequacies of pre-market chemical risk assessment's toxicity studies-the implications.
Tweedale, AC, 2017
)
0.46

Compound-Compound Interactions

ExcerptReferenceRelevance
" All methods gave recoveries >80% for the pesticide mixture, but extraction with sodium hydroxide in combination with solid-phase preconcentration was used for further recovery tests with soils of different properties spiked at four herbicide concentration levels (0."( Determination of bentazone, dichlorprop, and MCPA in different soils by sodium hydroxide extraction in combination with solid-phase preconcentration.
Christiansen, A; Thorstensen, CW, 2001
)
0.65

Bioavailability

ExcerptReferenceRelevance
" The present results have demonstrated the applicability of Fv/Fm parameter to access the early toxicity of bentazon, as well as other PSII-inhibition compounds, before significant changes occurred in the original concentration and bioavailability of these toxicants during longer exposure times."( Effects of the herbicide bentazon on growth and photosystem II maximum quantum yield of the marine diatom Skeletonema costatum.
Lombardi, AT; Macedo, RS; Omachi, CY; Rörig, LR, 2008
)
0.35
" To show the importance of physicochemical properties, the classic QSAR and CoMFA of neonicotinoids and prediction of bioavailability of pesticides in terms of membrane permeability in comparison with drugs are described."( Importance of physicochemical properties for the design of new pesticides.
Akamatsu, M, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
"A suite of dose-response bioassays with white mustard (Sinapis alba L) and sugar beet (Beta vulgaris L) in the greenhouse and with three herbicides was used to analyse how the fluorescence induction curves (Kautsky curves) were affected by the herbicides."( Linking fluorescence induction curve and biomass in herbicide screening.
Christensen, MG; Streibig, JC; Teicher, HB, 2003
)
0.32
" For mixtures with malathion on algae, dose-response surfaces were made and the results tested against the model of concentration addition (CA) and independent action (IA)."( Organophosphorous insecticides as herbicide synergists on the green algae Pseudokirchneriella subcapitata and the aquatic plant Lemna minor.
Abbaspoor, M; Cedergreen, N; Munkegaard, M, 2008
)
0.35
" The degradation kinetics was investigated under different conditions such as type of TiO2 (Anatase/Anatase-Rutile mixture), reaction pH, catalyst dosage and hydrogen peroxide (H202) concentration."( Photocatalytic degradation of herbicide bentazone in aqueous suspension of TiO2: mineralization, identification of intermediates and reaction pathways.
Haque, MM; Khan, A; Mir, NA; Muneer, M; Vijayalakshmi, S,
)
0.4
" Herbicide spray tests indicated that such transgenic rice plants can be killed selectively by a spray of bentazon at regular field application dosage for rice weed control."( A double built-in containment strategy for production of recombinant proteins in transgenic rice.
Shen, Z; Wang, D; Zhang, X; Zhao, S, 2014
)
0.4
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
xenobioticA xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
herbicideA substance used to destroy plant pests.
[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
benzothiadiazineHeterocyclic compound of a ring with sulfur and two nitrogen atoms fused to a benzene ring. Members inhibit sodium-potassium-chloride symporters and are used as diuretics.
[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 (9)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Chain A, 2-oxoglutarate OxygenaseHomo sapiens (human)Potency35.48130.177814.390939.8107AID2147
Chain A, ATP-DEPENDENT DNA HELICASE Q1Homo sapiens (human)Potency39.81070.125919.1169125.8920AID2549
GLI family zinc finger 3Homo sapiens (human)Potency61.06840.000714.592883.7951AID1259369
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency33.23050.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoid X nuclear receptor alphaHomo sapiens (human)Potency48.96620.000817.505159.3239AID1159527
farnesoid X nuclear receptorHomo sapiens (human)Potency0.00200.375827.485161.6524AID588527
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency0.00130.023723.228263.5986AID588543
aryl hydrocarbon receptorHomo sapiens (human)Potency79.43280.000723.06741,258.9301AID651777
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency0.21870.057821.109761.2679AID1159526
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (5)

Assay IDTitleYearJournalArticle
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID1091958Hydrophobicity, log P of the compound in octanol-water by shaking-flask method2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (145)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (2.76)18.7374
1990's18 (12.41)18.2507
2000's44 (30.34)29.6817
2010's58 (40.00)24.3611
2020's21 (14.48)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 53.40

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

MetricThis Compound (vs All)
Research Demand Index53.40 (24.57)
Research Supply Index5.08 (2.92)
Research Growth Index5.22 (4.65)
Search Engine Demand Index88.31 (26.88)
Search Engine Supply Index2.08 (0.95)

This Compound (53.40)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews5 (3.14%)6.00%
Case Studies5 (3.14%)4.05%
Observational0 (0.00%)0.25%
Other149 (93.71%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]