Page last updated: 2024-12-06

norflurazone

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

Description

Norflurazone is a herbicide that inhibits carotenoid biosynthesis. It is used to control weeds in a variety of crops, including corn, soybeans, and cotton. Norflurazone is a synthetic compound that was first synthesized in the 1960s. It is effective against a wide range of weeds, including grasses, broadleaves, and sedges. Norflurazone is absorbed by plant roots and leaves, and it inhibits the synthesis of carotenoids, which are essential for photosynthesis. The inhibition of carotenoid biosynthesis leads to a reduction in chlorophyll production, which in turn results in the death of the plant. Norflurazone is widely studied because of its potential to control weeds in a variety of crops. It is also being investigated for its potential to reduce the incidence of certain diseases in plants, such as rust and mildew. Norflurazone is relatively safe for humans and animals, but it can be toxic to fish and other aquatic organisms.'

norflurazone: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

norflurazon : A pyridazinone that is pyridazin-3(2H)-one which is substituted at positions 2, 4, and 5 by m-(trifluoromethyl)phenyl, chloro, and methylamino groups, respectively. A pre-emergence herbicide used to control grasses and broad-leafed weeds in a variety of crops. 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]

Cross-References

ID SourceID
PubMed CID33775
CHEMBL ID1881194
CHEBI ID50842
SCHEMBL ID54676
MeSH IDM0052729

Synonyms (82)

Synonym
norflurazon
3(2h)-pyridazinone, 4-chloro-5-(methylamino)-2-[3-(trifluoromethyl)phenyl]-
solicam
1-(3-trifluoromethylphenyl)-4-methylamino-5-chloropyridazone
norflurazone [iso-french]
norflurazone
caswell no. 195aa
san 97895
4-chloro-5-(methylamino)-2-(3-(trifluoromethyl)phenyl)-3(2h)-pyridazinone
3(2h)-pyridazinone, 4-chloro-5-(methylamino)-2-(3-(trifluoromethyl)phenyl)-
telok
einecs 248-397-1
h 9789
evital
monometflurazon
monometflurazone
norflurazon technical
h-9789
zorial rapid 80
evitol
epa pesticide chemical code 105801
4-chloro-5-(methylamino)-2-(alpha,alpha,alpha-trifluoro-m-tolyl)-3(2h)-pyridazinone
4-chloro-5-methylamino-2-(3-trifluoromethylphenyl)pyridazin-3-one
3(2h)-pyridazinone, 4-chloro-5-(methylamino)-2-(alpha,alpha,alpha-trifluoro-m-tolyl)-
norflurazon [ansi:bsi:iso]
san 9789 h
h-52,143
h 52143
zorial
solicam rapid
brn 0757115
san 9789
hsdb 6845
4-chloro-5-(methylamino)-2-[3-(trifluoromethyl)phenyl]-3(2h)-pyridazinone
CHEBI:50842 ,
NCGC00163841-01
27314-13-2
4-chloro-5-(methylamino)-2-[3-(trifluoromethyl)phenyl]pyridazin-3(2h)-one
NCGC00163841-02
norflurazon (nf)
NRF ,
4-chloro-5-(methylamino)-2-[3-(trifluoromethyl)phenyl]pyridazin-3-one
NCGC00163841-04
NCGC00163841-03
C18874
tox21_300701
NCGC00259592-01
dtxsid8024234 ,
tox21_202043
NCGC00254609-01
cas-27314-13-2
dtxcid304234
kes1hb07e4 ,
5-25-14-00201 (beilstein handbook reference)
unii-kes1hb07e4
FT-0673095
sandoz 9789
predict
1-(3-trifluoromethylphenyl)-4-methylamino-5-chloro-6-pyridazone
AKOS015903314
AB00081885-01
SCHEMBL54676
CHEMBL1881194
norflurazon [iso]
4-chloro-5-methylamino-2-(.alpha.,.alpha.,.alpha.-trifluoro-m-tolyl)pyridazin-3(2h)-one
norflurazon [hsdb]
norflurazon [mi]
san-9789
4-chloro-5-(methylamino)-2-(alpha,alpha,alpha-trifluoro-m-toluyl)-3-(2h)-pyridazinone
3(2h)-pyridazinone, 4-chloro-5-(methylamino)-2-(.alpha.,.alpha.,.alpha.-trifluoro-m-tolyl)-
4-chloro-5-(methylamino)-2-(.alpha.,.alpha.,.alpha.-trifluoro-m-tolyl)-3(2h)-pyridazinone
norflurazon, pestanal(r), analytical standard
sr-01000206068
SR-01000206068-1
norflurazon, analytical standard
norflurazon 10 microg/ml in acetonitrile
J-016727
4-chloro-5-(methylamino)-2-(3-(trifluoromethyl)phenyl)pyridazin-3(2h)-one ,
Q1321843
solicam;zorial;san 9789
CS-0064469
HY-114849

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" The aim of our study was to investigate toxic effects of norflurazon on non-targeted aquatic bioindicator organism, the planarian Polycelis felina (Daly."( Toxicity testing of herbicide norflurazon on an aquatic bioindicator species--the planarian Polycelis felina (Daly.).
Horvat, T; Kalafatić, M; Kopjar, N; Kovacević, G, 2005
)
0.33

Dosage Studied

ExcerptRelevanceReference
" Water samples were collected from the wetland upstream of the dosing system at 3 h intervals from the beginning through 360 h and at the exit point at 1, 2, and 3 h intervals for the periods of 0-24, 25-48 and 49-360 h after dosing, respectively."( Norflurazon and simazine removal from surface water using a constructed wetland.
Lin, Y; Lu, H; Wilson, PC, 2011
)
0.37
" Transformation efficiency and lethal norflurazon dosage were determined to evaluate the usefulness of syn-pds-int gene and functionality of the short promoter of pds."( Stable nuclear transformation of rhodophyte species Porphyridium purpureum: advanced molecular tools and an optimized method.
Buchholz, R; Lein, W; Lindenberger, CP; Prasad, B; Thiyam, G; Vadakedath, N, 2019
)
0.51
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
carotenoid biosynthesis inhibitorAny pathway inhibitor that acts on the carotenoid biosynthesis pathway.
herbicideA substance used to destroy plant pests.
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 (4)

ClassDescription
pyridazinone
(trifluoromethyl)benzenesAn organofluorine compound that is (trifluoromethyl)benzene and derivatives arising from substitution of one or more of the phenyl hydrogens.
organochlorine compoundAn organochlorine compound is a compound containing at least one carbon-chlorine bond.
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 (23)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
LuciferasePhotinus pyralis (common eastern firefly)Potency37.12250.007215.758889.3584AID1224835
pregnane X receptorRattus norvegicus (Norway rat)Potency15.84890.025127.9203501.1870AID651751
RAR-related orphan receptor gammaMus musculus (house mouse)Potency6.91340.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency27.30600.000714.592883.7951AID1259368
AR proteinHomo sapiens (human)Potency16.66400.000221.22318,912.5098AID1259243; AID1259247; AID588515; AID588516; AID743042; AID743054
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency15.08660.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency6.65600.003041.611522,387.1992AID1159552; AID1159553; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency51.56140.000817.505159.3239AID1159527; AID588544
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency20.11880.001530.607315,848.9004AID1224841; AID1224842; AID1224848; AID1224849; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency43.77650.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency18.64920.000229.305416,493.5996AID1259244; AID1259248; AID1259383; AID743069; AID743075; AID743078; AID743079; AID743080; AID743091
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency53.00410.001019.414170.9645AID743191
aryl hydrocarbon receptorHomo sapiens (human)Potency23.01200.000723.06741,258.9301AID651777; AID743085; AID743122
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency1.07260.001723.839378.1014AID743083
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency52.54930.000323.4451159.6830AID743065
histone deacetylase 9 isoform 3Homo sapiens (human)Potency30.85910.037617.082361.1927AID1259364; AID1259388
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency10.87070.000627.21521,122.0200AID720636
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency3.87360.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency3.87360.001551.739315,848.9004AID1259244
ATPase family AAA domain-containing protein 5Homo sapiens (human)Potency52.57000.011917.942071.5630AID651632; AID720516
Ataxin-2Homo sapiens (human)Potency50.55350.011912.222168.7989AID651632
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
15-cis-phytoene desaturaseSynechococcus elongatus PCC 7942 = FACHB-805IC50 (µMol)0.03030.02900.28500.7943AID1102389
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (18)

Processvia Protein(s)Taxonomy
cell population proliferationATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of B cell proliferationATPase family AAA domain-containing protein 5Homo sapiens (human)
nuclear DNA replicationATPase family AAA domain-containing protein 5Homo sapiens (human)
signal transduction in response to DNA damageATPase family AAA domain-containing protein 5Homo sapiens (human)
intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorATPase family AAA domain-containing protein 5Homo sapiens (human)
isotype switchingATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of DNA replicationATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of isotype switching to IgG isotypesATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA clamp unloadingATPase family AAA domain-containing protein 5Homo sapiens (human)
regulation of mitotic cell cycle phase transitionATPase family AAA domain-containing protein 5Homo sapiens (human)
negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage by p53 class mediatorATPase family AAA domain-containing protein 5Homo sapiens (human)
positive regulation of cell cycle G2/M phase transitionATPase family AAA domain-containing protein 5Homo sapiens (human)
negative regulation of receptor internalizationAtaxin-2Homo sapiens (human)
regulation of translationAtaxin-2Homo sapiens (human)
RNA metabolic processAtaxin-2Homo sapiens (human)
P-body assemblyAtaxin-2Homo sapiens (human)
stress granule assemblyAtaxin-2Homo sapiens (human)
RNA transportAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (8)

Processvia Protein(s)Taxonomy
protein bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
ATP bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
ATP hydrolysis activityATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA clamp unloader activityATPase family AAA domain-containing protein 5Homo sapiens (human)
DNA bindingATPase family AAA domain-containing protein 5Homo sapiens (human)
RNA bindingAtaxin-2Homo sapiens (human)
epidermal growth factor receptor bindingAtaxin-2Homo sapiens (human)
protein bindingAtaxin-2Homo sapiens (human)
mRNA bindingAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (11)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
Elg1 RFC-like complexATPase family AAA domain-containing protein 5Homo sapiens (human)
nucleusATPase family AAA domain-containing protein 5Homo sapiens (human)
cytoplasmAtaxin-2Homo sapiens (human)
Golgi apparatusAtaxin-2Homo sapiens (human)
trans-Golgi networkAtaxin-2Homo sapiens (human)
cytosolAtaxin-2Homo sapiens (human)
cytoplasmic stress granuleAtaxin-2Homo sapiens (human)
membraneAtaxin-2Homo sapiens (human)
perinuclear region of cytoplasmAtaxin-2Homo sapiens (human)
ribonucleoprotein complexAtaxin-2Homo sapiens (human)
cytoplasmic stress granuleAtaxin-2Homo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (23)

Assay IDTitleYearJournalArticle
AID1082556Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1103060Herbicidal activity against Glycine max (soybean) grown in slit loam soil at pH 7.6 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1082552Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082549Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1103061Herbicidal activity against Glycine max (soybean) grown in slit loam soil at pH 6.0 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1102388Inhibition of Capsicum annuum (pepper) zeta-carotene desaturase expressed in Escherichia coli using zeta-carotene as substrate after 8 hr by Dixon plot analysis2003Journal of agricultural and food chemistry, May-07, Volume: 51, Issue:10
Phytoene desaturase inhibition by O-(2-phenoxy)ethyl-N-aralkylcarbamates.
AID1082550Herbicidal activity against Stellaria media assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1103065Herbicidal activity against Glycine max (soybean) grown in sandy clay loam soil at pH 7.9 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1101632Competitive inhibition of Gentiana lutea desaturase using decyl plastoquinone as cofactor and phytoene as substrate at 0.1 uM after 2 hr by double reciprocal plot analysis2001Journal of agricultural and food chemistry, Nov, Volume: 49, Issue:11
Bleaching herbicide norflurazon inhibits phytoene desaturase by competition with the cofactors.
AID1103059Herbicidal activity against Glycine max (soybean) grown in loam soil at pH 5.8 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1101634Competitive inhibition of Synechococcus phytoene desaturase using NADP as cofactor and phytoene as substrate at 0.1 uM after 2 hr by double reciprocal plot analysis2001Journal of agricultural and food chemistry, Nov, Volume: 49, Issue:11
Bleaching herbicide norflurazon inhibits phytoene desaturase by competition with the cofactors.
AID1082553Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1101633Competitive inhibition of Synechococcus phytoene desaturase using decyl plastoquinone as cofactor and phytoene as substrate at 0.1 uM after 2 hr by double reciprocal plot analysis2001Journal of agricultural and food chemistry, Nov, Volume: 49, Issue:11
Bleaching herbicide norflurazon inhibits phytoene desaturase by competition with the cofactors.
AID1082558Herbicidal activity against Arabidopsis thaliana assessed as growth inhibition at 10 ppm by 96-well plate test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1103062Herbicidal activity against Glycine max (soybean) grown in clay soil at pH 8.0 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1103066Herbicidal activity against Glycine max (soybean) grown in sandy soil at pH 8.0 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1102389Inhibition of Synechococcus PCC 7942 phytoene desaturase expressed in Escherichia coli JM101 using phytoene as substrate after 8 hr by Dixon plot analysis2003Journal of agricultural and food chemistry, May-07, Volume: 51, Issue:10
Phytoene desaturase inhibition by O-(2-phenoxy)ethyl-N-aralkylcarbamates.
AID1103063Herbicidal activity against Glycine max (soybean) grown in loam soil at pH 5.5 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
AID1082554Herbicidal activity against Stellaria media assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082551Herbicidal activity against Lolium perenne (perennial ryegrass) assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082557Herbicidal activity against Poa annua assessed as growth inhibition at 32 ppm by 96-well plate test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082555Herbicidal activity against Lolium perenne (perennial ryegrass) assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1103064Herbicidal activity against Glycine max (soybean) grown in sandy clay loam soil at pH 5.7 assessed as chlorophyll bleaching effect on shoots compound treated to soil measured after 10 days relative to untreated control2004Journal of agricultural and food chemistry, Feb-25, Volume: 52, Issue:4
Effect of soil type on adsorption-desorption, mobility, and activity of the herbicide norflurazon.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (147)

TimeframeStudies, This Drug (%)All Drugs %
pre-199011 (7.48)18.7374
1990's22 (14.97)18.2507
2000's68 (46.26)29.6817
2010's43 (29.25)24.3611
2020's3 (2.04)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 32.24

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 Index32.24 (24.57)
Research Supply Index5.04 (2.92)
Research Growth Index4.86 (4.65)
Search Engine Demand Index44.85 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (32.24)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies1 (0.65%)4.05%
Observational0 (0.00%)0.25%
Other153 (99.35%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]