Page last updated: 2024-11-06

raiser

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

Description

raiser: an herbicide [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID91677
CHEMBL ID2272973
CHEBI ID5131
SCHEMBL ID54056
MeSH IDM0209177

Synonyms (50)

Synonym
AC-12495
r 40244
racer
3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)-2-pyrrolidone
3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)pyrrolidin-2-one
einecs 262-661-3
caswell no. 721b
(3rs,4rs;3rs,4sr)-3-chloro-4-chloromethyl-1-(alpha,alpha,alpha-trifluoro-m-tolyl)-2-pyrrolidone
flurochloridone [iso:bsi]
2-pyrrolidinone, 3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)-
fluorochloridone
3-chloro-4-(chloromethyl)-1-(3-(trifluoromethyl)phenyl)-2-pyrrolidinone
epa pesticide chemical code 128401
1-(m-trifluoromethylphenyl)-3-chloro-4-chloromethyl-2-pyrrolidone
3-chloro-4-(chloromethyl)-1-[3-(trifluoromethyl)phenyl]pyrrolidin-2-one
STK373128
raiser
61213-25-0
flurochloridone
BAS 00444577
FT-0653571
AKOS000545957
dtxcid8021987
NCGC00255939-01
dtxsid0041987 ,
cas-61213-25-0
tox21_302259
unii-ao023zb1bp
ao023zb1bp ,
flurochloridon
SCHEMBL54056
CHEMBL2272973
chebi:5131 ,
r-40244
n-(m-trifluoromethylphenyl)-3-chloro-4-chloromethyl-2-pyrrolidone
W-105176
3-chloro-4-(chloromethyl)-1-[3-(trifluoromethyl)phenyl]-2-pyrrolidinone #
2-pyrrolidinone, 3-chloro-4-(chloromethyl)-1-[3-(trifluoromethyl)phenyl]-
SR-01000362363-1
sr-01000362363
flurochloridon, pestanal(r), analytical standard
C75864
flurochloridone 100 microg/ml in acetonitrile
SY233452
mfcd00144317
AS-12674
Q18624139
r40244
AKOS016844370
CS-0081481

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" This study represents the first evidence of the acute toxic and genotoxic effects exerted by two FLC-based commercial formulations, Twin Pack Gold(®) and Rainbow(®), on tadpoles of an amphibian species native to Argentina under laboratory conditions."( Flurochloridone-based herbicides induced genotoxicity effects on Rhinella arenarum tadpoles (Anura: Bufonidae).
Larramendy, ML; Marino, D; Natale, GS; Nikoloff, N; Soloneski, S, 2014
)
0.4
" The aim of this study was to evaluate the acute toxic effects and the prevailing interactions on stage 36 tadpoles of the anuran species Rhinella arenarum when exposed to equitoxic and non-equitoxic combinations of these herbicide combinations."( Toxicity to Rhinella arenarum tadpoles (Anura, Bufonidae) of herbicide mixtures commonly used to treat fallow containing resistant weeds: glyphosate-dicamba and glyphosate-flurochloridone.
Brodeur, JC; Larramendy, ML; Ruiz de Arcaute, C; Soloneski, S, 2020
)
0.56

Pharmacokinetics

ExcerptReferenceRelevance
" This method has been successfully applied to a pilot FLC pharmacokinetic study after oral administration."( A quantitative determination of fluorochloridone in rat plasma by UPLC-MS/MS method: application to a pharmacokinetic study.
Chang, X; Fan, J; Hu, Y; Liu, S; Shi, J; Sun, J; Tang, L; Wei, L; Wu, C; Zhang, S; Zhou, Z, 2016
)
0.43

Dosage Studied

ExcerptRelevanceReference
" On the 1st, 60th, 75th and 90th days of the dosing phase, plasma of ten animals of all groups treated with FLC was collected for toxicokinetic analysis of FLC by an UPLC-MS/MS method."( Ninety day toxicity and toxicokinetics of fluorochloridone after oral administration in rats.
Chang, X; Cheng, X; Fan, J; Hu, Y; Li, R; Liu, S; Shi, J; Sun, J; Tang, L; Wang, Y; Wu, C; Xu, C; Zhang, S; Zhou, S; Zhou, Z, 2015
)
0.42
" Male and female rats were dosed for 9 and 2 consecutive weeks, intragastrically, prior to cohabitation and lasted throughout the mating period for males and continued until Gestation Day 7 (GD7) for females."( Low dose of flurochloridone affected reproductive system of male rats but not fertility and early embryonic development.
Chang, X; Fang, J; Li, R; Liu, P; Tang, L; Wang, Y; Zhang, Y; Zhang, Z; Zhou, S; Zhou, Z; Zhu, H, 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.
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
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 (3)

ClassDescription
pyrrolidinesAny of a class of heterocyclic amines having a saturated five-membered ring.
(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.
[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 (13)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency48.87990.006038.004119,952.5996AID1159521; AID1159523
GLI family zinc finger 3Homo sapiens (human)Potency45.49520.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency14.04300.000221.22318,912.5098AID1259243; AID1259247; AID743035; AID743063
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency40.81990.001022.650876.6163AID1224838; AID1224893
progesterone receptorHomo sapiens (human)Potency30.63790.000417.946075.1148AID1346795
retinoid X nuclear receptor alphaHomo sapiens (human)Potency0.07490.000817.505159.3239AID1159527; AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency36.24760.001530.607315,848.9004AID1224841; AID1224848; AID1224849; AID1259401; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency24.33650.005428.02631,258.9301AID1346982
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency21.87240.001019.414170.9645AID743191
aryl hydrocarbon receptorHomo sapiens (human)Potency42.13940.000723.06741,258.9301AID743085; AID743122
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency55.79400.000627.21521,122.0200AID743202; AID743219
[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)0.79430.02900.28500.7943AID1102389
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
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.
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.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (34)

TimeframeStudies, This Drug (%)All Drugs %
pre-19907 (20.59)18.7374
1990's1 (2.94)18.2507
2000's1 (2.94)29.6817
2010's15 (44.12)24.3611
2020's10 (29.41)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 80.65

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 Index80.65 (24.57)
Research Supply Index3.58 (2.92)
Research Growth Index6.18 (4.65)
Search Engine Demand Index134.67 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (80.65)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other35 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]