Page last updated: 2024-11-06

pretilachlor

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

Pretilachlor is a herbicide in the chloroacetanilide family that was introduced in 1978, primarily for use in controlling weeds in rice. It acts by inhibiting the synthesis of lipid molecules in plants. Research has focused on its effectiveness as a selective herbicide, its potential environmental impact, and its degradation pathways in soil and water. It is particularly important to study pretilachlor due to its widespread use in rice cultivation and its potential for persistence in the environment. Several studies have explored methods for reducing its environmental impact, including its degradation by microorganisms in soil.'

Cross-References

ID SourceID
PubMed CID91644
CHEMBL ID1867271
CHEBI ID34931
SCHEMBL ID63720
MeSH IDM0302729

Synonyms (42)

Synonym
BIDD:ER0510
2-chloro-2',6'-diethyl-n-(2-propoxyethyl)acetanilide
retilachlor
pretilachlor [bsi:iso]
cg 113
rifit
solnet
acetamide, 2-chloro-n-(2,6-diethylphenyl)-n-(2-propoxyethyl)-
2-chloro-n-(2,6-diethylphenyl)-n-(2-propoxyethyl)acetamide
pretilachlore
pretilachlore [iso-french]
brn 2754162
cga 26423
51218-49-6
pretilachlor
NCGC00166165-01
A828488
P1967
617k7lm10d ,
unii-617k7lm10d
FT-0630642
AKOS015889913
pretilachlor [mi]
pretilachlor [iso]
cg-113
cga-26423
SCHEMBL63720
chebi:34931 ,
CHEMBL1867271
DTXSID8058112
2-chloro-2',6'-diethyl-n-(2-propyloxyethyl)acetanilide
2-chloro-2',6'-diethyl-n-(2-n-propoxyethyl)-acetanilide
2-chloro-n-(2,6-diethylphenyl)-n-(2-propoxyethyl)acetamide #
mfcd00161476
pretilachlor, pestanal(r), analytical standard
pretilachlor 10 microg/ml in cyclohexane
Q3409268
CS-0014130
D92176
HY-B2035
BS-44191
BCA21849

Research Excerpts

Effects

Pretilachlor has been widely used during last few decades for weed management in paddy crop.

ExcerptReferenceRelevance
"The pretilachlor has been widely used worldwide and has contaminated the environment for many years. "( Revealing the driving synergistic degradation mechanism of Rhodococcus sp. B2 on the bioremediation of pretilachlor-contaminated soil.
Fang, S; Hong, Q; Liu, A; Liu, H; Liu, M; Liu, S; Lu, P; Wan, R; Yin, X, 2023
)
1.68
"Pretilachlor has been widely used during last few decades for weed management in paddy crop."( Ultimate fate, transformation, and toxicological consequences of herbicide pretilachlor to biotic components and associated environment: An overview.
Dhanda, V; Duhan, A; Kumar, R; Sangwan, S; Yadav, N, 2024
)
2.39

Treatment

recommended dose at 600g a.i. In pretilachlor treated soil, MBC increased through the first 15 days, and thereafter decreased to the initial level.

ExcerptReferenceRelevance
"Pretilachlor treatments, namely, recommended dose at 600 g a.i. "( Effect of Pretilachlor on Soil Enzyme Activities in Tropical Rice Soil.
Adak, T; Bagchi, TB; Berliner, J; Jena, M; Kumar, U; Mishra, BB; Munda, S; Saha, S; Sahoo, S, 2017
)
2.3
"In pretilachlor treated soil, MBC increased through the first 15 days, and thereafter decreased to the initial level."( Microbial biomass and carbon mineralization in agricultural soils as affected by pesticide addition.
Kumar, A; Mohanty, S; Nayak, AK; Panda, BB; Raja, R; Rath, PC; Shahid, M; Shukla, AK; Tripathi, R, 2012
)
0.89

Toxicity

ExcerptReferenceRelevance
"The objectives of the present study were to investigate the toxic effects of pretilachlor on zebrafish during its embryo development."( Pretilachlor has the potential to induce endocrine disruption, oxidative stress, apoptosis and immunotoxicity during zebrafish embryo development.
Cai, L; Chen, Y; Jiang, J; Wang, Q; Yu, R; Zhao, X, 2016
)
2.11
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
anilideAny aromatic amide obtained by acylation of aniline.
[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 (1)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
DNA polymerase kappa isoform 1Homo sapiens (human)Potency26.67950.031622.3146100.0000AID588579
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (53)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (1.89)18.2507
2000's10 (18.87)29.6817
2010's30 (56.60)24.3611
2020's12 (22.64)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 54.63

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 Index54.63 (24.57)
Research Supply Index3.99 (2.92)
Research Growth Index5.69 (4.65)
Search Engine Demand Index95.39 (26.88)
Search Engine Supply Index2.28 (0.95)

This Compound (54.63)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.89%)6.00%
Case Studies1 (1.89%)4.05%
Observational0 (0.00%)0.25%
Other51 (96.23%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]