Page last updated: 2024-12-07

clodinafop-propargyl

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

Description

Clodinafop-propargyl is a selective post-emergence herbicide that inhibits acetyl-CoA carboxylase (ACCase), an essential enzyme in fatty acid biosynthesis. It is widely used for controlling broadleaf weeds in cereal crops. Clodinafop-propargyl is applied as a granular or liquid formulation and is absorbed by the leaves and roots of plants. It is known to have a rapid mode of action and provides control of a wide range of weeds. The compound is typically applied to the soil surface or incorporated into the soil before planting. Studies on clodinafop-propargyl focus on its efficacy against different weed species, its impact on non-target organisms, and the development of resistance management strategies.'

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

clodinafop-propargyl : A carboxylic ester resulting from the formal condensation of the carboxy group of clodinafop with the hydroxy group of prop-2-yn-1-ol. It is widely used as a herbicide for the control of annual grass weeds in cereal crops. [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 CID92431
CHEMBL ID1898102
CHEBI ID132921
SCHEMBL ID63885
MeSH IDM0561020

Synonyms (63)

Synonym
AC-1858
NCGC00164311-01
prop-2-yn-1-yl (2r)-2-{4-[(5-chloro-3-fluoropyridin-2-yl)oxy]phenoxy}propanoate
clodinafop-propargyl
105512-06-9
topik
cga 184927
discover
clodinafop-propargyl [iso]
propanoic acid, 2-(4-((5-chloro-3-fluoro-2-pyridinyl)oxy)phenoxy)-, 2-propynyl ester, (r)-
hsdb 7007
NCGC00164311-02
(r)-2-(4-((5-chloro-3-fluoro-2-pyridinyl)oxy)phenoxy)propionic acid 2-propynyl ester
CHEBI:132921
2-propynyl (2r)-2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]propanoate
prop-2-ynyl (r)-2-[4-(5-chloro-3-fluoro-2-pyridyloxy)phenoxy]propionate
clodinafop propargyl ester
prop-2-ynyl (2r)-2-[4-(5-chloro-3-fluoropyridin-2-yl)oxyphenoxy]propanoate
prop-1-ynyl 2-[4-[(5-chloro-3-fluoro-2-pyridyl)oxy]phenoxy]propanoate
A801252
NCGC00164311-03
dtxcid4012354
tox21_300724
cas-105512-06-9
dtxsid6032354 ,
NCGC00254630-01
dndi1246788
CHEMBL1898102
unii-qeh394ty6y
propanoic acid, 2-(4-((5-chloro-3-fluoro-2-pyridinyl)oxy)phenoxy)-, 2-propynyl ester, (2r)-
discover herbicide
qeh394ty6y ,
AKOS015961771
clodinafop propargyl
2-propynyl (r)-2-[4-(5-chloro-3-fluoro-2-pyridinyloxy)phenoxy]propionate
propanoic acid, 2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]-, 2-propynyl ester, (2r)-
SCHEMBL63885
KS-5120
clodinafop-proargyl
(2r)-2-(4-((5-chloro-3-fluoro-2-pyridinyl)oxy)phenoxy)propanoic acid 2-propyn-1-yl ester
2-propynyl (r)-2-(4-(5-chloro-3-fluoro-2-pyridyloxy)phenoxy)propionate
cga-184927
clodinafop-propargyl [mi]
clodinafop-propargyl [hsdb]
propynyl (r)-2-(4-((5-chloro-3-fluoro-2-pyridinyl)oxy)phenoxy)propanoate
Q-101471
clodinafop-propargyl, pestanal(r), analytical standard
JBDHZKLJNAIJNC-LLVKDONJSA-N
126301-94-8
clodinafop-propargyl ester
clodinafop-propargyl ester 10 microg/ml in acetonitrile
clodinafop-propargyl ester 100 microg/ml in acetonitrile
(r)-prop-2-ynyl 2-(4-(5-chloro-3-fluoropyridin-2-yloxy)phenoxy)propanoate
mfcd01632328
(r)-prop-2-yn-1-yl 2-(4-((5-chloro-3-fluoropyridin-2-yl)oxy)phenoxy)propanoate
Q1102118
propanoic acid, 2-[4-[(5-chloro-3-fluoro-2-pyridinyl)oxy]phenoxy]-,2-propynyl ester, (2r)-
AMY3554
D89566
clodinafop-propargyl ester 1000 microg/ml in acetone
CS-0128860
HY-136380
C3552

Research Excerpts

Compound-Compound Interactions

ExcerptReferenceRelevance
" Based on the chiral HPLC method, enantioselective quantitative determination analysis methods for this herbicide combined with CP in diluted plasma were developed and validated."( Direct chiral resolution of cloquintocet-mexyl and its application to in vitro degradation combined with clodinafop-propargyl.
Liu, D; Shen, Z; Xu, X; Zhou, Z; Zhu, W, 2012
)
0.59

Dosage Studied

ExcerptRelevanceReference
" The aim of this paper is to assess selectivity of various herbicides in grass seed crops by using dose-response curves."( Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
Jensen, JE; Mathiesen, TJ; Ritz, C; Streibig, JC; Tind, T, 2009
)
0.35
" Dose-response experiment indicated that Lujiang population was highly resistant to fenoxaprop-p-ethyl (199."( Target-site mechanism of ACCase-inhibitors resistance in American sloughgrass (Beckmannia syzigachne Steud.) from China.
Du, L; Li, L; Liu, W; Wang, J; Yuan, G, 2014
)
0.4
" Dose-response experiments showed that the AHSX-1 population has evolved a very high level resistance to fenoxaprop-p-ethyl (RI = 275) and mesosulfuron-methyl (RI = 788)."( Multiple resistance to ACCase and AHAS-inhibiting herbicides in shortawn foxtail (Alopecurus aequalis Sobol.) from China.
Bi, Y; Du, L; Guo, W; Li, Q; Liu, W; Wang, J; Yuan, G; Zhang, C, 2015
)
0.42
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
EC 6.4.1.2 (acetyl-CoA carboxylase) inhibitorAn EC 6.4.1.* (C-C bond-forming ligase) inhibitor that interferes with the action of acetyl-CoA carboxylase (EC 6.4.1.2).
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 (6)

ClassDescription
carboxylic esterAn ester of a carboxylic acid, R(1)C(=O)OR(2), where R(1) = H or organyl and R(2) = organyl.
aromatic etherAny ether in which the oxygen is attached to at least one aryl substituent.
organochlorine compoundAn organochlorine compound is a compound containing at least one carbon-chlorine bond.
organofluorine compoundAn organofluorine compound is a compound containing at least one carbon-fluorine bond.
pyridinesAny organonitrogen heterocyclic compound based on a pyridine skeleton and its substituted derivatives.
propyzamideA member of the class of benzamides resulting from the formal condensation of the carboxy group of 3,5-dichlorobenzoic acid with the amino group of 2-methylbut-3-yn-2-amine. It is used as a systemic post-emergent herbicide for the control grass and broadleaf weeds in a wide range of in a wide variety of fruit and root crops.
[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 (7)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
AR proteinHomo sapiens (human)Potency0.65060.000221.22318,912.5098AID588515; AID743063
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency0.79610.000214.376460.0339AID588532; AID720692
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency38.37470.001530.607315,848.9004AID1224849
estrogen nuclear receptor alphaHomo sapiens (human)Potency21.29910.000229.305416,493.5996AID743069; AID743075; AID743078
thyroid stimulating hormone receptorHomo sapiens (human)Potency8.59100.001628.015177.1139AID1224843
thyroid hormone receptor beta isoform aHomo sapiens (human)Potency0.00790.010039.53711,122.0200AID588545
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency38.57080.000627.21521,122.0200AID651741
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (6)

Assay IDTitleYearJournalArticle
AID1112526Herbicidal activity against haloxyfop-R-methyl-sensitive Alopecurus japonicus (Japanese foxtail) biotype Js-S assessed as inhibition of shoot length after 14 days2012Pest management science, Sep, Volume: 68, Issue:9
Molecular bases for resistance to acetyl-coenzyme A carboxylase inhibitor in Japanese foxtail (Alopecurus japonicus).
AID1112527Herbicidal activity against haloxyfop-R-methyl-resistant Alopecurus japonicus (Japanese foxtail) biotype Js-R assessed as inhibition of shoot length after 14 days2012Pest management science, Sep, Volume: 68, Issue:9
Molecular bases for resistance to acetyl-coenzyme A carboxylase inhibitor in Japanese foxtail (Alopecurus japonicus).
AID1104238Selectivity index, ratio of ED10 for Festuca rubra L. to ED90 for Poa pratensis subsp. Pratensis2009Pest management science, Nov, Volume: 65, Issue:11
Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
AID1112525Resistance index, ratio of ED50 for haloxyfop-R-methyl-resistant Alopecurus japonicus (Japanese foxtail) biotype Js-R to ED50 for haloxyfop-R-methyl-sensitive Alopecurus japonicus (Japanese foxtail) biotype Js-S2012Pest management science, Sep, Volume: 68, Issue:9
Molecular bases for resistance to acetyl-coenzyme A carboxylase inhibitor in Japanese foxtail (Alopecurus japonicus).
AID1104245Herbicidal activity against Poa pratensis subsp. pratensis applied using logarithmic sprayer2009Pest management science, Nov, Volume: 65, Issue:11
Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
AID1104243Toxicity against Festuca rubra applied using logarithmic sprayer2009Pest management science, Nov, Volume: 65, Issue:11
Using a selectivity index to evaluate logarithmic spraying in grass seed crops.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (4.55)29.6817
2010's15 (68.18)24.3611
2020's6 (27.27)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 51.24

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

MetricThis Compound (vs All)
Research Demand Index51.24 (24.57)
Research Supply Index3.14 (2.92)
Research Growth Index6.10 (4.65)
Search Engine Demand Index75.08 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (51.24)

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%
Other22 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]