Page last updated: 2024-12-06

mepiquat

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

Description

Mepiquat chloride is a plant growth regulator that promotes flowering and fruiting in various crops. It is synthesized through a multi-step process involving the reaction of 2-chloroethyl methylamine with 1-methyl-3-pyrrolidinone. Mepiquat chloride is applied to crops as a foliar spray and acts by inhibiting the synthesis of gibberellins, plant hormones responsible for stem elongation. This inhibition promotes the development of compact plants with increased flower and fruit production. Mepiquat chloride is widely used in agriculture to enhance yield, improve fruit quality, and reduce the need for manual pruning. Researchers study mepiquat chloride to understand its mechanisms of action, optimize its application, and explore its potential in developing new agricultural technologies for sustainable crop production.'

mepiquat : A quaternary ammonium ion has that has two methyl groups and a pentamethylene-1,5-diyl group attached to the nitrogen. Its salts are used as plant growth inhibitors. [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 CID18743
CHEMBL ID2220867
CHEBI ID90548
SCHEMBL ID67996
MeSH IDM0141660

Synonyms (23)

Synonym
mepiquat [bsi:iso]
piperidinium, 1,1-dimethyl-
inchi=1/c7h16n/c1-8(2)6-4-3-5-7-8/h3-7h2,1-2h3/q+
1,1-dimethylpiperidinium
NCGC00164455-02
1,1-dimethylpiperidin-1-ium
NCGC00164455-03
1,1-dimethylpiperidinium ion
15302-91-7
s2sfz0z4tw ,
mepiquat
unii-s2sfz0z4tw
SCHEMBL67996
j8.555c ,
epa pesticide chemical code 109081
mepiquat [iso]
n,n-dimethylpiperidinium
CHEMBL2220867
AKOS024455953
DTXSID9042122
CHEBI:90548
mepiquatchlorid
Q27162610

Research Excerpts

Overview

Mepiquat chloride (MC) is a plant growth regulator widely used in cotton production. It is used to control vegetative overgrowth of cotton plants to achieve ideal plant architecture.

ExcerptReferenceRelevance
"Mepiquat chloride (MC) is a plant growth regulator widely used in cotton production to control vegetative overgrowth of cotton plants to achieve ideal plant architecture required for high yielding. "( Transcriptome Profiling Provides New Insights into the Molecular Mechanism Underlying the Sensitivity of Cotton Varieties to Mepiquat Chloride.
Li, Y; Liu, F; Sun, J; Tian, L; Wang, Z; Zhang, X; Zhu, Q, 2022
)
2.37
"Mepiquat chloride is an economical and safe retardant widely applied in cotton farming, but it is not uniformly effective."( Introducing selective agrochemical manipulation of gibberellin metabolism into a cereal crop.
Chen, Y; Duan, L; Li, Z; Peters, RJ; Tian, X; Wang, Q; Xing, J; Yin, P; Yu, H; Zhang, D; Zhang, J; Zhang, M; Zhang, R; Zhang, Y, 2020
)
1.28
"Mepiquat chloride (MC) is a plant growth regulator widely used in cotton (Gossypium hirsutum L.) production to suppress excessive vegetative growth, increase root growth and avoid yield losses. "( The effects of mepiquat chloride on the lateral root initiation of cotton seedlings are associated with auxin and auxin-conjugate homeostasis.
Chen, X; Hou, YX; Li, Z; Tan, G; Wang, B; Wang, M; Zhang, M, 2018
)
2.28
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
agrochemicalAn agrochemical is a substance that is used in agriculture or horticulture.
Maillard reaction productAny thermal degradation product obtained as a result of a chemical reaction between an amino acid and a reducing sugar (Maillard reaction, a non-enzymatic browning procedure that usually imparts flavour to starch-based food products).
plant growth retardantnull
[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
quaternary ammonium ionA derivative of ammonium, NH4(+), in which all four of the hydrogens bonded to nitrogen have been replaced with univalent (usually 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]

Research

Studies (44)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (2.27)18.7374
1990's0 (0.00)18.2507
2000's8 (18.18)29.6817
2010's23 (52.27)24.3611
2020's12 (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: 33.34

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 Index33.34 (24.57)
Research Supply Index3.87 (2.92)
Research Growth Index4.84 (4.65)
Search Engine Demand Index79.37 (26.88)
Search Engine Supply Index3.72 (0.95)

This Compound (33.34)

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%
Other47 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]