Compounds > acifluorfen-methyl
Page last updated: 2024-12-07

acifluorfen-methyl

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

Description

acifluorfen-methyl: acifluorfen methyl ester [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID91642
CHEMBL ID2269735
SCHEMBL ID39092
MeSH IDM0178606

Synonyms (25)

Synonym
acifluorfen-methyl
50594-67-7
methyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate
benzoic acid, 5-(2-chloro-4-(trifluoromethyl)phenoxy)-2-nitro-, methyl ester
unii-9261t4qe1k
9261t4qe1k ,
acifluorfen-methyl [iso]
methyl 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitro-benzoate
CHEMBL2269735
methyl 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrobenzoate
mc-10108
methyl acifluorfen
mc 10108
acifluorfen methyl ester
SCHEMBL39092
methyl 5-(2-chloro-4-trifluoromethylphenoxy)2-nitrobenzoate
DTXSID8041583
methyl 5-(2-chloro-4-(trifluoromethyl)phenoxy)-2-nitrobenzoate
AKOS033946821
Q27271483
acifluorfen-methyl 100 microg/ml in acetonitrile
HY-147365
CS-0567591
EN300-1703837
Z2574936371
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (2)

Assay IDTitleYearJournalArticle
AID1101430Inhibition of protoporphyrin oxidase in Cucumis sativus (cucumber) cotyledon disc assessed as increase in extraplastidic protoporphyrin 9 accumulation at 100 uM incubated in dim light for 2 hr by HPLC analysis relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Synthesis, herbicidal activity, and mode of action of IR 5790.
AID1101431Inhibition of protoporphyrin oxidase in Cucumis sativus (cucumber) cotyledon disc assessed as increase in extraplastidic protoporphyrin 9 accumulation at 10 uM incubated in dim light for 2 hr by HPLC analysis relative to control2001Journal of agricultural and food chemistry, May, Volume: 49, Issue:5
Synthesis, herbicidal activity, and mode of action of IR 5790.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's4 (80.00)18.2507
2000's1 (20.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.40

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 weak demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index12.40 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.20 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.40)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
galactose
galactopyranose : The pyranose form of galactose.		1.9910D-galactose;
galactopyranose		Escherichia coli metabolite;
mouse metabolite
nitrofen
nitrofen: structure		1.9810organic molecular entityEC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor;
herbicide
dithiothreitol
1,4-dimercaptobutane-2,3-diol : A glycol that is butane-2,3-diol in which a hydrogen from each of the methyl groups is replaced by a thiol group.. 1,4-dithiothreitol : The threo-diastereomer of 1,4-dimercaptobutane-2,3-diol.		1.97101,4-dimercaptobutane-2,3-diol;
butanediols;
dithiol;
glycol;
thiol		chelator;
human metabolite;
reducing agent
oxadiazon
oxadiazon: manufactured by the Societe Rhone-poulenc, France; structure		2.420aromatic ether
acifluorfen
[no description available]		2.3820aromatic ether;
benzoic acids;
C-nitro compound;
monocarboxylic acid;
organochlorine compound;
organofluorine compound		agrochemical;
EC 1.3.3.4 (protoporphyrinogen oxidase) inhibitor;
herbicide
oxadiazoles
Oxadiazoles: Compounds containing five-membered heteroaromatic rings containing two carbons, two nitrogens, and one oxygen atom which exist in various regioisomeric forms.		1.9910
heme
Heme: The color-furnishing portion of hemoglobin. It is found free in tissues and as the prosthetic group in many hemeproteins.. ferroheme : Any iron(II)--porphyrin coordination complex.. ferroheme b : Heme b in which the iron has oxidation state +2.. heme : A heme is any tetrapyrrolic chelate of iron.		1.9810
ConditionIndicatedRelationship StrengthStudiesTrials