Compounds > 2,6-difluorobenzamide
Page last updated: 2024-12-07

2,6-difluorobenzamide

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

Description

2,6-difluorobenzamide: structure given in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID87439
SCHEMBL ID203321
SCHEMBL ID11008706
MeSH IDM0209767

Synonyms (38)

Synonym
einecs 241-972-8
2,6-difluorobenzamide
benzamide, 2,6-difluoro-
inchi=1/c7h5f2no/c8-4-2-1-3-5(9)6(4)7(10)11/h1-3h,(h2,10,11
2,6-difluorobenzamide, 97%
18063-03-1
AC-10721
D1907
AKOS000119514
A25252
2,6-difluorobenzoic acid amide
unii-sj2rn214mk
ec 241-972-8
sj2rn214mk ,
FT-0610646
CK1202
lufenuron for veterinary use impurity a [ep impurity]
SCHEMBL203321
2,6 difluorobenzamide
2, 6 difluorobenzamide
2,6-difluoro-benzamide
SCHEMBL11008706
W-107808
PS-8830
mfcd00007972
DTXSID4073417
SY003317
cga 149772
CS-0017808
2,6-difluoro benzamide
2,6-difluorobenzoic amide
EN300-19935
Q15632832
AM10801
STL183292
benzamide, 2,6-difluoro-; 2,6-difluorobenzamide; lufenuron imp. a (ep)
SB67309
Z104476138

Research Excerpts

Toxicity

ExcerptReferenceRelevance
"The herbicides dichlobenil (2,6-dichlorobenzonitrile), chlorthiamid (2,6-dichlorothiobenzamide) and their environmental degradation product 2,6-dichlorobenzamide are irreversibly bound and toxic to the olfactory mucosa following single injections in mice (Brandt et al."( Tissue-binding and toxicity of compounds structurally related to the herbicide dichlobenil in the mouse olfactory mucosa.
Brandt, I; Brittebo, E; Eriksson, C, 1992)		0.28

Dosage Studied

ExcerptRelevanceReference
" The metabolic fate of the insecticide teflubenzuron, orally dosed to the male Wistar rat, was investigated."( Metabolism of the insecticide teflubenzuron in rats.
Cnubben, NH; De Kraker, JW; Koerts, J; Rietjens, IM; Soffers, AE, 1997)		0.3
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (11)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's2 (18.18)18.2507
2000's0 (0.00)29.6817
2010's7 (63.64)24.3611
2020's2 (18.18)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 23.59

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 Index23.59 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.43 (4.65)
Search Engine Demand Index23.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (23.59)

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%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
dichlobanil
2,6-dichlorobenzonitrile : A nitrile that is benzonitrile which is substituted by chlorines at positions 2 and 6. A cellulose synthesis inhibitor, it is used as a pre-emergent and early post-emergent herbicide.		1.9810dichlorobenzene;
nitrile		agrochemical;
cellulose synthesis inhibitor;
environmental contaminant;
herbicide;
xenobiotic
aniline
[no description available]		1.9910anilines;
primary arylamine
benzonitrile
benzonitrile : A nitrile that is hydrogen cyanide in which the hydrogen has been replaced by a phenyl group.		1.9810benzenes;
nitrile
thiazoles
[no description available]		2.11101,3-thiazoles;
mancude organic heteromonocyclic parent;
monocyclic heteroarene
2,6-difluorobenzoic acid
2,6-difluorobenzoic acid: structure given in first source		1.9910
1,4-benzodioxan
1,4-benzodioxan: structure in first source		2.1110
bromoxynil
bromoxynil: RN given refers to parent cpd; structure. 3,5-dibromo-4-hydroxybenzonitrile : A dibromobenzene that is 2,6-dibromophenol substituted by a cyano group at position 4.		1.9810dibromobenzene;
hydroxynitrile;
phenols		environmental contaminant;
herbicide;
xenobiotic
teflubenzuron
teflubenzuron: effective against development of house fly larvae (Musca domestica). teflubenzuron : A N-acylurea that is N-carbamoyl-2,6-difluorobenzamide substituted by a 3,5-dichloro-2,4-difluorophenyl group at the terminal nitrogen atom.		1.9910dichlorobenzene;
difluorobenzene;
N-acylurea		environmental contaminant;
insecticide;
xenobiotic
3-methoxybenzamide
[no description available]		2.610
pc190723
PC190723: Antibacterial; an inhibitor of FtsZ with potent and selective anti-staphylococcal activity including methicillin- and multi-drug-resistant Staphylococcus aureus; structure in first source		2.1110
ConditionIndicatedRelationship StrengthStudiesTrials
Colorectal Cancer
[description not available]		02.4110
Colorectal Neoplasms
Tumors or cancer of the COLON or the RECTUM or both. Risk factors for colorectal cancer include chronic ULCERATIVE COLITIS; FAMILIAL POLYPOSIS COLI; exposure to ASBESTOS; and irradiation of the CERVIX UTERI.		02.4110