Page last updated: 2024-12-05

triallate

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

Description

Triallate: A pre-emergence, selective herbicide for the control of wild oats in various crops. [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID5543
CHEMBL ID1884767
CHEBI ID81978
SCHEMBL ID62793
MeSH IDM0021887

Synonyms (105)

Synonym
BRD-K64698045-001-02-2
carbamic acid, diisopropylthio-, s-(2,3,3-trichloroallyl) ester
triallate
DIVK1C_006606
KBIO1_001550
einecs 218-962-7
triamyl
brn 1875853
n,n-diisopropyl-2,3,3-trichlorallyl-thiolcarbamat [german]
2,3,3-trichlorallyl-n,n-(diisopropyl)-thiocarbamat [german]
rcra waste no. u389
caswell no. 870a
dipthal
carbamothioic acid, bis(1-methylethyl)-, s-(2,3,3-trichloro-2-propenyl) ester
s-(2,3,3-trichloro-2-propenyl) bis(1-methylethyl)carbamothiote
2,3,3-trichloroallyl n,n-diisopropylthiocarbamate
epa pesticide chemical code 078802
nsc 379698
s-(2,3,3-trichloroallyl)diisopropylthiocarbamate
diisopropyltrichloroallylthiocarbamate
2,3,3-trichloro-2-propene-1-thiol diisopropylcarbamate
tri-allate [bsi:iso]
bis(1-methylethyl)carbamothioic acid, s-(2,3,3-trichloro-2-propenyl)ester
s-2,3,3-trichloroallyl n,n-diisopropylthiocarbamate
diisopropylthiocarbamic acid s-(2,3,3-trichloroallyl) ester
n-diisopropylthiocarbamic acid s-2,3,3-trichloro-2-propenyl ester
thiocarbamic acid, n-diisopropyl-, s-2,3,3-trichloroallyl ester
2,3,3-trichloroallyl diisopropylthiocarbamate
avadex bw
hsdb 1780
s-(2,3,3-trichloro-2-propenyl) bis(1-methylethyl)carbamothioate
triallat [german]
carbamothioic acid, bis(1-methylethyl)-, s-(2,3,3-trichloro-2-propenyl)ester
s-2,3,3-trichloroallyl-n,n-diisopropylthiolcarbamate
2-propene-1-thiol, 2,3,3-trichloro-, diisopropylcarbamate
ccris 5383
far-go
cp 23426
s-(2,3,3-trichloroallyl) diisopropylthiocarbamate
SPECTRUM_001889
SPECTRUM5_002006
BSPBIO_002429
2303-17-5
tri-allate
nsc379698
nsc-379698
KBIOSS_002419
KBIOGR_001149
KBIO2_007549
KBIO3_001929
KBIO2_002413
KBIO2_004981
SPECTRUM4_000685
SPECPLUS_000510
SPBIO_001628
SPECTRUM2_001844
SPECTRUM3_000845
s-(2,3,3-trichloroprop-2-en-1-yl) diisopropylthiocarbamate
NCGC00168339-01
NCGC00168339-02
s-2,3,3-trichloroallyl diisopropylthiocarbamate
s-(2,3,3-trichloroprop-2-enyl) n,n-di(propan-2-yl)carbamothioate
NCGC00168339-04
NCGC00168339-03
C18813
n,n-diisopropyl-2,3,3-trichlorallyl-thiolcarbamat
2,3,3-trichlorallyl-n,n-(diisopropyl)-thiocarbamat
triallat
unii-a9s097hs99
a9s097hs99 ,
dtxcid804344
NCGC00259366-01
dtxsid5024344 ,
cas-2303-17-5
tox21_300671
NCGC00254579-01
tox21_201817
2,3,3-trichloroallyl-n,n-diisopropyl-thiolcarbamate
AKOS016011225
CCG-39382
tri-allate [iso]
tri-allate [hsdb]
cp-23426
bis(1-methylethyl)carbamothioic acid s-(2,3,3-trichloro-2-propenyl) ester
triallate [mi]
chebi:81978 ,
CHEMBL1884767
SCHEMBL62793
n,n-diisopropyl-2,3,3-trichlorallyl-thiolcarbamate
showdown
s-(2,3,3-trichloro-2-propenyl) diisopropylthiocarbamate #
avadex be
MWBPRDONLNQCFV-UHFFFAOYSA-N
far-go/avadex bw
triallat, pestanal(r), analytical standard
triallat, analytical standard
tri-allate 100 microg/ml in acetonitrile
tri-allate 10 microg/ml in cyclohexane
FT-0748886
s-(2,3,3-trichloro-2-propenyl)bis(1-methylethyl)thiocarbamate
s-2,3,3-trichloroallyl diisopropylcarbamothioate
HY-119435
Q904371
CS-0068360
carbamothioic acid, n,n-bis(1-methylethyl)-, s-(2,3,3-trichloro-2-propen-1-yl) ester

Research Excerpts

Overview

Triallate is a selective herbicidal chemical used for control of wild oats in wheat.

ExcerptReferenceRelevance
"Triallate is a selective herbicidal chemical used for control of wild oats in wheat. "( A review of the genotoxicity of triallate.
Broeckaert, F; Healy, CE; Kier, LD; Martens, MA,
)
1.86

Effects

ExcerptReferenceRelevance
"Triallate has not produced any genotoxicity in in vitro DNA damage or unscheduled DNA synthesis assays using EUE cells, human lymphocytes, and rat and mouse hepatocytes."( A review of the genotoxicity of triallate.
Broeckaert, F; Healy, CE; Kier, LD; Martens, MA,
)
1.14

Toxicity

ExcerptReferenceRelevance
" In a series of in vivo genotoxicity assays (cytogenetics, micronucleus, dominant lethal, and unscheduled DNA synthesis), there has been no indication of any adverse genotoxic effect."( A review of the genotoxicity of triallate.
Broeckaert, F; Healy, CE; Kier, LD; Martens, MA,
)
0.41

Dosage Studied

ExcerptRelevanceReference
"Two allylthiocarbamate herbicides, diallate and triallate, were evaluated for neurotoxicity by oral and topical dosing studies with mature white leghorn hens."( Neurotoxicity of diallate and triallate when administered orally or topically to hens.
Francis, BM; Hansen, LG; Metcalf, RL; Reinders, JH, 1985
)
0.81
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
tertiary amineA compound formally derived from ammonia by replacing three hydrogen atoms by hydrocarbyl 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]

Protein Targets (14)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
pregnane X receptorRattus norvegicus (Norway rat)Potency44.66840.025127.9203501.1870AID651751
GLI family zinc finger 3Homo sapiens (human)Potency64.86010.000714.592883.7951AID1259369; AID1259392
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency54.48270.001022.650876.6163AID1224838; AID1224893
farnesoid X nuclear receptorHomo sapiens (human)Potency19.95260.375827.485161.6524AID588526
pregnane X nuclear receptorHomo sapiens (human)Potency24.64080.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency34.80600.000229.305416,493.5996AID588514; AID743079
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency7.93310.001024.504861.6448AID588535; AID743215
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency60.84620.001019.414170.9645AID743191
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency54.48270.001723.839378.1014AID743083
thyroid stimulating hormone receptorHomo sapiens (human)Potency18.09190.001628.015177.1139AID1224843; AID1224895
activating transcription factor 6Homo sapiens (human)Potency60.84620.143427.612159.8106AID1159516
v-jun sarcoma virus 17 oncogene homolog (avian)Homo sapiens (human)Potency36.59690.057821.109761.2679AID1159526; AID1159528
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency56.31780.000323.4451159.6830AID743065; AID743067
heat shock protein beta-1Homo sapiens (human)Potency60.84620.042027.378961.6448AID743210
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (14)

Assay IDTitleYearJournalArticle
AID1090120Growth inhibition of Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090128Inhibition of Arbidopsis thaliana C-terminal His-tagged KCS1 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090126Inhibition of Arbidopsis thaliana C-terminal His-tagged CER60 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID977602Inhibition of sodium fluorescein uptake in OATP1B3-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID1090129Inhibition of Arbidopsis thaliana C-terminal His-tagged FAE1 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090123Herbicidal activity against Arabidopsis thaliana assessed as apperance of fiddle head phenotype2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090127Inhibition of Arbidopsis thaliana C-terminal His-tagged KCS2 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1100793Binding affinity to SafBP receptor in Zea mays (maize) seedlings by [3H]Saf(R-29148) binding assay2000Journal of agricultural and food chemistry, Mar, Volume: 48, Issue:3
Comparative three-dimensional quantitative structure-activity relationship study of safeners and herbicides.
AID977599Inhibition of sodium fluorescein uptake in OATP1B1-transfected CHO cells at an equimolar substrate-inhibitor concentration of 10 uM2013Molecular pharmacology, Jun, Volume: 83, Issue:6
Structure-based identification of OATP1B1/3 inhibitors.
AID1090119Inhibition of Saccharomyces cerevisiae INVSc1 ELO at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090125Inhibition of Arbidopsis thaliana C-terminal His-tagged At1g04220 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1090124Inhibition of Arbidopsis thaliana C-terminal His-tagged At5g43760 expressed in Saccharomyces cerevisiae INVSc1 at 100 uM after 18 to 20 hr by GC/MS analysis2004Proceedings of the National Academy of Sciences of the United States of America, Aug-10, Volume: 101, Issue:32
Specific and differential inhibition of very-long-chain fatty acid elongases from Arabidopsis thaliana by different herbicides.
AID1159607Screen for inhibitors of RMI FANCM (MM2) intereaction2016Journal of biomolecular screening, Jul, Volume: 21, Issue:6
A High-Throughput Screening Strategy to Identify Protein-Protein Interaction Inhibitors That Block the Fanconi Anemia DNA Repair Pathway.
AID1159550Human Phosphogluconate dehydrogenase (6PGD) Inhibitor Screening2015Nature cell biology, Nov, Volume: 17, Issue:11
6-Phosphogluconate dehydrogenase links oxidative PPP, lipogenesis and tumour growth by inhibiting LKB1-AMPK signalling.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (44)

TimeframeStudies, This Drug (%)All Drugs %
pre-199017 (38.64)18.7374
1990's5 (11.36)18.2507
2000's10 (22.73)29.6817
2010's6 (13.64)24.3611
2020's6 (13.64)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 38.60

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

MetricThis Compound (vs All)
Research Demand Index38.60 (24.57)
Research Supply Index3.95 (2.92)
Research Growth Index4.63 (4.65)
Search Engine Demand Index56.07 (26.88)
Search Engine Supply Index2.11 (0.95)

This Compound (38.60)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (2.00%)5.53%
Reviews2 (4.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other47 (94.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]