Page last updated: 2024-12-05

ametryne

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

Description

ametryne: minor descriptor (72-83); on-line & Index Medicus search HERBICIDES, TRIAZINE (75-83) & HERBICIDES (72-74) & TRIAZINES (72-74); RN given refers to unlabeled cpd; structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

ametryn : A methylthio-1,3,5-triazine that is 2-(methylsulfanyl)-1,3,5-triazine substituted by an ethylamino and an isopropylamino group at positions 4 and 6 respectively. [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 CID13263
CHEMBL ID1235774
CHEBI ID22472
SCHEMBL ID65196
MeSH IDM0262488

Synonyms (126)

Synonym
AC-12557
CHEMBL1235774
1,3,5-triazine-2,4-diamine, n-ethyl-n'-(1-methylethyl)-6-(methylthio)-
C0260
(ethylamino)-4-(isopropylamino)-6-(methylthio)-s-triazine
evik 80w
2-ethylamino-4-isopropylamino-6-methylthio-s-trizaine
2-(ethylamino)-4-(isopropylamino)-6-(methylthio)triazine
CHEBI:22472 ,
n-ethyl-6-(methylsulfanyl)-n'-(propan-2-yl)-1,3,5-triazine-2,4-diamine
2-methylthio-4-ethylamino-6-isopropylamino-s-triazine
n-ethyl-n'-isopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine
n-ethyl-n'-(1-methylethyl)-6-(methylthio)-2,4-diaminetriazine
2-ethylamino-4-isopropylamino-6-methylmercapto-s-triazine
n(2)-ethyl-6-(methylsulfanyl)-n(4)-(propan-2-yl)-1,3,5-triazine-2,4-diamine
n(2)-ethyl-n(4)-isopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine
n-ethyl-n'-(1-methylethyl)-6-(methylthio)-1,3,5-triazine-2,4-diamine
OPREA1_869762
IDI1_016952
2-(ethylamino)-4-(isopropylamino)-6-(methylthio)-s-triazine
wln: t6n cn enj bs1 dmy1&1 fm2
2-(ethylamino)-4-(isopropylamino)-6-(methylmercapto)-s-triazine
1,5-triazine-2,4-diamine, n-ethyl-n'-(1-methylethyl)-6-(methylthio)-
2-(methylthio)-4-(ethylamino)-6-(isopropylamino)-s-triazine
nsc163044
2-(methylmercapto)-4-(ethylamino)-6-(isopropylamino)-s-triazine
ametryn
2-(ethylamino)-4-(isopropylamino)-6-(methylthio)-1,5-triazine
ametrex
2-(methylmercapto)-4-(isopropylamino)-6-(ethylamino)-s-triazine
nsc-163044
ametrine
s-triazine, 2-(ethylamino)-4-(isopropylamino)-6-(methylthio)-
gesapax
a 1093
g 34162
cemerin
ametryne
evik
834-12-8
SR-01000636076-1
ametryn, analytical standard
NCGC00163822-01
n-ethyl-n-isopropyl-6-methylthio-1,3,5-triazine-2,4-diamine
crisatrine
gestene
2-methylmercapto-4-isopropylamino-6-ethylamino-s-triazine
n2-ethyl-n4-isopropyl-6-methylthio-1,3,5-triazine-2,4-diamine
ametryn [ansi:bsi:iso]
geshpax
2-ethylamino-4-isopropylamino-6-methylthio-s-triazine
ai3-60365
epa pesticide chemical code 080801
brn 0613099
n-ethyl-n'-isopropyl-6-methylthio-1,3,5-triazine-2,4-diyldiamine
trinatox d
topazol
s-triazine, 2-ethylamino-4-isopropylamino-6-methylthio-
2-ethylamino-4-isopropylamino-6-methylthio-1,3,5-triazine
2-methylmercapto-4-ethylamino-6-isopropylamino-s-triazine
amephyt
hsdb 1710
nsc 163044
g-34162
gardopax
caswell no. 431
doruplant
primatol z 80
einecs 212-634-7
MAYBRIDGE3_005565
NCGC00163822-02
(2-ethylamino)-4-(isopropylamino)-6-(methylthio)-s-triazine
HMS1446M21
RYN ,
n-ethyl-n'-(1-methylethyl)-6-(methylsulfanyl)-1,3,5-triazine-2,4-diamine
4-n-ethyl-6-methylsulfanyl-2-n-propan-2-yl-1,3,5-triazine-2,4-diamine
FT-0652865
rqvybgpqfycbgx-uhfffaoysa-
n'-ethyl-6-methylsulfanyl-n-propan-2-yl-1,3,5-triazine-2,4-diamine
inchi=1/c9h17n5s/c1-5-10-7-12-8(11-6(2)3)14-9(13-7)15-4/h6h,5h2,1-4h3,(h2,10,11,12,13,14)
n4-ethyl-6-(methylthio)-n2-propan-2-yl-1,3,5-triazine-2,4-diamine
n4-ethyl-6-methylsulfanyl-n2-propan-2-yl-1,3,5-triazine-2,4-diamine
A840571
NCGC00163822-04
NCGC00163822-03
C18700
NCGC00258965-01
dtxsid1023869 ,
dtxcid303869
cas-834-12-8
tox21_201414
NCGC00254574-01
tox21_300666
CCG-46374
AKOS005203488
ec 212-634-7
1spq95183y ,
unii-1spq95183y
S10164
n2-ethyl-n4-isopropyl-6-(methylthio)-1,3,5-triazine-2,4-diamine
SCHEMBL65196
ametryn [hsdb]
ametryn [mi]
ametryn [iso]
2-(methylthio)-4-(1-methylethylamino)-6-(ethylamino)-1,3,5-triazine
mfcd00055398
n-ethyl-n'-isopropyl-6-(methylsulfanyl)-1,3,5-triazine-2,4-diamine
W-104145
evik 80w (salt/mix)
mebatryne
n-ethyl-n'-isopropyl-6-methylthio-1,3,5-triazine-2,4-diamine
ametryn, pestanal(r), analytical standard
ametryn 100 microg/ml in acetonitrile
ametryn 10 microg/ml in acetonitrile
Q2844856
2-methylthio-4-ethylamino-6-isopropylamino-1,3,5-triazine
AS-16080
a 1093; amephyt; ametrex;ametryne
AMY22120
BRD-K33455047-001-01-5
ametryn 1000 microg/ml in acetone
n~2~-ethyl-6-(methylsulfanyl)-n~4~-(propan-2-yl)-1,3,5-triazine-2,4-diamine
CS-0012880
HY-B0866
20b - triazines and urea herbicides in wastewater
08b - triazines and urea herbicides in clean water

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Genotoxicity tests showed that formulations of nanocapsules containing the herbicides were less toxic than the free herbicides."( Poly(ε-caprolactone)nanocapsules as carrier systems for herbicides: physico-chemical characterization and genotoxicity evaluation.
de Lima, R; dos Santos, NZ; Fraceto, LF; Grillo, R; Maruyama, CR; Rosa, AH, 2012
)
0.38

Dosage Studied

ExcerptRelevanceReference
" Removal rates of ametryn were greatly affected by H(2)O(2) dosage and initial concentrations of ametryn, but appeared to be slightly influenced by initial pH."( Ametryn degradation in the ultraviolet (UV) irradiation/hydrogen peroxide (H2O2) treatment.
Deng, Y; Gao, NY; Zhao, D, 2009
)
0.35
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (2)

RoleDescription
herbicideA substance used to destroy plant pests.
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
[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 (2)

ClassDescription
diamino-1,3,5-triazineAny member of the class of 1,3,5-triazines that consists of a 1,3,5-triazine skeleton substituted by two amino groups.
methylthio-1,3,5-triazine
[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 (12)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
RAR-related orphan receptor gammaMus musculus (house mouse)Potency68.58960.006038.004119,952.5996AID1159521
GLI family zinc finger 3Homo sapiens (human)Potency2.06880.000714.592883.7951AID1259369; AID1259392
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency34.20740.001022.650876.6163AID1224838; AID1224839; AID1224893
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency19.82960.003041.611522,387.1992AID1159552; AID1159555
retinoid X nuclear receptor alphaHomo sapiens (human)Potency21.87240.000817.505159.3239AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency68.58960.001530.607315,848.9004AID1224841
pregnane X nuclear receptorHomo sapiens (human)Potency38.21100.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency47.63980.000229.305416,493.5996AID1259244; AID1259248; AID743079
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency54.94100.001024.504861.6448AID743212
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency68.58960.000323.4451159.6830AID743066
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency54.48270.001557.789015,848.9004AID1259244
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency54.48270.001551.739315,848.9004AID1259244
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Ceullar Components (1)

Processvia Protein(s)Taxonomy
plasma membraneGlutamate receptor 2Rattus norvegicus (Norway rat)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (24)

Assay IDTitleYearJournalArticle
AID1082552Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082551Herbicidal activity against Lolium perenne (perennial ryegrass) assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082567Insecticidal activity against Aphididae (aphids) assessed as mortality at 1000 ppm by leaf-disk assay2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082547Fungicidal activity against Alternaria solani assessed as inhibition of mycelia growth at 2 ppm2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082554Herbicidal activity against Stellaria media assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082557Herbicidal activity against Poa annua assessed as growth inhibition at 32 ppm by 96-well plate test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082556Herbicidal activity against Amaranthus retroflexus assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082555Herbicidal activity against Lolium perenne (perennial ryegrass) assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082548Fungicidal activity against Pythium dissimile assessed as inhibition of mycelia growth at 2 ppm2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082550Herbicidal activity against Stellaria media assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082560Herbicidal activity against Brassica napus (oilseed rape) at 1.5 kg/ha postemergence treatment measured after 10 days by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082544Fungicidal activity against Zymoseptoria tritici assessed as inhibition of mycelia growth at 100 ppm2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082549Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 1 kg/ha preemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082546Fungicidal activity against Fusarium graminearum assessed as inhibition of mycelia growth at 2 ppm2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082565Insecticidal activity against Plutella xylostella (diamondback moth) assessed as mortality at 1000 ppm by artificial diet assay2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082543Fungicidal activity against Phytophthora infestans assessed as inhibition of mycelia growth at 200 ppm2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082566Insecticidal activity against Lepidoptera Heliothis virescens (tobacco budworm) assessed as mortality at 1000 ppm by leaf-disk assay2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082553Herbicidal activity against Digitaria sanguinalis (hairy crabgrass) assessed as growth inhibition at 1 kg/ha postemergence treatment by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082558Herbicidal activity against Arabidopsis thaliana assessed as growth inhibition at 10 ppm by 96-well plate test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082561Herbicidal activity against Echinochloa crus-galli (barnyard grass) at 1.5 kg/ha preemergence treatment measured after 10 days by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082559Herbicidal activity against Echinochloa crus-galli (barnyard grass) at 1.5 kg/ha postemergence treatment measured after 10 days by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1082562Herbicidal activity against Brassica napus (oilseed rape) at 1.5 kg/ha preemergence treatment measured after 10 days by glasshouse test2011Journal of agricultural and food chemistry, Nov-09, Volume: 59, Issue:21
Design, synthesis, and biological activities of arylmethylamine substituted chlorotriazine and methylthiotriazine compounds.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).2014Journal of biomolecular screening, Jul, Volume: 19, Issue:6
A High-Throughput Assay to Identify Inhibitors of the Apicoplast DNA Polymerase from Plasmodium falciparum.
AID1794808Fluorescence-based screening to identify small molecule inhibitors of Plasmodium falciparum apicoplast DNA polymerase (Pf-apPOL).
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (86)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (3.49)18.7374
1990's8 (9.30)18.2507
2000's24 (27.91)29.6817
2010's41 (47.67)24.3611
2020's10 (11.63)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 27.83

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 Index27.83 (24.57)
Research Supply Index4.49 (2.92)
Research Growth Index5.13 (4.65)
Search Engine Demand Index34.37 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (27.83)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.14%)6.00%
Case Studies1 (1.14%)4.05%
Observational0 (0.00%)0.25%
Other86 (97.73%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]