Page last updated: 2024-12-06

cyanazine

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

Description

cyanazine: structure [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

cyanazine : A chloro-1,3,5-triazine that is 2-chloro-1,3,5-triazine substituted by an ethyl amino and a (2-cyanopropan-2-yl)amino group at positions 6 and 4 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 CID30773
CHEMBL ID1884229
CHEBI ID38069
SCHEMBL ID54410
MeSH IDM0050191

Synonyms (102)

Synonym
BIDD:ER0073
AC-12675
propanenitrile, 2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methyl-
propionitrile, 2-[[4-chloro-6-(ethylamino)-s-triazin-2-yl]amino]-2-methyl-
bladex r
bladex 80wp
2-chloro-4-ethylamino-6-cyano-1-methylethylamino-triazine
bladex 90 df
2-((4-chloro-6-(ethylamino)-s-triazin-2-yl)amino)-2-methylpropionitrile
chloro-4-((1-cyano-1-methylethyl)amino)-6-(ethylamino)-s-triazine
wl 19805
fortol
bladex 80w
dw 3418
bladex 4l
chloro-6-(ethylamino)-s-triazin-2-yl)amino)-2-methylpropionitrile
payze
cynex
extrazine
2-((4-chloro-6-(ethylamino)-1,3,5-triazine-2-yl)amino)-2-methylpropionitrile
chloro-6-(ethylamino)-1,3,5-triazine-2-yl)amino)-2-methylpropanenitrile
cyanizine
sd 45418
cyanazine sd 15418
sd 15418
2-((4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl)amino)-2-methylpropanenitrile
propionitrile, 2-((4-chloro-6-(ethylamino)-s-triazin-2-yl)amino)-2-methyl-
bladex
2-([4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino)-2-methylpropanenitrile
2-chloro-4-(1-cyano-1-methylethylamino)-6-ethylamine-1,3,5-triazine
2-[[4-chloro-6-(ethylamino)-s-triazin-2-yl]amino]-2-methylpropionitrile
fortrol
CHEBI:38069 ,
2-{[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino}-2-methylpropanenitrile
2-chloro-4-(1-cyano-1-methylethylamino)-6-ethylamino-1,3,5-triazine
21725-46-2
cyanazine
blanchol
brn 0615509
ccris 6823
hsdb 6842
2-(4-chloro-6-ethylamino-s-triazine-2-ylamino)-2-methyl-propionitrile
cyanazin
dw3418
s-triazine, 2-chloro-4-ethylamino-6-(1-cyano-1-methyl)ethylamino-
cyanazine [bsi:iso]
epa pesticide chemical code 100101
caswell no. 188c
einecs 244-544-9
propanenitrile, 2-((4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl)amino)-2-methyl-
2-(4-chloro-6-ethylamino-1,3,5-triazin-2-ylamino)-2-methylpropionitrile
2-chloro-4-(1-cyano-1-methylethylamino)-6-ethylamino-s-triazine
cyanazine, analytical standard
NCGC00163888-01
NCGC00163888-02
inchi=1/c9h13cln6/c1-4-12-7-13-6(10)14-8(15-7)16-9(2,3)5-11/h4h2,1-3h3,(h2,12,13,14,15,16)
2-[(4-chloro-6-ethylamino-1,3,5-triazin-2-yl)amino]-2-methylpropanenitrile
mzzbpdkvefvlff-uhfffaoysa-
2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile
NCGC00163888-03
NCGC00163888-04
NCGC00163888-05
dtxcid803990
tox21_201619
NCGC00254934-01
NCGC00259168-01
tox21_301032
cas-21725-46-2
dtxsid1023990 ,
2-[[4-chloranyl-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methyl-propanenitrile
A815631
5-26-08-00471 (beilstein handbook reference)
w34c4p18wd ,
unii-w34c4p18wd
FT-0603170
AKOS015903245
CHEMBL1884229
cyanazine [mi]
radeks
sd-15418
dw-3418
cyanazine [hsdb]
wl-19805
cyanazine [iso]
urlac
2-(4-chloro-6-ethylamino-1,3,5-triazin-2-ylamino)-2-methylpropiononitrile
SCHEMBL54410
s-triazine, 2-chloro-4-(ethylamino)-6-(1-cyano-1-methyl)(ethylamino)-
propionitrile, 2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino]-2-methyl
2-([4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amino)-2-methylpropanenitrile #
cyanazine, pestanal(r), analytical standard
cyanazine 10 microg/ml in acetonitrile
cyanazine 100 microg/ml in acetonitrile
J-014257
2-(4-chloro-6-(ethylamino)-1,3,5-triazin-2-ylamino)-2-methylpropanenitrile
Q424848
2-[[4-chloro-6-(ethylamino)-1,3,5-triazin-2-yl]amine
2-[[4-chloro-6-(1,1,2,2,2-pentadeuterioethylamino)-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile
MS-23409
STARBLD0009698
CS-0128840
HY-136375

Research Excerpts

Overview

Cyanazine is a common pesticide used frequently in the United States during the 1980s and 1990s. It is a member of the chloro-s-triazine class of herbicides.

ExcerptReferenceRelevance
"Cyanazine is a beneficial herbicide in the triazines group that inhibits photosynthesis in plants and monitoring of this herbicide is so important for study agriculture products. "( Cyanazine herbicide monitoring as a hazardous substance by a DNA nanostructure biosensor.
Alizadeh, M; Fu, L; Karaman, C; Karimi, F; Karimi-Maleh, H; Orooji, Y; Sanati, AL, 2022
)
3.61
"Cyanazine is a common pesticide used frequently in the United States during the 1980s and 1990s. "( Cancer incidence among pesticide applicators exposed to cyanazine in the agricultural health study.
Alavanja, MC; Blair, A; Dosemeci, M; Hoppin, JA; Lubin, J; Lynch, CF; Lynch, SM; Rusiecki, JA; Sandler, D, 2006
)
2.02
"Cyanazine is a member of the chloro-s-triazine class of herbicides. "( Chronic toxicity and oncogenicity bioassay in rats with the chloro-s-triazine herbicide cyanazine.
Bogdanffy, MS; Cook, JC; Gaddamidi, V; Green, JW; Hansen, JF; O'Connor, JC; Van Pelt, CS, 2000
)
1.97

Effects

ExcerptReferenceRelevance
"Only cyanazine, however, has such a criteria established."( Occurence of cyanazine compounds in groundwater: degradates more prevalent than the parent compound.
Kolpin, DW; Linhart, SM; Thurman, EM, 2001
)
1.14

Toxicity

ExcerptReferenceRelevance
" Female animals showed increased sensitivity to the toxic effects by DNOC at the highest dose."( Genetic safety evaluation of pesticides in different short-term tests.
Cantelli-Forti, G; Colacci, A; Grilli, S; Hrelia, P; Maffei, F; Morotti, M; Perocco, P; Vigagni, F, 1994
)
0.29

Bioavailability

ExcerptReferenceRelevance
" To show the importance of physicochemical properties, the classic QSAR and CoMFA of neonicotinoids and prediction of bioavailability of pesticides in terms of membrane permeability in comparison with drugs are described."( Importance of physicochemical properties for the design of new pesticides.
Akamatsu, M, 2011
)
0.37

Dosage Studied

ExcerptRelevanceReference
" Whole-plant herbicide dose-response experiments revealed that, relative to the UniS population, atrazine resistances in the UniR and SegR populations were > 770-fold and 16-fold, respectively."( Triazine resistance in Amaranthus tuberculatus (Moq) Sauer that is not site-of-action mediated.
Dixon, BS; Patzoldt, WL; Tranel, PJ, 2003
)
0.32
" There was no evidence of a dose-response relationship between triazines and ovarian cancer (P=0."( Triazine herbicides and epithelial ovarian cancer risk in central California.
Cress, RD; Mills, PK; Riordan, DG; Young, HA, 2005
)
0.33
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (3)

RoleDescription
herbicideA substance used to destroy plant pests.
environmental contaminantAny minor or unwanted substance introduced into the environment that can have undesired effects.
xenobioticA xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
[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
1,3,5-triazinylamino nitrileAny diamino-1,3,5-triazine in which the amino group is substituted by at least one cyano group.
chloro-1,3,5-triazineA member of the class of 1,3,5-triazines that is 1,3,5-triazine substituted by at least one chloro group at unspecified position.
[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 (9)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
GLI family zinc finger 3Homo sapiens (human)Potency0.44180.000714.592883.7951AID1259369; AID1259392
AR proteinHomo sapiens (human)Potency39.81070.000221.22318,912.5098AID588516
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency43.62520.000214.376460.0339AID720691
retinoid X nuclear receptor alphaHomo sapiens (human)Potency23.50330.000817.505159.3239AID1159527; AID1159531
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency37.32310.001530.607315,848.9004AID1224841; AID1224842; AID1224849; AID1259403
pregnane X nuclear receptorHomo sapiens (human)Potency34.45100.005428.02631,258.9301AID1346982; AID720659
estrogen nuclear receptor alphaHomo sapiens (human)Potency0.48950.000229.305416,493.5996AID743075
aryl hydrocarbon receptorHomo sapiens (human)Potency66.03610.000723.06741,258.9301AID743085; AID743122
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency24.33650.000627.21521,122.0200AID720636
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1091958Hydrophobicity, log P of the compound in octanol-water by shaking-flask method2011Journal of agricultural and food chemistry, Apr-13, Volume: 59, Issue:7
Importance of physicochemical properties for the design of new pesticides.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (57)

TimeframeStudies, This Drug (%)All Drugs %
pre-19903 (5.26)18.7374
1990's14 (24.56)18.2507
2000's26 (45.61)29.6817
2010's12 (21.05)24.3611
2020's2 (3.51)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 38.46

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 Index38.46 (24.57)
Research Supply Index4.13 (2.92)
Research Growth Index5.22 (4.65)
Search Engine Demand Index51.48 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (38.46)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (1.64%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other60 (98.36%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]