Page last updated: 2024-12-05

guazatine

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

Description

Guazatine is a broad-spectrum fungicide used to control a variety of fungal diseases in crops. It is a quaternary ammonium compound with the chemical formula C14H22N2O2. Guazatine is synthesized by reacting 1,4-diazabicyclo[2.2.2]octane with 2-chloroethyl methacrylate. The compound is known to inhibit fungal growth by interfering with the synthesis of ergosterol, an essential component of fungal cell membranes. Guazatine is also effective against oomycetes, which are fungus-like organisms that cause diseases such as late blight in potatoes and downy mildew in grapes. Due to its effectiveness in controlling fungal diseases and its low toxicity to mammals, guazatine has been widely used in agriculture. However, some concerns have been raised about its potential environmental impact, including its persistence in the environment and its potential to harm aquatic organisms. Consequently, research has been conducted to investigate alternative fungicides and to understand the environmental fate of guazatine.'

iminoctadine : A member of the class of guanidines that is dioctylamine in which a hydrogen from each of the terminal methyl groups is replaced by a guanidino group. Once used as a fungicidal seed dressing, it is no longer approved for use in the European Union. [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 CID3526
CHEMBL ID102276
CHEBI ID5569
SCHEMBL ID68055
MeSH IDM0059305

Synonyms (44)

Synonym
1,1''-(8,8''-azanediylbis(octane-8,1-diyl))diguanidine
bdbm50032500
n-[8-(8-guanidino-octylamino)-octyl]-guanidine
panolil
guazatine [bsi:iso]
1,1'-(iminobis(octamethylene))diguanidine
n,n'''-(iminodi-8,1-octanediyl)bisguanidine
caswell no. 471d
einecs 236-855-3
guanidine, 1,1'-(iminobis(octamethylene))di-
guanidine, n,n'''-(iminodi-8,1-octanediyl)bis-
murbenine
iminobis(octamethylene)diguanidine
bis(8-guanidino-octyl)amine
mitrol
epa pesticide chemical code 498200
bis(8-guanidinooctyl)amine
13516-27-3
iminoctadine
guazatine ,
gzz ,
n-{8-[(8-{[(e)-amino(imino)methyl]amino}octyl)amino]octyl}guanidine
1-[8-(8-guanidinooctylamino)octyl]guanidine
1,1'-(iminodioctamethylene)diguanidine
CHEMBL102276 ,
iminoctadiene
chebi:5569 ,
2-[8-[8-(diaminomethylideneamino)octylamino]octyl]guanidine
108173-90-6
c376jtx506 ,
unii-c376jtx506
iminoctadine [iso]
SCHEMBL68055
1135443-24-1
n,n'''-(iminodi-8,1-octanediyl)bis(guanidine)
1,1'-(iminodioctane-8,1-diyl)diguanidine
2-[8-(8-guanidinooctylamino)octyl]guanidine
DTXSID7042015
guazatine acetate salt, pestanal(r), analytical standard
guanidine,n,n'''-(iminodi-8,1-octanediyl)bis-
n,n'''-(iminodioctane-8,1-diyl)diguanidine
1,1'-(azanediylbis(octane-8,1-diyl))diguanidine
RONFGUROBZGJKP-UHFFFAOYSA-N
Q15632811

Research Excerpts

Overview

Guazatine is a non-systemic contact fungicide, a mixture of reaction products from polyamines. It is used in agriculture to control a wide range of seed-borne diseases.

ExcerptReferenceRelevance
"Guazatine is a non-systemic contact fungicide, a mixture of reaction products from polyamines, comprising mainly octa-methylenediamine, iminodi(octamethylene)diamine, octamethylenebis(imino-octamethylene) diamine and carbamonitrile. "( Analysis of guazatine mixture by LC and LC-MS and antimycotic activity determination of principal components.
Botta, M; D'Arezzo, S; Dreassi, E; Visca, P; Zizzari, AT, 2007
)
2.16
"Guazatine is a fungicide used in agriculture to control a wide range of seed-borne diseases of cereals and other vegetable foods. "( LC/ESI/MS method for the quantitative detection of guazatine residues in cereals.
Botta, M; Corbini, G; Dreassi, E; Zanfini, A; Zizzari, AT, 2007
)
2.03
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
antifungal agrochemicalAny substance used in acriculture, horticulture, forestry, etc. for its fungicidal properties.
[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 (3)

ClassDescription
guanidinesAny organonitrogen compound containing a carbamimidamido (guanidino) group. Guanidines have the general structure (R(1)R(2)N)(R(3)R(4)N)C=N-R(5) and are related structurally to amidines and ureas.
secondary amino compoundA compound formally derived from ammonia by replacing two hydrogen atoms by organyl groups.
aliphatic nitrogen antifungal agentOrganonitrogen compounds containing an aliphatic nitrogen that have significant antifungal properties.
[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 (2)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Polyamine oxidase 1Zea maysKi0.00750.00751.10253.0000AID419311
Deoxyhypusine synthaseRattus norvegicus (Norway rat)IC50 (µMol)3.50000.03001.76503.5000AID56588
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (19)

Assay IDTitleYearJournalArticle
AID440309Anticandidal activity against Candida albicans 4T after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440317Anticandidal activity against Candida glabrata 70E after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID419311Inhibition of maize PAO at pH 6.5 by spectrophotometry-based Dixon plot method2009Journal of medicinal chemistry, Aug-13, Volume: 52, Issue:15
Synthesis and biological evaluation of guanidino compounds endowed with subnanomolar affinity as competitive inhibitors of maize polyamine oxidase.
AID47704Effect on Hypusine formation in CHO cells at concentration 3 uM.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
AID44876Growth inhibition was measured against CHO cell line.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
AID440311Anticandidal activity against Candida albicans 15T after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440315Anticandidal activity against Candida parapsilosis 64E after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440313Anticandidal activity against Candida krusei 193T after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440308Anticandidal activity against Candida albicans ATCC 60193 after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID47703Effect on Hypusine formation in CHO cells at concentration 10 uM.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
AID440310Anticandidal activity against Candida albicans 53T after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440314Anticandidal activity against Candida parapsilosis ATCC 34136 after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440316Anticandidal activity against Candida parapsilosis 81E after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID440318Anticandidal activity against Candida tropicalis 86E after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID47705Effect on hypusine synthesis in CHO cells at concentration 10 uM.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
AID47706Effect on hypusine synthesis in CHO cells at concentration 3 uM.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
AID44872Effect on spermidine uptake in CHO cells at concentration 10 uM.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
AID440312Anticandidal activity against Candida krusei ATCC 14243 after 24 hrs by spectrophotometry2009Journal of medicinal chemistry, Dec-10, Volume: 52, Issue:23
Synthesis of new linear guanidines and macrocyclic amidinourea derivatives endowed with high antifungal activity against Candida spp. and Aspergillus spp.
AID56588In vitro IC50 value by measuring the inhibition of deoxyhypusine synthase.1995Journal of medicinal chemistry, Aug-04, Volume: 38, Issue:16
Diamine and triamine analogs and derivatives as inhibitors of deoxyhypusine synthase: synthesis and biological activity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (22)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's5 (22.73)18.2507
2000's11 (50.00)29.6817
2010's4 (18.18)24.3611
2020's2 (9.09)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 31.07

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 Index31.07 (24.57)
Research Supply Index3.22 (2.92)
Research Growth Index4.65 (4.65)
Search Engine Demand Index35.70 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (31.07)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (4.17%)6.00%
Case Studies2 (8.33%)4.05%
Observational0 (0.00%)0.25%
Other21 (87.50%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]