Compounds > ammelide
Page last updated: 2024-11-05

ammelide

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

Description

Ammelide, a triazine derivative, is a key intermediate in the synthesis of melamine, a valuable industrial chemical. It is typically produced through the hydrolysis of melamine. Its unique chemical structure and reactivity have attracted research interest for various applications. Ammelide has potential applications in areas such as flame retardants, polymers, and pharmaceuticals due to its nitrogen-rich nature and ability to form hydrogen bonds. The study of ammelide helps in understanding the reactivity and properties of triazines and their potential applications in various fields.'

ammelide: structure given in first source; RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID12584
CHEBI ID28134
SCHEMBL ID36691
MeSH IDM0184118

Synonyms (46)

Synonym
nsc8146
nsc-8146
CHEBI:28134
6-amino-1,3,5-triazine-2,4(1h,3h)-dione
1,3,5-triazine-2,4(1h,3h)-dione, 6-amino-
ammedlide
6-amino-1,3,5-triazine-2,4-diol
ammelide
2,4-dihydroxy-6-amino-1,3,5-triazine
C08734
645-93-2
dihydro-6-imino-1,3,5-triazine-2,4(1h,3h)-dione
cyanuric acid monoamide
melanuric acid
A0645
6-amino-1h-1,3,5-triazine-2,4-dione
A834821
6-azanyl-1h-1,3,5-triazine-2,4-dione
6-amino-s-triazine-2,4-diol
AKOS006222979
j604qc4098 ,
einecs 211-456-7
ai3-61038
unii-j604qc4098
nsc 8146
FT-0622302
6-amino-2,4-dihydroxy-1,3,5-triazine
AKOS022175465
SCHEMBL36691
167613-80-1
DTXSID10214757 ,
6-amino-1,3,5-triazine-2,4(1h,3h)-dione, aldrichcpr
mfcd00049046
ammelide, analytical standard
AS-60764
T71177
terbutylazine metabolite mt24
Q4747226
STL186172
terbuthylazine-tp mt24 (lm1)
SB73399
1,3,5-triazine-2,4-diol,6-amino-(9ci)
ammelide; 98%
EN300-1461831
cid 5281299
Z1203578012

Research Excerpts

[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
dihydroxy-1,3,5-triazine
monoamino-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]

Research

Studies (20)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's1 (5.00)18.2507
2000's5 (25.00)29.6817
2010's13 (65.00)24.3611
2020's1 (5.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 52.09

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

MetricThis Compound (vs All)
Research Demand Index52.09 (24.57)
Research Supply Index3.04 (2.92)
Research Growth Index5.38 (4.65)
Search Engine Demand Index79.51 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (52.09)

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%
Other20 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
citric acid, anhydrous
Citric Acid: A key intermediate in metabolism. It is an acid compound found in citrus fruits. The salts of citric acid (citrates) can be used as anticoagulants due to their calcium chelating ability.. citric acid : A tricarboxylic acid that is propane-1,2,3-tricarboxylic acid bearing a hydroxy substituent at position 2. It is an important metabolite in the pathway of all aerobic organisms.		2.0710tricarboxylic acidantimicrobial agent;
chelator;
food acidity regulator;
fundamental metabolite
urea
pseudourea: clinical use; structure. isourea : A carboximidic acid that is the imidic acid tautomer of urea, H2NC(=NH)OH, and its hydrocarbyl derivatives.		2.1310isourea;
monocarboxylic acid amide;
one-carbon compound		Daphnia magna metabolite;
Escherichia coli metabolite;
fertilizer;
flour treatment agent;
human metabolite;
mouse metabolite;
Saccharomyces cerevisiae metabolite
methacrylic acid
methacrylic acid: RN given refers to parent cpd. methacrylic acid : An alpha,beta-unsaturated monocarboxylic acid that is acrylic acid in which the hydrogen at position 2 is substituted by a methyl group.		2.1110alpha,beta-unsaturated monocarboxylic acid
propazine
propazine: relatively non-toxic triazine herbicide; minor descriptor (75-82); online & Index Medicus search TRIAZINES (75-82). propazine : A diamino-1,3,5-triazine that is N,N'-di(propan-2-yl)-1,3,5-triazine-2,4-diamine substituted by a chloro group at position 6.		2.1510chloro-1,3,5-triazine;
diamino-1,3,5-triazine		environmental contaminant;
herbicide;
xenobiotic
trimethylchlorosilane
trimethylsilyl chloride: structure in first source. chlorotrimethylsilane : A silyl chloride consisting of a central silicon atom covalently bound to one chloro and three methyl groups. Chlorotrimethylsilane is a derivatisation agent used in gas chromatography/mass spectrometry applications.		2.0510silyl chloridechromatographic reagent
phencyclidine
Phencyclidine: A hallucinogen formerly used as a veterinary anesthetic, and briefly as a general anesthetic for humans. Phencyclidine is similar to KETAMINE in structure and in many of its effects. Like ketamine, it can produce a dissociative state. It exerts its pharmacological action through inhibition of NMDA receptors (RECEPTORS, N-METHYL-D-ASPARTATE). As a drug of abuse, it is known as PCP and Angel Dust.. phencyclidine : A member of the class of piperidines that is piperidine in which the nitrogen is substituted with a 1-phenylcyclohexyl group. Formerly used as an anaesthetic agent, it exhibits both hallucinogenic and neurotoxic effects.		2.2510benzenes;
piperidines		anaesthetic;
neurotoxin;
NMDA receptor antagonist;
psychotropic drug
melamine
melamine: RN given refers to parent cpd; structure. melamine : A trimer of cyanamide, with a 1,3,5-triazine skeleton.		4.22160triamino-1,3,5-triazinexenobiotic metabolite
cyanuric acid
cyanuric acid: RN given refers to parent cpd. isocyanuric acid : The keto tautomer of cyanuric acid.. cyanuric acid : The enol tautomer of isocyanuric acid.		4.141501,3,5-triazinanes;
1,3,5-triazines;
heteroaryl hydroxy compound		xenobiotic
2-chloro-4,6-diamino-s-triazine
[no description available]		2.0110chloro-1,3,5-triazine;
diamino-1,3,5-triazine
gold
Gold: A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.		2.0710copper group element atom;
elemental gold
cyromazine
cyromazine: RN given refers to parent cpd		2.5220triamino-1,3,5-triazinemouse metabolite;
triazine insecticide
n,n-bis(trimethylsilyl)-2,2,2-trifluoroacetamide
[no description available]		2.0510
melamine formaldehyde
[no description available]		2.0610
ammonium citrate
[no description available]		2.0710ammonium salt;
citrate salt		buffer;
food emulsifier
ammeline
ammeline: causes retinal degeneration		4.23160diamino-1,3,5-triazine;
monohydroxy-1,3,5-triazine
ConditionIndicatedRelationship StrengthStudiesTrials
Sensitivity and Specificity
Binary classification measures to assess test results. Sensitivity or recall rate is the proportion of true positives. Specificity is the probability of correctly determining the absence of a condition. (From Last, Dictionary of Epidemiology, 2d ed)		03.1550