Page last updated: 2024-11-05

1-aminomethylphosphonic acid

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

Description

1-Aminomethylphosphonic acid (AMPA) is a naturally occurring amino phosphonic acid. It is a structural analog of glycine with a phosphonic acid group replacing the carboxylic acid group. AMPA is found in various organisms, including bacteria, fungi, and plants. It plays a role in various biological processes, including phosphorylation reactions, the regulation of enzyme activity, and the synthesis of bioactive compounds. The compound is synthesized through a variety of methods including enzymatic synthesis, chemical synthesis, and fermentation. Its effects are varied and are influenced by its interactions with different biological systems. It has shown inhibitory effects on some enzymes, and the ability to stimulate the growth of plants and microorganisms. The biological activity of AMPA has led to its being investigated for potential applications in areas such as agriculture, medicine, and biotechnology. It is studied to understand its biochemical functions, potential applications, and its impact on biological systems.'

1-aminomethylphosphonic acid: RN given refers to parent cpd [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

(aminomethyl)phosphonic acid : A member of the class of phosphonic acids that is phosphonic acid substituted by an aminomethyl group. It is a metabolite of the herbicide glyphosate. [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 CID14017
CHEMBL ID41873
CHEBI ID28812
SCHEMBL ID66605
MeSH IDM0110971

Synonyms (51)

Synonym
CHEBI:28812 ,
ccris 9453
phosphonic acid, aminomethyl-
unii-90825o5c1u
90825o5c1u ,
BB 0218000
nsc-30076
(aminomethyl)phosphonic acid
phosphonic acid, (aminomethyl)-
nsc30076
amino methane phosphoric acid
aminomethanephosphonic acid
(1-aminomethyl)phosphonic acid
phosphaglycine
aminomethylphosphonic acid
1-aminomethylphosphonic acid
1066-51-9
(aminomethyl)phosphonic acid, 99%
caswell no. 037c
nsc 30076
1-aminomethylphosphonate
epa pesticide chemical code 207800
amep
A1072
AKOS000348731
ammonium-methanephosphonic acid anion
CHEMBL41873 ,
GEO-00169
FT-0622293
aminomethyl)phosphonic acid, (
SCHEMBL66605
DG-0043
phosphonic acid, p-(aminomethyl)-
DTXSID5037490
mfcd00008105
J-001622
(aminomethyl)phosphonic acid, analytical standard
aminomethyl phosphonic acid (ampa) 10 microg/ml in water
aminomethyl phosphonic acid (ampa)
aminomethyl phosphonic acid (ampa) 100 microg/ml in water
BBL101930
STL555727
glyphosat-trimesium metabolite
glyphosate metabolite
glyphosate tp
SY011283
BCP11241
Q19367475
CS-0085750
807 - glyphosate and ampa in grain flour
EN300-7401424

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Likewise there were no adverse effects in reproductive tissues from animals treated with glyphosate, AMPA, or POEA in chronic and/or subchronic studies."( Safety evaluation and risk assessment of the herbicide Roundup and its active ingredient, glyphosate, for humans.
Kroes, R; Munro, IC; Williams, GM, 2000
)
0.31

Dosage Studied

ExcerptRelevanceReference
" We observed a dose-response relationship between consumption of whole grain bread and higher urinary glyphosate concentrations."( Urinary concentrations and determinants of glyphosate and glufosinate in pregnant Canadian participants in the MIREC study.
Arbuckle, TE; Ashley-Martin, J; Bienvenu, JF; Borghese, MM; Bouchard, MF; Brion, O; Fisher, M; Foster, WG; Gaudreau, E; Huang, R; Lanphear, B; MacPherson, S; Owen, J, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
phosphonic acidsHP(=O)(OH)2 (phosphonic acid) and its P-substituted derivatives.
one-carbon compoundAn organic molecular entity containing a single carbon atom (C1).
[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 (1)

Inhibition Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Cytosol aminopeptidaseHomo sapiens (human)Ki1,040.00000.00060.16010.4200AID101210
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Biological Processes (1)

Processvia Protein(s)Taxonomy
proteolysisCytosol aminopeptidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (7)

Processvia Protein(s)Taxonomy
aminopeptidase activityCytosol aminopeptidaseHomo sapiens (human)
carboxypeptidase activityCytosol aminopeptidaseHomo sapiens (human)
protein bindingCytosol aminopeptidaseHomo sapiens (human)
metalloexopeptidase activityCytosol aminopeptidaseHomo sapiens (human)
manganese ion bindingCytosol aminopeptidaseHomo sapiens (human)
metalloaminopeptidase activityCytosol aminopeptidaseHomo sapiens (human)
peptidase activityCytosol aminopeptidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (5)

Processvia Protein(s)Taxonomy
nucleusCytosol aminopeptidaseHomo sapiens (human)
trans-Golgi networkCytosol aminopeptidaseHomo sapiens (human)
focal adhesionCytosol aminopeptidaseHomo sapiens (human)
extracellular exosomeCytosol aminopeptidaseHomo sapiens (human)
cytoplasmCytosol aminopeptidaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID101210Inhibition of Leucine aminopeptidase isolated from porcine kidney.1987Journal of medicinal chemistry, Sep, Volume: 30, Issue:9
Phosphorus amino acid analogues as inhibitors of leucine aminopeptidase.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (65)

TimeframeStudies, This Drug (%)All Drugs %
pre-19907 (10.77)18.7374
1990's7 (10.77)18.2507
2000's9 (13.85)29.6817
2010's17 (26.15)24.3611
2020's25 (38.46)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 10.97

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

MetricThis Compound (vs All)
Research Demand Index10.97 (24.57)
Research Supply Index4.29 (2.92)
Research Growth Index5.26 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (10.97)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews5 (6.94%)6.00%
Case Studies1 (1.39%)4.05%
Observational0 (0.00%)0.25%
Other66 (91.67%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]