Page last updated: 2024-12-05

4-aminophenylacetic acid

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

Description

4-aminophenylacetic acid, also known as p-aminophenylacetic acid, is a naturally occurring amino acid that has been found in various plants and microorganisms. It is a precursor to the synthesis of several important compounds, including the neurotransmitter dopamine. The synthesis of 4-aminophenylacetic acid typically involves the reaction of 4-nitrophenylacetic acid with a reducing agent, such as iron or tin. The resulting 4-aminophenylacetic acid can then be used as a starting material for the production of other pharmaceuticals. 4-aminophenylacetic acid has been studied for its potential therapeutic applications, particularly in the treatment of Parkinson's disease. It is also used as an intermediate in the synthesis of several other drugs and chemicals. Its importance in research lies in its role as a precursor to dopamine and its potential to serve as a therapeutic agent.'

4-aminophenylacetic acid: peptide mimic; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID14533
CHEMBL ID3278327
SCHEMBL ID39103
MeSH IDM0285128

Synonyms (73)

Synonym
BB 0244247
(4-amino-phenyl)-acetic acid
2-(4-aminophenyl)-acetic acid
acetic acid, (p-aminophenyl)-
p-aminophenylacetic acid
(para-aminophenyl)acetic acid
4-aminobenzeneacetic acid
nsc-7929
4-aminophenylacetic acid
1197-55-3
benzeneacetic acid, 4-amino-
nsc7929
ccris 3157
nsc 7929
einecs 214-828-7
p-amino-alpha-toluic acid
brn 2208094
4-carboxymethylaniline
OPREA1_658624
(p-aminophenyl)acetic acid
2-(4-aminophenyl)acetic acid
inchi=1/c8h9no2/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4h,5,9h2,(h,10,11
4-aminophenylacetic acid, 98% ,
A0393
AKOS000104762
(4-aminophenyl)acetic acid
STL139160
(4-aminophenyl)acetate
unii-1ied47a544
3-14-00-01182 (beilstein handbook reference)
1ied47a544 ,
FT-0617595
BBL018950
AM20060949
AE-508/40191188
4-(carboxymethyl)aniline
p-amino-.alpha.-toluic acid
p-aminophenylacetic acid [mi]
4-aminophenylaceticacid
CHEMBL3278327
SCHEMBL39103
SY001637
mfcd00007916
DTXSID1061609
2-(4-amino phenyl)-acetic acid
para-aminophenylacetic acid
p-aminophenyl acetic acid
(p-aminophenyl)-acetic acid
4-aminophenyl-acetic acid
4-amino phenyl acetic acid
(4-aminophenyl)-acetic acid
2-(4aminophenyl)acetic acid
4-amino-phenylacetic acid
4-amino-phenyl acetic acid
4-amino-phenyl-acetic acid
(4-amino-phenyl)acetic acid
4-aminobenzene acetic acid
4-amino phenylacetic acid
4-aminophenyl acetic acid
STR03492
BS-3833
4-(aminophenyl)acetic acid
W-108499
bdbm231635
4-aminophenylacetic acid, vetec(tm) reagent grade, 98%
CS-W018535
F0001-0324
BP-24384
BCP24945
Q15726001
AC7503
EN300-20755
Z104481066
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Protein Targets (1)

Activation Measurements

ProteinTaxonomyMeasurementAverageMin (ref.)Avg (ref.)Max (ref.)Bioassay(s)
Olfactory receptor class A-like protein 1Danio rerio (zebrafish)EC50 (µMol)91.70001.90001.90001.9000AID1802885
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (3)

Assay IDTitleYearJournalArticle
AID1146772Dissociation constant, pKa of the compound1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
P-Aminobenzoic acid derivatives as inhibitors of the cell-free H2-pteroate synthesizing system of Escherichia coli.
AID1146770Competitive inhibition of Escherichia coli B H2-pteroate synthetase assessed as decrease in H2-pteroate formation using [7-14C]-PABA as substrate treated with enzyme for 10 mins prior to substrate challenge for 40 mins by radioassay method1977Journal of medicinal chemistry, Feb, Volume: 20, Issue:2
P-Aminobenzoic acid derivatives as inhibitors of the cell-free H2-pteroate synthesizing system of Escherichia coli.
AID1802885Functional Calcium Imaging Assay from Article 10.1074/jbc.M114.573162: \\ORA1, a zebrafish olfactory receptor ancestral to all mammalian V1R genes, recognizes 4-hydroxyphenylacetic acid, a putative reproductive pheromone.\\2014The Journal of biological chemistry, Jul-11, Volume: 289, Issue:28
ORA1, a zebrafish olfactory receptor ancestral to all mammalian V1R genes, recognizes 4-hydroxyphenylacetic acid, a putative reproductive pheromone.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (11)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (18.18)18.7374
1990's2 (18.18)18.2507
2000's3 (27.27)29.6817
2010's3 (27.27)24.3611
2020's1 (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: 28.80

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 Index28.80 (24.57)
Research Supply Index2.48 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index29.80 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (28.80)

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%
Other11 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]