Page last updated: 2024-12-04

4-hydroxymandelic acid

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

Description

4-hydroxymandelic acid: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

4-hydroxymandelic acid : A 2-hydroxy carboxylic acid that is mandelic acid bearing a phenolic hydroxy substituent at position 4. [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 CID328
CHEMBL ID2087618
CHEBI ID16388
SCHEMBL ID352555
MeSH IDM0063252

Synonyms (80)

Synonym
AC-19775
CHEBI:16388 ,
4-hydroxyphenylglycolic acid
hydroxy(4-hydroxyphenyl)acetic acid
p-hydroxymandelic acid
d-p-hydroxymandelate
4-hydroxymandelic acid
d-4-hydroxymandelate
1198-84-1
dl-4-hydroxymandelic acid
dl-alpha,4-dihydroxyphenylacetic acid
H0660
2-hydroxy-2-(4-hydroxyphenyl)acetic acid
A804384
A837374
2-(4-hydroxyphenyl)-2-oxidanyl-ethanoic acid
AKOS009156762
dl-4-hydroxymandelicacid
p-hydroxy mandelic acid monohydrate
4-hydroxy-dl-mandelic acid
hv52gs53ba ,
unii-hv52gs53ba
(rs)-p-hydroxymandelic acid
einecs 214-839-7
p-hydroxyphenylglycolic acid
einecs 230-569-2
alpha,4-dihydroxybenzeneacetic acid
2-(4-hydroxyphenyl)-2-hydroxyacetic acid
dl-p-hydroxymandelic acid
dl-p-hydroxyphenylglycolic acid
mandelic acid, p-hydroxy-
(+-)-4-hydroxymandelic acid
benzeneacetic acid, alpha,4-dihydroxy-
(+-)-p-hydroxymandelic acid
4'-hydroxymandelic acid
(+-)-alpha,4-dihydroxybenzeneacetic acid
CHEMBL2087618
FT-0625408
FT-0618716
AE-562/40848536
SCHEMBL352555
racemic parahydroxymandelic acid
4-hydroxy-mandelic acid
parahydroxymandelic acid
benzeneacetic acid, .alpha.,4-dihydroxy-
.alpha.,4-dihydroxybenzeneacetic acid
mfcd00004234
2-(4'-hydroxyphenyl)-2-hydroxyethanoic acid
p-hydroxyphenylglycolate
alpha,4-dihydroxy-benzeneacetate
4-hydroxy-dl-mandelate
(+/-)-alpha,4-dihydroxy-benzeneacetate
dl-p-hydroxyphenylglycolate
(rs)-p-hydroxymandelate
2-(4-hydroxyphenyl)-2-hydroxyacetate
dl-4-hydroxymandelate
p-hydroxymandelate
alpha,4-dihydroxybenzeneacetate
(+/-)-alpha,4-dihydroxy-benzeneacetic acid
p-hydroxy-mandelate
delta-p-hydroxymandelate
delta-4-hydroxymandelate
p-hydroxy-mandelic acid
alpha,4-dihydroxy-benzeneacetic acid
dl-p-hydroxymandelate
4-hydroxyphenylglycolate
HY-113027
CS-0059383
DTXSID70862596
h-d-ala-pro-ohhcl
DS-18506
Q10395570
D95528
2-hydroxy-2-(4-hydroxyphenyl)aceticacid
benzeneacetic acid, ?,4-dihydroxy-
(+/-)-.alpha.,4-dihydroxybenzeneacetic acid
(+/-)-p-hydroxymandelic acid
(+/-)-4-hydroxymandelic acid
EN300-204954
SY113769

Research Excerpts

Overview

4-Hydroxymandelic acid (4-HMA) is a valuable aromatic fine chemical. It is widely used for production of pharmaceuticals and food additives.

ExcerptReferenceRelevance
"4-Hydroxymandelic acid (4-HMA) is a valuable aromatic fine chemical and widely used for production of pharmaceuticals and food additives. "( Engineering Escherichia coli for production of 4-hydroxymandelic acid using glucose-xylose mixture.
Li, BZ; Li, FF; Qiao, JJ; Zhao, GR; Zhao, Y, 2016
)
2.13
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
metaboliteAny intermediate or product resulting from metabolism. The term 'metabolite' subsumes the classes commonly known as primary and secondary metabolites.
[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
2-hydroxy carboxylic acid
phenolsOrganic aromatic compounds having one or more hydroxy groups attached to a benzene or other arene ring.
[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]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID685295Inhibition of recombinant human IDO expressed in Escherichia coli using L-tryptophan as substrate at 200 uM after 60 mins by spectrophotometry2012Journal of natural products, Aug-24, Volume: 75, Issue:8
Halicloic acids A and B isolated from the marine sponge Haliclona sp. collected in the Philippines inhibit indoleamine 2,3-dioxygenase.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (25)

TimeframeStudies, This Drug (%)All Drugs %
pre-19906 (24.00)18.7374
1990's5 (20.00)18.2507
2000's5 (20.00)29.6817
2010's7 (28.00)24.3611
2020's2 (8.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 26.94

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 Index26.94 (24.57)
Research Supply Index3.30 (2.92)
Research Growth Index4.62 (4.65)
Search Engine Demand Index24.28 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (26.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (4.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other24 (96.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]