Page last updated: 2024-11-08

3-hydroxyhippuric acid

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

Description

3-hydroxyhippuric acid: a kynureninase inhibitor; structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

m-hydroxyhippuric acid : An N-acylglycine that is hippuric acid (N-benzoylglycine) substituted at position 3 on the phenyl ring by a hydroxy group. [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 CID450268
CHEMBL ID447627
CHEBI ID70824
SCHEMBL ID600772
MeSH IDM0529684

Synonyms (42)

Synonym
unii-17hcx0hnrt
17hcx0hnrt ,
glycine, n-(3-hydroxybenzoyl)-
3xh ,
3-hydroxyhippuric acid
3-hydroxybenzoylglycine
[(3-hydroxybenzoyl)amino]acetic acid
n-(3-hydroxybenzoyl)glycine
m-hydroxyhippuric acid
2-[(3-hydroxybenzoyl)amino]acetic acid
2-[(3-hydroxyphenyl)formamido]acetic acid
DB07069
n-m-hydroxylbenzoylglycine
bdbm50265459
CHEMBL447627 ,
chebi:70824 ,
AKOS000128280
1637-75-8
EN300-54417
(3-hydroxybenzoylamino)acetic acid
hippuric acid, m-hydroxy-
hydroxyhippuric acid, m-
SCHEMBL600772
(3-hydroxy-benzoyl amino)-acetic acid
XDOFWFNMYJRHEW-UHFFFAOYSA-N
(3-hydroxy-benzoylamino)-acetic acid
mfcd09044170
HMS3604N06
DTXSID30167650
J-010089
BS-13947
(3-hydroxybenzoyl)glycine
HY-113085
CS-0059522
n-[(3-hydroxyphenyl)carbonyl]glycine
Q27095984
3-hydroxyhippuricacid
B2699-167342
m-hydroxyhippuricacid
n-(3-hydroxybenzoyl)-glycine
Z239129930
[(3-hydroxyphenyl)formamido]acetic acid
[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
N-acylglycineAn N-acyl-amino acid in which amino acid specified is glycine.
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]

Pathways (1)

PathwayProteinsCompounds
Flavan-3-ol metabolic pathway070

Protein Targets (1)

Inhibition Measurements

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

Biological Processes (9)

Processvia Protein(s)Taxonomy
tryptophan catabolic processKynureninaseHomo sapiens (human)
NAD biosynthetic processKynureninaseHomo sapiens (human)
quinolinate biosynthetic processKynureninaseHomo sapiens (human)
response to type II interferonKynureninaseHomo sapiens (human)
'de novo' NAD biosynthetic process from tryptophanKynureninaseHomo sapiens (human)
response to vitamin B6KynureninaseHomo sapiens (human)
anthranilate metabolic processKynureninaseHomo sapiens (human)
L-kynurenine catabolic processKynureninaseHomo sapiens (human)
tryptophan catabolic process to kynurenineKynureninaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Molecular Functions (4)

Processvia Protein(s)Taxonomy
pyridoxal phosphate bindingKynureninaseHomo sapiens (human)
kynureninase activityKynureninaseHomo sapiens (human)
protein homodimerization activityKynureninaseHomo sapiens (human)
3-hydroxykynureninase activityKynureninaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Ceullar Components (4)

Processvia Protein(s)Taxonomy
nucleoplasmKynureninaseHomo sapiens (human)
mitochondrionKynureninaseHomo sapiens (human)
cytosolKynureninaseHomo sapiens (human)
cytoplasmKynureninaseHomo sapiens (human)
[Information is prepared from geneontology information from the June-17-2024 release]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID412639Inhibition of human kynureninase2009Journal of medicinal chemistry, Jan-22, Volume: 52, Issue:2
Crystal structure of the Homo sapiens kynureninase-3-hydroxyhippuric acid inhibitor complex: insights into the molecular basis of kynureninase substrate specificity.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (5)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (20.00)29.6817
2010's3 (60.00)24.3611
2020's1 (20.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.76

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 Index20.76 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index5.08 (4.65)
Search Engine Demand Index15.26 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.76)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials1 (20.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other4 (80.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]