3-hydroxyhippuric acid: a kynureninase inhibitor; structure in first source
m-hydroxyhippuric acid : An N-acylglycine that is hippuric acid (N-benzoylglycine) substituted at position 3 on the phenyl ring by a hydroxy group.
ID Source | ID |
---|---|
PubMed CID | 450268 |
CHEMBL ID | 447627 |
CHEBI ID | 70824 |
SCHEMBL ID | 600772 |
MeSH ID | M0529684 |
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 |
Role | Description |
---|---|
metabolite | Any 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] |
Class | Description |
---|---|
N-acylglycine | An N-acyl-amino acid in which amino acid specified is glycine. |
phenols | Organic 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] |
Pathway | Proteins | Compounds |
---|---|---|
Flavan-3-ol metabolic pathway | 0 | 70 |
Protein | Taxonomy | Measurement | Average | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Process | via Protein(s) | Taxonomy |
---|---|---|
tryptophan catabolic process | Kynureninase | Homo sapiens (human) |
NAD biosynthetic process | Kynureninase | Homo sapiens (human) |
quinolinate biosynthetic process | Kynureninase | Homo sapiens (human) |
response to type II interferon | Kynureninase | Homo sapiens (human) |
'de novo' NAD biosynthetic process from tryptophan | Kynureninase | Homo sapiens (human) |
response to vitamin B6 | Kynureninase | Homo sapiens (human) |
anthranilate metabolic process | Kynureninase | Homo sapiens (human) |
L-kynurenine catabolic process | Kynureninase | Homo sapiens (human) |
tryptophan catabolic process to kynurenine | Kynureninase | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
pyridoxal phosphate binding | Kynureninase | Homo sapiens (human) |
kynureninase activity | Kynureninase | Homo sapiens (human) |
protein homodimerization activity | Kynureninase | Homo sapiens (human) |
3-hydroxykynureninase activity | Kynureninase | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Process | via Protein(s) | Taxonomy |
---|---|---|
nucleoplasm | Kynureninase | Homo sapiens (human) |
mitochondrion | Kynureninase | Homo sapiens (human) |
cytosol | Kynureninase | Homo sapiens (human) |
cytoplasm | Kynureninase | Homo sapiens (human) |
[Information is prepared from geneontology information from the June-17-2024 release] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID412639 | Inhibition of human kynureninase | 2009 | Journal 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] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (20.00) | 29.6817 |
2010's | 3 (60.00) | 24.3611 |
2020's | 1 (20.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (20.76) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 1 (20.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 4 (80.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |