Page last updated: 2024-11-07

4-chloro-3-hydroxyanthranilic acid

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

Description

4-chloro-3-hydroxyanthranilic acid is a synthetic derivative of anthranilic acid that has shown promising activity as an antibacterial agent. It is synthesized through a multi-step process involving the chlorination and hydroxylation of anthranilic acid. Studies have shown that this compound exhibits significant antibacterial activity against a range of Gram-positive and Gram-negative bacteria, including strains resistant to conventional antibiotics. The compound's mechanism of action is thought to involve interference with bacterial cell wall synthesis. Further research is ongoing to explore its potential as a novel therapeutic agent for bacterial infections. The compound's unique chemical structure and potent antibacterial activity make it an attractive target for further investigation in the development of new antibiotics.'
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4-chloro-3-hydroxyanthranilic acid: metabolite of 6-chlorotryptophan; inhibitor of 3-hydroxyanthranilic acid oxidase [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID114947
CHEMBL ID1230244
SCHEMBL ID2408682
MeSH IDM0086681

Synonyms (22)

Synonym
CHEMBL1230244
4-chloro-3-hydroxyanthranilic acid
DB04598
2-amino-4-chloro-3-hydroxybenzoic acid
23219-33-2
benzoic acid, 2-amino-4-chloro-3-hydroxy-
4-chloro-3-hydroxyanthranilate
unii-r67leh4x5q
r67leh4x5q ,
4-cl-3-hana
AKOS022642585
SCHEMBL2408682
DTXSID30177794
EN300-222755
BS-16721
Q27095338
mfcd20639114
D80855
CS-0161456
2-amino-4-chloro-3-hydroxybenzoicacid
PD005976
Z1262513945
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (1)

Assay IDTitleYearJournalArticle
AID1065667Chemical stability in PBS buffer assessed as auto-oxidative degradation after 24 hrs by HPLC analysis2013Journal of medicinal chemistry, Dec-12, Volume: 56, Issue:23
2-Aminonicotinic acid 1-oxides are chemically stable inhibitors of quinolinic acid synthesis in the mammalian brain: a step toward new antiexcitotoxic agents.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (20)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (10.00)18.7374
1990's11 (55.00)18.2507
2000's5 (25.00)29.6817
2010's2 (10.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 11.94

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

MetricThis Compound (vs All)
Research Demand Index11.94 (24.57)
Research Supply Index3.04 (2.92)
Research Growth Index4.98 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (11.94)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews1 (5.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other19 (95.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]