Page last updated: 2024-12-06

6-amino-1,2-benzopyrone

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

Description

6-Amino-1,2-benzopyrone, also known as 6-amino-coumarin, is a synthetic derivative of coumarin. It has been investigated for its potential biological activities, including antibacterial, antifungal, and anticancer properties. Research suggests that its effects might stem from its ability to inhibit enzyme activity and influence cellular processes. Further studies are necessary to fully elucidate its mechanisms of action and potential therapeutic applications.'

6-amino-1,2-benzopyrone: selective inhibitor of adenosine diphosphoribosyl transferase; RN given refers to the parent compound [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID46153
CHEMBL ID1829962
SCHEMBL ID483027
MeSH IDM0184980

Synonyms (33)

Synonym
HMS1749K04
BB 0245754
6-amino-2h-1-benzopyran-2-one
6-amino-chromen-2-one
OPREA1_467607
OPREA1_644760
nsc613801
6-amino-1,2-benzopyrone
coumarin, 6-amino-
6-abp
6-aminocoumarin
6-aminochromen-2-one
2h-1-benzopyran-2-one, 6-amino-
6-amino-2h-chromen-2-one
STK140470
AKOS000111175
(2-oxochromen-6-yl)azanium chloride
CHEMBL1829962
14415-44-2
EN300-51130
unii-s9w3l9r2na
s9w3l9r2na ,
FT-0684448
SCHEMBL483027
6-amino-2h-chromen-2-one #
4jq ,
DTXSID70162624
mfcd00115435
6-amino-chromen-2-one, aldrichcpr
Z56754502
CS-0207101
AS-42838
Q27454762
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Bioassays (4)

Assay IDTitleYearJournalArticle
AID619823Vasorelaxant activity in Wistar rat thoracic aortic ring assessed as inhibition of norepinephrine hydrochloride-induced contraction treated after noradrenaline challenge2011Bioorganic & medicinal chemistry, Oct-15, Volume: 19, Issue:20
Design, synthesis and vasorelaxant evaluation of novel coumarin-pyrimidine hybrids.
AID619824Aqueous solubility, log S of the compound2011Bioorganic & medicinal chemistry, Oct-15, Volume: 19, Issue:20
Design, synthesis and vasorelaxant evaluation of novel coumarin-pyrimidine hybrids.
AID588519A screen for compounds that inhibit viral RNA polymerase binding and polymerization activities2011Antiviral research, Sep, Volume: 91, Issue:3
High-throughput screening identification of poliovirus RNA-dependent RNA polymerase inhibitors.
AID540299A screen for compounds that inhibit the MenB enzyme of Mycobacterium tuberculosis2010Bioorganic & medicinal chemistry letters, Nov-01, Volume: 20, Issue:21
Synthesis and SAR studies of 1,4-benzoxazine MenB inhibitors: novel antibacterial agents against Mycobacterium tuberculosis.
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (13)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's3 (23.08)18.2507
2000's1 (7.69)29.6817
2010's8 (61.54)24.3611
2020's1 (7.69)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 12.16

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 Index12.16 (24.57)
Research Supply Index2.83 (2.92)
Research Growth Index5.00 (4.65)
Search Engine Demand Index0.00 (26.88)
Search Engine Supply Index0.00 (0.95)

This Compound (12.16)

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%
Other16 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]