Page last updated: 2024-11-11

noreugenin

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

Description

noreugenin : A member of the class of chromones in which the 1,4-benzopyrone skeleton is substituted with a methyl group at position 2 and with hydroxy groups at positions 5 and 7. A natural product, it is found in Pisonia aculeata. [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]

FloraRankFlora DefinitionFamilyFamily Definition
Pisoniagenus[no description available]NyctaginaceaeA plant family of the order Caryophyllales, subclass Caryophyllidae, class Magnoliopsida.[MeSH]

Cross-References

ID SourceID
PubMed CID5375252
CHEMBL ID507707
CHEBI ID67375
SCHEMBL ID168822

Synonyms (33)

Synonym
5,7-dihydroxy-2-methyl-chromen-4-one
5,7-dihydroxy-2-methyl-4h-chromen-4-one
5,7-dihydroxy-2-methylchromone
noreugenin
chebi:67375 ,
CHEMBL507707
5,7-dihydroxy-2-methylchromen-4-one
AKOS006277487
1013-69-0
m0kfc1q5jc ,
unii-m0kfc1q5jc
5,7-dihydroxy-2-methyl-4h-1-benzopyran-4-one
4h-1-benzopyran-4-one, 5,7-dihydroxy-2-methyl-
C20462
SCHEMBL168822
4h-1-benzopyran-4-one,5,7-dihydroxy-2-methyl-
dihydroxy methylchromone [inci]
dihydroxymethylchromone
chromone, 5,7-dihydroxy-2-methyl-
5,7-dihydroxy-2-methyl-4h-chromen-4-one #
5,7-dihydroxy-2-methylchromome
2-methyl-5,7-dihydroxychromone
DTXSID80143828
mfcd03001435
A897187
2-methyl-5,7-dihydroxychromon
Q27135833
HY-N3029
CS-0023039
FT-0775292
AS-78622
5,7-dihydroxy-2-methylbenzopyran-4-one
SY310866
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Roles (1)

RoleDescription
plant metaboliteAny eukaryotic metabolite produced during a metabolic reaction in plants, the kingdom that include flowering plants, conifers and other gymnosperms.
[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
chromonesA chromenone that consists of a 1,4-benzopyrone skeleton and its substituted derivatives thereof.
resorcinolsAny benzenediol in which the two hydroxy groups are meta to one another.
[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
pentaketide chromone biosynthesis06

Bioassays (13)

Assay IDTitleYearJournalArticle
AID1675368Antifungal activity against Cryptococcus neoformans after 48 hrs by microdilution assay2020Journal of natural products, 08-28, Volume: 83, Issue:8
Synthesis and Antifungal Activity of Chromones and Benzoxepines from the Leaves of
AID421967Cytotoxicity against human HT-29 cells by MTT assay2009Journal of natural products, May-22, Volume: 72, Issue:5
Cytotoxic and HIF-1alpha inhibitory compounds from Crossosoma bigelovii.
AID421965Cytotoxicity against human A549 cells by MTT assay2009Journal of natural products, May-22, Volume: 72, Issue:5
Cytotoxic and HIF-1alpha inhibitory compounds from Crossosoma bigelovii.
AID37426Inhibitory activity against yeast alpha-glucosidase; mild activity observed2004Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
Yeast and mammalian alpha-glucosidase inhibitory constituents from Himalayan rhubarb Rheum emodi Wall.ex Meisson.
AID332930Cytotoxicity against human H9 cells after 3 days1994Journal of natural products, Jan, Volume: 57, Issue:1
Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids.
AID1675365Antifungal activity against Candida albicans ATCC 10231 after 24 hrs by microdilution assay2020Journal of natural products, 08-28, Volume: 83, Issue:8
Synthesis and Antifungal Activity of Chromones and Benzoxepines from the Leaves of
AID332931Therapeutic index, ratio of IC50 for human H9 cells to EC50 for HIV1 3B1994Journal of natural products, Jan, Volume: 57, Issue:1
Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids.
AID332929Antiviral activity against HIV1 3B infected in human H9 cells assessed as inhibition of viral replication after 3 days by p24 antigen capture assay1994Journal of natural products, Jan, Volume: 57, Issue:1
Anti-AIDS agents, 10. Acacetin-7-O-beta-D-galactopyranoside, an anti-HIV principle from Chrysanthemum morifolium and a structure-activity correlation with some related flavonoids.
AID1675366Antifungal activity against Candida albicans ATCC 10231 after 48 hrs by microdilution assay2020Journal of natural products, 08-28, Volume: 83, Issue:8
Synthesis and Antifungal Activity of Chromones and Benzoxepines from the Leaves of
AID1675367Antifungal activity against Cryptococcus neoformans after 24 hrs by microdilution assay2020Journal of natural products, 08-28, Volume: 83, Issue:8
Synthesis and Antifungal Activity of Chromones and Benzoxepines from the Leaves of
AID606810Antitubercular activity against Mycobacterium tuberculosis H37Rv after 2 weeks by agar plate assay2011Journal of natural products, May-27, Volume: 74, Issue:5
Antitubercular chromones and flavonoids from Pisonia aculeata.
AID421966Cytotoxicity against human MCF7 cells by MTT assay2009Journal of natural products, May-22, Volume: 72, Issue:5
Cytotoxic and HIF-1alpha inhibitory compounds from Crossosoma bigelovii.
AID37282Inhibitory activity against rat alpha-glucosidase; mild activity observed2004Bioorganic & medicinal chemistry letters, Jul-16, Volume: 14, Issue:14
Yeast and mammalian alpha-glucosidase inhibitory constituents from Himalayan rhubarb Rheum emodi Wall.ex Meisson.
[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's1 (20.00)18.2507
2000's2 (40.00)29.6817
2010's1 (20.00)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: 22.17

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 Index22.17 (24.57)
Research Supply Index1.79 (2.92)
Research Growth Index4.66 (4.65)
Search Engine Demand Index18.60 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (22.17)

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%
Other5 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]