Page last updated: 2024-08-01 16:25:10

3',4',7-trihydroxyflavone

Description

3',4',7-trihydroxyflavone: from the Sudanese medicinal plant Albizia zygia; structure in first source [MeSH]

7,3',4'-Trihydroxyflavone : no description available [CHeBI]

Cross-References

ID SourceID
PubMed CID5322065
CHEMBL ID301624
SCHEMBL ID34405
CHEBI ID196247
MeSH IDM0593193

Synonyms (38)

Synonym
3'',4'',7-trihydroxyflavon
2-(3,4-dihydroxy-phenyl)-7-hydroxy-chromen-4-one
bdbm50077325
7,3'',4''-trihydroxyflavone
2-(3,4-dihydroxyphenyl)-7-hydroxy-4h-chromen-4-one
brn 0253031
7,3',4'-trihydroxyflavone
2-(3,4-dihydroxyphenyl)-7-hydroxy-4h-1-benzopyran-4-one
4h-1-benzopyran-4-one, 2-(3,4-dihydroxyphenyl)-7-hydroxy-
2150-11-0
3',4',7-trihydroxyflavone
CHEMBL301624 ,
3',4',7-trihydroxyflavon
LMPK12110042
2-(3,4-dihydroxyphenyl)-7-hydroxychromen-4-one
CHEBI:196247
flavone, 7,3',4'-trihydroxy-
5-18-04-00590 (beilstein handbook reference)
15z ,
AKOS016009456
FT-0634068
4HLF
SCHEMBL34405
Q-100553
PVFGJHYLIHMCQD-UHFFFAOYSA-N
DTXSID30175836
mfcd00017434
2-(3,4-dihydroxyphenyl)-7-hydroxy-chromen-4-one
7, 3',4'-trihydroxyflavone
104666-14-0
Q23055239
flavone, 3',4',7-trihydroxy- (6ci,7ci,8ci); 2-(3,4-dihydroxyphenyl)-7-hydroxy-4h-1-benzopyran-4-one; 3',4',7-trihydroxyflavone; 3',4',7-trihydroxylflavone; 5-deoxyluteolin; 7,3',4'-trihydroxyflavone
t 414
D81760
BS-49064
3 inverted exclamation marka,4 inverted exclamation marka,7-trihydroxyflavone
HY-N2736
CS-0023236

Drug Classes (1)

ClassDescription
flavonesA member of the class of flavonoid with a 2-aryl-1-benzopyran-4-one (2-arylchromen-4-one) skeleton and its substituted derivatives.

Protein Targets (7)

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)
Telomerase reverse transcriptaseHomo sapiens (human)IC5040.0000AID281989
Poly [ADP-ribose] polymerase tankyrase-1Homo sapiens (human)IC500.6378AID735786
Poly [ADP-ribose] polymerase 1Homo sapiens (human)IC507.5429AID735783
Polyunsaturated fatty acid 5-lipoxygenaseHomo sapiens (human)IC502.0000AID1063904
Aldo-keto reductase family 1 member B1Bos taurus (cattle)IC506.5200AID34338
Poly [ADP-ribose] polymerase tankyrase-2Homo sapiens (human)IC500.8705AID735784

Other Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)
Seed linoleate 13S-lipoxygenase-1Glycine max (soybean)Km143.9300AID1063899; AID1063900
Seed linoleate 13S-lipoxygenase-1Glycine max (soybean)Vmax0.0085AID1063899; AID1063900

Bioassays (33)

Assay IDTitleYearJournalArticle
AID1668637Inhibition of human liver FBP1 at 200 uM incubated for 5 mins by fluorescence method relative to control2020Journal of natural products, 05-22, Volume: 83, Issue:5
ISSN: 1520-6025
Structural Specificity of Flavonoids in the Inhibition of Human Fructose 1,6-Bisphosphatase.
AID426715Antiplasmodial activity against chloroquine-sensitive Plasmodium falciparum D102009Journal of natural products, Jul, Volume: 72, Issue:7
ISSN: 1520-6025
Antiplasmodial isoflavanones from the roots of Sophora mollis.
AID765677Inhibition of oxidative burst in PMA-stimulated human neutrophils assessed as inhibition of H2O2-induced oxidation of amplex red incubated for 5 mins prior to PMA challenge by fluorescence assay2013European journal of medicinal chemistry, Sep, Volume: 67ISSN: 1768-3254Modulation of human neutrophils' oxidative burst by flavonoids.
AID596670Induction of adipogenesis in mouse 3T3L1 cells assessed as increase in triglyceride level at 1 uM on day 8 relative to control2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
ISSN: 1464-3391
Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells.
AID1063900Activity at soybean LOX-1 using linoleic acid as substrate at 10 uM preincubated for 5 mins followed by substrate addition by Michaelis-Menten plot analysis2014European journal of medicinal chemistry, Jan-24, Volume: 72ISSN: 1768-3254Inhibition of LOX by flavonoids: a structure-activity relationship study.
AID180466Inhibitory effect on the oxidative degradation of membrane lipids (lipid peroxidation assay) in microsomes of rat.2000Journal of medicinal chemistry, Oct-05, Volume: 43, Issue:20
ISSN: 0022-2623
Synthesis of novel 3,7-substituted-2-(3',4'-dihydroxyphenyl)flavones with improved antioxidant activity.
AID1063899Activity at soybean LOX-1 using linoleic acid as substrate at 25 uM preincubated for 5 mins followed by substrate addition by Michaelis-Menten plot analysis2014European journal of medicinal chemistry, Jan-24, Volume: 72ISSN: 1768-3254Inhibition of LOX by flavonoids: a structure-activity relationship study.
AID749999Binding affinity to recombinant paraoxonase-1 (unknown origin) expressed in Escherichia coli after 5 mins by Trp-fluorescence quenching method2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
ISSN: 1464-3391
The effects and mechanism of flavonoid-rePON1 interactions. Structure-activity relationship study.
AID281989Inhibition of human telomerase from HEK293 cell extracts by Flash-Plate assay2004Journal of medicinal chemistry, Dec-16, Volume: 47, Issue:26
ISSN: 0022-2623
Catecholic flavonoids acting as telomerase inhibitors.
AID765681Inhibition of oxidative burst in PMA-stimulated human neutrophils assessed as inhibition of ROS-induced luminol oxidation incubated for 5 mins prior to PMA challenge by chemiluminescence assay2013European journal of medicinal chemistry, Sep, Volume: 67ISSN: 1768-3254Modulation of human neutrophils' oxidative burst by flavonoids.
AID735784Inhibition of human 6XHis-tagged TNKS2 ART domain (946 to 1161 amino acid residues) expressed in Escherichia coli Rosetta2 (DE3) by fluorescence assay2013Journal of medicinal chemistry, May-09, Volume: 56, Issue:9
ISSN: 1520-4804
Screening and structural analysis of flavones inhibiting tankyrases.
AID34338Inhibition of ALR2 (aldose reductase) of bovine lens1999Journal of medicinal chemistry, Jun-03, Volume: 42, Issue:11
ISSN: 0022-2623
1-Benzopyran-4-one antioxidants as aldose reductase inhibitors.
AID765679Inhibition of oxidative burst in PMA-stimulated human neutrophils assessed as inhibition of superoxide anion radical-induced lucigenin oxidation incubated for 5 mins prior to PMA challenge by chemiluminescence assay2013European journal of medicinal chemistry, Sep, Volume: 67ISSN: 1768-3254Modulation of human neutrophils' oxidative burst by flavonoids.
AID596672Induction of adipogenesis in mouse 3T3L1 cells assessed as increase in triglyceride level at 10 uM on day 8 relative to control2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
ISSN: 1464-3391
Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells.
AID735786Inhibition of human 6XHis-tagged TNKS1 SAM-ART domain (1030 to 1317 amino acid residues) by fluorescence assay2013Journal of medicinal chemistry, May-09, Volume: 56, Issue:9
ISSN: 1520-4804
Screening and structural analysis of flavones inhibiting tankyrases.
AID426717Selectivity index, ratio of IC50 for CHO cells to IC50 for chloroquine-sensitive Plasmodium falciparum D102009Journal of natural products, Jul, Volume: 72, Issue:7
ISSN: 1520-6025
Antiplasmodial isoflavanones from the roots of Sophora mollis.
AID1063904Inhibition of 5-LOX-mediated LTB4 production in human neutrophils using arachidonic acid as substrate preincubated for 10 mins followed by substrate addition measured after 8 mins by enzyme immunoassay2014European journal of medicinal chemistry, Jan-24, Volume: 72ISSN: 1768-3254Inhibition of LOX by flavonoids: a structure-activity relationship study.
AID426716Cytotoxicity against CHO cells by MTT assay2009Journal of natural products, Jul, Volume: 72, Issue:7
ISSN: 1520-6025
Antiplasmodial isoflavanones from the roots of Sophora mollis.
AID201080Minimum inhibitory concentration, that inhibits growth of Staphylococcus aureus in the presence of subinhibitory (30 ug/mL) Berberine; Inactive2001Journal of medicinal chemistry, Jan-18, Volume: 44, Issue:2
ISSN: 0022-2623
Flavonolignan and flavone inhibitors of a Staphylococcus aureus multidrug resistance pump: structure-activity relationships.
AID749998Binding affinity to recombinant paraoxonase-1 (unknown origin) expressed in Escherichia coli2013Bioorganic & medicinal chemistry, Jun-01, Volume: 21, Issue:11
ISSN: 1464-3391
The effects and mechanism of flavonoid-rePON1 interactions. Structure-activity relationship study.
AID502292Antioxidant activity assessed as DDPH radical scavenging activity2010Bioorganic & medicinal chemistry letters, Sep-15, Volume: 20, Issue:18
ISSN: 1464-3405
Relationships between structures of hydroxyflavones and their antioxidative effects.
AID1063895Mixed noncompetitive type inhibition of soybean LOX-1 using linoleic acid as substrate preincubated for 5 mins followed by substrate addition by Lineweaver-Burk plot analysis2014European journal of medicinal chemistry, Jan-24, Volume: 72ISSN: 1768-3254Inhibition of LOX by flavonoids: a structure-activity relationship study.
AID765682Cytotoxicity against human neutrophils assessed as cell viability at 100 uM after 1 hr by trypan blue exclusion assay2013European journal of medicinal chemistry, Sep, Volume: 67ISSN: 1768-3254Modulation of human neutrophils' oxidative burst by flavonoids.
AID1063894Binding affinity to soybean LOX-1 at 1248 uM by STD-[1H] NMR spectroscopic analysis2014European journal of medicinal chemistry, Jan-24, Volume: 72ISSN: 1768-3254Inhibition of LOX by flavonoids: a structure-activity relationship study.
AID605243Agonist activity at TrkB in E17 rat primary cortical neurons assessed as AKT phosphorylation at Ser 473 at 500 nM after 15 mins by ELISA2010Journal of medicinal chemistry, Dec-09, Volume: 53, Issue:23
ISSN: 1520-4804
A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect.
AID232853Antioxidant activity was determined using trolox equivalent antioxidant capacity assay.2000Journal of medicinal chemistry, Oct-05, Volume: 43, Issue:20
ISSN: 0022-2623
Synthesis of novel 3,7-substituted-2-(3',4'-dihydroxyphenyl)flavones with improved antioxidant activity.
AID596671Induction of adipogenesis in mouse 3T3L1 cells assessed as increase in triglyceride level at 3 uM on day 8 relative to control2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
ISSN: 1464-3391
Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells.
AID765674Inhibition of oxidative burst in PMA-stimulated human neutrophils assessed as inhibition of HOCl-induced oxidation of APF after 6 mins by fluorescence assay2013European journal of medicinal chemistry, Sep, Volume: 67ISSN: 1768-3254Modulation of human neutrophils' oxidative burst by flavonoids.
AID596673Induction of adipogenesis in mouse 3T3L1 cells assessed as increase in triglyceride level at 30 uM on day 8 relative to control2011Bioorganic & medicinal chemistry, May-01, Volume: 19, Issue:9
ISSN: 1464-3391
Structural requirements of flavonoids for the adipogenesis of 3T3-L1 cells.
AID735783Inhibition of human recombinant ARTD1 by fluorescence assay2013Journal of medicinal chemistry, May-09, Volume: 56, Issue:9
ISSN: 1520-4804
Screening and structural analysis of flavones inhibiting tankyrases.
AID1239713Anti-platelet activity in rat platelet rich plasma assessed as inhibition of ADP and calcium-induced platelet aggregation at 100 uM pre-incubated at 37 degC for 10 mins and measured 30 mins after ADP and calcium addition2015Bioorganic & medicinal chemistry letters, Aug-15, Volume: 25, Issue:16
ISSN: 1464-3405
Potential therapeutic agents for circulatory diseases from Bauhinia glauca Benth.subsp. pernervosa. (Da Ye Guan Men).
AID1334868Inhibition of LPS-stimulated nitric oxide production in ddy mouse peritoneal macrophages measured after 20 hrs by Greiss method2017Bioorganic & medicinal chemistry, 01-15, Volume: 25, Issue:2
ISSN: 1464-3391
Structure-activity relationship of the inhibitory effects of flavonoids on nitric oxide production in RAW264.7 cells.
AID977608Experimentally measured binding affinity data (IC50) for protein-ligand complexes derived from PDB2013Journal of medicinal chemistry, May-09, Volume: 56, Issue:9
ISSN: 1520-4804
Screening and structural analysis of flavones inhibiting tankyrases.

Research

Studies (24)

TimeframeStudies, This Drug (%)All Drugs %
pre-19901 (4.17)18.7374
1990's1 (4.17)18.2507
2000's4 (16.67)29.6817
2010's16 (66.67)24.3611
2020's2 (8.33)2.80

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%
Other24 (100.00%)84.16%
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
flavoxatecarboxylic ester;
flavones;
piperidines;
tertiary amino compound
antispasmodic drug;
muscarinic antagonist;
parasympatholytic
00low000000
flavoneflavonesmetabolite;
nematicide
00low000000
5-hydroxyflavoneflavones00low000000
flavodic acidflavones00low000000
3-methylflavone-8-carboxylic acidflavones;
oxo monocarboxylic acid
EC 3.1.4.* (phosphoric diester hydrolase) inhibitor00low000000
4'-amino-6-hydroxyflavoneflavones00low000000
2'-hydroxyflavoneflavones00low000000
2-(3,4-dihydroxyphenyl)-7,8-dihydroxy-1-benzopyran-4-oneflavones00low000000
2-[(4-oxo-2-phenyl-1-benzopyran-3-yl)oxy]acetic acidflavones00low000000
cochliophilin aflavones00low000000
2-[[5-[2-[(2-methylpropan-2-yl)oxy]-2-oxoethoxy]-4-oxo-2-phenyl-1-benzopyran-7-yl]oxy]acetic acid tert-butyl esterflavones;
tert-butyl ester
00low000000
Isolicoflavonolflavones00low000000
Licoflavone Aflavones00low000000
5,7,2'-trihydroxyflavoneflavones00low000000
morusinolflavones00low000000
Norartocarpetinflavones00low000000
Licoflavone Bflavones00low000000
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
protocatechuic acidcatechols;
dihydroxybenzoic acid
antineoplastic agent;
EC 1.1.1.25 (shikimate dehydrogenase) inhibitor;
EC 1.14.11.2 (procollagen-proline dioxygenase) inhibitor;
human xenobiotic metabolite;
plant metabolite
201520159.0low000010
gallic acidtrihydroxybenzoic acidantineoplastic agent;
antioxidant;
apoptosis inducer;
astringent;
cyclooxygenase 2 inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
geroprotector;
human xenobiotic metabolite;
plant metabolite
201520159.0low000010
dimethyl sulfoxidesulfoxide;
volatile organic compound
alkylating agent;
antidote;
Escherichia coli metabolite;
geroprotector;
MRI contrast agent;
non-narcotic analgesic;
polar aprotic solvent;
radical scavenger
2010201014.0low000100
naringenin4'-hydroxyflavanones;
trihydroxyflavanone
2013201410.5low000020
catechinhydroxyflavan2013201311.0low000010
7,8-dihydroxyflavonedihydroxyflavoneantidepressant;
antineoplastic agent;
antioxidant;
plant metabolite;
tropomyosin-related kinase B receptor agonist
2001201019.0medium000300
aspirinbenzoic acids;
phenyl acetates;
salicylates
anticoagulant;
antipyretic;
cyclooxygenase 1 inhibitor;
cyclooxygenase 2 inhibitor;
drug allergen;
EC 1.1.1.188 (prostaglandin-F synthase) inhibitor;
geroprotector;
non-narcotic analgesic;
non-steroidal anti-inflammatory drug;
plant activator;
platelet aggregation inhibitor;
prostaglandin antagonist;
teratogenic agent
201520159.0low000010
chloroquineaminoquinoline;
organochlorine compound;
secondary amino compound;
tertiary amino compound
anticoronaviral agent;
antimalarial;
antirheumatic drug;
autophagy inhibitor;
dermatologic drug
2009200915.0low000100
masoprocolcatechols;
lignan;
tetrol
antioxidant;
ferroptosis inhibitor;
geroprotector;
plant metabolite
2014201410.0low000010
troglitazonechromanes;
thiazolidinone
anticoagulant;
anticonvulsant;
antineoplastic agent;
antioxidant;
EC 6.2.1.3 (long-chain-fatty-acid--CoA ligase) inhibitor;
ferroptosis inhibitor;
hypoglycemic agent;
platelet aggregation inhibitor;
vasodilator agent
2011201113.0low000010
adenosine monophosphateadenosine 5'-phosphate;
purine ribonucleoside 5'-monophosphate
adenosine A1 receptor agonist;
cofactor;
EC 3.1.3.1 (alkaline phosphatase) inhibitor;
EC 3.1.3.11 (fructose-bisphosphatase) inhibitor;
fundamental metabolite;
micronutrient;
nutraceutical
202020204.0low000010
methyl gallategallate esteranti-inflammatory agent;
antioxidant;
plant metabolite
201520159.0low000010
catechincatechinantioxidant;
plant metabolite
2011201511.0low000020
emetineisoquinoline alkaloid;
pyridoisoquinoline
antiamoebic agent;
anticoronaviral agent;
antiinfective agent;
antimalarial;
antineoplastic agent;
antiprotozoal drug;
antiviral agent;
autophagy inhibitor;
emetic;
expectorant;
plant metabolite;
protein synthesis inhibitor
2009200915.0low000100
flavanoneflavanones2011201113.0low000010
kainic aciddicarboxylic acid;
L-proline derivative;
non-proteinogenic L-alpha-amino acid;
pyrrolidinecarboxylic acid
antinematodal drug;
excitatory amino acid agonist
2010201014.0low000100
flavoneflavonesmetabolite;
nematicide
2010202010.5low000150
syringic acidbenzoic acids;
dimethoxybenzene;
phenols
plant metabolite201520159.0low000010
eriodictyolflavanones2013201410.5high000020
3-hydroxyflavoneflavonols;
monohydroxyflavone
1999201117.3low001110
isovanillic acidmethoxybenzoic acid;
monohydroxybenzoic acid
antibacterial agent;
plant metabolite
201520159.0low000010
4-aminobenzhydrazide2013201311.0low000010
butylated hydroxytoluenephenolsantioxidant;
ferroptosis inhibitor;
food additive;
geroprotector
1999199925.0low001000
silybinaromatic ether;
benzodioxine;
flavonolignan;
polyphenol;
secondary alpha-hydroxy ketone
antineoplastic agent;
antioxidant;
hepatoprotective agent;
plant metabolite
2001200123.0low000100
baicalindihydroxyflavone;
glucosiduronic acid;
glycosyloxyflavone;
monosaccharide derivative
antiatherosclerotic agent;
antibacterial agent;
anticoronaviral agent;
antineoplastic agent;
antioxidant;
cardioprotective agent;
EC 2.7.7.48 (RNA-directed RNA polymerase) inhibitor;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor;
ferroptosis inhibitor;
neuroprotective agent;
non-steroidal anti-inflammatory drug;
plant metabolite;
prodrug
202020204.0low000010
5-hydroxyflavoneflavones1999202012.8medium001130
epicatechincatechin;
polyphenol
antioxidant2011201113.0low000010
gallocatecholcatechin;
flavan-3,3',4',5,5',7-hexol
antioxidant;
food component;
plant metabolite
2011201113.0low000010
6-hydroxyflavonehydroxyflavonoid2010201014.0low000100
hesperetin3'-hydroxyflavanones;
4'-methoxyflavanones;
monomethoxyflavanone;
trihydroxyflavanone
antineoplastic agent;
antioxidant;
plant metabolite
2013201311.0low000010
nobiletinmethoxyflavoneantineoplastic agent;
plant metabolite
2011201113.0low000010
4'-methoxyflavoneether;
flavonoids
2001200123.0low000100
5,7,4'-trimethylapigeninether;
flavonoids
2011201113.0low000010
5,7-dimethoxyflavonedimethoxyflavoneplant metabolite2001201118.0low000110
3,5,7,3',4'-pentamethoxyflavone2011201113.0low000010
liquiritigenin4',7-dihydroxyflavanonehormone agonist;
plant metabolite
201720177.0low000010
aromadedrin4'-hydroxyflavanones;
dihydroflavonols;
secondary alpha-hydroxy ketone;
tetrahydroxyflavanone
metabolite201720177.0low000010
glabridinhydroxyisoflavansantiplasmodial drug2013201311.0low000010
3',4'-dihydroxyflavone2004202011.9high000250
3,3',4'-trihydroxyflavonehydroxyflavan2000202014.0low001110
inerminmaackiain2009200915.0medium000100
2'-hydroxyflavoneflavones2010201014.0medium000100
4'-hydroxyflavone2001202012.4high000230
sorbinilazaspiro compound;
chromanes;
imidazolidinone;
organofluorine compound;
oxaspiro compound
antioxidant;
EC 1.1.1.21 (aldehyde reductase) inhibitor
1999199925.0low001000
naringenin(2S)-flavan-4-one;
naringenin
expectorant;
plant metabolite
201320207.3low000030
taxifolintaxifolinmetabolite201320208.3low000030
eriodictyol3'-hydroxyflavanones;
tetrahydroxyflavanone
201120208.2low000040
farrerolorganic molecular entitymetabolite201520159.0low000010
5,6,7-trimethoxyflavonetrimethoxyflavoneanti-HSV-1 agent;
plant metabolite
202020204.0low000010
e-z cinnamic acidcinnamic acidplant metabolite201520159.0low000010
3,2'-dihydroxyflavone2010201014.0high000200
7-methoxyflavoneether;
flavonoids
1999199925.0low001000
negleteinether;
flavonoids
202020204.0low000010
5,7,3',4'-tetramethylluteolin2001201118.0high000110
isoliquiritigeninchalconesantineoplastic agent;
biological pigment;
EC 1.14.18.1 (tyrosinase) inhibitor;
GABA modulator;
geroprotector;
metabolite;
NMDA receptor antagonist
2009201114.0low000110
7,8,3'-trihydroxyflavone2004201016.0high000300
3',4'-dimethoxyflavone2001200123.0low000100
2-(3,4-dihydroxyphenyl)-7,8-dihydroxy-1-benzopyran-4-oneflavones2004201017.0high000200
7,8,4'-trihydroxyflavone2001201019.0high000300
quercetin7-hydroxyflavonol;
pentahydroxyflavone
antibacterial agent;
antineoplastic agent;
antioxidant;
Aurora kinase inhibitor;
chelator;
EC 1.10.99.2 [ribosyldihydronicotinamide dehydrogenase (quinone)] inhibitor;
geroprotector;
phytoestrogen;
plant metabolite;
protein kinase inhibitor;
radical scavenger
1999202012.7low001270
biochanin a4'-methoxyisoflavones;
7-hydroxyisoflavones
antineoplastic agent;
EC 3.5.1.99 (fatty acid amide hydrolase) inhibitor;
phytoestrogen;
plant metabolite;
tyrosine kinase inhibitor
2011201113.0low000010
acacetindihydroxyflavone;
monomethoxyflavone
anticonvulsant;
plant metabolite
201320208.0low000040
apigenintrihydroxyflavoneantineoplastic agent;
metabolite
201120209.6low000070
luteolin3'-hydroxyflavonoid;
tetrahydroxyflavone
angiogenesis inhibitor;
anti-inflammatory agent;
antineoplastic agent;
apoptosis inducer;
c-Jun N-terminal kinase inhibitor;
EC 2.3.1.85 (fatty acid synthase) inhibitor;
immunomodulator;
nephroprotective agent;
plant metabolite;
radical scavenger;
vascular endothelial growth factor receptor antagonist
1999202012.4low001180
quercitrinalpha-L-rhamnoside;
monosaccharide derivative;
quercetin O-glycoside;
tetrahydroxyflavone
antileishmanial agent;
antioxidant;
EC 1.1.1.184 [carbonyl reductase (NADPH)] inhibitor;
EC 1.1.1.21 (aldehyde reductase) inhibitor;
EC 1.14.18.1 (tyrosinase) inhibitor;
plant metabolite
201520159.0low000010
scopoletinhydroxycoumarinplant growth regulator;
plant metabolite
2009200915.0low000100
herbacetin7-hydroxyflavonol;
pentahydroxyflavone
angiogenesis inhibitor;
anti-inflammatory agent;
antilipemic drug;
antineoplastic agent;
apoptosis inducer;
EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor;
EC 4.1.1.17 (ornithine decarboxylase) inhibitor;
plant metabolite
202020204.0low000010
gossypetin7-hydroxyflavonol;
hexahydroxyflavone
plant metabolite2010202011.2low000220
chrysoeriolmonomethoxyflavone;
trihydroxyflavone
antineoplastic agent;
antioxidant;
metabolite
201320208.5low000040
quercetin 3-o-methyl ethermonomethoxyflavone;
tetrahydroxyflavone
antimicrobial agent;
metabolite
201520159.0low000010
ayanindihydroxyflavone;
trimethoxyflavone
plant metabolite2011201113.0low000010
quercetin 3-o-glucopyranosidebeta-D-glucoside;
monosaccharide derivative;
quercetin O-glucoside;
tetrahydroxyflavone
antineoplastic agent;
antioxidant;
antipruritic drug;
bone density conservation agent;
geroprotector;
histamine antagonist;
osteogenesis regulator;
plant metabolite
2011201511.0low000020
rutindisaccharide derivative;
quercetin O-glucoside;
rutinoside;
tetrahydroxyflavone
antioxidant;
metabolite
202020204.0low000010
kaempferol7-hydroxyflavonol;
flavonols;
tetrahydroxyflavone
antibacterial agent;
geroprotector;
human blood serum metabolite;
human urinary metabolite;
human xenobiotic metabolite;
plant metabolite
201020209.7low000150
genistein7-hydroxyisoflavonesantineoplastic agent;
EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor;
geroprotector;
human urinary metabolite;
phytoestrogen;
plant metabolite;
tyrosine kinase inhibitor
2011201312.0low000020
buteinchalcones;
polyphenol
antineoplastic agent;
antioxidant;
EC 1.1.1.21 (aldehyde reductase) inhibitor;
geroprotector;
hypoglycemic agent;
plant metabolite;
radiosensitizing agent;
tyrosine kinase inhibitor
2011201113.0low000010
okaninbenzenetriol;
chalcones
plant metabolite2004200420.0low000100
5,7-dihydroxychromonechromones201520159.0low000010
apigenin dimethyletherdimethoxyflavone;
monohydroxyflavone
plant metabolite2011201113.0low000010
baicaleintrihydroxyflavoneangiogenesis inhibitor;
anti-inflammatory agent;
antibacterial agent;
anticoronaviral agent;
antifungal agent;
antineoplastic agent;
antioxidant;
apoptosis inducer;
EC 1.13.11.31 (arachidonate 12-lipoxygenase) inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor;
EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor;
EC 4.1.1.17 (ornithine decarboxylase) inhibitor;
ferroptosis inhibitor;
geroprotector;
hormone antagonist;
plant metabolite;
prostaglandin antagonist;
radical scavenger
2010202010.3low000120
chrysin7-hydroxyflavonol;
dihydroxyflavone
anti-inflammatory agent;
antineoplastic agent;
antioxidant;
EC 2.7.11.18 (myosin-light-chain kinase) inhibitor;
hepatoprotective agent;
plant metabolite
2001202012.4low000230
datiscetin7-hydroxyflavonol;
tetrahydroxyflavone
2010201014.0low000100
3,7,4'-trihydroxyflavonehydroxyflavan202020204.0low000010
diosmetin3'-hydroxyflavonoid;
monomethoxyflavone;
trihydroxyflavone
angiogenesis inhibitor;
anti-inflammatory agent;
antineoplastic agent;
antioxidant;
apoptosis inducer;
bone density conservation agent;
cardioprotective agent;
plant metabolite;
tropomyosin-related kinase B receptor agonist;
vasodilator agent
2001201712.8low000130
fisetin3'-hydroxyflavonoid;
7-hydroxyflavonol;
tetrahydroxyflavone
anti-inflammatory agent;
antioxidant;
EC 5.99.1.3 [DNA topoisomerase (ATP-hydrolysing)] inhibitor;
geroprotector;
metabolite;
plant metabolite
2000201117.0low001110
galangin7-hydroxyflavonol;
trihydroxyflavone
antimicrobial agent;
EC 3.1.1.3 (triacylglycerol lipase) inhibitor;
plant metabolite
201020209.0low000110
gossypin7-hydroxyflavonol;
glycosyloxyflavone;
monosaccharide derivative;
pentahydroxyflavone
neuroprotective agent;
plant metabolite
202020204.0low000010
hyperosidebeta-D-galactoside;
monosaccharide derivative;
quercetin O-glycoside;
tetrahydroxyflavone
hepatoprotective agent;
plant metabolite
201520159.0low000010
3-methylquercetin7-hydroxyflavonol;
monomethoxyflavone;
tetrahydroxyflavone
anticoagulant;
EC 1.14.18.1 (tyrosinase) inhibitor;
metabolite
201520159.0low000010
morin7-hydroxyflavonol;
pentahydroxyflavone
angiogenesis modulating agent;
anti-inflammatory agent;
antibacterial agent;
antihypertensive agent;
antineoplastic agent;
antioxidant;
EC 5.99.1.2 (DNA topoisomerase) inhibitor;
hepatoprotective agent;
metabolite;
neuroprotective agent
201020209.0low000110
myricetin7-hydroxyflavonol;
hexahydroxyflavone
antineoplastic agent;
antioxidant;
cyclooxygenase 1 inhibitor;
food component;
geroprotector;
hypoglycemic agent;
plant metabolite
201020209.5low000130
norwogonintrihydroxyflavoneantioxidant;
metabolite
2010202010.7medium000210
quercetagetinflavonols;
hexahydroxyflavone
antioxidant;
antiviral agent;
plant metabolite
202020204.0low000010
rhamnetinmonomethoxyflavone;
tetrahydroxyflavone
anti-inflammatory agent;
antioxidant;
metabolite
2011201113.0low000010
robinetin7-hydroxyflavonol;
pentahydroxyflavone
plant metabolite2010201710.5low000110
scutellareintetrahydroxyflavonemetabolite201020209.0low000110
tamarixetin7-hydroxyflavonol;
monomethoxyflavone;
tetrahydroxyflavone
antioxidant;
metabolite
201720177.0low000010
tricetinpentahydroxyflavoneantineoplastic agent;
metabolite
2010201014.0low000100
tricin3'-methoxyflavones;
dimethoxyflavone;
trihydroxyflavone
EC 1.14.99.1 (prostaglandin-endoperoxide synthase) inhibitor;
metabolite
201720177.0low000010
wogonindihydroxyflavone;
monomethoxyflavone
angiogenesis inhibitor;
antineoplastic agent;
cyclooxygenase 2 inhibitor;
plant metabolite
2011201113.0low000010
daidzein7-hydroxyisoflavonesantineoplastic agent;
EC 2.7.7.7 (DNA-directed DNA polymerase) inhibitor;
EC 3.2.1.20 (alpha-glucosidase) inhibitor;
phytoestrogen;
plant metabolite
2011201312.0low000020
5'-methoxyhydnocarpin2001200123.0medium000100
7-hydroxyflavonehydroxyflavonoid1999202012.8low001140
tectochrysinmonohydroxyflavone;
monomethoxyflavone
antidiarrhoeal drug;
antineoplastic agent;
plant metabolite
2011201113.0low000010
4',7-dihydroxyflavonedihydroxyflavonemetabolite1999202011.7medium001050
astragalinbeta-D-glucoside;
kaempferol O-glucoside;
monosaccharide derivative;
trihydroxyflavone
plant metabolite;
trypanocidal drug
2011201113.0low000010
ombuinedimethoxyflavone;
flavonols;
trihydroxyflavone
anti-inflammatory agent;
plant metabolite
2011201113.0low000010
5-hydroxy-3,3',4',7-tetramethoxyflavone3'-methoxyflavones;
monohydroxyflavone;
tetramethoxyflavone
plant metabolite2011201113.0low000010
6,7-dihydroxyflavone1999201019.5low001100
7-hydroxy-3-(4-methoxyphenyl)-4-methylcoumarinhydroxycoumarin;
monomethoxybenzene
2010201014.0medium000100
7-hydroxyisoflavone7-hydroxyisoflavonesEC 1.14.14.14 (aromatase) inhibitor;
metabolite
2010201014.0low000100
3,7-dihydroxyflavonehydroxyflavan2010201014.0low000100
4',7,8-trihydroxyisoflavoneisoflavones2009200915.0low000100
guajavarin201520159.0low000010
3,7-dimethylgalangin2011201113.0medium000010
SubstanceStudiesClassesRolesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
gallic acidtrihydroxybenzoic acidantineoplastic agent;
antioxidant;
apoptosis inducer;
astringent;
cyclooxygenase 2 inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
geroprotector;
human xenobiotic metabolite;
plant metabolite
201820186.0low000010
chloramphenicolC-nitro compound;
carboxamide;
diol;
organochlorine compound
antibacterial drug;
antimicrobial agent;
Escherichia coli metabolite;
geroprotector;
Mycoplasma genitalium metabolite;
protein synthesis inhibitor
201820186.0low000010
benzofurans201820186.0low000010
1,1-diphenyl-2-picrylhydrazyl201720177.0low000010
butinflavanones201820186.0low000010
apigenintrihydroxyflavoneantineoplastic agent;
metabolite
201720177.0low000010
sulfuretin1-benzofurans201820186.0low000010
baicaleintrihydroxyflavoneangiogenesis inhibitor;
anti-inflammatory agent;
antibacterial agent;
anticoronaviral agent;
antifungal agent;
antineoplastic agent;
antioxidant;
apoptosis inducer;
EC 1.13.11.31 (arachidonate 12-lipoxygenase) inhibitor;
EC 1.13.11.33 (arachidonate 15-lipoxygenase) inhibitor;
EC 3.4.21.26 (prolyl oligopeptidase) inhibitor;
EC 3.4.22.69 (SARS coronavirus main proteinase) inhibitor;
EC 4.1.1.17 (ornithine decarboxylase) inhibitor;
ferroptosis inhibitor;
geroprotector;
hormone antagonist;
plant metabolite;
prostaglandin antagonist;
radical scavenger
201720177.0low000010
ConditionIndicatedStudiesFirst YearLast YearAverage AgeRelationship StrengthTrialspre-19901990's2000's2010'spost-2020
Bone Loss, Osteoclastic0201520178.0high000020

Bioavailability (1)

ArticleYear
A synthetic 7,8-dihydroxyflavone derivative promotes neurogenesis and exhibits potent antidepressant effect.
Journal of medicinal chemistry, , Dec-09, Volume: 53, Issue:23
2010

Natural Sources (1)

ArticleYear
Screening and structural analysis of flavones inhibiting tankyrases.
Journal of medicinal chemistry, , May-09, Volume: 56, Issue:9
2013