Page last updated: 2024-08-05 15:35:07

EC 1.17.3.2 (xanthine oxidase) inhibitor

An EC 1.17.3.* (oxidoreductase acting on CH or CH2 with oxygen as acceptor) inhibitor that interferes with the action of xanthine oxidase (EC 1.17.3.2).

ChEBI ID: 35634

Members (8)

MemberDefinitionClass
2-amino-4-hydroxy-6-formylpteridinePterin carrying a formyl group at position 6.6-formylpterin
8-azaadenineA triazolopyrimidine that is [1,2,3]triazolo[4,5-d]pyrimidine bearing an amino substituent at position 7.8-azaadenine
allopurinolA bicyclic structure comprising a pyrazole ring fused to a hydroxy-substituted pyrimidine ring.allopurinol
aspalathinA member of the class of dihydrochalcones that is the 2-C-beta-D-glucopyranide of phloroglucinol and which is substituted at position 4 by a 3-(3,4-dihydroxyphenyl)propanoyl group. A metabolite of red bush, Aspalathus linearis (and present in the herbal tea made from the leaves), aspalathin exhibits significant hypoglycemic activity.aspalathin
febuxostatA 1,3-thiazolemonocarboxylic acid that is 4-methyl-1,3-thiazole-5-carboxylic acid which is substituted by a 3-cyano-4-(2-methylpropoxy)phenyl group at position 2. It is an orally-active, potent, and selective xanthine oxidase inhibitor used for the treatment of chronic hyperuricaemia in patients with gout.febuxostat
oxypurinolA pyrazolopyrimidine that is 4,5,6,7-tetrahydro-H-pyrazolo[3,4-d]pyrimidine substituted by oxo groups at positions 4 and 6.alloxanthine
pedalitinA tetrahydroxy-monohydroxy-flavone, with the four hydroxy groups at C-3',-4',-5 and 6, and the methoxy group at C-7. It has been isolated from a number of plant species, including Eremosparton songoricum, Rabdosia japonica and Ruellia tuberosa.pedalitin
procyanidin C1A proanthocyanidin consisting of three (-)-epicatechin units joined by two successive (4beta->8)-linkages.procyanidin C1

Research

Studies (14,806)

TimeframeStudies, Drugs with This Role(%)All Drugs %
pre-19904,236 (28.61)18.7374
1990's3,665 (24.75)18.2507
2000's2,868 (19.37)29.6817
2010's3,048 (20.59)24.3611
2020's989 (6.68)2.80

Study Types

Publication TypeStudies, Drugs with this Role (%)All Drugs (%)
Trials922 (5.58%)5.53%
Reviews1,255 (7.59%)6.00%
Case Studies1,030 (6.23%)4.05%
Observational69 (0.42%)0.25%
Other13,258 (80.19%)84.16%

Protein Targets (74)

Potency Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
acetylcholinesteraseHomo sapiens (human)Potency29.220622
AR proteinHomo sapiens (human)Potency4.3072910
aryl hydrocarbon receptorHomo sapiens (human)Potency0.028222
Ataxin-2Homo sapiens (human)Potency0.149611
ATPase family AAA domain-containing protein 5Homo sapiens (human)Potency0.158722
Bloom syndrome protein isoform 1Homo sapiens (human)Potency0.398122
Cellular tumor antigen p53Homo sapiens (human)Potency31.622811
Chain A, Beta-lactamaseEscherichia coli K-12Potency5.011911
cytochrome P450 2C9, partialHomo sapiens (human)Potency27.540411
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_aHomo sapiens (human)Potency0.042211
estrogen nuclear receptor alphaHomo sapiens (human)Potency13.8448710
estrogen receptor 2 (ER beta)Homo sapiens (human)Potency14.613623
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency34.9212619
euchromatic histone-lysine N-methyltransferase 2Homo sapiens (human)Potency0.025111
EWS/FLI fusion proteinHomo sapiens (human)Potency29.565911
farnesoid X nuclear receptorHomo sapiens (human)Potency15.871622
GVesicular stomatitis virusPotency27.540411
gemininHomo sapiens (human)Potency0.838422
GLI family zinc finger 3Homo sapiens (human)Potency7.527222
glucocorticoid receptor [Homo sapiens]Homo sapiens (human)Potency7.789412
Glutamate receptor 2Rattus norvegicus (Norway rat)Potency35.231512
histone deacetylase 9 isoform 3Homo sapiens (human)Potency0.454022
HLA class I histocompatibility antigen, B alpha chain Homo sapiens (human)Potency27.540411
IDH1Homo sapiens (human)Potency25.929011
Inositol hexakisphosphate kinase 1Homo sapiens (human)Potency27.540412
Interferon betaHomo sapiens (human)Potency27.540411
interleukin 8Homo sapiens (human)Potency74.978011
lamin isoform A-delta10Homo sapiens (human)Potency6.309611
LuciferasePhotinus pyralis (common eastern firefly)Potency0.172622
nuclear factor erythroid 2-related factor 2 isoform 1Homo sapiens (human)Potency50.789622
nuclear receptor subfamily 1, group I, member 3Homo sapiens (human)Potency0.068033
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency18.832211
peroxisome proliferator-activated receptor deltaHomo sapiens (human)Potency10.590111
pregnane X nuclear receptorHomo sapiens (human)Potency34.347812
progesterone receptorHomo sapiens (human)Potency28.897622
RAR-related orphan receptor gammaMus musculus (house mouse)Potency0.010822
ras-related protein Rab-9AHomo sapiens (human)Potency1.000011
retinoic acid nuclear receptor alpha variant 1Homo sapiens (human)Potency0.080833
retinoid X nuclear receptor alphaHomo sapiens (human)Potency9.122322
SMAD family member 2Homo sapiens (human)Potency15.417222
SMAD family member 3Homo sapiens (human)Potency15.417222
survival motor neuron protein isoform dHomo sapiens (human)Potency1.000011
TAR DNA-binding protein 43Homo sapiens (human)Potency35.481311
TDP1 proteinHomo sapiens (human)Potency5.804811
thioredoxin reductaseRattus norvegicus (Norway rat)Potency0.100011
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency15.758524
thyroid stimulating hormone receptorHomo sapiens (human)Potency7.785733
transcriptional regulator ERG isoform 3Homo sapiens (human)Potency0.794311
vitamin D (1,25- dihydroxyvitamin D3) receptorHomo sapiens (human)Potency7.396122
Voltage-dependent calcium channel gamma-2 subunitMus musculus (house mouse)Potency35.231512

Inhibition Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
72 kDa type IV collagenaseHomo sapiens (human)IC5031.400011
AlbuminHomo sapiens (human)IC500.001311
Aldo-keto reductase family 1 member B1Rattus norvegicus (Norway rat)IC500.302011
Alpha-glucosidase Blautia obeumIC5060.000011
ATP-binding cassette sub-family C member 3Homo sapiens (human)IC50133.000012
Bile salt export pumpHomo sapiens (human)IC5091.966723
Broad substrate specificity ATP-binding cassette transporter ABCG2Homo sapiens (human)IC500.027011
Canalicular multispecific organic anion transporter 1Homo sapiens (human)IC50133.000012
Histamine H3 receptorCavia porcellus (domestic guinea pig)IC504.360012
Matrix metalloproteinase-9Homo sapiens (human)IC5053.200011
Multidrug resistance-associated protein 4Homo sapiens (human)IC5067.450012
Nuclear receptor ROR-gammaMus musculus (house mouse)IC505.562512
Polyphenol oxidase 2Agaricus bisporusIC501,000.000011
Shiga toxin subunit AShigella dysenteriaeIC5023.900011
Xanthine dehydrogenase Rhodobacter capsulatusKi0.103611
Xanthine dehydrogenase/oxidaseBos taurus (cattle)IC509.96295158
Xanthine dehydrogenase/oxidaseHomo sapiens (human)IC509.56464346
Xanthine dehydrogenase/oxidaseBos taurus (cattle)Ki0.720655
Xanthine dehydrogenase/oxidaseHomo sapiens (human)Ki1.53241012
Xanthine dehydrogenase/oxidase [Includes: Xanthine dehydrogenase Rattus norvegicus (Norway rat)IC506.989244

Activation Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Adenosine receptor A2aHomo sapiens (human)Kd77.000011
Flavin reductase (NADPH)Homo sapiens (human)Kd1.625912
Purine nucleoside phosphorylaseMycobacterium tuberculosis H37RvKd897.164012
Xanthine dehydrogenase/oxidaseBos taurus (cattle)Kd0.000511

Other Measurements

ProteinTaxonomyMeasurementAverage (mM)Bioassay(s)Drugs
Hypoxanthine-guanine phosphoribosyltransferaseHomo sapiens (human)Km91.450022
LactoperoxidaseBos taurus (cattle)Km8.410011
Xanthine dehydrogenase/oxidaseHomo sapiens (human)Kis0.000911
Xanthine dehydrogenase/oxidaseBos taurus (cattle)Km58.375044