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oxopurine

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ChEBI ID: 25810

Members (89)

MemberDefinitionRole
1-methyluric acidAn oxopurine that is 7,9-dihydro-1H-purine-2,6,8(3H)-trione substituted by a methyl group at N-1. It is one of the metabolites of caffeine found in human urine.1-methyluric acid
1,3-dimethyl-8-(3-methyl-1-piperidinyl)-7-[2-[(5-methyl-1,3,4-thiadiazol-2-yl)thio]ethyl]purine-2,6-dione1,3-dimethyl-8-(3-methyl-1-piperidinyl)-7-[2-[(5-methyl-1,3,4-thiadiazol-2-yl)thio]ethyl]purine-2,6-dione
1,3-dimethyl-8-[[methyl-(phenylmethyl)amino]methyl]-7-(2-methylpropyl)purine-2,6-dione1,3-dimethyl-8-[[methyl-(phenylmethyl)amino]methyl]-7-(2-methylpropyl)purine-2,6-dione
1,3-dimethyl-8-[2-(1-pyrrolidinyl)ethylthio]-6-sulfanylidene-7H-purin-2-one1,3-dimethyl-8-[2-(1-pyrrolidinyl)ethylthio]-6-sulfanylidene-7H-purin-2-one
1,3-dimethyl-8-[methyl-(phenylmethyl)amino]-7-[2-(2-pyrimidinylthio)ethyl]purine-2,6-dione1,3-dimethyl-8-[methyl-(phenylmethyl)amino]-7-[2-(2-pyrimidinylthio)ethyl]purine-2,6-dione
1,3-dimethyluric acidAn oxopurine that is 7,9-dihydro-1H-purine-2,6,8(3H)-trionesubstituted by methyl groups at N-1 and N-3.1,3-dimethyluric acid
1,3-dipropyl-8-cyclopentylxanthineAn oxopurine that is 7H-xanthine substituted at positions 1 and 3 by propyl groups and at position 8 by a cyclohexyl group.DPCPX
1,3-dipropyl-8-phenylxanthine8-phenyl-1,3-dipropyl-7H-purine-2,6-dione
1,3,7-trimethyl-8-(phenylmethyl)purine-2,6-dione1,3,7-trimethyl-8-(phenylmethyl)purine-2,6-dione
1,3,7-trimethylurateAn oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8, and the nitrogens at positions 1, 3, and 7 are substituted by methyl groups. It is a metabolite of caffeine.1,3,7-trimethyluric acid
1,3,7,9-tetramethyluric acidAn oxopurine that is uric acid in which the hydrogens at positions 1,3,7 and 9 are replaced by methyl groups. It is a purine alkaloid that is found in Chinese tea known as kucha (Camellia assamica var. kucha) and exhibits anti-inflammatory and analgesic properties.1,3,7,9-tetramethyluric acid
1,7-dimethyluric acidAn oxopurine that is 7,9-dihydro-1H-purine-2,6,8(3H)-trione substituted by methyl groups at N-1 and N-7. It is a metabolite of caffeine and is often found in human urine samples.1,7-dimethyluric acid
1',3'-dimethylspiro[1H-indole-3,8'-7,9-dihydropurine]-2,2',6'-trione1',3'-dimethylspiro[1H-indole-3,8'-7,9-dihydropurine]-2,2',6'-trione
2-(1,3-dimethyl-2,6-dioxo-7-purinyl)-N-(phenylmethyl)-N-(2-pyridinyl)acetamide2-(1,3-dimethyl-2,6-dioxo-7-purinyl)-N-(phenylmethyl)-N-(2-pyridinyl)acetamide
2-(1,3-dimethyl-2,6-dioxo-7-purinyl)-N-[3-[(4-methoxyphenyl)sulfamoyl]-4-methylphenyl]acetamide2-(1,3-dimethyl-2,6-dioxo-7-purinyl)-N-[3-[(4-methoxyphenyl)sulfamoyl]-4-methylphenyl]acetamide
2-(1,3-dimethyl-2,6-dioxo-7-purinyl)-N'-[2-(2-ethoxyphenoxy)-1-oxoethyl]acetohydrazide2-(1,3-dimethyl-2,6-dioxo-7-purinyl)-N'-[2-(2-ethoxyphenoxy)-1-oxoethyl]acetohydrazide
2-[(7-ethyl-1,3-dimethyl-2,6-dioxo-8-purinyl)thio]-N-(6-methyl-2-pyridinyl)acetamide2-[(7-ethyl-1,3-dimethyl-2,6-dioxo-8-purinyl)thio]-N-(6-methyl-2-pyridinyl)acetamide
2-[[3-methyl-7-(3-methylbutyl)-2,6-dioxo-8-purinyl]thio]propanoic acid methyl ester2-[[3-methyl-7-(3-methylbutyl)-2,6-dioxo-8-purinyl]thio]propanoic acid methyl ester
2,8-dihydroxyadenineAn oxopurine that is adenine bearing two oxo substituents at positions 2 and 8.2,8-dihydroxyadenine; 2,8-dioxoadenine
3-butyl-8-(2-fluorophenyl)-7-(phenylmethyl)purine-2,6-dione3-butyl-8-(2-fluorophenyl)-7-(phenylmethyl)purine-2,6-dione
3-methyl-7-(2-phenylethyl)-8-(propylamino)purine-2,6-dione3-methyl-7-(2-phenylethyl)-8-(propylamino)purine-2,6-dione
3-methyl-7-(phenylmethyl)-8-(propan-2-ylthio)purine-2,6-dione3-methyl-7-(phenylmethyl)-8-(propan-2-ylthio)purine-2,6-dione
3-methyl-7-[(4-methylphenyl)methyl]-8-[2-(1-piperidinyl)ethylthio]purine-2,6-dione3-methyl-7-[(4-methylphenyl)methyl]-8-[2-(1-piperidinyl)ethylthio]purine-2,6-dione
3-methyl-7-pentyl-8-(2-phenylethylthio)purine-2,6-dione3-methyl-7-pentyl-8-(2-phenylethylthio)purine-2,6-dione
3,5-dimethyl-4-isoxazolecarboxylic acid (3-butyl-2,6-dioxo-7-propyl-8-purinyl)methyl ester3,5-dimethyl-4-isoxazolecarboxylic acid (3-butyl-2,6-dioxo-7-propyl-8-purinyl)methyl ester
3,7-dimethyl-1-(phenylmethyl)-8-[(phenylmethyl)amino]purine-2,6-dione3,7-dimethyl-1-(phenylmethyl)-8-[(phenylmethyl)amino]purine-2,6-dione
3,7-dimethyluric acidAn oxopurine that is 7,9-dihydro-1H-purine-2,6,8(3H)-trione substituted by methyl groups at N-3 and N-7.3,7-dimethyluric acid
4-[(1,3-dimethyl-2,6-dioxo-7H-purin-8-yl)methylamino]benzoic acid4-[(1,3-dimethyl-2,6-dioxo-7H-purin-8-yl)methylamino]benzoic acid
4-[[7-[(4-fluorophenyl)methyl]-1,3-dimethyl-2,6-dioxo-8-purinyl]methyl]-1-piperazinecarboxylic acid ethyl ester4-[[7-[(4-fluorophenyl)methyl]-1,3-dimethyl-2,6-dioxo-8-purinyl]methyl]-1-piperazinecarboxylic acid ethyl ester
4-[7-(2-methoxyethyl)-2,6-dioxo-3-(phenylmethyl)-8-purinyl]benzonitrile4-[7-(2-methoxyethyl)-2,6-dioxo-3-(phenylmethyl)-8-purinyl]benzonitrile
5-hydroxyisourateAn oxopurine that is 5,7-dihydro-1H-purine-2,6,8(9H)-trione in which the hydrogen at position 5 is substituted by a hydroxy group.5-hydroxyisouric acid
6-thiouric acid6-Thiourate
7-(2-chloroethyl)theophylline7-(2-chloroethyl)-1,3-dimethylpurine-2,6-dione
7-(2-methoxyethyl)-3-methyl-8-(phenylthio)purine-2,6-dione7-(2-methoxyethyl)-3-methyl-8-(phenylthio)purine-2,6-dione
7-(3-methoxypropyl)-3-(phenylmethyl)-8-(3-thiophenyl)purine-2,6-dione7-(3-methoxypropyl)-3-(phenylmethyl)-8-(3-thiophenyl)purine-2,6-dione
7-[(2-chloro-6-fluorophenyl)methyl]-1,3-dimethyl-8-(1-piperidinylmethyl)purine-2,6-dione7-[(2-chloro-6-fluorophenyl)methyl]-1,3-dimethyl-8-(1-piperidinylmethyl)purine-2,6-dione
7-[(2-chloro-6-fluorophenyl)methyl]-1,3-dimethyl-8-[(3-methyl-1-piperidinyl)methyl]purine-2,6-dione7-[(2-chloro-6-fluorophenyl)methyl]-1,3-dimethyl-8-[(3-methyl-1-piperidinyl)methyl]purine-2,6-dione
7-[(3-bromophenyl)methyl]-1,3-dimethyl-8-(2-methylpropylamino)purine-2,6-dione7-[(3-bromophenyl)methyl]-1,3-dimethyl-8-(2-methylpropylamino)purine-2,6-dione
7-[(4-fluorophenyl)methyl]-1,3-dimethyl-8-[(2-oxo-2-thiophen-2-ylethyl)thio]purine-2,6-dione7-[(4-fluorophenyl)methyl]-1,3-dimethyl-8-[(2-oxo-2-thiophen-2-ylethyl)thio]purine-2,6-dione
7-[2-(1,3-benzothiazol-2-ylthio)ethyl]-1,3-dimethyl-8-(3-methyl-1-piperidinyl)purine-2,6-dione7-[2-(1,3-benzothiazol-2-ylthio)ethyl]-1,3-dimethyl-8-(3-methyl-1-piperidinyl)purine-2,6-dione
7-[2-hydroxy-3-(2-methylphenoxy)propyl]-3-methyl-8-(propan-2-ylthio)purine-2,6-dione7-[2-hydroxy-3-(2-methylphenoxy)propyl]-3-methyl-8-(propan-2-ylthio)purine-2,6-dione
7-ethylguanine7-Ethylguanine
7-methylxanthineAn oxopurine that is xanthine in which the hydrogen attached to the nitrogen at position 7 is replaced by a methyl group. It is an intermediate metabolite in the synthesis of caffeine.7-methylxanthine
8-(1,3-benzothiazol-2-ylthio)-3-methyl-7-pentylpurine-2,6-dione8-(1,3-benzothiazol-2-ylthio)-3-methyl-7-pentylpurine-2,6-dione
8-(2,5-dimethylphenoxy)-1,3-dimethyl-7-prop-2-enylpurine-2,6-dione8-(2,5-dimethylphenoxy)-1,3-dimethyl-7-prop-2-enylpurine-2,6-dione
8-(3-ethoxypropylamino)-1,3-dimethyl-7H-purine-2,6-dione8-(3-ethoxypropylamino)-1,3-dimethyl-7H-purine-2,6-dione
8-(4-methoxyphenyl)-7-methyl-3-(phenylmethyl)purine-2,6-dione8-(4-methoxyphenyl)-7-methyl-3-(phenylmethyl)purine-2,6-dione
8-(butan-2-ylthio)-7-[(4-chlorophenyl)methyl]-3-methylpurine-2,6-dione8-(butan-2-ylthio)-7-[(4-chlorophenyl)methyl]-3-methylpurine-2,6-dione
8-[(1-ethyl-3-piperidinyl)thio]-1,3-dimethyl-6-sulfanylidene-7H-purin-2-one8-[(1-ethyl-3-piperidinyl)thio]-1,3-dimethyl-6-sulfanylidene-7H-purin-2-one
8-[[4-[2-furanyl(oxo)methyl]-1-piperazinyl]methyl]-1,3-dimethyl-7-[(2-methylphenyl)methyl]purine-2,6-dione8-[[4-[2-furanyl(oxo)methyl]-1-piperazinyl]methyl]-1,3-dimethyl-7-[(2-methylphenyl)methyl]purine-2,6-dione
8-[[4-[2-furanyl(oxo)methyl]-1-piperazinyl]methyl]-1,3-dimethyl-7-propylpurine-2,6-dione8-[[4-[2-furanyl(oxo)methyl]-1-piperazinyl]methyl]-1,3-dimethyl-7-propylpurine-2,6-dione
8-anilino-1,3-dimethyl-7H-purine-2,6-dione8-anilino-1,3-dimethyl-7H-purine-2,6-dione
8-cyclopentyl-1,3-dimethylxanthine8-cyclopentyl-1,3-dimethyl-7H-purine-2,6-dione
8-hydroxyadenineAn oxopurine that is adenine bearing a single oxo substituent at position 8.8-hydroxyadenine; 8-oxoadenine
8-hydroxyguanineAn oxopurine that is guanine in which the hydrogen at position 8 is replaced by an oxo group and in which the nitrogens at positions 7 and 9 each bear a hydrogen.7,8-dihydro-8-oxoguanine
8-methoxymethyl-3-isobutyl-1-methylxanthine8-(methoxymethyl)-1-methyl-3-(2-methylpropyl)-7H-purine-2,6-dione
8-nitroguanine8-Nitroguanine
8-oxyguanineAn oxopurine that is guanine which is substituted by an oxo group at position 8.8-oxoguanine
9-carboxymethoxymethylguanine9-Carboxymethoxymethylguanine
acefylline2-(1,3-dimethyl-2,6-dioxo-7-purinyl)acetic acid
acyclovirAn oxopurine that is guanine substituted by a (2-hydroxyethoxy)methyl substituent at position 9. Used in the treatment of viral infections.acyclovir
bamifyllinebamifylline
cafedrinecafedrine
cipamfyllinecipamfylline
denbufylline1,3-dibutyl-7-(2-oxopropyl)purine-2,6-dione
doxofyllineAn oxopurine that is a derivative of xanthine, methylated at N-1 and N-3 and carrying a 1,3-dioxolan-2-ylmethyl group at N-7, used in the treatment of asthma.doxofylline
dyphyllineAn oxopurine that is theophylline bearing a 2,3-dihydroxypropyl group at the 7 position. It has broncho- and vasodilator properties, and is used in the treatment of asthma, cardiac dyspnea, and bronchitis. It is also an ingredient in preparations that have been promoted for coughs.dyphylline
enprofyllineXanthine bearing a propyl substituent at position 3. A bronchodilator, it is used for the symptomatic treatment of asthma and chronic obstructive pulmonary disease, and in the management of cerebrovascular insufficiency, sickle cell disease, and diabetic neuropathy.enprofylline
entecavirGuanine substituted at the 9 position by a 4-hydroxy-3-(hydroxymethyl)-2-methylidenecyclopentyl group. A synthetic analogue of 2'-deoxyguanosine, it is a nucleoside reverse transcriptase inhibitor with selective antiviral activity against hepatitis B virus. Entecavir is phosphorylated intracellularly to the active triphosphate form, which competes with deoxyguanosine triphosphate, the natural substrate of hepatitis B virus reverse transcriptase, inhibiting every stage of the enzyme's activity, although it has no activity against HIV. It is used for the treatment of chronic hepatitis B.entecavir (anhydrous)
etamiphyllineetamiphylline
etofylline7-(2-hydroxyethyl)-1,3-dimethylpurine-2,6-dione
etofylline clofibrateetofylline clofibrate
fenethyllinefenetylline
furafyllineFurafylline
ganciclovirAn oxopurine that is guanine substituted by a [(1,3-dihydroxypropan-2-yl)oxy]methyl group at position 9. Ganciclovir is an antiviral drug used to treat or prevent AIDS-related cytomegalovirus infections.ganciclovir
guanineA 2-aminopurine carrying a 6-oxo substituent.guanine
hypoxanthineA purine nucleobase that consists of purine bearing an oxo substituent at position 6.hypoxanthine
isoguanineAn oxopurine that is 3,7-dihydro-purin-2-one in which the hydrogen at position 6 is substituted by an amino group.isoguanine
istradefyllineistradefylline
mrs 1754N-(4-cyanophenyl)-2-[4-(2,6-dioxo-1,3-dipropyl-7H-purin-8-yl)phenoxy]acetamide
pentifyllinepentifylline
pentoxifyllinePentoxifylline
propentofyllinePropentofylline
proxyphyllineProxyphylline
psb 11154-(2,6-dioxo-1-propyl-3,7-dihydropurin-8-yl)benzenesulfonic acid
psb 36LSM-1748
reproterolreproterol
rolofyllineRolofylline
theodrenalinetheodrenaline

Research

Studies (39,148)

TimeframeStudies, Drugs in This Class (%)All Drugs %
pre-19907,358 (18.80)18.7374
1990's9,309 (23.78)18.2507
2000's10,743 (27.44)29.6817
2010's9,360 (23.91)24.3611
2020's2,378 (6.07)2.80

Study Types

Publication TypeStudies, Drugs in This Class (%)All Drugs (%)
Trials3,600 (7.64%)5.53%
Reviews4,065 (8.63%)6.00%
Case Studies5,558 (11.80%)4.05%
Observational151 (0.32%)0.25%
Other33,734 (71.61%)84.16%