Chemical Formula: C11H14N4O4

Chemical Formula C11H14N4O4

Found 39 metabolite its formula value is C11H14N4O4

   

1-(3-Carboxypropyl)-3,7-dimethylxanthine

4-(3,7-dimethyl-2,6-dioxo-2,3,6,7-tetrahydro-1H-purin-1-yl)butanoic acid

C11H14N4O4 (266.1015004)


   

3-Deazaadenosine

2-{4-amino-1H-imidazo[4,5-c]pyridin-1-yl}-5-(hydroxymethyl)oxolane-3,4-diol

C11H14N4O4 (266.1015004)


   

7-Deaza-2'-deoxyguanosine

2-amino-7-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H,4H,7H-pyrrolo[2,3-d]pyrimidin-4-one

C11H14N4O4 (266.1015004)


   

Doxofylline

7-[(1,3-dioxolan-2-yl)methyl]-1,3-dimethyl-2,3,6,7-tetrahydro-1H-purine-2,6-dione

C11H14N4O4 (266.1015004)


R - Respiratory system > R03 - Drugs for obstructive airway diseases > R03D - Other systemic drugs for obstructive airway diseases > R03DA - Xanthines D019141 - Respiratory System Agents > D018927 - Anti-Asthmatic Agents > D001993 - Bronchodilator Agents D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents D004791 - Enzyme Inhibitors > D010726 - Phosphodiesterase Inhibitors D019141 - Respiratory System Agents > D000996 - Antitussive Agents C471 - Enzyme Inhibitor > C744 - Phosphodiesterase Inhibitor D002491 - Central Nervous System Agents Doxofylline is an orally active PDE IV inhibitor and A1AR antagonist. Doxofylline reduces inflammation in epithelial cells via inhibiting mitochondrial ROS production and amelioration of multiple cellular pathways (NLRP3-TXNIP inflammasome activation). Doxophylline can be used in studies of asthma, chronic obstructive pulmonary disease, and bronchospasm[1][2][3].

   

Forodesine

7-[3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-3H,4H,5H-pyrrolo[3,2-d]pyrimidin-4-one

C11H14N4O4 (266.1015004)


   

2,2-Dimethylpropanal 2,4-dinitrophenylhydrazone

1-(2,2-dimethylpropylidene)-2-(2,4-dinitrophenyl)hydrazine

C11H14N4O4 (266.1015004)


   

(2S)-3-(4H-Imidazol-4-yl)-2-[[(2S)-5-oxopyrrolidine-2-carbonyl]amino]propanoic acid

2-{[hydroxy(5-hydroxy-3,4-dihydro-2H-pyrrol-2-yl)methylidene]amino}-3-(4H-imidazol-4-yl)propanoate

C11H14N4O4 (266.1015004)


   

tubercidin

2-{4-amino-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-5-(hydroxymethyl)oxolane-3,4-diol

C11H14N4O4 (266.1015004)


   
   

3-(hydroxymethyl)-5-(6-hydroxy-9h-purin-9-yl)cyclopentane-1,2-diol

3-(hydroxymethyl)-5-(6-hydroxy-9h-purin-9-yl)cyclopentane-1,2-diol

C11H14N4O4 (266.1015004)


   

2,6-Bis[(2-hydroxyethyl)amino]-3-nitrobenzonitrile

2,6-Bis[(2-hydroxyethyl)amino]-3-nitrobenzonitrile

C11H14N4O4 (266.1015004)


   

1-(3-Carboxypropyl)-3,7-dimethylxanthine

1-(3-Carboxypropyl)-3,7-dimethylxanthine

C11H14N4O4 (266.1015004)


CONFIDENCE standard compound; INTERNAL_ID 2785 INTERNAL_ID 2785; CONFIDENCE standard compound CONFIDENCE standard compound; INTERNAL_ID 8711

   
   
   

7-Deaza-2-deoxyguanosine

2-amino-7-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-pyrrolo[2,3-d]pyrimidin-4-one

C11H14N4O4 (266.1015004)


   

1H-Purine-8-butanoicacid, 2,3,6,9-tetrahydro-1,3-dimethyl-2,6-dioxo-

1H-Purine-8-butanoicacid, 2,3,6,9-tetrahydro-1,3-dimethyl-2,6-dioxo-

C11H14N4O4 (266.1015004)


   

isovaleraldehyde 2,4-dinitrophenylhydrazone

isovaleraldehyde 2,4-dinitrophenylhydrazone

C11H14N4O4 (266.1015004)


   

tubercidin

7-Deazaadenosine(Tubercidin)

C11H14N4O4 (266.1015004)


An N-glycosylpyrrolopyrimidine that is adenosine in which the in the 5-membered ring that is not attached to the ribose moiety is replaced by a carbon. Tubercidin is produced in the culture broth of Streptomyces tubericidus. C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents Tubercidin (7-Deazaadenosine) is an antibiotic obtained from Streptomyces tubercidicus. Tubercidin inhibits the growth of Streptococcus faecalis (8043) with an IC50 of 0.02 μM[1]. Tubercidin inhibits polymerases by incorporating DNA or RNA, thereby inhibiting DNA replication, RNA and protein synthesis[2]. Tubercidin is a weak inhibitor of adenosine phosphorylase, and interferes with the phosphorylation of adenosine and AMP[1]. Tubercidin has antiviral activity[2]. Tubercidin (7-Deazaadenosine) is an antibiotic obtained from Streptomyces tubercidicus. Tubercidin inhibits the growth of Streptococcus faecalis (8043) with an IC50 of 0.02 μM[1]. Tubercidin inhibits polymerases by incorporating DNA or RNA, thereby inhibiting DNA replication, RNA and protein synthesis[2]. Tubercidin is a weak inhibitor of adenosine phosphorylase, and interferes with the phosphorylation of adenosine and AMP[1]. Tubercidin has antiviral activity[2].

   

n-valeraldehyde 2,4-dinitrophenylhydrazone

n-valeraldehyde 2,4-dinitrophenylhydrazone

C11H14N4O4 (266.1015004)


   

1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purine-7-butyric acid

1,2,3,6-tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purine-7-butyric acid

C11H14N4O4 (266.1015004)


   
   

Forodesine

Forodesine

C11H14N4O4 (266.1015004)


C471 - Enzyme Inhibitor > C2151 - Purine Nucleoside Phosphorylase Inhibitor

   

9H-Purine, 6-methyl-9-b-D-ribofuranosyl-

9H-Purine, 6-methyl-9-b-D-ribofuranosyl-

C11H14N4O4 (266.1015004)


6-Methylpurine riboside is a purine nucleoside analogue. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc[1].

   

9-(2-C-Methyl-β-D-ribofuranosyl)purine

9-(2-C-Methyl-β-D-ribofuranosyl)purine

C11H14N4O4 (266.1015004)


   
   
   

2,2-Dimethylpropanal 2,4-dinitrophenylhydrazone

2,2-Dimethylpropanal 2,4-dinitrophenylhydrazone

C11H14N4O4 (266.1015004)


   

Pyroglutamylhistidine

Pyroglutamylhistidine

C11H14N4O4 (266.1015004)


   

7-[(2S,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one

7-[(2S,3S,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidin-2-yl]-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one

C11H14N4O4 (266.1015004)


   

Doxofylline

Doxofylline

C11H14N4O4 (266.1015004)


R - Respiratory system > R03 - Drugs for obstructive airway diseases > R03D - Other systemic drugs for obstructive airway diseases > R03DA - Xanthines D019141 - Respiratory System Agents > D018927 - Anti-Asthmatic Agents > D001993 - Bronchodilator Agents D018373 - Peripheral Nervous System Agents > D001337 - Autonomic Agents D004791 - Enzyme Inhibitors > D010726 - Phosphodiesterase Inhibitors D019141 - Respiratory System Agents > D000996 - Antitussive Agents C471 - Enzyme Inhibitor > C744 - Phosphodiesterase Inhibitor D002491 - Central Nervous System Agents Doxofylline is an orally active PDE IV inhibitor and A1AR antagonist. Doxofylline reduces inflammation in epithelial cells via inhibiting mitochondrial ROS production and amelioration of multiple cellular pathways (NLRP3-TXNIP inflammasome activation). Doxophylline can be used in studies of asthma, chronic obstructive pulmonary disease, and bronchospasm[1][2][3].

   

3-(4H-imidazol-4-yl)-2-[(5-oxopyrrolidine-2-carbonyl)amino]propanoic acid

3-(4H-imidazol-4-yl)-2-[(5-oxopyrrolidine-2-carbonyl)amino]propanoic acid

C11H14N4O4 (266.1015004)


   

dehydrodeoxycoformycin

dehydrodeoxycoformycin

C11H14N4O4 (266.1015004)


A coformycin that is dehydrocoformycin with the hydroxy group at position 2 replaced with a hydrogen.

   
   
   

2-(6-hydroxypurin-9-yl)-3,5-dimethyloxolane-3,4-diol

2-(6-hydroxypurin-9-yl)-3,5-dimethyloxolane-3,4-diol

C11H14N4O4 (266.1015004)


   

(2r,3r,4r,5r)-2-(6-hydroxypurin-9-yl)-3,5-dimethyloxolane-3,4-diol

(2r,3r,4r,5r)-2-(6-hydroxypurin-9-yl)-3,5-dimethyloxolane-3,4-diol

C11H14N4O4 (266.1015004)


   

2-(hydroxymethyl)-5-{4-imino-3h,5h-pyrrolo[3,2-d]pyrimidin-7-yl}oxolane-3,4-diol

2-(hydroxymethyl)-5-{4-imino-3h,5h-pyrrolo[3,2-d]pyrimidin-7-yl}oxolane-3,4-diol

C11H14N4O4 (266.1015004)


   

(2r,3s,4r,5s)-2-(hydroxymethyl)-5-{4-imino-3h,5h-pyrrolo[3,2-d]pyrimidin-7-yl}oxolane-3,4-diol

(2r,3s,4r,5s)-2-(hydroxymethyl)-5-{4-imino-3h,5h-pyrrolo[3,2-d]pyrimidin-7-yl}oxolane-3,4-diol

C11H14N4O4 (266.1015004)