Chemical Formula: C10H15N3O4

Chemical Formula C10H15N3O4

Found 31 metabolite its formula value is C10H15N3O4

5-Methyldeoxycytidine

4-amino-1-[(2R,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methyl-1,2-dihydropyrimidin-2-one

C10H15N3O4 (241.1063)


5-Methyldeoxycytidine is a dinucleotide. Methylation of cytosine-guanine dinucleotide sequences (CpG dinucleotides) catalyzed by DNA methyltransferase, particularly in the 5′-promoter regions of mammalian genes, forms 5-methyldeoxycytidine (5-mdc) whose levels may regulate gene expression. Levels of 5-mdc and the expression of nm23-H1 (an anti-metastatic gene identified in and human cancer lines) are highly correlated with human hepatoma cells with different invasion activities. DNA hypermethylation is a common finding in malignant cells and has been explored as a therapeutic target for hypomethylating agents. The levels of 5-mdc in the urine of patients with breast cancer is not significantly different than controls. (PMID: 17044778, 17264127, 16799933) [HMDB] 5-Methyldeoxycytidine is a dinucleotide. Methylation of cytosine-guanine dinucleotide sequences (CpG dinucleotides) catalyzed by DNA methyltransferase, particularly in the 5′-promoter regions of mammalian genes, forms 5-methyldeoxycytidine (5-mdc) whose levels may regulate gene expression. Levels of 5-mdc and the expression of nm23-H1 (an anti-metastatic gene identified in and human cancer lines) are highly correlated with human hepatoma cells with different invasion activities. DNA hypermethylation is a common finding in malignant cells and has been explored as a therapeutic target for hypomethylating agents. The levels of 5-mdc in the urine of patients with breast cancer is not significantly different than controls. (PMID: 17044778, 17264127, 16799933). 5-Methyl-2'-deoxycytidine in single-stranded DNA can act in cis to signal de novo DNA methylation[1][2]. 5-Methyl-2'-deoxycytidine in single-stranded DNA can act in cis to signal de novo DNA methylation[1][2].

   

3'-Amino-3'-deoxythimidine

1-[4-amino-5-(hydroxymethyl)oxolan-2-yl]-4-hydroxy-5-methyl-1,2-dihydropyrimidin-2-one

C10H15N3O4 (241.1063)


3-Amino-3-deoxythimidine is a metabolite of zidovudine. Zidovudine or azidothymidine (AZT) (also called ZDV) is a nucleoside analog reverse-transcriptase inhibitor (NRTI), a type of antiretroviral drug used for the successful treatment of HIV/AIDS infectiousness. It is a therapeutic analog of thymidine. AZT is the first U.S. government-approved treatment for HIV therapy, prescribed under the names Retrovir and Retrovis. (Wikipedia)

   

1-[(2R,4R,5R)-5-(Aminomethyl)-4-hydroxyoxolan-2-yl]-5-methylpyrimidine-2,4-dione

1-[5-(aminomethyl)-4-hydroxyoxolan-2-yl]-5-methyl-1,2,3,4-tetrahydropyrimidine-2,4-dione

C10H15N3O4 (241.1063)


   

epsilon-Maleimido-lysine

2,6-diamino-6-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)hexanoic acid

C10H15N3O4 (241.1063)


   

SCHEMBL17867375

SCHEMBL17867375

C10H15N3O4 (241.1063)


   

2-Deoxy-3-methylcytidine

2-Deoxy-3-methylcytidine

C10H15N3O4 (241.1063)


   

1-beta-ribofuranosylbrunfelsamidine

1-beta-ribofuranosylbrunfelsamidine

C10H15N3O4 (241.1063)


   

3-Methyl-deoxycytidine

3-Methyl-deoxycytidine

C10H15N3O4 (241.1063)


   

5-Methyl-deoxycytidine

5-Methyl-deoxycytidine

C10H15N3O4 (241.1063)


   

5-Methyl-deoxycytosine

5-Methyl-deoxycytosine

C10H15N3O4 (241.1063)


   

3-Amino-3-deoxythymidine

3-Amino-3-deoxythymidine

C10H15N3O4 (241.1063)


   

Bis-1,4-(2-hydroxyethylamino)-2-nitrobenzene

Bis-1,4-(2-hydroxyethylamino)-2-nitrobenzene

C10H15N3O4 (241.1063)


   

2-((TERT-BUTOXYCARBONYLAMINO)METHYL)-1H-IMIDAZOLE-5-CARBOXYLIC ACID

2-((TERT-BUTOXYCARBONYLAMINO)METHYL)-1H-IMIDAZOLE-5-CARBOXYLIC ACID

C10H15N3O4 (241.1063)


   

Thymidine,5-amino-5-deoxy-

Thymidine,5-amino-5-deoxy-

C10H15N3O4 (241.1063)


   

HC ORANGE NO. 2

HC ORANGE NO. 2

C10H15N3O4 (241.1063)


   

5-(2-HYDROXYETHYL)-2-MORPHOLINOPYRIMIDINE-4,6-DIOL

5-(2-HYDROXYETHYL)-2-MORPHOLINOPYRIMIDINE-4,6-DIOL

C10H15N3O4 (241.1063)


   

2,2-[(4-amino-3-nitrophenyl)imino]bis-Ethanol

2,2-[(4-amino-3-nitrophenyl)imino]bis-Ethanol

C10H15N3O4 (241.1063)


   

6-[(4,6-dioxo-1H-pyrimidin-2-yl)amino]hexanoic acid

6-[(4,6-dioxo-1H-pyrimidin-2-yl)amino]hexanoic acid

C10H15N3O4 (241.1063)


   

4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid

4-((tert-butoxycarbonyl)amino)-1-methyl-1H-imidazole-2-carboxylic acid

C10H15N3O4 (241.1063)


   

6-[(2-Methoxyethyl)amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxaldehyde

6-[(2-Methoxyethyl)amino]-1,3-dimethyl-2,4-dioxo-1,2,3,4-tetrahydro-5-pyrimidinecarboxaldehyde

C10H15N3O4 (241.1063)


   

2,6-DIBROMOISONICOTINICACID

2,6-DIBROMOISONICOTINICACID

C10H15N3O4 (241.1063)


   

1-TERT-BUTYL 3-METHYL 4-AMINO-1H-PYRAZOLE-1,3-DICARBOXYLATE

1-TERT-BUTYL 3-METHYL 4-AMINO-1H-PYRAZOLE-1,3-DICARBOXYLATE

C10H15N3O4 (241.1063)


   

2,6-diamino-6-(2,5-dioxopyrrol-1-yl)hexanoic acid

2,6-diamino-6-(2,5-dioxopyrrol-1-yl)hexanoic acid

C10H15N3O4 (241.1063)


   

5-Methyl-2-deoxycytidine

5-Methyl-2-deoxycytidine

C10H15N3O4 (241.1063)


5-Methyl-2'-deoxycytidine in single-stranded DNA can act in cis to signal de novo DNA methylation[1][2]. 5-Methyl-2'-deoxycytidine in single-stranded DNA can act in cis to signal de novo DNA methylation[1][2].

   

1-[4-Amino-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

1-[4-Amino-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione

C10H15N3O4 (241.1063)


   

5-Methyl-2'-deoxycytidine

5-Methyl-2'-deoxycytidine

C10H15N3O4 (241.1063)


   

Methyldeoxycytidine

Methyldeoxycytidine

C10H15N3O4 (241.1063)


   

2’-Deoxy-N4-methylcytidine

2’-Deoxy-N4-methylcytidine

C10H15N3O4 (241.1063)


2’-Deoxy-N4-methylcytidine is a purine nucleoside analog. 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].

   

methyl 2-{[hydroxy(methoxy)methylidene]amino}-3-(3-methylimidazol-4-yl)propanoate

methyl 2-{[hydroxy(methoxy)methylidene]amino}-3-(3-methylimidazol-4-yl)propanoate

C10H15N3O4 (241.1063)


   

3-hydroxy-2-{[hydroxy(5-imino-4-methylidenepyrrolidin-2-yl)methylidene]amino}butanoic acid

3-hydroxy-2-{[hydroxy(5-imino-4-methylidenepyrrolidin-2-yl)methylidene]amino}butanoic acid

C10H15N3O4 (241.1063)


   

(2s,3r)-3-hydroxy-2-({hydroxy[(2s)-5-imino-4-methylidenepyrrolidin-2-yl]methylidene}amino)butanoic acid

(2s,3r)-3-hydroxy-2-({hydroxy[(2s)-5-imino-4-methylidenepyrrolidin-2-yl]methylidene}amino)butanoic acid

C10H15N3O4 (241.1063)