Exact Mass: 212.0797

Exact Mass Matches: 212.0797

Found 33 metabolites which its exact mass value is equals to given mass value 212.0797, within given mass tolerance error 0.001 dalton. Try search metabolite list with more accurate mass tolerance error 0.0002 dalton.

2',3'-Dideoxyuridine

1-[5-(hydroxymethyl)oxolan-2-yl]-1,2,3,4-tetrahydropyrimidine-2,4-dione

C9H12N2O4 (212.0797)


   

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

1-(4-Nitrophenyl)-2-aminopropane-1,3-diol, (S)-hydroxybutanedioate (2:1) (S-(r*,r*))-isomer

C9H12N2O4 (212.0797)


   

2?,3?-Dideoxyuridine

2?,3?-Dideoxyuridine

C9H12N2O4 (212.0797)


   

surugapyrrole A

surugapyrrole A

C9H12N2O4 (212.0797)


A pyrrolecarboxamide obtained by the formal condensation of 1-hydroxy-4-methyl-1H-pyrrole-2-carboxylic acid with the amino group of 3-aminopropanoic acid. It is isolated from the culture broth of Streptomyces sp.USF-6280 and exhibits DPPH radical scavenging activity.

   

2,3-Dideoxyuridine

2,3-Dideoxyuridine

C9H12N2O4 (212.0797)


D009676 - Noxae > D000963 - Antimetabolites > D015224 - Dideoxynucleosides

   

4-Hydroxy-3,5-dimethoxybenzoic acid

4-Hydroxy-3,5-dimethoxybenzoic acid

C9H12N2O4 (212.0797)


   

Levoamine (Chloramphenicol D base)

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

C9H12N2O4 (212.0797)


   

METHYL 5,6-DIHYDROXY-2-ISOPROPYLPYRIMIDINE-4-CARBOXYLATE

METHYL 5,6-DIHYDROXY-2-ISOPROPYLPYRIMIDINE-4-CARBOXYLATE

C9H12N2O4 (212.0797)


   

4-((3-Hydroxypropyl)amino)-3-nitrophenol

4-((3-Hydroxypropyl)amino)-3-nitrophenol

C9H12N2O4 (212.0797)


   

3-phenylpropyldimethylchlorosilane

3-phenylpropyldimethylchlorosilane

C11H17ClSi (212.0788)


   

1-(p-nitrophenyl)-2-amino-1,3-propanediol

1-(p-nitrophenyl)-2-amino-1,3-propanediol

C9H12N2O4 (212.0797)


   

Methyl Ester L-Lysine Diisocyanate

Methyl Ester L-Lysine Diisocyanate

C9H12N2O4 (212.0797)


   

(2,4-DICHLORO-PHENYL)-ACETYLCHLORIDE

(2,4-DICHLORO-PHENYL)-ACETYLCHLORIDE

C9H12N2O4 (212.0797)


   

Ethyl 4,6-dimethoxypyrimidine-2-carboxylate

Ethyl 4,6-dimethoxypyrimidine-2-carboxylate

C9H12N2O4 (212.0797)


   

3,5-Pyrazoledicarboxylic acid diethyl ester

3,5-Pyrazoledicarboxylic acid diethyl ester

C9H12N2O4 (212.0797)


   

2-(5-methoxy-2-nitroanilino)ethanol

2-(5-methoxy-2-nitroanilino)ethanol

C9H12N2O4 (212.0797)


   

2-[3-(methylamino)-4-nitrophenoxy]ethanol

2-[3-(methylamino)-4-nitrophenoxy]ethanol

C9H12N2O4 (212.0797)


   

benzylhydrazine oxalate

benzylhydrazine oxalate

C9H12N2O4 (212.0797)


   

Chlorodimethyl(2-phenylpropan-2-yl)silane

Chlorodimethyl(2-phenylpropan-2-yl)silane

C11H17ClSi (212.0788)


   

Pyridine,3,5-diethoxy-2-nitro-(9CI)

Pyridine,3,5-diethoxy-2-nitro-(9CI)

C9H12N2O4 (212.0797)


   

Diethyl 1H-imidazole-4,5-dicarboxylate

Diethyl 1H-imidazole-4,5-dicarboxylate

C9H12N2O4 (212.0797)


   

DIMETHYL 1-AMINO-3-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE

DIMETHYL 1-AMINO-3-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE

C9H12N2O4 (212.0797)


   

Diethyl 3-amino-1H-pyrrole-2,4-dicarboxylate

Diethyl 3-amino-1H-pyrrole-2,4-dicarboxylate

C9H12N2O4 (212.0797)


   

Benzoic acid,4-hydroxy-3,5-dimethoxy-, hydrazide

Benzoic acid,4-hydroxy-3,5-dimethoxy-, hydrazide

C9H12N2O4 (212.0797)


   

2-NITRO-N-HYDROXYETHYL-p-ANISIDINE

2-NITRO-N-HYDROXYETHYL-p-ANISIDINE

C9H12N2O4 (212.0797)


   

3-(4,6-dimethoxypyrimidin-2-yl)propanoicacid

3-(4,6-dimethoxypyrimidin-2-yl)propanoicacid

C9H12N2O4 (212.0797)


   

2,5-Dideoxyuridine

2,5-Dideoxyuridine

C9H12N2O4 (212.0797)


   

3-Amino-6-Hydroxy-Tyrosine

3-Amino-6-Hydroxy-Tyrosine

C9H12N2O4 (212.0797)


   

2-((4-Methoxy-3-nitrophenyl)amino)ethanol

2-((4-Methoxy-3-nitrophenyl)amino)ethanol

C9H12N2O4 (212.0797)


   

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

(1R,2R)-2-Amino-1-(4-nitrophenyl)propane-1,3-diol

C9H12N2O4 (212.0797)


   

Cyclo(Asp-Pro)

Cyclo(Asp-Pro)

C9H12N2O4 (212.0797)


   

2',3'-Dideoxyuridine

2',3'-Dideoxyuridine

C9H12N2O4 (212.0797)


2',3'-Dideoxyuridine 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 (2s)-2-amino-3-(3-hydroxy-4-oxopyridin-1-yl)propanoate

methyl (2s)-2-amino-3-(3-hydroxy-4-oxopyridin-1-yl)propanoate

C9H12N2O4 (212.0797)