Exact Mass: 130.0088

Exact Mass Matches: 130.0088

Found 27 metabolites which its exact mass value is equals to given mass value 130.0088, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

Fluorouracil

5-fluoro-1,2,3,4-tetrahydropyrimidine-2,4-dione

C4H3FN2O2 (130.0179)


Fluorouracil is only found in individuals that have used or taken this drug. It is a pyrimidine analog that is an antineoplastic antimetabolite. It interferes with DNA synthesis by blocking the thymidylate synthetase conversion of deoxyuridylic acid to thymidylic acid. [PubChem]The precise mechanism of action has not been fully determined, but the main mechanism of fluorouracil is thought to be the binding of the deoxyribonucleotide of the drug (FdUMP) and the folate cofactor, N5–10-methylenetetrahydrofolate, to thymidylate synthase (TS) to form a covalently bound ternary complex. This results in the inhibition of the formation of thymidylate from uracil, which leads to the inhibition of DNA and RNA synthesis and cell death. Fluorouracil can also be incorporated into RNA in place of uridine triphosphate (UTP), producing a fraudulent RNA and interfering with RNA processing and protein synthesis. L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BC - Pyrimidine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C471 - Enzyme Inhibitor > C2021 - Thymidylate Synthase Inhibitor CONFIDENCE standard compound; EAWAG_UCHEM_ID 2566 D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents 5-Fluorouracil (5-FU) is an analogue of uracil and a potent antitumor agent. 5-Fluorouracil affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools. 5-Fluorouracil induces apoptosis and can be used as a chemical sensitizer[1][2]. 5-Fluorouracil also inhibits HIV[3].

   

4-Hydroxy-5-methyl-3(2H)-thiophenone

4-hydroxy-5-methyl-2,3-dihydrothiophen-3-one

C5H6O2S (130.0088)


Roasted meat-like flavour component. Roasted meat-like flavour component

   

s-Triazol-3-ol, 5-nitro-

5-nitro-1H-1,2,4-triazol-3-ol

C2H2N4O3 (130.0127)


   

Fluoruracil

1-fluoro-1,2,3,4-tetrahydropyrimidine-2,4-dione

C4H3FN2O2 (130.0179)


D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents

   

4-Hydroxy-5-methyl-3(2H)-thiophenone

4-hydroxy-5-methyl-2,3-dihydrothiophen-3-one

C5H6O2S (130.0088)


   

1,3,4-thiadiazol-2-ylboronic acid

1,3,4-thiadiazol-2-ylboronic acid

C2H3BN2O2S (130.0008)


   

6-fluorouracil

6-fluorouracil

C4H3FN2O2 (130.0179)


   

4-BROMOMETHYL-PIPERIDINE

4-BROMOMETHYL-PIPERIDINE

C6H7ClO (130.0185)


   

3-methylidenecyclobutane-1-carbonyl chloride

3-methylidenecyclobutane-1-carbonyl chloride

C6H7ClO (130.0185)


   

1-CYCLOPENTENE-1-CARBONYL CHLORIDE

1-CYCLOPENTENE-1-CARBONYL CHLORIDE

C6H7ClO (130.0185)


   

5-fluorouracil-15n2

5-fluorouracil-15n2

C4H3FN2O2 (130.0179)


   

Sorbic chloride

Sorbic chloride

C6H7ClO (130.0185)


   

5-Fluoropyrimidine-4,6-diol

5-Fluoropyrimidine-4,6-diol

C4H3FN2O2 (130.0179)


   

magnesium methyl carbonate

magnesium methyl carbonate

C3H6MgO4 (130.0117)


   

3-Hydroxy-4-methyl-2(5H)-thiophenone

3-Hydroxy-4-methyl-2(5H)-thiophenone

C5H6O2S (130.0088)


   

Hydrazine sulfate

Hydrazine sulfate

H6N2O4S (130.0048)


   

4-Amino-2-chloro-1,3,5-triazine

4-Amino-2-chloro-1,3,5-triazine

C3H3ClN4 (130.0046)


   

2H-Thiopyran-3,5(4H,6H)-dione

2H-Thiopyran-3,5(4H,6H)-dione

C5H6O2S (130.0088)


   

5-fluorouracil, [2-14c]

5-fluorouracil, [2-14c]

C4H3FN2O2 (130.0179)


   
   

chondroitinase abc

chondroitinase abc

C4H3FN2O2 (130.0179)


   

4-nitro-1,2,5-oxadiazol-3-amine

4-nitro-1,2,5-oxadiazol-3-amine

C2H2N4O3 (130.0127)


   

4-Hydroxy-1,2,5-oxadiazole-3-carboxylic acid

4-Hydroxy-1,2,5-oxadiazole-3-carboxylic acid

C3H2N2O4 (130.0015)


   

s-Triazol-3-ol, 5-nitro-

s-Triazol-3-ol, 5-nitro-

C2H2N4O3 (130.0127)


   

2-Oxosuccinamate

2-Oxosuccinamate

C4H4NO4- (130.014)


   

Iminoaspartate(1-)

Iminoaspartate(1-)

C4H4NO4- (130.014)


A dicarboxylic acid monoanion that is the conjugate base of iminoaspartic acid and the major microspecies at pH 7.3 (according to Marvin v 6.2.0.).

   

Fluorouracil

2,4-Pyrimidinediol, 5-fluoro- (9CI)

C4H3FN2O2 (130.0179)


L - Antineoplastic and immunomodulating agents > L01 - Antineoplastic agents > L01B - Antimetabolites > L01BC - Pyrimidine analogues C274 - Antineoplastic Agent > C186664 - Cytotoxic Chemotherapeutic Agent > C272 - Antimetabolite D007155 - Immunologic Factors > D007166 - Immunosuppressive Agents C471 - Enzyme Inhibitor > C2021 - Thymidylate Synthase Inhibitor D009676 - Noxae > D000963 - Antimetabolites D000970 - Antineoplastic Agents 5-Fluorouracil (5-FU) is an analogue of uracil and a potent antitumor agent. 5-Fluorouracil affects pyrimidine synthesis by inhibiting thymidylate synthetase thus depleting intracellular dTTP pools. 5-Fluorouracil induces apoptosis and can be used as a chemical sensitizer[1][2]. 5-Fluorouracil also inhibits HIV[3].