Chemical Formula: C6H8N2O3
Chemical Formula C6H8N2O3
Found 74 metabolite its formula value is C6H8N2O3
4-Imidazolone-5-propionic acid
4-Imidazolone-5-propanoate is a metabolite of histidine metabolism. It is produced from urocanic acid by the enzyme urocanate hydratase [EC:4.2.1.49]. 4-Imidazolone-5-propionic acid can spontaneously decay to 4-oxoglutaramate or formylisoglutamine. It is also converted to N-forminimo-L-glutamate by the enzyme imidazolonepropionase [EC:3.5.2.7]. [HMDB] 4-Imidazolone-5-propanoate is a metabolite of histidine metabolism. It is produced from urocanic acid by the enzyme urocanate hydratase [EC:4.2.1.49]. 4-Imidazolone-5-propionic acid can spontaneously decay to 4-oxoglutaramate or formylisoglutamine. It is also converted to N-forminimo-L-glutamate by the enzyme imidazolonepropionase [EC:3.5.2.7].
Imidazole lactate
Imidazolelactic acid is the component of normal human urine. (PMID: 5856262). histidine loading causes an increase in the excretion of imidazolelactic acid. (PMID: 6021220). During pregnancy the values for imidazolelactic acid in urine is increased 3-fold. An interaction of allergic reactions and anomalies in the metabolism of the sex hormones are considered to form the basis of the pregnancy-specific illnesses that were studied. (PMID: 5789877). Urinary excretion of imidazolelactic acid is also an indication for folic acid and vitamin B12 deficiency. (PMID: 4645251). Imidazolelactic acid is the component of normal human urine. (PMID: 5856262)
5-Hydroxymethyl-4-methyluracil
5-Hydroxymethyl-6-methyl- 2,4-(1H,3H)-pyrimidinedione. Uracil derivative used in combination with toxic antibiotics to lessen their toxicity; also to stimulate leukopoiesis and immunity. [HMDB] 5-Hydroxymethyl-6-methyl- 2,4-(1H,3H)-pyrimidinedione. Uracil derivative used in combination with toxic antibiotics to lessen their toxicity; also to stimulate leukopoiesis and immunity.
5-(2-carboxylatoethyl)-4-oxo-4,5-dihydro-1H-imidazol-5-ide
5-(2-carboxylatoethyl)-4-oxo-4,5-dihydro-1H-imidazol-5-ide is classified as an imidazolyl carboxylic acid or an Imidazolyl carboxylic acid derivative. Imidazolyl carboxylic acids are organic compounds containing a carboxylic acid chain (of at least 2 carbon atoms) linked to an imidazole ring. 5-(2-carboxylatoethyl)-4-oxo-4,5-dihydro-1H-imidazol-5-ide is considered to be soluble (in water) and acidic
ETHYL 2-OXO-2,3-DIHYDRO-1H-IMIDAZOLE-4-CARBOXYLATE
5,5-DimethylBarbituric Acid
CONFIDENCE standard compound; INTERNAL_ID 249; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4668; ORIGINAL_PRECURSOR_SCAN_NO 4666 CONFIDENCE standard compound; INTERNAL_ID 249; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4666; ORIGINAL_PRECURSOR_SCAN_NO 4665 CONFIDENCE standard compound; INTERNAL_ID 249; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4689; ORIGINAL_PRECURSOR_SCAN_NO 4687 CONFIDENCE standard compound; INTERNAL_ID 249; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4687; ORIGINAL_PRECURSOR_SCAN_NO 4686 CONFIDENCE standard compound; INTERNAL_ID 249; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4764; ORIGINAL_PRECURSOR_SCAN_NO 4763 CONFIDENCE standard compound; INTERNAL_ID 249; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4680; ORIGINAL_PRECURSOR_SCAN_NO 4679
1H-Imidazole-5-carboxylicacid,2-methoxy-1-methyl-(9CI)
5-[hydroxy(methoxy)methylidene]-3-methylimidazol-4-one
4-Oxazolecarboxylicacid,2-(aminomethyl)-,methylester(9CI)
2-(3-METHYL-5-OXO-4,5-DIHYDRO-1H-PYRAZOL-1-YL)ACETIC ACID
1H-Imidazole-4-carboxylicacid,1-(2-hydroxyethyl)-(9CI)
1H-Pyrazole-3-carboxylicacid, 4,5-dihydro-5-oxo-, ethyl ester
Methyl 5-hydroxy-1-methyl-1H-pyrazole-3-carboxylate
5-Hydroxymethyl-1H-imidazole-4-carboxylic acid methyl ester
1H-Imidazole-4-carboxylicacid,5-ethyl-2,3-dihydro-2-oxo-(9CI)
5-Methyl-1,3,4-oxadiazole-2-carboxylic acid ethyl ester
1H-Imidazole-2-carboxylicacid,1-(methoxymethyl)-(9CI)
2-(3-methyl-5-oxo-1,4-dihydropyrazol-4-yl)acetic acid
1H-Imidazole-4-carboxylicacid,2-(methoxymethyl)-(9CI)
Methyl 3-Hydroxy-1-Methyl-1H-Pyrazole-5-Carboxylate
1-methyl-6-oxo-1,4,5,6-tetrahydropyridazine-3-carboxylic acid
5-Isoxazolecarboxylicacid,4-amino-3-methyl-,methylester(9CI)
(S)-3-(4-oxo-4,5-dihydro-1H-imidazol-5-yl)propanoic acid
3-(4-oxo-4,5-Dihydro-1H-imidazol-5-yl)propanoic acid
An imidazol-4-one having a 2-carboxyethyl substituent at the 5-position.
3-(imidazol-5-yl)lactic acid
A 2-hydroxy monocarboxylic acid that is lactic acid in which one of the methyl hydrogens has been replaced by an imidazol-5-yl group.
3-(imidazol-1-yl)lactic acid
An imidazolyl carboxylic acid that is lactic acid in which one of the methyl hydrogens is substituted by an imidazol-1-yl group.