All terms in CHEBI
| Label | Id | Description |
|---|---|---|
| germacrene D | CHEBI_49045 | |
| (+)-germacrene D | CHEBI_49046 | |
| germacrene | CHEBI_36743 | |
| CHEBI_49047 | CHEBI_49047 | |
| CHEBI_355508 | CHEBI_355508 | |
| CHEBI_49048 | CHEBI_49048 | |
| 3-oxo-3-ureidopropanoic acid | CHEBI_49049 | [The ureido derivative of malonic acid.] |
| 3-oxo-3-ureidopropanoate | CHEBI_58775 | [Conjugate base of 3-oxo-3-ureidopropanoic acid.] |
| ureidoglycolic acid | CHEBI_49050 | |
| glycolic acid | CHEBI_17497 | [A 2-hydroxy monocarboxylic acid that is acetic acid where the methyl group has been hydroxylated.] |
| 5,7-dihydro-1H-purine-2,6,8(9H)-trione | CHEBI_49051 | |
| uric acid | CHEBI_27226 | [An oxopurine that is the final oxidation product of purine metabolism.] |
| 2,6-dihydroxy-7,9-dihydro-8H-purin-8-one | CHEBI_46811 | |
| 1H-purine-2,6,8-triol | CHEBI_46823 | |
| 7,9-dihydro-1H-purine-2,6,8(3H)-trione | CHEBI_17775 | [An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.] |
| 7H-purine-2,6,8-triol | CHEBI_46817 | |
| 9H-purine-2,6,8-triol | CHEBI_46814 | |
| (R)-2-(carboxymethyl)-5-oxo-2,5-dihydro-2-furoic acid | CHEBI_49030 | [The (R)-enantiomer of 2-(carboxymethyl)-5-oxo-2,5-dihydro-2-furoic acid.] |
| 2-(carboxymethyl)-5-oxo-2,5-dihydro-2-furoic acid | CHEBI_16993 | [A 5-oxo-2-furylacetic acid having a carboxy group at the 2-position.] |
| (R)-2-(carboxylatomethyl)-5-oxo-2,5-dihydro-2-furoate | CHEBI_58771 | [Dicarboxylate anion of (R)-2-(carboxymethyl)-5-oxo-2,5-dihydro-2-furoic acid.] |