All terms in CHEBI
| Label | Id | Description |
|---|---|---|
| N-acetyl-L-citrulline | CHEBI_49002 | [The L-enantiomer of N-acetylcitrulline.] |
| N-acetylcitrulline | CHEBI_49006 | [An N-acetyl-amino acid that is the N(alpha)-acetyl derivative of citrulline.] |
| N-acetyl-L-citrullinate | CHEBI_58765 | [An N-acyl-L-alpha-amino acid anion that is the conjugate base of N-acetyl-L-citrulline, obtained by deprotonation of the carboxy group; major species at pH 7.3.] |
| 4-O-phosphonato-D-erythronate(3-) | CHEBI_58766 | [Trianion of 4-phospho-D-erythronic acid arising from deprotonation of phosphate and carboxylic acid functions.] |
| N-acetyl-LL-2,6-diaminopimelic acid | CHEBI_49004 | |
| N-acetyl-LL-2,6-diaminopimelate(1-) | CHEBI_58767 | [Conjugate base of N-acetyl-LL-2,6-diaminopimelic acid.] |
| N-acetyl-LL-2,6-diaminopimelate(2-) | CHEBI_18317 | [A dicarboxylic acid dianion resulting from removal of a proton from both carboxy groups of N-acetyl-LL-2,6-diaminopimelic acid.] |
| deferasirox | CHEBI_49005 | [A member of the class of triazoles, deferasirox is 1,2,4-triazole substituted by a 4-carboxyphenyl group at position 1 and by 2-hydroxyphenyl groups at positions 3 and 5. An orally active iron chelator, it is used to manage chronic iron overload in patients receiving long-term blood transfusions.] |
| 2,2'-(1-phenyl-1H-1,2,4-triazole-3,5-diyl)diphenol | CHEBI_855 | [A member of the class of triazoles that is 1-phenyl-1H-1,2,4-triazole substituted by 2-hydroxyphenyl groups at positions 3 and 5.] |
| (1R,6S)-1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylic acid | CHEBI_49008 | [The (1R,6S)-diastereomer of 1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylic acid.] |
| cis-1,6-dihydroxy-4-methylcyclohexa-2,4-dienecarboxylic acid | CHEBI_17095 | [A cyclohexadienecarboxylic acid that is cyclohexa-2,4-dienecarboxylic acid which is substituted at positions 1 and 6 by hydroxy groups which are both on the same side of the plane of the cyclohexadiene ring.] |
| (1R,6S)-1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylate | CHEBI_58768 | [Conjugate base of (1R,6S)-1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylic acid.] |
| (1S,6R)-1,6-dihydroxy-4-methylcyclohexa-2,4-diene-1-carboxylic acid | CHEBI_49009 | |
| CHEBI_40686 | CHEBI_40686 | |
| CHEBI_40688 | CHEBI_40688 | |
| L-2-aminoheptanoic acid | CHEBI_40682 | [An optically active form of 2-aminoheptanoic acid having L-configuration.] |
| 2-aminoheptanoic acid | CHEBI_64304 | [An alpha-amino acid that is heptanoic acid in which one of the hydrogens at position 2 is replaced by an amino group.] |
| (4S)-2-(3-methoxyphenyl)-4-(methylamino)-3,4-dihydro-2H-thieno[3,2-e][1,2]thiazine-6-sulfonamide 1,1-dioxide | CHEBI_40681 | |
| N-[3-(dimethylamino)propyl]-2-({[4-({[4-(formylamino)-1-methyl-1H-pyrrol-2-yl]carbonyl}amino)-1-methyl-1H-pyrrol-2-yl]carbonyl}amino)-5-(1-methylethyl)-1,3-thiazole-4-carboxamide | CHEBI_40658 | |
| 1,3-thiazolecarboxamide | CHEBI_48890 |