All terms in CHEBI
| Label | Id | Description |
|---|---|---|
| octyl beta-D-glucopyranoside | CHEBI_41128 | [An beta-D-glucoside in which the anomeric hydrogen of beta-D-glucopyranose is substituted by an octyl group.] |
| CHEBI_41124 | CHEBI_41124 | |
| CHEBI_41125 | CHEBI_41125 | |
| (3S)-3-hydroxy-L-aspartic acid residue | CHEBI_41121 | |
| (3S)-3-hydroxy-L-aspartic acid | CHEBI_10696 | [The (3S)-diastereomer of 3-hydroxy-L-aspartic acid.] |
| Dolichotheline | CHEBI_80664 | |
| 1-Indolizidinone | CHEBI_80665 | |
| indolizines | CHEBI_38485 | |
| norbelladine | CHEBI_80666 | [A phenethylamine alkaloid that is tyramine in which one of the amino hydrogens has been replaced by a 3,4-dihydroxybenzyl group.] |
| norbelladine(1+) | CHEBI_134001 | [An organic cation obtained by protonation of the secondary amino group of norbelladine; major species at pH 7.3.] |
| 4'-O-methylnorbelladine | CHEBI_80667 | [A phenethylamine alkaloid that is norbelladine in which the phenolic hydrogen at position 4' has been replaced by a methyl group.] |
| 4'-O-methylnorbelladine(1+) | CHEBI_133993 | [An organic cation obtained by protonation of the secondary amino group of 4'-O-methylnorbelladine; major species at pH 7.3.] |
| 5-L-Glutamyl-D-glutamyl-peptide | CHEBI_80660 | |
| DNA 2,6-diamino-5-formamido-3,4-dihydro-4-oxopyrimidine | CHEBI_80661 | |
| mannopine | CHEBI_80662 | [A hexitol derivative that is D-mannitol in which the hydroxy group at position 1 is replaced by the alpha-amino group of L-glutamine. It is produced in crown gall tumours induced in a wide range of dicotyledenous plants by Agrobacterium tumefaciens.] |
| amino acid opine | CHEBI_83229 | [Any opine whose structure is based on the condensation of an amino acid with a carbohydrate or a keto-acid.] |
| hexitol derivative | CHEBI_63430 | [An alditol derivative that is formally obtained from a hexitol.] |
| dicarboxylic acid monoamide | CHEBI_35735 | |
| Plastoquinone-1 | CHEBI_80663 | |
| prenylquinone | CHEBI_26255 | [A quinone substituted by a polyprenyl-derived side-chain. Prenylquinones occur in all living cells. Due to their amphiphilic character, they are mainly located in biological membranes where they function as electron and proton carriers in the photosynthetic and respiratory electron transport chains. Some prenylquinones also perform more specialised roles sucy as antioxidants and enzyme cofactors. Prenylquinones are classified according to ring structure: the main classes are menaquinones, phylloquinones, ubiquinones and plastoquinones.] |