All terms in CHEBI
| Label | Id | Description |
|---|---|---|
| (3S)-3-methyl-2-oxo-3-phenylpropanoate | CHEBI_74119 | [A 2-oxo monocarboxylic acid anion that is the conjugate base of (3S)-3-methyl-2-oxo-3-phenylpropanoic acid, obtained by deprotonation of the carboxy group.] |
| (3S)-3-methyl-2-oxo-3-phenylpropanoic acid | CHEBI_74122 | [A 2-oxo monocarboxylic acid that is pyruvic acid in which two of the methyl hydrogens are substituted by phenyl and methyl groups (the S-enantiomer).] |
| tricin 7-O-neohesperidoside | CHEBI_131777 | [A glycosyloxyflavone that is 3',5'-di-O-methyltricetin (tricin) in which the phenolic hydrogen at position 7 has been replaced by a neohesperidosyl group.] |
| neohesperidoside | CHEBI_25495 | [A glycoside containing alpha-L-rhamnopyranosyl-(1->2)-beta-D-glucopyranosyl residue as the sugar unit.] |
| indole-5-carboxylic acid | CHEBI_131778 | [An indolecarboxylic acid in which the carboxy group is the only substituent and is located at position 5.] |
| isoorientin 2''-O-glucoside | CHEBI_131779 | [A tetrahydroxyflavone that consists of isoorientin having a beta-glucosyl residue attached at position 2''.] |
| isoorientin | CHEBI_17965 | [A flavone C-glycoside consisting of luteolin having a beta-D-glucosyl residue at the 6-position.] |
| xestospongin C | CHEBI_131784 | [An organic heteropentacyclic compound that is isolated from the marine sponge Xestospongia exigua.] |
| IP3 receptor antagonist | CHEBI_131186 | [An antagonist that binds to and deactivates IP3 receptors.] |
| Ro 5-3335 | CHEBI_131785 | [A 1,4-benzodiazepinone that is nordazepam in which the phenyl substituent has been replaced by a 1H-pyrrol-2-yl group. It inhibits gene expression in HIV-1 at the transcriptional level through interference with Tat-mediated transactivation.] |
| HIV-1 Tat inhibitor | CHEBI_131791 | [An inhibitor of gene expression of human immunodeficiency virus type 1 (HIV-1) at the transcriptional level through interference with Tat-mediated transactivation.] |
| anti-HIV-1 agent | CHEBI_64947 | [An anti-HIV agent that destroys or inhibits the replication of HIV-1, the more infective and more virulent of the two types of HIV virus.] |
| RUNX1 inhibitor | CHEBI_131789 | [An inhibitor that interferes with RUNX1 (runt-related transcription factor 1), a transcription factor protein that regulates the differentiation of haematopoietic stem cells into mature blood cells.] |
| Gly-Met | CHEBI_74120 | [A dipeptide formed from glycine and L-methionine residues.] |
| Gly-Met zwitterion | CHEBI_74393 | [A peptide zwitterion obtained by transfer of a proton from the carboxy to the amino terminus of Gly-Met.] |
| O-dodecanedioylcarnitine | CHEBI_74121 | [An O-acylcarnitine having 11-carboxyundecanoyl as the acyl substituent.] |
| dodecanedioic acid | CHEBI_4676 | [An alpha,omega-dicarboxylic acid that is dodecane in which the methyl groups have been oxidised to the corresponding carboxylic acids.] |
| dopamine receptor D2 antagonist | CHEBI_131787 | [An antagonist that binds to and deactivates the dopamine receptor D2, the main receptor for all antipsychotic drugs.] |
| 2-hydroxyisobutanoyl-CoA(4-) | CHEBI_131780 | [An acyl-CoA(4-) obtained by deprotonation of the phosphate and diphosphate OH groups of 2-hydroxyisobutanoyl-CoA; major species at pH 7.3] |
| 2-hydroxyisobutanoyl-CoA | CHEBI_132116 | [A hydroxyacyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of 2-hydroxyisobutanoic acid.] |