Terminology Service < Semantic Lookup Platform

All terms in CHEBI

Label	Id	Description
2-Phenyl-1,3-propanediol monocarbamate	CHEBI_80585
3-Carbamoyl-2-phenylpropionaldehyde	CHEBI_80586
phenylacetaldehydes	CHEBI_25973
cytosine	CHEBI_16040	[An aminopyrimidine that is pyrimidin-2-one having the amino group located at position 4.]
pyrimidine nucleobase	CHEBI_26432	[A nucleobase whose skeleton is derived from pyrimidine.]
phosphoguanidinoacetic acid	CHEBI_16034	[A guanidinoacetate having a phospho group attached to the primary amino part of the guanidine moiety.]
guanidinoacetic acids	CHEBI_24439
phosphoramide	CHEBI_17102	[A compound in which one or more of the OH groups of phosphoric acid have been replaced with an amino or substituted amino group. The term is commonly confined to the phosphoric triamides, P(=O)(NR2)3, since replacement of one or two OH groups produces phosphoramidic acids: P(=O)(OH)(NR2)2 , P(=O)(OH)2(NR2).]
phosphonatoguanidiniumylacetate(2-)	CHEBI_57612	[Dianion of phosphoguanidinoacetic acid having anionic carboxylic acid and phosphoramido groups and a protonated imino group.]
2'-hydroxy-2,3-dihydrodaidzein	CHEBI_16035	[A hydroxyisoflavanone that is 2,3-dihydrodaidzein with an additonal hydroxy substituent at position 2'.]
daidzein	CHEBI_28197	[A member of the class of 7-hydroxyisoflavones that is 7-hydroxyisoflavone substituted by an additional hydroxy group at position 4'.]
ethyl (S)-3-hydroxyhexanoate	CHEBI_16036	[The (S)-enantiomer of ethyl 3-hydroxyhexanoate.]
ethyl 3-hydroxyhexanoate	CHEBI_23997	[A fatty acid ester that is the ethyl ester of 3-hydroxyhexanoic acid.]
ethyl (R)-3-hydroxyhexanoate	CHEBI_16641	[The (R)-enantiomer of ethyl 3-hydroxyhexanoate.]
2-nitropropane	CHEBI_16037	[A secondary nitroalkane that is propane in which a hydrogen at position 2 has been replaced by a nitro group. Mainly used as a solvent (b.p. 120degreeC).]
secondary nitroalkane	CHEBI_139218	[A nitroalkane in which the nitro group, -NO2, is attached to a saturated carbon atom which has two other carbon atoms attached to it. Major microspecies at pH 7.3.]
carcinogenic agent	CHEBI_50903	[A role played by a chemical compound which is known to induce a process of carcinogenesis by corrupting normal cellular pathways, leading to the acquistion of tumoral capabilities.]
hepatotoxic agent	CHEBI_50908	[A role played by a chemical compound exihibiting itself through the ability to induce damage to the liver in animals.]
polar aprotic solvent	CHEBI_48358	[A solvent with a comparatively high relative permittivity (or dielectric constant), greater than ca. 15, and a sizable permanent dipole moment, that cannot donate suitably labile hydrogen atoms to form strong hydrogen bonds.]
acyldolichol	CHEBI_16030	[Dolichol esterified at the terminal hydroxy group.]