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All terms in CHEBI

Label	Id	Description
chelator	CHEBI_38161	[A ligand with two or more separate binding sites that can bind to a single metallic central atom, forming a chelate.]
5-bromo-4-chloro-3-indolyl beta-D-galactoside	CHEBI_75055	[An indolyl carbohydrate that is the beta-D-galactoside of 3-hydroxy-1H-indole in which the indole moiety is substituted at positions 4 and 5 by chlorine and bromine, respectively. It is used to test for the presence of an enzyme, beta-galactosidase, which cleaved the glycosidic bond to give 5-bromo-4-chloro-3-hydroxy-1H-indole, which immediately dimerises to give an intensely blue product.]
beta-D-galactoside	CHEBI_28034	[Any D-galactoside having beta-configuration at its anomeric centre.]
D-aldohexose derivative	CHEBI_63387	[An aldohexose derivative that has D-configuration.]
chromogenic compound	CHEBI_75050	[Colourless, endogenous or exogenous pigment precursors that may be transformed by biological mechanisms into coloured compounds. They are used in biochemical assays and in diagnosis as indicators, particularly in the form of enzyme substrates.]
N-[(5-acetyl-3-thienyl)methyl]-2-chloroacetamide semicarbazone	CHEBI_75056	[A semicarbazone obtained by formal condensation of the keto group of N-[(5-acetyl-3-thienyl)methyl]-2-chloroacetamide with the hydrazino group of semicarbazide.]
semicarbazone	CHEBI_87210	[A hydrazone resulting from the formal condensation of an aldehyde or ketone with the non-acylated nitrogen of semicarbazide or its substituted derivatives.]
semicarbazide	CHEBI_28306	[A monocarboxylic acid amide that is urea where one of the amino groups has been replaced with hydrazine.]
chloroacetic acid	CHEBI_27869	[A chlorocarboxylic acid that is acetic acid carrying a 2-chloro substituent.]
2-amino-5-chloro-cis,cis-muconate 6-semialdehyde zwitterion	CHEBI_75057	[An amino acid zwitterion obtained by transfer of a proton from the amino to the carboxy group of 2-amino-5-chloro-cis,cis-muconic 6-semialdehyde]
2-amino-5-chloro-cis,cis-muconic 6-semialdehyde	CHEBI_75320	[A muconic semialdehyde having amino and chloro substituents at positions 2 and 5 respectively.]
4-nitrophenyl phthalimidoacetate	CHEBI_75058	[A carboxylic ester obtained by formal condensation of the carboxy group of phthalimidoacetic acid with the phenolic hydroxy group of 4-nitrophenol.]
glycine	CHEBI_15428	[The simplest (and the only achiral) proteinogenic amino acid, with a hydrogen atom as its side chain.]
4-methyl-2-oxochromen-7-yl {[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-4-oxochromen-7-yl]oxy}acetate	CHEBI_75059	[A carboxylic ester obtained by formal condensation of that carboxy group of {[3-(2,3-dihydro-1,4-benzodioxin-6-yl)-2-methyl-4-oxochromen-7-yl]oxy}acetic acid with the hydroxy group of 7-hydroxy-4-methylchromen-2-one.]
one-colour indicator	CHEBI_50411	[A colour indicator that is colourless on one side of the transition interval.]
2-amino-5-chlorophenol	CHEBI_75051	[Phenol carrying amino and chloro substituents at positions 2 and 5 respectively. It is part of the degradation pathway of 4-chloronitrobenzene, CHEBI:34399.]
PC(18:1(11Z)/18:4(6Z,9Z,12Z,15Z))	CHEBI_89694
PC(18:1(11Z)/20:3(8Z,11Z,14Z))	CHEBI_89695
PC(18:1(11Z)/20:4(8Z,11Z,14Z,17Z))	CHEBI_89696
PC(18:1(11Z)/20:4(5Z,8Z,11Z,14Z))	CHEBI_89697