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All terms in CHEBI

Label	Id	Description
O(3)-{N-acetyl-beta-D-glucosaminyl-(1->3)-beta-D-galactosyl-(1->3)-[N-acetyl-beta-D-glucosaminyl-(1->6)]-N-acetyl-alpha-D-galactosaminyl}-L-threonine residue	CHEBI_139612	[An L-alpha-amino acid residue derived from O(3)-{N-acetyl-beta-D-glucosaminyl-(1->3)-beta-D-galactosyl-(1->3)-[N-acetyl-beta-D-glucosaminyl-(1->6)]-N-acetyl-alpha-D-galactosaminyl}-L-threonine.]
L-threonine residue	CHEBI_30013
calcidiol 3-O-(beta-D-glucuronide)	CHEBI_139613	[A steroid glucosiduronic acid that is calcidiol in which the hydroxy hydrogen at position 3 has been replaced by a beta-D-glucuronyl residue.]
calcidiol 3-O-(beta-D-glucuronate)	CHEBI_139278	[A steroid glucuronide anion that is the conjugate base of calcidiol 3-O-(beta-D-glucuronide) arising from deprotonation of the carboxylic acid function; major species at pH 7.3.]
ascr#1(1-)	CHEBI_139614	[A monocarboxylic acid anion resulting from the deprotonation of the carboxy group of ascr#1. The conjugate base of ascr#1 and the major species at pH 7.3.]
ascr#1	CHEBI_78786	[An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (6R)-6-hydroxyheptanoic acid with ascarylopyranose (the alpha anomer). It is a major component of the dauer pheromone, used by the nematode Caenorhabditis elegans as a population-density signal to promote entry into an alternate larval stage, the nonfeeding and highly persistent dauer diapause. It has also been found in Pristionchus pacificus and the sour paste nematode Panagrellus redivivus.]
ascr#10(1-)	CHEBI_139615	[A monocarboxylic acid anion resulting from the deprotonation of the carboxy group of ascr#10. The conjugate base of ascr#10 and the major species at pH 7.3.]
ascr#10	CHEBI_78838	[An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (8R)-8-hydroxynonanoic acid with ascarylopyranose (the alpha anomer). A metabolite of the nematode Caenorhabditis elegans, it is the direct biosynthetic precursor to ascr#3. It has also been detected in the sour paste nematode, Panagrellus redivivus.]
ascr#10-CoA	CHEBI_139616	[CoA ester of ascr#10]
ascr#10-CoA(4-)	CHEBI_139617	[Conjugate base of ascr#10-CoA]
ascr#11(1-)	CHEBI_139618	[Conjugate base of ascr#11]
ascr#11	CHEBI_78743	[An (omega-1)-hydroxy fatty acid ascaroside consisting of ascarylopyranose linked glycosidically to the alcoholic hydroxy group of (3R)-3-hydroxybutanoic acid.]
ascr#11-CoA	CHEBI_139619	[CoA ester of ascr#11]
ascr#11-CoA(4-)	CHEBI_139620	[Conjugate base of ascr#11-CoA]
ascr#12(1-)	CHEBI_139621	[Conjugate base of ascr#12]
ascr#12	CHEBI_78841	[An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (5R)-5-hydroxyhexanoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematodes Caenorhabditis elegans and Pristionchus pacificus.]
ascr#12-CoA	CHEBI_139622	[CoA ester of ascr#12]
ascr#12-CoA(4-)	CHEBI_139623	[Conjugate base of ascr#12-CoA]
ascr#13(1-)	CHEBI_139624	[Conjugate base of ascr#13]
ascr#13	CHEBI_78851	[An (omega-1)-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of (2E,6R)-6-hydroxyhept-2-enoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.]