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All terms in CHEBI

Label	Id	Description
oscr#10(1-)	CHEBI_139965	[A hydroxy fatty acid ascaroside anion that is the conjugate base of oscr#10, obtained by deprotonation of the carboxy group; major species at pH 7.3.]
oscr#10	CHEBI_79134	[An omega-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of 9-hydroxynonanoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.]
oscr#10-CoA	CHEBI_139966	[An acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of oscr#12.]
oscr#10-CoA(4-)	CHEBI_139967	[An acyl-CoA(4-) obtained by deprotonation of the phosphate and diphosphate groups of oscr#10-CoA; major species at pH 7.3.]
oscr#12(1-)	CHEBI_139968	[A hydroxy fatty acid ascaroside anion that is the conjugate base of oscr#12, obtained by deprotonation of the carboxy group; major species at pH 7.3.]
oscr#12	CHEBI_79135	[An omega-hydroxy fatty acid ascaroside obtained by formal condensation of the alcoholic hydroxy group of 6-hydroxyhexanoic acid with ascarylopyranose (the alpha anomer). It is a metabolite of the nematode Caenorhabditis elegans.]
9-(6-deoxy-beta-D-allofuranosyl)-6-methyl-9H-purine	CHEBI_41867
CHEBI_41864	CHEBI_41864
sebacic acid	CHEBI_41865	[An alpha,omega-dicarboxylic acid that is the 1,8-dicarboxy derivative of octane.]
alpha,omega-dicarboxylic acid	CHEBI_28383
sebacate	CHEBI_132954	[A dicarboxylic acid anion obtained by deprotonation of at least one of the carboxy groups of sebacic acid.]
sebacate(2-)	CHEBI_76283	[A dicarboxylic acid dianion obtained by deprotonation of both carboxy groups of suberic acid; major species at pH 7.3.]
CHEBI_41866	CHEBI_41866
CHEBI_718203	CHEBI_718203
CHEBI_41860	CHEBI_41860
bkos#14	CHEBI_139906
bkos#14(1-)	CHEBI_139907	[Conjugate base of bkos#14]
bkos#14-CoA	CHEBI_139908	[CoA ester of bkos#14]
bkos#14-CoA(4-)	CHEBI_139909	[Conjugate base of bkos#14-CoA]
dexamethasone	CHEBI_41879	[A fluorinated steroid that is 9-fluoropregna-1,4-diene substituted by hydroxy groups at positions 11, 17 and 21, a methyl group at position 16 and oxo groups at positions 3 and 20. It is a synthetic member of the class of glucocorticoids.]