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All terms in CHEBI

Label	Id	Description
Cer(d42:2)	CHEBI_85812	[A ceramide in which the acyl group and the sphingoid base contain a total of 42 carbon atoms and 2 double bonds.]
(R)-3-hydroxytetradecanoyl-CoA	CHEBI_74458	[A 3-hydroxy fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of (R)-3-hydroxytetradecanoic acid.]
(R)-3-hydroxytetradecanoyl-CoA(4-)	CHEBI_74277	[A 3-hydroxy fatty acyl-CoA(4-) obtained by deprotonation of the phosphate and diphosphate OH groups of (R)-3-hydroxytetradecanoyl-CoA.]
(R)-3-hydroxytetradecanoic acid	CHEBI_42539	[A 3-hydroxytetradecanoic acid that has R configuration at position 3. It plays an intermediate role in fatty acid biosynthesis.]
(R)-3-hydroxypalmitoyl-CoA	CHEBI_74459	[A 3-hydroxy fatty acyl-CoA that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of (R)-3-hydroxypalmitic acid.]
(R)-3-hydroxypalmitoyl-CoA(4-)	CHEBI_74278	[A 3-hydroxy fatty acyl-CoA(4-) obtained by deprotonation of the phosphate and diphosphate OH groups of (R)-3-hydroxypalmitoyl-CoA.]
(R)-3-hydroxypalmitic acid	CHEBI_38247
5-chloro-7-iodoquinolin-8-ol	CHEBI_74460	[A monohydroxyquinoline that is quinolin-8-ol in which the hydrogens at positions 5 and 7 are replaced by chlorine and iodine, respectively. It has antibacterial and atifungal properties, and is used in creams for the treatment of skin infections. It has also been investigated as a chelator of copper and zinc ions for the possible treatment of Alzheimer's disease.]
lysophosphatidylinositol 14:0(1-)	CHEBI_74461	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 14 carbons and zero double bonds.]
lysophosphatidyl-1D-myo-inositol(1-)	CHEBI_68498	[An anionic phospholipid obtained by deprotonation of the phosphate OH group of any lysophosphatidyl-1D-myo-inositol; major species at pH 7.3.]
lysophosphatidylinositol 14:1(1-)	CHEBI_74462	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 14 carbons and 1 double bond.]
lysophosphatidylinositol 16:0(1-)	CHEBI_74463	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 16 carbons and 0 double bonds.]
lysophosphatidylinositol 16:1(1-)	CHEBI_74464	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 16 carbons and 1 double bond.]
lysophosphatidylinositol 18:0(1-)	CHEBI_74465	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 18 carbons and 0 double bonds.]
lysophosphatidylinositol 18:1(1-)	CHEBI_74466	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 18 carbons and 1 double bond.]
lysophosphatidylinositol 18:1	CHEBI_90456	[A lysophosphatidyl-1D-myo-inositol in which the remaining acyl group (position not specified) contains 18 carbons and 1 double bond.]
lysophosphatidylinositol 20:1(1-)	CHEBI_74467	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 20 carbons and 0 double bonds.]
lysophosphatidylinositol 22:0(1-)	CHEBI_74468	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 22 carbons and 0 double bonds.]
lysophosphatidylinositol 26:0(1-)	CHEBI_74469	[A lysophosphatidyl-1D-myo-inositol(1-) in which the remaining acyl group (position not specified) contains 26 carbons and 0 double bonds.]
lysophosphatidylcholine 24:0	CHEBI_74470	[A lysophosphatidylcholine in which the remaining acyl group (position not specified) contains 24 carbons and 0 double bonds.]