All terms in CHEBI
| Label | Id | Description |
|---|---|---|
| 5-methyluridine 5'-monophosphate residue | CHEBI_74675 | [A nucleotide residue derived from 5-methyluridine 5'-monophosphate.] |
| senegasaponin b | CHEBI_74448 | [A triterpenoid saponin isolated from Polygala senega var latifolia and has been shown to exhibit hypoglycemic activity.] |
| 4-methoxycinnamic acid | CHEBI_48541 | [A methoxycinnamic acid having a single methoxy substituent at the 4-position on the phenyl ring.] |
| N(6)-methyladenosine 5'-monophosphate(1-) residue | CHEBI_74449 | [An organic anionic group obtained by deprotonation of the free phosphate OH group of N(6)-methyladenosine 5'-monophosphate residue.] |
| N(6)-methyladenosine 5'-monophosphate residue | CHEBI_74676 | [A nucleotide residue derived from N(6)-methyladenosine 5'-monophosphate.] |
| N-(15Z)-tetracosenoylsphingosine | CHEBI_74450 | [An N-tetracosenoylsphingosine in which the double bond in the ceramide acyl group is located at position 15 (the Z-geoisomer.] |
| N-tetracosenoylsphingosine | CHEBI_74457 | [An acylsphingosine in which the acyl moiety contains 24 carbons and 1 double bond.] |
| (R)-3-hydroxylauroyl-CoA | CHEBI_74451 | [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-hydroxydodecanoic acid.] |
| (R)-3-hydroxylauroyl-CoA(4-) | CHEBI_74276 | [An (R)-3-hydroxyacyl-CoA(4-) obtained by deprotonation of the phosphate and diphosphate OH groups of (R)-3-hydroxylauroyl-CoA.] |
| (R)-3-hydroxylauric acid | CHEBI_43197 | [The (R)-enantiomer of 3-hydroxylauric acid. An intermediate in fatty acid biosynthesis.] |
| NMNH | CHEBI_74452 | [A nicotinamide mononucleotide that is obtained by addition of hydride to position 4 on the pyridine ring of NMN(+).] |
| NMNH(2-) | CHEBI_90832 | [An organophosphate oxoanion arising from deprotonation of the phosphate OH groups of NMNH; major species at pH 7.3.] |
| senegasaponin a | CHEBI_74453 | [A triterpenoid saponin isolated from Polygala senega var latifolia and has been shown to exhibit hypoglycemic activity.] |
| 5-aminomethyl-2-thiouridine 5'-monophosphate zwitterion residue | CHEBI_74454 | [A zwitterionic group obtained by transfer of a proton from the phosphate to the amino group of 5-aminomethyl-2-thiouridine 5'-monophosphate residue.] |
| zwitterionic group | CHEBI_64768 | [A neutral group having formal unit electrical charges of opposite sign on non-adjacent atoms.] |
| 5-aminomethyl-2-thiouridine 5'-monophosphate residue | CHEBI_74677 | [A nucleotide residue derived from 5-aminomethyl-2-thiouridine 5'-monophosphate.] |
| 5-methylaminomethyl-2-thiouridine 5'-monophosphate zwitterion residue | CHEBI_74455 | [A zwitterionic group obtained by transfer of a proton from the amino to the phosphate group of 5-methylaminomethyl-2-thiouridine 5'-monophosphate residue.] |
| 5-methylaminomethyl-2-thiouridine 5'-monophosphate residue | CHEBI_74679 | [A nucleotide residue derived from 5-methylaminomethyl-2-thiouridine 5'-monophosphate.] |
| 4-hydroxy-5-methyl-3-furanone | CHEBI_74456 | [A member of the class of furans that is 5-methyl-2,3-dihydrofuran with a hydroxy group at position 4 and a keto group at position 3.] |
| 5-methyl-2,3-dihydrofuran | CHEBI_51677 |