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All terms in CHEBI

Label	Id	Description
LSM-4916	CHEBI_94289
(Z)-4-methoxy-2,2-bipyridine-6-carbaldehyde oxime	CHEBI_69235	[A pyridine alkaloid that is 2,2'-bipyridine substituted by a methoxy group at position 4 and a (Z)-(hydroxyimino)methyl group at position 6. It has been isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus.]
falcarindiol	CHEBI_69236
pinusolide	CHEBI_69237
caerulomycin K	CHEBI_69230	[A pyridine alkaloid that is 2-phenylpyridine substituted by a methoxy group at position 4 and a (E)-(hydroxyimino)methyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.]
caerulomycin A	CHEBI_69231	[A pyridine alkaloid that is 2,2'-bipyridine substituted by a methoxy group at position 4 and a (E)-(hydroxyimino)methyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.]
caerulomycin C	CHEBI_69232	[A pyridine alkaloid that is 2,2'-bipyridine substituted by methoxy groups at positions 3 and 4 and a (E)-(hydroxyimino)methyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.]
caerulomycinamide	CHEBI_69233	[A pyridine alkaloid that is 2,2'-bipyridine substituted by a methoxy group at position 4 and an aminocarbonyl group at position 6. Isolated from the marine-derived actinomycete Actinoalloteichus cyanogriseus, it exhibits antineoplastic activity.]
(3S)-3-hydroxy-D-aspartic acid	CHEBI_60893	[A 3-hydroxy-D-aspartic acid in which the carbon bearing the hydroxy substituent has S configuration.]
3-hydroxy-D-aspartic acid	CHEBI_60887	[A 3-hydroxyaspartic acid that has R configuration at the carbon bearing the amino group.]
(3S)-3-hydroxy-D-aspartate(1-)	CHEBI_60894	[A D-alpha-amino acid anion which is obtained from (3S)-3-hydroxy-D-aspartic acid by formal deprotonation of both carboxyl groups and protonation of the amino group.]
(3R)-3-hydroxy-L-aspartic acid	CHEBI_17576
2-(4-chlorophenyl)-6-(phenacylthio)-2,3-dihydrothiopyran-4-one	CHEBI_94274
(3R)-3-hydroxy-L-aspartate(1-)	CHEBI_58196	[Conjugate base of (3R)-3-hydroxy-L-aspartic acid arising from deprotonation of the two carboxy groups and protonation of the amino group; major species at pH 7.3.]
4,6-dimethyl-N-phenyl-2-quinolinamine	CHEBI_94275
2-[[3-[[2-(dimethylamino)phenyl]methyl]-2-pyridin-4-yl-1,3-diazinan-1-yl]methyl]-N,N-dimethylaniline	CHEBI_94276
poly(hexafluorobutyl methacrylamide) polymer	CHEBI_60896	[A polyacrylamide polymer, composed of poly(hexafluorobutyl methacrylamide) macromolecules.]
poly(hexafluorobutyl methacrylamide) macromolecule	CHEBI_53381	[A macromolecule composed of repeating N-(1,1,2,2,3,3-hexafluorobutyl)-2-methylpropanamide units.]
N-[4-[[(4-chlorophenyl)-oxomethyl]amino]phenyl]-2-hydroxybenzamide	CHEBI_94277
(3R)-3-hydroxy-D-aspartic acid	CHEBI_60897	[A 3-hydroxy-D-aspartic acid in which the carbon bearing the hydroxy substituent has R configuration.]