Terminology Service < Semantic Lookup Platform

All terms in CHEBI

Label	Id	Description
himachalol	CHEBI_5719
himachalane sesquiterpenoid	CHEBI_36746
hippeastrine	CHEBI_5724	[An indole alkaloid isolated from the Amaryllidaceae family and has been shown to exhibit cytotoxic activity.]
2-[(2S)-2-[(2R)-2-morpholinyl]-2-phenylethyl]phenol	CHEBI_125470
CHEBI_5725	CHEBI_5725
(2S)-2-[[(2S)-2-[[(2S)-2-amino-3-methyl-1-oxobutyl]amino]-3-methyl-1-oxobutyl]amino]-3-methylbutanoic acid	CHEBI_125471
Hircinol	CHEBI_5726
N-(6-acetamidohexyl)acetamide	CHEBI_125472
Hirsutic acid C	CHEBI_5727
(4-chlorophenyl)-[4-(8-nitro-5-quinolinyl)-1-piperazinyl]methanone	CHEBI_125473
himbacine	CHEBI_5720	[A piperidine alkaloid that is decahydronaphtho[2,3-c]furan-1(3H)-one substituted by a methyl group at position 3 and a 2-[(2R,6S)-1,6-dimethylpiperidin-2-yl]ethenyl group at position 4. It has been isolated from the bark of Australian magnolias.]
piperidine alkaloid	CHEBI_26147
muscarinic antagonist	CHEBI_48876	[A drug that binds to but does not activate muscarinic cholinergic receptors, thereby blocking the actions of endogenous acetylcholine or exogenous agonists.]
4-aminoimidazole	CHEBI_16607	[An aminoimidazole that is 1H-imidazole substituted by an amino group at position 4.]
4-[3-(dimethylamino)propylamino]phenol	CHEBI_125474
hinokiflavone	CHEBI_5721	[A biflavonoid that is apigenin substituted by a 4-(5,7-dihydroxy-4-oxo-4H-chromen-2-yl)phenoxy group at position 6. A diflavonyl ether, it is isolated from Rhus succedanea and has been found to possess significant cytotoxic potential.]
hydroxyflavone	CHEBI_24698	[Any flavone in which one or more ring hydrogens are replaced by hydroxy groups.]
biflavonoid	CHEBI_50128	[A flavonoid oligomer that is obtained by the oxidative coupling of at least two units of aryl-substituted benzopyran rings or its substituted derivatives, resulting in the two ring systems being joined together by a single atom or bond.]
apigenin	CHEBI_18388	[A trihydroxyflavone that is flavone substituted by hydroxy groups at positions 4', 5 and 7. It induces autophagy in leukaemia cells.]
5alpha-cholest-8-en-3beta-ol	CHEBI_16608	[A cholestanoid that is 5alpha-cholestane substituted by a beta-hydroxy group at position 3.]