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All terms in CHEBI

Label	Id	Description
3-methylbutanoic acid [(2S,3S,4R,6S)-6-[[(2R,3S,4R,5R,6S)-6-[[(4R,5S,6S,7R,9R,10R,16R)-4-acetyloxy-10-hydroxy-5-methoxy-9,16-dimethyl-2-oxo-7-(2-oxoethyl)-1-oxacyclohexadeca-11,13-dien-6-yl]oxy]-4-(dimethylamino)-5-hydroxy-2-methyl-3-oxanyl]oxy]-3-hydroxy-2,4-dimethyl-4-oxanyl] ester	CHEBI_94651
2-(4,5,6,7-tetraiodo-1,3-dioxo-2-isoindolyl)acetic acid	CHEBI_94656
N,N-dimethyl-9-[3-(1-piperazinyl)propylidene]-2-thioxanthenesulfonamide	CHEBI_94657
2-amino-5-[(4-hydroxyphenyl)methylidene]-4-thiazolone	CHEBI_94658
(5S)-5-methylimidazolidine-2,4-dione	CHEBI_94659
2-methylpropanethioic acid S-[7-oxo-7-[(4-phenyl-2-thiazolyl)amino]heptyl] ester	CHEBI_94652
LSM-5644	CHEBI_94653
(2R)-2-[2-[[(2R)-1-hydroxybutan-2-yl]amino]ethylamino]-1-butanol	CHEBI_94654
2,2-dimethylpropanoyloxymethyl (2S,5S,6R)-6-(azepan-1-ylmethylideneamino)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate	CHEBI_94655
formamidines	CHEBI_51917	[Amidines with the general formula R(1)N=CHNR(2)R(3) (R(1), R(2), R(3) can be H).]
penicillanic acid ester	CHEBI_51212
pivaloyloxymethyl ester	CHEBI_136685	[A acetal obtained from a carboxylic acid by replacement of the hydrogen attached to the carboxy group by a pivaloyloxymethyl group.]
Mycinamicin VIII	CHEBI_80020
Protomycinolide IV	CHEBI_80021
Tubulysin E	CHEBI_80037
Spinosyn H	CHEBI_80038
Spinosyn J	CHEBI_80039
syringolin A	CHEBI_80033	[A syrbactin that has a (3E,9E)-2,7-dioxo-1,6-diazacyclododeca-3,9-diene skeleton that is substituted by an isopropyl group at position 5 and by a [(2S)-2-({[(1S)-1-carboxy-2-methylpropyl]carbamoyl}amino)-3-methylbutanoyl]nitrilo group at the 8-pro-S position. It is produced by the pathogenic bacterium Pseudomonas syringae pv. syringae.]
syrbactin	CHEBI_82671	[A class of azamacrocyclic natural products with a 2,7-dioxo-1,6-diazacyclododecane skeleton that includes the syringolin, glidobactin and cepafungin natural product families. In addition to their related molecular frameworks, members of the class share similar biosynthesis pathways and identical modes-of-action, being irreversible proteasome inhibitor that inhibit all three activities of eukaryotic proteasomes.]
homodetic cyclic peptide	CHEBI_24613	[A homodetic cyclic peptide is a cyclic peptide in which the ring consists solely of amino-acid residues in peptide linkages.]