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Substance chimique
A maltose that has β-configuration at the reducing end anomeric centre.
The β-isomer of mannobiose.
A melibiose that has β-configuration at the anomeric hydroxy group.
A bile acid anion resulting from deprotonation of the carboxy group of β-muricholic acid (i.e. the conjugate base of β-muricholic acid). It is the major species at pH 7.3.
A member of the class of muricholic acids in which the hydroxy groups at positions 6 and 7 both have β configuration.
A member of the class of choloyl-CoAs that results from the formal condensation of the thiol group of coenzyme A with the carboxy group of β-muricholic acid.
A steroidal acyl-CoA(4−) obtained by deprotonation of phosphate and diphosphate functions of β-muricholoyl-CoA; major species at pH 7.3.
A monoterpene that is octa-1,6-diene bearing methylene and methyl substituents at positions 3 and 7 respectively.
An extended flavonoid resulting from the formal fusion of a benzene ring with the f side of flavone.
An α-amino acid ester obtained by the fromal condensation of N -acetylphenylalanine with 2-naphthol.
A limonoid found in Azadirachta indica .
A 4,4a-dimethyl-6-(prop-1-en-2-yl)-2,3,4,4a,5,6,7,8-octahydronaphthalen-2-ol with (2 S ,4 R ,4a S ,6 R ) stereochemistry.
The trans -stereoisomer of ocimene.
A triterpenoid that is ethane in which each carbon has been substituted by a (4a S ,6 S ,8a S )-6-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,5,6,7,8,8a-octahydronaphthalen-1-yl group.
An oxyketone with the general formula R 2 C(=O) (R≠H) where one or more of the R groups contains an oxy (‒O‒) group and the oxy and carbonyl groups are separated by a carbon atom.
A morphinane alkaloid with formula C 17 H 22 N 2 O 3 .
An organic heterotetracyclic compound that is α-peltatin in which the phenolic hydroxy group of the 4-hydroxy-3,5-dimethoxyphenyl substitutent had been converted into the corresponding methyl ether.
One of a pair of phellandrene cyclic monoterpene double-bond isomers in which one double bond is exocyclic ( cf . α-phellandrene, where both of them are endoocyclic).
