Term Name: rifamycin SV hemiaminal
Synonyms: (2S,12Z,14E,16S,17S,18R,19R,20R,21S,22R,23S,24E)-5,7,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,6,11-trioxo-1,2,6,7-tetrahydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate
Definition: A member of the class of rifamycins that is rifamycin SV in which the enol hydroxy group at position 6 has undergone tautomerisation to the corresponding ketone, with concomitant hydroxylation at position 7 (where the lactam nitrogen is attached) to give the corresponding hemiaminal.
Ontology: ChEBI [CHEBI:142732]  ( EBI )

Relationships
is a type of: acetate ester aromatic ketone cyclic ketal enol lactam macrocycle N-acyl hemiaminal naphthofuran organic heterotetracyclic compound rifamycins
has_functional_parent: rifamycin SV
inverse is_conjugate_base_of: rifamycin SV hemiaminal(1-)
is_conjugate_acid_of: rifamycin SV hemiaminal(1-)