Antibiotics and Antimycotics

5-chloro-2-hydroxypyridine acts as donor ligand and exists in zwitterionic form, i.e. 5-chloropyridinium-2-olate in copper complexes Usually used to study the effect of dicumarol on xanthine dehydrogenase and mechanism of mitomycin C bioreduction by

5-chloro-2-hydroxypyridine acts as donor ligand and exists in zwitterionic form, i.e. 5-chloropyridinium-2-olate in copper complexes Usually used to study the effect of dicumarol on xanthine dehydrogenase and mechanism of mitomycin C bioreduction by

5-Nitroisoquinoline reacted with vinylmagnesium bromide to form a number of pyrroloisoquinolines. 5-Nitroisoquinoline derivatives (potential antimalarial drugs) were evaluated for mutagenic (MUT) and chromosome-damaging (CHR) activities by the

5-Nitroisoquinoline reacted with vinylmagnesium bromide to form a number of pyrroloisoquinolines. 5-Nitroisoquinoline derivatives (potential antimalarial drugs) were evaluated for mutagenic (MUT) and chromosome-damaging (CHR) activities by the

5-Nitroisoquinoline reacted with vinylmagnesium bromide to form a number of pyrroloisoquinolines. 5-Nitroisoquinoline derivatives (potential antimalarial drugs) were evaluated for mutagenic (MUT) and chromosome-damaging (CHR) activities by the

5-Nitroisoquinoline reacted with vinylmagnesium bromide to form a number of pyrroloisoquinolines. 5-Nitroisoquinoline derivatives (potential antimalarial drugs) were evaluated for mutagenic (MUT) and chromosome-damaging (CHR) activities by the

5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid.

5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid.

5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid.

5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid.

5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid.

6-(2,3-dihydro-1,4-benzodioxin-5-yl)-N-[3-[(dimethylamino)methyl]phenyl]-2-methoxy-pyridin-3-amine.