Separation, structural determination and biological evaluation of the thymidylate synthase inhibitor 3,3-di-(4 '-hydroxyphenyl)-6(7)-chloro-1-oxo-1H,3H-naphtho[1,8-cd]pyran
Mp. Costi et al., Separation, structural determination and biological evaluation of the thymidylate synthase inhibitor 3,3-di-(4 '-hydroxyphenyl)-6(7)-chloro-1-oxo-1H,3H-naphtho[1,8-cd]pyran, J HETERO CH, 36(4), 1999, pp. 1043-1048
The chloro substituted 3,3-di-(4'-hydroxyphenyl)-1-oxo-1H,3H-naphtho[1,8-cd
]pyran was synthesized in a 40/60 mixture of C-6 or C-7 substituted isomers
, respectively. The two isomers were separated by hplc. The X-ray crystal s
tructure of the mixture was obtained. Both the mixture and the single isome
rs were tested against Lactobacillus Casei thymidylate synthase. The X-ray
analysis clearly revealed co-crystallization of the two isomeric species. T
he apparent Ki of the mixture was 0.8 muM, while those of the C-6 and C-7 s
ubstituted isomers were 0.42 and 0.52 muM, respectively, thus showing that
the position of the chlorine in the naphthalene ring was not critical for e
nzymatic activity.