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

Citation
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
Citations number
22
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF HETEROCYCLIC CHEMISTRY
ISSN journal
0022152X → ACNP
Volume
36
Issue
4
Year of publication
1999
Pages
1043 - 1048
Database
ISI
SICI code
0022-152X(199907/08)36:4<1043:SSDABE>2.0.ZU;2-R
Abstract
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.