PT  - JOURNAL ARTICLE
AU  - V H DuVernay
AU  - D Eubanks
AU  - R Perales
AU  - A W Prestayko
AU  - S T Crooke
TI  - The antitumor effects of anthracyclines. II. The stereospecificity of the carbomethoxy group at position 10 of the class II anthracycline molecule.
DP  - 1982 Jan 01
TA  - Molecular Pharmacology
PG  - 196--203
VI  - 21
IP  - 1
4099  - http://molpharm.aspetjournals.org/content/21/1/196.short
4100  - http://molpharm.aspetjournals.org/content/21/1/196.full
SO  - Mol Pharmacol1982 Jan 01; 21
AB  - The effects of marcellomycin, musettamycin, and their respective position 10 epimers mimimycin and collinemycin were compared in several systems both in vivo and in vitro. The results of these studies showed that the epimerization of the carbomethoxy-group at position 10 of the Class II anthracycline aglycone resulted in a 3-fold to 20-fold decrease in DNA-binding ability. The reduced DNA binding ability of these compounds is correlated with a 2-fold to 17-fold decrease in whole cellular nucleic acid synthesis inhibitory potency, a 2-fold to 4-fold decrease in vitro antitumor potency, and a 4-fold to 32-fold reduction in in vivo antitumor potency. These results further support the concept that a major portion of the antitumor activity of Class II anthracyclines is related to their avidity for DNA interactions and resultant disruption of normal template function. Previous studies from this laboratory have demonstrated that the 10-carbomethoxy group is essential for nucleolar RNA synthesis inhibition and Class II anthracycline antitumor activity. The current study further demonstrates that the stereochemical orientation of the carbomethoxy group at position 10 of the aglycone is also important in conferring Class II anthracycline antitumor activity.