Synthesis and antitumor activity of 2-deamino- and N2-(.gamma.-hydroxypropyl)actinomycin D

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Abstract
2-Deamino- and N2-(.gamma.-hydroxypropyl)actinomycin D were synthesized by modification of the parent actinomycin D molecule at the 2 position of the phenoxazinone moiety. The common intermediate was 2-deamino-2-chloroactinomycin D. Catalytic hydrogenation of this material afforded the 2-deamino derivative while treatment with .gamma.-hydroxypropylamine yielded the N2-(.gamma.-hydroxypropyl) derivative. These 2-substituted actinomycin D derivates were less potent in microbiological assays than the parent compound. Evaluation of activity in vivo against 3 murine tumor systems indicated that optimal dose levels of 2-deaminoactinomycin D were 50 times greater than toxic dose levels of actinomycin D. N2-(.gamma.-Hydroxypropyl)actinomycin D exhibited antitumor activity similar to the parent compound.

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