https://ack-signal.com/index.p....hp/three-new-p-couma
g., FL) had been investigated along with their mode of interactions with CT-DNA. All of the enamine derivatives (7a-o) with 86-168 µM IC50 values demonstrated stronger antiproliferative task than the beginning particles (3a-o) contrary to the cancer cells. While, among the enamine derivatives, the substances 7e, 7f, 7k and 7l exhibited higher cytotoxic effectiveness than the control drugs (5-fluorouracil and cisplatin) resistant to the Hep3B mobile line, these compounds didn't display any
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