郑懿雅, 高怡生. 肿瘤的化学治疗——ⅩⅩⅩⅧ.氯霉素同型物的合成J. 药学学报, 1979, 14(10): 628-631.
引用本文: 郑懿雅, 高怡生. 肿瘤的化学治疗——ⅩⅩⅩⅧ.氯霉素同型物的合成J. 药学学报, 1979, 14(10): 628-631.
Zheng Yiya Kao Yeesheng, . TUMOUR CHEMOTHERAPHY ⅩⅩⅩⅧ SYNTHESIS OF ANALOGUES OF CHLORAMPHENICOLJ. Acta Pharmaceutica Sinica, 1979, 14(10): 628-631.
Citation: Zheng Yiya Kao Yeesheng, . TUMOUR CHEMOTHERAPHY ⅩⅩⅩⅧ SYNTHESIS OF ANALOGUES OF CHLORAMPHENICOLJ. Acta Pharmaceutica Sinica, 1979, 14(10): 628-631.

肿瘤的化学治疗——ⅩⅩⅩⅧ.氯霉素同型物的合成

TUMOUR CHEMOTHERAPHY ⅩⅩⅩⅧ SYNTHESIS OF ANALOGUES OF CHLORAMPHENICOL

  • Abstract: In view of the tumour inhibitory effect of AT-16, a Schiff's base prepared by condensing 1-p-nitrophenyl-2-aminopropandiol (1, 3) with p-bis (2-chloroethyl) aminobenzaldehyde, several other Schiff's bases were prepared by condensing 1-p-methoxyphenyl2-aminopropane diol (1, 3) with aromatic aldehyde containing N, N, -bis (2-chloroethyl) amino group. Analogys of chloramphenicol in which the nitro group was replaced by methoxy group and the dichloroacetyl group by the moiety of plant growth inhibitors, 2, 4-dichlorophenoxyacetic acid and 2, 4, 5-trichlorophenoxyacetic acid, were also reported.Among these compounds, it was found that the Schiff's base of 4-N, N-bis (2-chloroethyl) amino-3-methyl-benzaldehyde(Ⅳb) possessed a moderate inhibiting action against S-180 in mice.

     

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