Journal of Medicinal Chemistry p. 2114 - 2117 (1986)
Update date:2022-08-02
Topics:
Morris-Natschke, Susan
Surles, Jefferson R.
Daniel, Larry W.
Berens, Michael E.
Modest, Edward J.
Piantadosi, Claude
Five sulfur-containing phospholipid analogues (compounds 1-5) of alkyl lysophospholipid (1-O-alkyl-2-O-methyl-rac-glycero-3-phosphocholine, ALP) were synthesized and tested for inhibition of neoplastic cell proliferation with two human ovarian carcinoma cell lines in a clonogenic assay and with the HL-60 promyelocytic leukemia cell line.Compared with 1-O-octadecyl-2-O-methyl-rac-glycero-3-phosphocholine (ET-18-OMe), the most active reference analogue, these thio analogues are at least as active against HL-60 cells, and the 1-S-hexadecyl-2-O-ethyl analogue (2) is twice as active in the clonogenic assays.
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(1986)