The dinuclear organoplatinum(IV) compound {Pt(CH(3))(3)}(2)(μ-I)(2)(μ-adenine) (abbreviated Pt(2)ad), obtained by treating cubic [Pt(CH(3))(3)(μ(3)-I)](4) with two equivalents of adenine, was isolated and structurally characterized by single crystal X-ray diffraction. The National Cancer Institute Developmental Therapeutics Program's in vitro sulforhodamine B assays showed Pt(2)ad to be particularly cytotoxic against central nervous system cancer cell line SF-539, and human renal carcinoma cell line RXF-393. Furthermore, Pt(2)ad displayed some degree of cytotoxicity against non-small cell lung cancer (NCI-H522), colon cancer (HCC-2998, HCT-116, HT29, and SW-620), melanoma (LOX-IMVI, MALME-3M, M14, MDA-MB-435, SK-MEL-28, and UACC-62), ovarian cancer (OVCAR-5), renal carcinoma (A498), breast cancer (BT-549 and MDA-MB-468), and triple-negative breast cancer (MDA-MB-231).
Synthesis, Structure and Anticancer Activity of a Dinuclear Organoplatinum(IV) Complex Stabilized by Adenine.
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作者:O'Brie Alisha M, Howard William A, Wheeler Kraig A
| 期刊: | bioRxiv | 影响因子: | 0.000 |
| 时间: | 2024 | 起止号: | 2024 Feb 18 |
| doi: | 10.1101/2024.02.14.580361 | ||
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