2020
DOI: 10.1080/00958972.2020.1844883
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Synthesis, crystal structures and biological activity of palladium(II) complexes with 1-methyl-1H-1,2,3,4-tetrazole-5-thiol and substituted 2,2′-bipyridines

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Cited by 3 publications
(1 citation statement)
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“…The presence of two purine-like nucleobases led to the strongest inhibitory effect against the PDE3A, while the insertion of a pyrimidine-like nucleobase also led to an enhanced inhibitory effect against the PDE3A and cytotoxicity activity against the HeLa and MCF-7 cell lines. Rashidipour et al [ 63 ] reported the effectiveness of 60 on SKBR-3 cell proliferation as being similar to that of cisplatin, and the DNA-binding assay uncovered the ability of the compound to bind to DNA and alter its structure (see Figure 12 ).…”
Section: Five-membered Heterocyclic Compoundsmentioning
confidence: 99%
“…The presence of two purine-like nucleobases led to the strongest inhibitory effect against the PDE3A, while the insertion of a pyrimidine-like nucleobase also led to an enhanced inhibitory effect against the PDE3A and cytotoxicity activity against the HeLa and MCF-7 cell lines. Rashidipour et al [ 63 ] reported the effectiveness of 60 on SKBR-3 cell proliferation as being similar to that of cisplatin, and the DNA-binding assay uncovered the ability of the compound to bind to DNA and alter its structure (see Figure 12 ).…”
Section: Five-membered Heterocyclic Compoundsmentioning
confidence: 99%