2015
DOI: 10.1016/j.saa.2014.09.136
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A mononuclear zinc(II) complex with piroxicam: Crystal structure, DNA- and BSA-binding studies; in vitro cell cytotoxicity and molecular modeling of oxicam complexes

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Cited by 25 publications
(10 citation statements)
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“…The target sequences of virus and fluorescent dyes labeled complementary probe DNA were summarized in Table 2 . MOF could bind with DNA in a variety of ways, mainly including covalent, electrostatic, insert, or groove bonding ( Jannesari et al, 2015 ; Liu et al, 2020b ; Yang et al, 2019b ) ( Fig. 3 C).…”
Section: Viral Nucleic Acid Detection Based On Mofmentioning
confidence: 99%
“…The target sequences of virus and fluorescent dyes labeled complementary probe DNA were summarized in Table 2 . MOF could bind with DNA in a variety of ways, mainly including covalent, electrostatic, insert, or groove bonding ( Jannesari et al, 2015 ; Liu et al, 2020b ; Yang et al, 2019b ) ( Fig. 3 C).…”
Section: Viral Nucleic Acid Detection Based On Mofmentioning
confidence: 99%
“…For example meloxicam acted as monodentate nitrogen donor ligand to Pt II , and coordinated in a bidentate fashion to Ni II through the thiazole nitrogen and amidate oxygen atoms . Similarly, piroxicam coordinated monodentately to Ru II (arene), by its pyridyl nitrogen, and it can act also as an N,O ‐chelator through its amidate oxygen and pyridyl nitrogen to metal ions such as Co II , Ru II , Cu II , and Zn II . In case of hard Sn IV , piroxicam coordinated as an O,O ‐chelator via its enolate and amidate oxygen atoms, whereas the analogous benzothiazine lornoxicam coordinated as a tridentate N , N,O ‐chelator by employing an enolate oxygen and pyridyl and amide nitrogen donors.…”
Section: Introductionmentioning
confidence: 99%
“…In case of hard Sn IV , piroxicam coordinated as an O,O ‐chelator via its enolate and amidate oxygen atoms, whereas the analogous benzothiazine lornoxicam coordinated as a tridentate N , N,O ‐chelator by employing an enolate oxygen and pyridyl and amide nitrogen donors. Many of the metal complexes of oxicam‐based ligands have demonstrated biological applications, such as in DNA cleavage, or as antitumor agents …”
Section: Introductionmentioning
confidence: 99%
“…Synthesis of Bi-complex was carried out according to previously reported procedure with minor modifications [2]. Na-piroxicam was made by adding 0.001 g of NaOH in ethanolic solution of piroxicam (0.09 g, 0.3 mmol).…”
Section: Synthesismentioning
confidence: 99%
“…Piroxicam [4-hydroxy-2-methyl-N-2-(pyridyl)-2H-1,2benzothiazine-3-carboxamide 1,1-dioxide] is a very effective antiinflammatory drug and biologically active as an analgesic, antipyretic, hypoglycemic and antihypertensive [1]. Chemo preventive and chemo suppressive effects in different cancers i.e colon, lung and breast cancers have also been studied [2]. This important member of oxicam class is a strong chelator for d-block divalent metal ions of the periodic table, via nitrogen atoms from the pyridyl the amide oxygen atom or thiazolyl rings [3].…”
mentioning
confidence: 99%