A. Sanjeev, N. Naresh Reddy, M. Kumara Swamy, Rohini Rondla, S. R. Reddy, P. Muralidhar Reddy
{"title":"新型Co(II)、Ni(II)、Cu(II)和zn (II)配合物(E)-4-((喹啉-8-酰基)甲基)苯-1,2,3-三醇配体的合成、表征及体外抗癌研究","authors":"A. Sanjeev, N. Naresh Reddy, M. Kumara Swamy, Rohini Rondla, S. R. Reddy, P. Muralidhar Reddy","doi":"10.14233/ajomc.2021.ajomc-p345","DOIUrl":null,"url":null,"abstract":"Herein, a new tridentate (NNO) Schiff base ligand, (E)-4-[(quinoline-8-ylimino)methyl]benzene-1,2,3-\ntriol derived from the condensation of 8-aminoquinoline with 2,3,4-trihydroxy benzaldehyde is reported.\nThe ligand was complexed with certain metal ions like Co(II) (1), Ni(II) (2), Cu(II) (3), Zn(II) (4) and\nwere characterized by various spectroscopic and analytical techniques such as FT-IR, UV-Vis, 1H\nNMR, 13C NMR, ESI-Mass, ESR, elemental analysis and magnetic susceptibility. Spectral data revealed\noctahedral geometry for cobalt(II), nickel(II), copper(II) complexes and tetrahedral geometry for zinc(II)\ncomplex. All the metal(II) complexes along with the Schiff base ligand were screened for their anticancer\nactivities. The CT-DNA binding studies revealed high binding propensity for metal complexes with\nKb values 1.50 × 104 M-1 for 1; 3.62 × 104 M-1 for 2; 2.53 × 104 M-1 for 3 and 1.8 × 104 M-1 for 4,\nrespectively. Anticancer studies against A549 & MCF-7 demonstrated excellent antiproliferative activity\nwith IC50 values in the range 17.62-48.82 μM. A standard drug cisplatin was employed to compare the\nactivity of metal complexes. The complexes exhibited remarkable antitumour activity due to their\nhigh binding ability with DNA. It is interesting to observe that the complexes did not produce any\ncytotoxicity towards the normal cell lines.","PeriodicalId":8846,"journal":{"name":"Asian Journal of Organic & Medicinal Chemistry","volume":"27 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis, Characterization and in vitro Anticancer Studies of New Co(II), Ni(II), Cu(II) and\\nZn(II) Complexes of (E)-4-((Quinoline-8-ylimino)methyl)benzene-1,2,3-triol Ligand\",\"authors\":\"A. Sanjeev, N. Naresh Reddy, M. Kumara Swamy, Rohini Rondla, S. R. Reddy, P. Muralidhar Reddy\",\"doi\":\"10.14233/ajomc.2021.ajomc-p345\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, a new tridentate (NNO) Schiff base ligand, (E)-4-[(quinoline-8-ylimino)methyl]benzene-1,2,3-\\ntriol derived from the condensation of 8-aminoquinoline with 2,3,4-trihydroxy benzaldehyde is reported.\\nThe ligand was complexed with certain metal ions like Co(II) (1), Ni(II) (2), Cu(II) (3), Zn(II) (4) and\\nwere characterized by various spectroscopic and analytical techniques such as FT-IR, UV-Vis, 1H\\nNMR, 13C NMR, ESI-Mass, ESR, elemental analysis and magnetic susceptibility. Spectral data revealed\\noctahedral geometry for cobalt(II), nickel(II), copper(II) complexes and tetrahedral geometry for zinc(II)\\ncomplex. All the metal(II) complexes along with the Schiff base ligand were screened for their anticancer\\nactivities. The CT-DNA binding studies revealed high binding propensity for metal complexes with\\nKb values 1.50 × 104 M-1 for 1; 3.62 × 104 M-1 for 2; 2.53 × 104 M-1 for 3 and 1.8 × 104 M-1 for 4,\\nrespectively. Anticancer studies against A549 & MCF-7 demonstrated excellent antiproliferative activity\\nwith IC50 values in the range 17.62-48.82 μM. A standard drug cisplatin was employed to compare the\\nactivity of metal complexes. The complexes exhibited remarkable antitumour activity due to their\\nhigh binding ability with DNA. It is interesting to observe that the complexes did not produce any\\ncytotoxicity towards the normal cell lines.\",\"PeriodicalId\":8846,\"journal\":{\"name\":\"Asian Journal of Organic & Medicinal Chemistry\",\"volume\":\"27 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-12-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic & Medicinal Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14233/ajomc.2021.ajomc-p345\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Asian Journal of Organic & Medicinal Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14233/ajomc.2021.ajomc-p345","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis, Characterization and in vitro Anticancer Studies of New Co(II), Ni(II), Cu(II) and
Zn(II) Complexes of (E)-4-((Quinoline-8-ylimino)methyl)benzene-1,2,3-triol Ligand
Herein, a new tridentate (NNO) Schiff base ligand, (E)-4-[(quinoline-8-ylimino)methyl]benzene-1,2,3-
triol derived from the condensation of 8-aminoquinoline with 2,3,4-trihydroxy benzaldehyde is reported.
The ligand was complexed with certain metal ions like Co(II) (1), Ni(II) (2), Cu(II) (3), Zn(II) (4) and
were characterized by various spectroscopic and analytical techniques such as FT-IR, UV-Vis, 1H
NMR, 13C NMR, ESI-Mass, ESR, elemental analysis and magnetic susceptibility. Spectral data revealed
octahedral geometry for cobalt(II), nickel(II), copper(II) complexes and tetrahedral geometry for zinc(II)
complex. All the metal(II) complexes along with the Schiff base ligand were screened for their anticancer
activities. The CT-DNA binding studies revealed high binding propensity for metal complexes with
Kb values 1.50 × 104 M-1 for 1; 3.62 × 104 M-1 for 2; 2.53 × 104 M-1 for 3 and 1.8 × 104 M-1 for 4,
respectively. Anticancer studies against A549 & MCF-7 demonstrated excellent antiproliferative activity
with IC50 values in the range 17.62-48.82 μM. A standard drug cisplatin was employed to compare the
activity of metal complexes. The complexes exhibited remarkable antitumour activity due to their
high binding ability with DNA. It is interesting to observe that the complexes did not produce any
cytotoxicity towards the normal cell lines.