Synthesis of Piperidine Conjugated Dihydroquinazolin-4(1H)-ones and their Antiproliferative Activity, Molecular Docking Studies and DFT Calculations

被引:6
作者
Narasimhamurthy, Kereyagalahally Honneshappa [1 ]
Chandra [2 ]
Swaroop, Toreshettahally Ramesh [1 ]
Jagadish, Swamy [3 ]
Rangappa, Kanchugarakoppal Subbegowda [4 ]
机构
[1] Manasagangotri Univ Mysore, Dept Studies Organ Chem, Mysuru 570006, India
[2] Natl Inst Engn, Dept Phys, Mysuru 570008, India
[3] Univ Mysore, Dept Studies Biochem, Manasagangotri 570006, Mysuru, India
[4] Univ Mysore, Dept Studies Chem, Manasagangotri 570006, Mysuru, India
关键词
Piperidine-conjugated dihydroquinazolinones; cytotoxicity; human colorectal carcinoma; colon adenocarcinoma; VEGFR2 tyrosine kinase inhibitors; DFT; TUMOR-GROWTH; INHIBITS ANGIOGENESIS; POTENT INHIBITOR; IN-VITRO; DERIVATIVES; RECEPTOR; CANCER; APOPTOSIS; SERIES;
D O I
10.2174/1570180816666190613120349
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Background: Xanthatin, fluoropyrimidine and thienopyrimidine, pyrazolopyrimidine, pyrimidine carboxamides, and SKLB1002 are reported as VEGFR2 tyrosine kinase inhibitors. Recently, many studies related to different heterocycles conjugated with dihydroquinazolinones are known to have very good biological activities. In this study, we are intended to explore the cytotoxic studies of piperidine conjugated dihydroquinazolinones against colorectal/colon cancer cell lines and along with molecular docking studies and DFT calculations. Methods: The colorectal/colon cell lines HCT116 and A549 cell lines were treated with these compounds and cytotoxic activities were evaluated by MTT dye uptake method. We performed molecular modelling for compound 3d using the Auto Dock software. The binding of compound 3d with target proteins was studied with the collection of experimentally determined PDB database. Optimized geometry by DFT calculations was performed with B3LYP/6-31G (d) basis set. Results: Piperidine-conjugated dihydroquinazolinone analogues displayed anticancer activity. Particularly, the compound 3d with electron-with drawing substituents on a phenyl ring showed significant cytotoxicity against HCT116 and A549 cell lines. Molecular docking studies proved that the compound 3d has good fitting by forming hydrogen bonds with amino acid residues at the active sites of VEGFR2. The HOMO, LUMO, their energies and UV visible spectrum were predicted using DFT calculations. Conclusion: Four piperidine-conjugated dihydroquinazolinones were synthesized and evaluated against colorectal and colon cancer cell lines. Compound 3d significantly inhibited the growth of HCT116 and A549. Molecular docking studies displayed good fitting of compound 3d by forming different H-bonds with the amino acid at the active sites of the VEGFR2 target. Using a theoretical approach, we optimized HOMO and LUMO plots for the compound 3d.
引用
收藏
页码:85 / 93
页数:9
相关论文
共 46 条
  • [1] [Anonymous], OMCIJ
  • [2] [Anonymous], THESIS
  • [3] [Anonymous], INT J CHEM
  • [4] [Anonymous], IJNTPS
  • [5] [Anonymous], J MOL MED CLIN APPL
  • [6] Discovery of Potent VEGFR-2 Inhibitors based on Furopyrimidine and Thienopyrimidne Scaffolds as Cancer Targeting Agents
    Aziz, Marwa A.
    Serya, Rabah A. T.
    Lasheen, Deena S.
    Abdel-Aziz, Amal Kamal
    Esmat, Ahmed
    Mansour, Ahmed M.
    Singab, Abdel Nasser B.
    Abouzid, Khaled A. M.
    [J]. SCIENTIFIC REPORTS, 2016, 6
  • [7] Baldazzi C, 1996, ARZNEIMITTELFORSCH, V46, P911
  • [8] Phase II study of sunitinib as second-line treatment for advanced gastric cancer
    Bang, Yung-Jue
    Kang, Yoon-Koo
    Kang, Won K.
    Boku, Narikazu
    Chung, Hyun C.
    Chen, Jen-Shi
    Doi, Toshihiko
    Sun, Yan
    Shen, Lin
    Qin, Shukui
    Ng, Wai-Tong
    Tursi, Jennifer M.
    Lechuga, Maria J.
    Lu, Dongrui Ray
    Ruiz-Garcia, Ana
    Sobrero, Alberto
    [J]. INVESTIGATIONAL NEW DRUGS, 2011, 29 (06) : 1449 - 1458
  • [9] Constitutive Endocytosis of VEGFR2 Protects the Receptor against Shedding
    Basagiannis, Dimitris
    Christoforidis, Savvas
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2016, 291 (32) : 16892 - 16903
  • [10] Novel 7-methoxy-6-oxazol-5-yl-2,3-dihydro-1H-quinazolin-4-ones as IMPDH inhibitors
    Birch, HL
    Buckley, GM
    Davies, N
    Dyke, HJ
    Frost, EJ
    Gilbert, PJ
    Hannah, DR
    Haughan, AF
    Madigan, MJ
    Morgan, T
    Pitt, WR
    Ratcliffe, AJ
    Ray, NC
    Richard, MD
    Sharpe, A
    Taylor, AJ
    Whitworth, JM
    Williams, SC
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2005, 15 (23) : 5335 - 5339