Synthesis and in vitro antiproliferative activity of diphenyl(sulphonylpiperidin-4-yl)methanol derivatives

被引:0
|
作者
S. B. Benaka Prasad
K. Vinaya
C. S. Ananda Kumar
Sanjay Swarup
K. S. Rangappa
机构
[1] University of Mysore,Department of Studies in Chemistry
[2] National University of Singapore,Department of Biological Sciences
来源
关键词
Diphenyl(pyridin-4-yl)methanol; Sulfonyl chloride; MTT assay; Antiproliferative activity; Cancer therapy; Cell proliferation;
D O I
暂无
中图分类号
学科分类号
摘要
A series of novel diphenyl(piperidin-4-yl)methanol derivatives 10(a–n) were synthesized and characterized by 1H NMR, LC/MS, FTIR, and elemental analyses. All the synthesized compounds were evaluated for cell proliferation by MTT assay. The antiproliferative effects of the synthesized compounds were tested against viable human skin fibroblast cell line and carcinoma cell lines, namely HeLa cells, HT-29 cells, MCF-7 cells, and HepG-2 cells in comparing the positive and negative control. Among the synthesized compounds, (10b) and (10g) have been identified as potent antiproliferative agents.
引用
收藏
页码:220 / 235
页数:15
相关论文
共 50 条
  • [41] Synthesis, characterization and in vitro antiproliferative effects of isosteviol derivatives
    Qi, Xin-Xin
    Wang, Pan-Pan
    Cui, Lan-Tian
    Jin, Mei
    Zhao, Long-Xuan
    Li, Gao
    JOURNAL OF ASIAN NATURAL PRODUCTS RESEARCH, 2024, 26 (07) : 812 - 823
  • [42] Synthesis and antiproliferative activity of novel 4-substituted-phenoxy-benzamide derivatives
    Sun, Chi-Yu
    Li, Yang-Sheng
    Shi, Ai-Long
    Li, Ya-Fei
    Cao, Rui-Fang
    Ding, Huai-Wei
    Yin, Qing-Qing
    Zhang, Li-Juan
    Zheng, Hua-Chuan
    Song, Hong-Rui
    CHINESE CHEMICAL LETTERS, 2015, 26 (10) : 1307 - 1310
  • [43] Synthesis and antiproliferative activity of novel 4-azasteroidal-17-hydrazone derivatives
    Chen, Shao-Rui
    Wu, Hao
    Zhao, Hai-Yan
    Zhang, Yu-Mei
    Li, Peng-Qi
    Zhao, Lian-Mei
    JOURNAL OF CHEMICAL RESEARCH, 2019, 43 (3-4) : 130 - 134
  • [44] Synthesis and antiproliferative activity of novel 4-substituted-phenoxy-benzamide derivatives
    Chi-Yu Sun
    Yang-Sheng Li
    Ai-Long Shi
    Ya-Fei Li
    Rui-Fang Cao
    Huai-Wei Ding
    Qing-Qing Yin
    Li-Juan Zhang
    Hua-Chuan Zheng
    Hong-Rui Song
    ChineseChemicalLetters, 2015, 26 (10) : 1307 - 1310
  • [45] Synthesis, in vitro antiproliferative and antimycobacterial activity of thiazolidine-2,4dione and hydantoin derivatives
    Angelova, V. T.
    Vacheva, V.
    Vassilev, N.
    Buyukliev, R.
    Mihaylova, R.
    Momekov, G.
    BULGARIAN CHEMICAL COMMUNICATIONS, 2017, 49 (03): : 643 - 651
  • [46] Synthesis and antiproliferative activity in vitro of new 2-aminobenzimidazole derivatives.: Part 2
    Nawrocka, W
    Sztuba, B
    Liszkiewicz, H
    Kowalska, MW
    Wietrzyk, J
    Nevozhai, D
    Opolski, A
    POLISH JOURNAL OF CHEMISTRY, 2005, 79 (04) : 709 - 716
  • [47] Synthesis and In Vitro Antiproliferative Activity of Novel Androst-5-ene Triazolyl and Tetrazolyl Derivatives
    Kadar, Zalan
    Kovacs, Dora
    Frank, Eva
    Schneider, Gyula
    Huber, Judit
    Zupko, Istvan
    Bartok, Tibor
    Woelfling, Janos
    MOLECULES, 2011, 16 (06) : 4786 - 4806
  • [48] DESIGN, SYNTHESIS, IN VITRO ANTIPROLIFERATIVE ACTIVITY EVALUATION OF 2-ALICANOYLAMIDOTHIOPHENE-3-CARBOXAMIDE DERIVATIVES
    Zhang, Jiefeng
    Guan, Fengjie
    Qiu, Jiakun
    Fang, Yanfen
    Yu, Lifang
    Li, Jingya
    Yang, Fan
    Zhang, Xiongwen
    Li, Jia
    Tang, Jie
    HETEROCYCLES, 2016, 92 (12) : 2145 - 2165
  • [49] Synthesis and in vitro antiproliferative and antibacterial activity of new thiazolidine-2,4-dione derivatives
    Trotsko, Nazar
    Przekora, Agata
    Zalewska, Justyna
    Ginalska, Grazyna
    Paneth, Agata
    Wujec, Monika
    JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2017, 33 (01) : 17 - 24
  • [50] Synthesis and in vitro antiproliferative activity of novel pyrazolo[3,4-d]pyrimidine derivatives
    Abdou, Nermin S.
    Serya, Rabah A. T.
    Esmat, Ahmed
    Tolba, Mai F.
    Ismail, Nasser S. M.
    Abouzid, Khaled A. M.
    MEDCHEMCOMM, 2015, 6 (08) : 1518 - 1534