Novel cyanoacetamide integrated phenothiazines: Synthesis, characterization, computational studies and in vitro antioxidant and anticancer evaluations

被引:37
作者
Krishnan, Kannan Gokula [1 ]
Kumar, Chandran Udhaya [1 ]
Lim, Wei-Meng [2 ]
Mai, Chun-Wai [2 ,3 ]
Thanikachalam, Punniyakoti, V [2 ]
Ramalingan, Chennan [1 ]
机构
[1] Kalasalingam Acad Res & Educ, Sch Adv Sci, Dept Chem, Krishnankoil 626126, Tamil Nadu, India
[2] Int Med Univ, Sch Pharm, 126 Jalan Jalil Perkasa 19, Kuala Lumpur 57000, Malaysia
[3] Int Med Univ, Ctr Canc & Stem Cell Res, IRDI, 126 Jalan Jalil Perkasa 19, Kuala Lumpur 57000, Malaysia
关键词
Anticancer; Antioxidant; Computation; Cyanoacetamide; Phenothiazine; HETEROCYCLES; PLATFORM; DESIGN;
D O I
10.1016/j.molstruc.2019.127037
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of novel phenothiazine based cyanoacrylamides 6a-d have been synthesized from phenothiazine through multistep synthetic strategy. The structure of these novel molecules (6a-d) has been determined by FT-IR, H-1 NMR and C-13 NMR spectral techniques. Computational studies were carried out for the synthesized compounds 6a-d using DFT method with B3LYP/6-311G(d,p) basis set. The target compounds 6a-d have been screened for their in vitro antioxidant and anticancer activity. The antioxidant data revealed that the compounds 6c and 6d exhibited high radical scavenging activity with IC50 value of 37.32 and 39.07 mu M, respectively. Furthermore, all the synthesized compounds displayed significant in-vitro anticancer activity against both the pancreatic tumor cells AsPC1 and SW1990. Particularly, the compound 6c exhibited the highest activity among the molecules tested against both the tumor cells viz., AsPC1 and SW1990. (C) 2019 Elsevier B.V. All rights reserved.
引用
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页数:10
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