Chandra, Dattatray and Banerjee, Priyabrata and Saha, Sourav Kr and Bhanda, Sujit and Patil, Rajendra and Sunita Salunke-Gawalia, Sunita (2019) n-alkylamino analogs of Vitamin K3: Electrochemical, DFT and anticancer activity of their oxidized and one electron reduced form. Journal of Molecular Structure, 1179. pp. 443-452.

Full text not available from this repository.

Abstract

Synthesis, characterization and anticancer activity of reduced form of n-alkylamino analogs of Vitamin K3 (1Na to 8Na) are undertaken. Molecular structure and molecular association of oxidized form of 2-ethylamino-3-methyl-1,4-naphthoquinone (2) and 2-hexylamino-3-methyl-1,4-naphthoquinone (6) were studied by single crystal X-ray analysis. 2 crystallize in monoclinic C2/c and 6 in P21 space group. The reduced form of eight homologated analogs of 2-(n-alkylamino)-3-methyl-1,4-naphthoquinone (1Na to 8Na) were synthesized using sodium metal as reductant at 0 °C in methanol. The formations of naphthosemiquinone radical in 1 to 6 have been confirmed from their EPR spectra. Polycrystalline powder X-band EPR spectra of 1 to 6 shows signals ∼2.0020 ± 0.0026 at 133 K. Anticancer activity of 2-(n-alkylamino)-3-methyl-1,4-naphthoquinone (1Na to 8Na) and one electron reduced forms have been evaluated against breast cancer (HeLa) cell line, 1 and 1Na showed promising anticancer activity.

Item Type:	Article
Subjects:	Chemistry
Depositing User:	Dr. Arup Kr. Nandi
Date Deposited:	15 Jan 2021 07:12
Last Modified:	15 Jan 2021 07:12
URI:	http://cmeri.csircentral.net/id/eprint/652

Actions (login required)

View Item