2. Academic Validation
  3. Synthesis, docking and ADMET studies of novel chalcone triazoles for anti-cancer and anti-diabetic activity

Synthesis, docking and ADMET studies of novel chalcone triazoles for anti-cancer and anti-diabetic activity

  • Eur J Med Chem. 2015 Mar 26:93:564-73. doi: 10.1016/j.ejmech.2015.02.027.
Yakaiah Chinthala 1,  Sneha Thakur 1,  Shalini Tirunagari 1,  Srinivas Chinde 2,  Anand Kumar Domatti 3,  Niranjana Kumar Arigari 1,  Srinivas K V N S 1,  Sarfaraz Alam 4,  Kotesh Kumar Jonnala 5,  Feroz Khan 4,  Ashok Tiwari 3,  Paramjit Grover 2
Affiliations

Affiliations

  • 1 Natural Product Chemistry, CSIR-Central Institute of Medicinal and Aromatic Plants-Research Centre, Boduppal, Hyderabad 500092, India.
  • 2 Toxicology Unit, Biology Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India.
  • 3 Medicinal Chemistry and Pharmacology Division, CSIR-Indian Institute of Chemical Technology, Hyderabad 500007, India.
  • 4 Metabolic and Structural Biology Department, CSIR-CIMAP, Lucknow 226015, UP, India.
  • 5 Natural Product Chemistry, CSIR-Central Institute of Medicinal and Aromatic Plants-Research Centre, Boduppal, Hyderabad 500092, India. Electronic address: koteshkumarj@yahoo.com.
PMID: 25743216 DOI: 10.1016/j.ejmech.2015.02.027
Abstract

A series of novel chalcone-triazole derivatives were synthesized and screened for in vitro Anticancer activity on the human Cancer cell lines IMR32 (neuroblastoma), HepG2 (hepatoma) and MCF-7 (breast adenocarcinoma), DU-145 (prostate carcinoma), and A549 (lung adenocarcinoma). Among the tested compounds, 4r showed the most promising Anticancer activity in all the cell lines whereas, compounds 4c (IC50 65.86 μM), 4e (IC50 66.28 μM), 4o (IC50 35.81 μM), 4q (IC50 50.82 μM) and 4s (IC50 48.63 μM) showed better activity than the standard doxorubicin (IC50 69.33 μM) in A549 cell line alone. Rat intestinal α-glucosidase inhibitory activity of the synthesized derivatives showed 4m (IC50 67.77 μM), 4p (IC50 74.94 in μM) and 4s (IC50 102.10 μM) as most active compared to Others. The in silico docking of synthesized derivatives 4a-4t with DNA Topoisomerase IIα revealed the LibDock score in the range of 71.2623-118.29 whereas, compounds 4h, 4m, 4p and 4s with docking target α-glucosidase were in the range of 100.372-107.784.

Keywords

1,2,3-Triazoles; Anticancer activity; Chromanochalcones; Molecular docking; α-Glucosidase inhibition.

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