000 a
999 _c16256
_d16256
003 OSt
005 20220208113052.0
008 220208b xxu||||| |||| 00| 0 eng d
040 _aAIKTC-KRRC
_cAIKTC-KRRC
100 _915916
_aKotha, Anusha
245 _aDithiocarbamate substituted phenothiazine derivatives: in silicoexperiments, synthesis,and biological evaluation
250 _aVol.13(10)
260 _aM P
_bInnovare Academic Sciences Pvt Ltd
_c2021
300 _a25-30p.
520 _aObjective: The present study was designed to study the anticancer activity of a series of novel analogs of phenothiazine with dithiocarbamate as a side chain.Methods: A novel series of derivatives containing dithiocarbamate as a side chain at the tenth position of phenothiazine nucleus were synthesized, characterized by spectral analysis, and evaluated for their antimitotic and antioxidant activity using germinated Bengal gram seeds and 2,2-diphenyl-1-picrylhydrazyl (DPPH)method,respectively. A quantitative estimate of drug-likeness was also performed,which calculated the molecular properties and screenedthe molecules based on drug-likeness rules.Further, molecular docking study was performed for finding the binding affinity with tubulin protein to rationalize their anticancer activity.Results: The results revealed that the antioxidant activity of compounds3e, 3g, 3i, 3j andstandard Ascorbic acid were 10 mmol, 14 mmol, 16 mmol, 16 mmoland 35 mmol,respectively. Further compounds 3e, 3g, 3h and 3i have shown promising antimitotic activity. Compound 3i (-9 K. Cal/mol) showed the highest binding energies towards tubulin protein when compared to standard drug colchicine (-8.6 K. Cal/mol). Among all, compound 3i showed promising antimitoticand antioxidant activity, which correlated with insilico docking studies.Conclusion: Dithiocarbamate substituted phenothiazine derivatives proved to be encouraging leads as tubulin inhibitors.
650 0 _94639
_aPHARMACEUTICS
700 _915917
_a Muni Sireesha, S.
773 0 _tInternational journal of pharmacy and pharmaceutical science
_dBhopal Innovare Academic Sciences Pvt Ltd
_x2656-0097
856 _uhttps://innovareacademics.in/journals/index.php/ijpps/article/view/41882/25491
_yClick here
942 _2ddc
_cAR