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Dimethyl sulfoxide (dmso)

Manufactured by Bruker

DMSO is a solvent commonly used in analytical and preparative applications. It has a high dielectric constant, making it a useful solvent for a variety of organic and inorganic compounds. DMSO is compatible with many laboratory instruments and can be used to dissolve samples for analysis.

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3 protocols using dimethyl sulfoxide (dmso)

1

Detailed Analytical Methods for Novel Compounds

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DMEM, FBS, L-glutamine, penicillin-streptomycin and SYBR Gold (molecular biology grade) were procured from Invitrogen. Caspase-3 assay kit was procured from Thermo Scientific. All single stranded oligonucleotide sequences (Table S1) and the primers for RT-PCR (Table S2) were purchased from Integrated DNA technologies (IDT). DMSO, MTT, Hoechst 33258 and DAPI were obtained from Sigma Aldrich (Merck). All other chemicals were of analytical reagent grade and used without further purification unless otherwise stated. Ultrapure water (double-distilled) obtained from Milli-Q Gradient ultrapure water system (Millipore) and was used in all experiments. 1H and 13C NMR spectra were recorded on Bruker AV-400 MHz spectrometer with chemical shifts reported as parts per million (ppm) (in DMSO-d6, tetramethylsilane as an internal standard) at 20 °C. UV-vis absorption and emission spectra were measured in quartz cuvettes of 1 cm path length. HRMS were obtained on Agilent Technologies 6538 UHD Accurate-Mass Q-TOF LC/MS spectrometer. HPLC traces were obtained from Shimadzu analytical HPLC.
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2

Synthesis and Characterization of Fluorescent Probes

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All chemicals and reagents were purchased from commercial suppliers and used without further purification. All solvents were purified by a solvent purifier prior to ACC1 and ACC2 probe synthesis by standard methods. Stock solutions of the probe were prepared by dissolving in DMSO (Sigma-Aldrich, St. Louis, MO, USA). A full description of the synthesis of the probe and its intermediates is presented in the ESI Methods section. The synthesis results were characterized by 1H-NMR, 13C-NMR, and ESI high-resolution mass spectrometry. 1H-NMR and 13C-NMR spectra were recorded using a Bruker 600 MHz spectrometer using CDCl3, methanol-d4, and DMSO-d6 as solvents. The chemical shifts are reported in ppm, and the coupling constant is given in Hz. The spectra of the probe in the absorption and emission spectra were recorded using a UV-vis spectrophotometer (S-3100) and a fluorescence spectrophotometer (FluoroMate FS-2) with a 1 cm quartz cell, respectively. The fluorescence quantum yield was determined using Rhodamine 6G (Φ = 0.98 in MeOH) as the reference.
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3

Synthesis and Characterization of Dehydroacetic Acid-based Chalcones

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DMEM, foetal bovine serum (FBS) and l-glutamine were purchased from Sigma-Aldrich, USA. Penicillin was purchased from HiMedia, India. HEK-293 and T24 cells were procured from NCCS, Pune, India. MTT reagent (3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide was purchased from HiMedia, India. DMSO was purchased from HiMedia, India.
All melting points are uncorrected. The Infra-Red (IR) spectra for all the compounds were recorded on an FT-IR instrument (JASCO 4700). 1H NMR spectra were recorded on a BRUKER 400 spectrometer at 300 MHz in CDCl3 or DMSO-d6 using TMS as the internal standard, while 13C NMR was recorded on the same spectrometer at 75 MHz. Mass spectra were recorded on LCMS 8045, SHIMADZU Scientific. Elemental analysis was carried out using FLASH 2000 HT Analyzer. UV–visible spectrum was recorded using Cary 5000 Model, NIR-UV Spectrometer. Silica gel (ACME, 100–200 mesh) was used for column chromatography. Reagent grade solvents were used as per the standard protocols. The starting materials such as dehydroacetic acid, sarcosine, isatin and hydrazine were purchased commercially and dehydroacetic acid-based chalcones were synthesized as described in the literature46 (link).
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