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Method Article

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay

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DOI:

10.3791/61950

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February 9th, 2021

In This Article

Summary

Here, we describe a bioassay using 3-(4′,5′-dimethylthiazol-2′-yl)-2,5- diphenyltetrazolium bromide (MTT) to test previously synthesized spirocyclic oximes.

Abstract

Spirocyclic heterocycles have recently been reported in literature to be potential drugs for cancer therapy. The synthesis of these novel orthogonal ring systems is challenging. An efficient methodology to synthesize these compounds was recently published that described the solid phase synthesis in four steps rather than the previously reported five steps. The advantage of this shorter synthesis is the elimination of the use of toxic reagents. Low-loading Regenerating Michael (REM) linker-based resin was found to be crucial in the synthesis as high-loading versions prevented the addition of reagents containing bulky phenyl and aromatic side chains. The colorimetric 3-(4′,5′-dimethylthiazol-2′-yl)-2,5- diphenyltetrazolium bromide (MTT) assay was used to examine the cytotoxicity of micromolar concentrations of these novel spirocyclic molecules in vitro. MTT is readily available commercially and produces relatively fast, reliable results, making this assay ideal for these spirocyclic heterocycles. Orthogonal ring structures as well as furfurylamine (a precursor in the synthesis method containing a similar 5-member ring motif) were tested.

Introduction

Small-molecule inhibition of the interaction of E3 ubiquitin-ligase mouse double minute 2 homolog (MDM2) with p53 is known to restore p53-mediated induction of tumor cell apoptosis1,2,3. MDM2 is a negative regulator of the p53 pathway and is often overexpressed in cancer cells4,5,6,7,8,9. Recent crystallographic and biochemical studies have revealed that small molecules containing....

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Protocol

NOTE: Several chemicals and biological reagents used in this protocol are toxic and carcinogenic. Consult relevant material safety data sheets (MSDS) prior to use. Use appropriate personal protective gears (Occupational Safety and Health Administration-approved safety goggles, proper gloves, lab coats, full-length pants, and closed-toe shoes) prior to starting the experiment. In addition, adopt appropriate safety practices when performing synthesis and handling toxic chemicals and reagents (fume hood).

1. Solid phase synthesis of spirocyclic heterocycles 6 and 7

NOTE: Synthesis was based on previously published wor....

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Results

Spirocyclic oximes 6 and 7 were synthesized using a modified protocol (Figure 1). Michael addition of furfurylamine to an REM linker 1b afforded polymer-bound resin 2. The progress of the reaction was monitored by infrared (IR) spectroscopy by detecting the disappearance of the α,β-unsaturated ester at 1722 cm-1 (Figure 3). Spirocyclic-bound resin 4 was formed from 2 via a transient intermediate 3. Methanolic hydrolysis of 4 produced 3-[(3E)-.......

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Discussion

The synthesis of the spirocyclic compounds was based on previous research conducted by this laboratory, but with some modifications (Figure 1)11,12. The progress of each reaction step was monitored by IR spectroscopy. Michael addition of the REM linker 1 with furfurylamine afforded polymer-bound 2 (IR 1722 cm-1 → 1731 cm-.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

This work was funded by a grant from the Faculty Research Council to K.S.H. (Office of Research and Grants, Azusa Pacific University-USA). A.N.G. and J.F.M. are recipients of the Scholarly Undergraduate Research Experience (SURE) Fellowship. S.K.M. and B.M.R. are recipients of the STEM Research Fellowship Grants (Center for Research in Science, Azusa Pacific University-USA). We are grateful to Dr. Matthew Berezuk and Dr. Philip Cox for guidance on the bioassays.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
CELLS
COS-7 cells (ATCC CRL-1651)ATCCCRL-1651African green monkey kidney cells
CHEMICALS
1-BromooctaneSigma-Aldrich152951Alkyl-halide
AllylbromideSigma-Aldrich337528Alkyl-halide
BenzylbromideSigma-AldrichB17905Alkyl-halide
CisplatinCayman Chemical13119Cytotoxicity control
Dichloromethane (DCM)Sigma-Aldrich270997Solvent
Dimethylformamide (DMF)Sigma-Aldrich227056Solvent
Dimethylsulfoxide (DMSO)Sigma-Aldrich276855Solvent
DMEM, high glucose, with L-glutamineGenesee Scientific25-500Cell culture media
FBS (Fetal bovine serum)Sigma-AldrichF4135Cell culture media
FurfurylamineAcros Organics119800050reagent 
IodomethaneSigma-Aldrich289566Alkyl-halide
MethanolSigma-Aldrich34860Solvent
MTT ((3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide)EMD MilliporeCalbiochem 475989-1GMReagent
Phosphate-buffered Saline (PBS)Genesee Scientific25-507Cell culture media
REM ResinNova Biochem8551010005Polymer support; 0.500 mmol/g loading
trans-β-nitrostyreneSigma-AldrichN26806Nitro-olefin reagent
TolueneSigma-Aldrich244511Solvent
Triethylamine (TEA)Sigma-AldrichT0886Reagent for beta-elimination
Trimethylsilyl chloride (TMSCl)Sigma-Aldrich386529Reagent; CAUTION - highly volatile; creates HCl gas
GLASSWARE/INSTRUMENTATION
25 mL solid-phase reaction vesselChemglassCG-1861-02Glassware with filter
96 Well plate readerPromega (Turner Biosystems)9310-011Instrument
AVANCE III NMR SpectrometerBrukerN/AInstrument; 300 MHz; Solvents: CDCl3 and CD3OH
Thermo Scientific Nicole iS5Thermo ScientificIQLAADGAAGFAHDMAZAInstrument
Wrist-Action ShakerBurrell Scientific757950819Instrument

References

  1. Shangary, S., Wang, S. Small-molecule inhibitors of the MDM2-p53 protein-protein interaction to reactivate p53 function: a novel approach for cancer therapy. Annual Review of Pharmacology and Toxicology. 49, 223-241 (2009).
  2. Zhao, Y., Aguilar, A., Bernard, D., Wang, S.

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Tags

Solid Phase SynthesisMTT Cytotoxicity AssayInfrared SpectroscopyCell Viability TestFurfurylamine PrecursorCisplatin Positive ControlRegenerating Michael LinkerLow-Loading Resin