1,3-Dipolar Cycloaddition Reaction: Synthesis of Novel 5,6-Dehydronorcantharidin Derivatives of Substituted Aromatic Amines with Potential antitumor Activities.

ChemInform ◽  
2005 ◽  
Vol 36 (27) ◽  
Author(s):  
Li-Ping Deng ◽  
Fang-Ming Liu ◽  
Hou-Yong Wang
Keyword(s):  
Aromatic Amines ◽  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
Reaction Synthesis ◽  
Antitumor Activities ◽  
Derivatives Of ◽  
Potential Antitumor

Norcantharidin analogues — Synthesis and evaluation of growth inhibition in a panel of selected tumor-cell lines

2007 ◽  
Vol 85 (11) ◽  
pp. 938-944 ◽  
Author(s):  
Liping Deng ◽  
Li Shen ◽  
Jing Zhang ◽  
Bo Yang ◽  
Qiaojun He ◽  
...  
Keyword(s):  
Tumor Cell ◽  
Growth Inhibition ◽  
Cell Lines ◽  
Antiproliferative Activity ◽  
Aromatic Amines ◽  
Cycloaddition Reaction ◽  
Dipolar Cycloaddition ◽  
Tumor Cell Lines ◽  
Derivatives Of

A series of norcantharidin (NCTD) analogues have been synthesized by [3+2]1,3-dipolar cycloaddition reaction of norcantharidin derivatives of substituted aromatic amines with four nitrile oximes. All analogues have been screened for their antiproliferative activity in vitro against a panel of tumor cell lines: KB, SGC-7901, HL60, Bel-7402, HO-8910, and ECA109, producing IC50 values from 0.36 µmol/L to >100 µmol/L. Compound 9d showed potency for the treatment of hepatoma, with IC50 value to Bel-7402 cell line comparable to that of norcantharidin.Key words: norcantharidin analogues, isoxazoline, growth inhibition.

scholarly journals Synthesis and spectroscopic properties of β-triazoloporphyrin–xanthone dyads

2015 ◽  
Vol 11 ◽  
pp. 1434-1440 ◽  
Author(s):  
Dileep Kumar Singh ◽  
Mahendra Nath
Keyword(s):  
Fluorescence Spectra ◽  
Photophysical Properties ◽  
Bathochromic Shift ◽  
Cycloaddition Reaction ◽  
Spectroscopic Characterization ◽  
Spectroscopic Properties ◽  
Dipolar Cycloaddition ◽  
Free Base ◽  
Acidic Conditions ◽  
Derivatives Of

A novel series of β-triazoloporphyrin–xanthone conjugates and xanthone-bridged β-triazoloporphyrin dyads has been synthesized in moderate to good yields through Cu(I)-catalyzed Huisgen 1,3-dipolar cycloaddition reaction of copper(II) 2-azido-5,10,15,20-tetraphenylporphyrin or zinc(II) 2-azidomethyl-5,10,15,20-tetraphenylporphyrin with various alkyne derivatives of xanthones in DMF containing CuSO4 and ascorbic acid at 80 °C. Furthermore, these metalloporphyrins underwent demetalation under acidic conditions to afford the corresponding free-base porphyrins in good to excellent yields. After successful spectroscopic characterization, these porphyrins have been evaluated for their photophysical properties. The preliminary results revealed a bathochromic shift in the UV–vis and fluorescence spectra of these porphyrin–xanthone dyads.

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