scholarly journals Curcumin analogues for possible cancer treatment A QSAR and partial ordering study

2021 ◽  
Vol 1 (2) ◽  
pp. 001-016
Author(s):  
Lars Carlsen ◽  
Poul Erik Hansen ◽  
Bahjat A Saeed ◽  
Rita S Elias

The possible effect of curcumin as a potential natural cancer treatment drug has been intensively discussed. In the present study the probabilities of a series of curcumin analogues to possess potential as antineoplastic, prostate cancer treatment and anticarcinogenic agents has been studied theoretically applying a selection of quantitative structure-activity relation and absorption, distribution, metabolism, and excretion (ADME) approaches. From spectroscopic studies it is evident that these compounds can be found in both enol and diketo forms, the former in general the more predominant in non-polar solvents, whereas in polar solvents, like water an increasing amount of the diketo form can be noted. Hence, the probabilities for both the enols and diketo forms to possess the above-mentioned effects were studied. In most cases the enol form shows the highest probabilities for being effective although the differences are not significant. Thus, it is suggested to look at the sum of effects of the keto and the enol forms in relation to the possible therapeutic effects of the compounds here studied.

2007 ◽  
Vol 10 (6) ◽  
pp. A346
Author(s):  
SD Ramsey ◽  
SD Zeliadt ◽  
IJ Hall ◽  
JW Lee ◽  
DU Ekwueme ◽  
...  

1962 ◽  
Vol 40 (12) ◽  
pp. 2272-2277 ◽  
Author(s):  
T. R. Kasturi ◽  
B. N. Mylari ◽  
A. Balasubramanian ◽  
C. N. R. Rao

1,2-Dicyano esters show an absorption band around 245 mμ in alcoholic solutions which is not found in non-polar and other polar solvents. This anomalous behavior has been found to be due to the unusual solvent dependence of the equilibrium between the keto and enol forms. The intensity of the absorption band in alcoholic solutions decreases with increase in concentration of the 1,2-dicyano ester, indicating association of the enol form. The keto–enol equilibrium is also found to be sensitive to the substituent R of the alcohol ROH.


2004 ◽  
Vol 171 (4S) ◽  
pp. 284-284
Author(s):  
Yi Lu ◽  
Jun Zhang ◽  
Ben Beheshti ◽  
Ximing J. Yang ◽  
Syamal K. Bhattacharya ◽  
...  

2020 ◽  
Author(s):  
Luke Adams ◽  
Lorna E. Wilkinson-White ◽  
Menachem J. Gunzburg ◽  
Stephen J. Headey ◽  
Martin J. Scanlon ◽  
...  

The development of low-affinity fragment hits into higher affinity leads is a major hurdle in fragment-based drug design. Here we demonstrate an approach for the Rapid Elaboration of Fragments into Leads (REFiL) applying an integrated workflow that provides a systematic approach to generate higher-affinity binders without the need for structural information. The workflow involves the selection of commercial analogues of fragment hits to generate preliminary structure-activity relationships. This is followed by parallel microscale chemistry using chemoinformatically designed reagent libraries to rapidly explore chemical diversity. Upon completion of a fragment screen against Bromodomain-3 extra terminal (BRD3-ET) domain we applied the REFiL workflow, which allowed us to develop a series of tetrahydrocarbazole ligands that bind to the peptide binding site of BRD3-ET. With REFiL we were able to rapidly improve binding affinity >30-fold. The REFiL workflow can be applied readily to a broad range of protein targets without the need of a structure, allowing the efficient evolution of low-affinity fragments into higher affinity leads and chemical probes.<br>


2017 ◽  
Vol 5 (4) ◽  
pp. e219-e228 ◽  
Author(s):  
Stephanie R. Reading ◽  
Kimberly R. Porter ◽  
Jeffrey M. Slezak ◽  
Teresa N. Harrison ◽  
Joy S. Gelfond ◽  
...  

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