Design and in vitro biological evaluation of substituted chalcones synthesized from nitrogen mustards as potent microtubule targeted anticancer agents

2017 ◽  
Vol 41 (10) ◽  
pp. 4096-4109 ◽  
Author(s):  
X. Janet Sabina ◽  
J. Karthikeyan ◽  
Gunasekaran Velmurugan ◽  
M. Muthu Tamizh ◽  
A. Nityananda Shetty

Six chalcones were synthesized and their structures determined by single crystal X-ray diffraction studies. They exhibited enhanced anticancer activity and tubulin inhibition.

Molecules ◽  
2018 ◽  
Vol 23 (12) ◽  
pp. 3253 ◽  
Author(s):  
Ioana Vlaicu ◽  
Gheorghe Borodi ◽  
Gina Scăețeanu ◽  
Mariana Chifiriuc ◽  
Luminița Măruțescu ◽  
...  

Five new copper(II) acrylate complexes (acr is the acrylate anion: C3H3O2) with imidazole derivatives (2-methylimidazole/2-MeIm, 5-methylimidazole/5-MeIm, 2-ethylimidazole/2-EtIm) of type: cis-[Cu(2-RIm)2(acr)2]·xH2O ((1): R = –CH3, x = 2; (4): R = –CH2–CH3, x = 0), trans-[Cu(2-RIm)2(acr)2] ((2): R = –CH3; (5): R = –CH2–CH3) and trans-[Cu(5-RIm)2(acr)2] ((3): R = –CH3) have been prepared and characterized by elemental analysis, Fourier Transform Infrared spectrometry (FTIR), Electron Paramagnetic Resonance (EPR), electronic reflectance spectroscopy, scanning electron microscopy, and mass spectrometry. The single crystal X-ray diffraction study of complexes (2) and (5) reveals that the copper(II) ion is located on an inversion center and show elongated octahedral geometry completed by two coplanar bidentate acrylates and two unidentate imidazole derivatives displayed in trans positions. For complex (4) the single crystal X-ray diffraction shows that the copper(II) ion is in a distorted octahedral environment which can be easily confused with a trigonal prism completed by two bidentate acrylates and two unidentate imidazole derivatives displayed in cis positions. These results indicate the fact that complexes (4) and (5) are the geometric isomers of the same compound bis(acrylate)-bis(2-ethylimidazole)-copper(II). Complexes (1) and (2), as well as (4) and (5), were produced simultaneously in the reaction of the corresponding copper(II) acrylate with imidazole derivatives in methanol solution. Furthermore, in order to be able to formulate potential applications of the obtained compounds, our next goal was to investigate the in vitro antimicrobial activity of the synthesized complexes against Gram-positive and Gram-negative bacteria, as well as fungal strains, of both clinical and ecological importance (biodeterioration of historical buildings). The trans isomers (2) and (5), followed by (4) have shown the broadest range of antimicrobial activity. In case of (1) and (2) isomers, the trans isomer (2) was significantly more active than cis (1), while the cis isomer (4) proved to be more active than trans (5). Taken together, the biological evaluation results indicate that the trans (2) was the most active complex, demonstrating its potential for the development of novel antimicrobial agents, with potential applications in the biomedical and restoration of architectural monuments fields.


2020 ◽  
Vol 12 (1) ◽  
pp. 19-35 ◽  
Author(s):  
Dimitrios Trafalis ◽  
Panagiotis Dalezis ◽  
Elena Geromichalou ◽  
Sofia Sagredou ◽  
Eleni Sflakidou ◽  
...  

Aim: Steroidal prodrugs of nitrogen mustards such as estramustine and prednimustine have proven effective anticancer agents in clinical use since the 1970s. In this work, we aimed to develop steroidal prodrugs of the novel nitrogen mustard POPAM-NH2. POPAM-NH2 is a melphalan analogue that was coupled with three different steroidal lactams. Methodology: The new conjugates were preclinically tested for anticancer activity against nine human and one rodent cancer experimental models, in vitro and in vivo. Results & conclusion: All the steroidal alkylators showed high antitumor activity, in vitro and in vivo, in the experimental systems tested. Moreover, these hybrid compounds showed by far superior anticancer activity compared with the alkylating agents, melphalan and POPAM-NH2.


2015 ◽  
Vol 10 (2) ◽  
pp. 1934578X1501000
Author(s):  
Yen-You Lin ◽  
Su-June Tsai ◽  
Michael Y. Chiang ◽  
Zhi-Hong Wen ◽  
Jui-Hsin Su

Chemical investigation of a crinoid Himerometra magnipinna has afforded three anthraquinones (1–3), including one new metabolite, (+)-rhodoptilometrin (1). The structures of these compounds were elucidated on the basis of their spectroscopic data and the absolute configuration of 1 was further confirmed by single-crystal X-ray diffraction analysis. In the in vitro anti-inflammatory effects test, compound 2 was found to significantly inhibit the accumulation of the pro-inflammatory iNOS protein of the LPS-stimulated RAW264.7 macrophage cells.


Author(s):  
Mamatha S. V ◽  
S. L. Belagali ◽  
Mahesh Bhat ◽  
Vijay M. Kumbar

Background: Coumarin and benzophenone possess a vast sphere of biological activities whereas thiazoles display various pharmacological properties. Hence we focused on incorporation of coumarin and thiazole core to the benzophenone skeleton to enhance the bioactivity anticipating their interesting biological properties. Objective: The objective of the current work is synthesis and biological evaluation of a novel series of coumarin fused thiazole derivatives. Methods: A novel series of Coumarin conjugated thiazolyl acetamide hybrid derivatives were synthesized by multistep reaction sequence and were characterized by the FT-IR, LCMS and NMR spectral techniques. The newly synthesized compounds were screened for anticancer activity by in-silico and in-vitro methods. The cytotoxicity of the synthesized unique compounds had been executed for two different cancer cell lines MCF-7 (Breast cancer) and KB (Oral cancer) in comparison with standard paclitaxel by MTT assay. Results: The compound 7f is the potent motif with an acceptable range of IC 50 values for anticancer activity were 63.54 µg/ml and 55.67 µg/ml, against the MCF-7 and KB cell lines, respectively. Molecule docking model revealed that this compound formed three conventional hydrogen bonds with the active sites of the amino acids MET 769, ARG 817 and LYS 721. Conclusion: Compound 7f with two methyl groups on the phenoxy ring and one 4-position methoxy group on the benzoyl ring, showed a significant cytotoxic effect. An advantageous level of low toxicity against normal cell line (L292) by MTT assay was determined.


Author(s):  
Vinutha V. Salian ◽  
Badiadka Narayana ◽  
Balladka K. Sarojini ◽  
Madan S. Kumar ◽  
Govinahalli S. Nagananda ◽  
...  

2019 ◽  
Vol 43 (9) ◽  
pp. 3665-3672 ◽  
Author(s):  
Edmore F. Kangara ◽  
Tebogo Peega ◽  
Leonie Harmse ◽  
Juanita L. van Wyk ◽  
Demetrius C. Levendis ◽  
...  

Conformers of [Pt(phen)(L1-κS)2] observed in solution as a result of π-stacking interactions between the unusual κS-coordinated N,N-diethyl-N′-1-naphthoylthioureato ligands and 1,10-phenanthroline.


2017 ◽  
Vol 41 (13) ◽  
pp. 5639-5650 ◽  
Author(s):  
Ya-Ru Qiu ◽  
Ru-Fen Zhang ◽  
Shao-Liang Zhang ◽  
Shuang Cheng ◽  
Qian-Li Li ◽  
...  

A cluster of novel organotin(iv) complexes were designed, synthesized, and characterized by elemental analysis, FT-IR, and NMR (1H, 13C, and 119Sn) spectroscopy as well as single-crystal X-ray diffraction.


2010 ◽  
Vol 63 (11) ◽  
pp. 1514 ◽  
Author(s):  
Brendan Gleeson ◽  
Anthony Deally ◽  
Helge Müller-Bunz ◽  
Siddappa Patil ◽  
Matthias Tacke

From the reaction of 6‐(4‐methoxymethyl‐phenyl) fulvene (1a), 6‐(N‐methyl‐pyrrole) fulvene (1b), and 6‐(4‐dimethylamino‐phenyl) fulvene (1c) with LiBEt3H, the corresponding lithium cyclopentadienide intermediates (2a–c) were synthesized. These intermediates were then transmetallated to vanadium with VCl4 to yield the substituted vanadocene dichlorides bis‐[(4‐methoxymethyl‐benzyl)cyclopentadienyl] vanadium(iv) dichloride (3a), bis‐[(N‐methylpyrrole)2‐methylcyclopentadienyl] vanadium(iv) dichloride (3b), and bis‐[(p‐dimethylaminobenzyl)cyclopentadienyl] vanadium(iv) dichloride (3c). The vanadocene dichloride 3a was characterized by single crystal X‐ray diffraction. All three vanadocenes had their cytotoxicity investigated through MTT based preliminary in vitro testing on the human renal cell line Caki‐1 in order to determine their IC50 values. Vanadocenes 3a–b were found to have IC50 values of 6.5 and 5.2 µM, respectively, while 3c displayed a superior value of 1.7 µM.


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