Neutral and ion-pair silver(I) complexes of Schiff bases derived from methyl and ethyl carbazates with glyoxylic acid: Synthesis, structure, thermal behavior and cytotoxic activity

2019 ◽  
Vol 497 ◽  
pp. 119072 ◽  
Author(s):  
S. Poornima ◽  
S. Packiaraj ◽  
A. Pushpaveni ◽  
S. Govindarajan ◽  
R.J. Butcher ◽  
...  
2020 ◽  
Vol 1200 ◽  
pp. 127082 ◽  
Author(s):  
Mansura Huseynova ◽  
Vaqif Farzaliyev ◽  
Ajdar Medjidov ◽  
Mahizar Aliyeva ◽  
Parham Taslimi ◽  
...  

2018 ◽  
Vol 34 (5) ◽  
pp. 2350-2360 ◽  
Author(s):  
Kany A. Abdulqader ◽  
Ahmed W. Naser ◽  
Muthanna S. Farhan ◽  
Sabah J. Salih

A series of 1,2,3-triazole, oxadiazole and aza-β-lactam derivatives were synthesized through consecutive reaction began from o-(N-propargyl) sulfonamido benzoic acid (1a). The reaction of (1a) with absolute ethanol in the presence of concentrated H2SO4 resulted in the formation of ester derivative (2a). The product of the previous reaction was reacted with 80% hydrazine hydrate to prepare benzohydrazide derivative (3a). 1,3,4-oxadiazole compound (4a) was obtained by condensation of compound (3a) with CS2 in presence KOH . Compound (3a) react with Phenyl isocyanates to give Carboxamide derivative (5a), that Condensation either with 2,4-dimethoxybenzaldhyde and p-hydroxybenzaldehyde to prepare the Schiff bases (6a-b). The cycloaddotion of Schiff-bases (6a-b) with phenyl isocyanate gave aza-β-lactams (7a-b). Benzamide derivatives (8a-c) were prepared via the reaction of compound (1a) with aniline derivatives, such as (p-toluidine, o-nitroaniline and m-nitroaniline). In a regioselective reaction 1,4-disubstituted-1,2,3-triazole derivative (9a-j) were synthesized via the click reaction of compounds 4a,5a and (8a-c) with benzyl azide and p-bromobenzyl azide. The compounds were identified using the spectral methods shown in the work. Cytotoxic effects of some final prepared compounds were studied in one cultured cellular models (MCF7 cell line) breast cancer (at various concentrations) by MTT assay, compound (9j) showed the better cytotoxic activity among the tested compounds.


2018 ◽  
Vol 13 (8) ◽  
pp. 1012-1023 ◽  
Author(s):  
Bhyranalyar N. Veerabhadraswamy ◽  
Doddamane S. Shankar Rao ◽  
Channabasaveshwar V. Yelamaggad

1990 ◽  
Vol 35 (3) ◽  
pp. 621-623 ◽  
Author(s):  
K. Scott ◽  
A.P. Colbourne ◽  
S.D. Perry

2014 ◽  
Vol 9 (12) ◽  
pp. 1934578X1400901
Author(s):  
Uppuluri V. Mallavadhani ◽  
Banita Pattnaik ◽  
Nitasha Suri ◽  
Ajit K. Saxena

Ursolic acid (1), a natural pentacyclic triterpenic acid, afforded a variety of ring-C transformed products (5–11) when treated with N-bromosuccinimide under the influence of a range of protective groups and solvents. The synthesized compounds have been evaluated for cytotoxic activity against prostate PC 3, leukemia THP 1, cervical Hela and lung A-549 cancer cell lines. Among the tested analogs, compounds 5, 8, 9 and 10 showed potent activity against PC 3, THP 1 and Hela cell lines. Especially, compound 10 showed enhanced activity against the Hela cell line than the parent compound. Compounds 5, 8 and 9 showed comparable activities against PC 3 and THP 1 cell lines.


2019 ◽  
Vol 1185 ◽  
pp. 8-20 ◽  
Author(s):  
Naghmana Kausar ◽  
Shahzad Muratza ◽  
Muhammad Asam Raza ◽  
Hummera Rafique ◽  
Muhammad Nadeem Arshad ◽  
...  

1997 ◽  
Vol 69 (23) ◽  
pp. 4814-4818 ◽  
Author(s):  
Naoki Hirayama ◽  
Isao Takeuchi ◽  
Takaharu Honjo ◽  
Koji Kubono ◽  
Hisao Kokusen

2014 ◽  
Vol 55 (6) ◽  
pp. 1067-1074 ◽  
Author(s):  
S. I. Dorovskikh ◽  
N. V. Kuratieva ◽  
S. V. Tkachev ◽  
S. V. Trubin ◽  
P. A. Stabnikov ◽  
...  

2016 ◽  
Vol 10 (5) ◽  
pp. 766-773 ◽  
Author(s):  
Md. Rabiul Hasan ◽  
Mohammad Amzad Hossain ◽  
Md. Abdus Salam ◽  
Mohammad Nasir Uddin

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