Histamine Antagonists. III. 1- and 1,4-Substituted Piperazine Derivatives

1949 ◽  
Vol 71 (8) ◽  
pp. 2734-2736 ◽  
Author(s):  
K. E. Hamlin ◽  
Arthur W. Weston ◽  
Francis E. Fischer ◽  
R. J. Michaels
2004 ◽  
Vol 1 (2) ◽  
pp. 93-98 ◽  
Author(s):  
H. S. Patel ◽  
H. D. Desai ◽  
H. J. Mistry

NovelN-substituted piperazine derivatives containing sulfonyloxy aniline moiety have been prepared. The various 4-sulfonyloxy aniline (SA) derivatives (2a-h) have been prepared by the condensation reaction ofN-Acetyl Sulfanilyl chloride (ASC) and sodium phenates followed by hydrolysis. The SA derivatives are then reacted with chloro acetyl chloride to give corresponding (N-Chloroacetyl) derivatives (3a-h). These derivatives are then reacted withN-phenyl piperazine to yield the corresponding piperazine derivatives (4a-h).


2019 ◽  
Vol 16 (5) ◽  
pp. 547-555 ◽  
Author(s):  
Asaf Evrim Evren ◽  
Leyla Yurttaş ◽  
Busra Eksellı ◽  
Gulsen Akalın-Cıftcı

Background: Cancer cells are described as an unregulated growth and spread of abnormal cells. Recently, cancer has become the most important major reason for deaths in the world. Methods: For anticancer activity, we have used the MTT method and determine the early/late apoptosis by flow cytometry. Results: The title compounds were procured by reacting 2-chloro-N-[4-(pyridin-4-yl)thiazol-2- yl]acetamide with some substituted piperazine derivatives. The in vitro anticancer activity of synthesized compounds was tested against C6 rat glioma cells and A549 human lung carcinoma cells. As a result, the compounds 3d, 3e, 3f and 3g have shown anticancer activity against both cell line. Conclusion: Specifically, compound 3f was determined as the most active compound against C6 rat glioma cells. Also, as understood, the core structure which is substituted with piperazine bridge, the heterocyclic aromatic derivatives are more active than phenyl or benzyl derivatives.


1999 ◽  
Vol 10 (4) ◽  
pp. 799-811 ◽  
Author(s):  
Aurelio Ortiz ◽  
Norberto Farfán ◽  
Herbert Höpfl ◽  
Rosa Santillan ◽  
Marı́a E. Ochoa ◽  
...  

ChemInform ◽  
2012 ◽  
Vol 43 (10) ◽  
pp. no-no
Author(s):  
H. Marona ◽  
M. Kubacka ◽  
B. Filipek ◽  
A. Siwek ◽  
M. Dybaia ◽  
...  

2015 ◽  
Vol 25 (7) ◽  
pp. 1427-1430 ◽  
Author(s):  
Maria N. Modica ◽  
Sebastiano Intagliata ◽  
Valeria Pittalà ◽  
Loredana Salerno ◽  
Maria A. Siracusa ◽  
...  

2017 ◽  
Vol 10 (3) ◽  
pp. 178-189
Author(s):  
Kommula Dileep ◽  
Mohana Rao Katiki ◽  
Busam Ramalingeswara Rao ◽  
V. P. S. Vishnu Vardhan ◽  
Ramakrishna Sistla ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document