Synthesis and investigation of viral-inhibitory activity of nitrogen-containing derivatives of adamantane

1991 ◽  
Vol 25 (7) ◽  
pp. 485-488 ◽  
Author(s):  
Yu. N. Klimochkin ◽  
I. K. Moiseev ◽  
G. V. Vladyko ◽  
L. V. Korobchenko ◽  
E. I. Boreko
RSC Advances ◽  
2014 ◽  
Vol 4 (97) ◽  
pp. 54217-54225 ◽  
Author(s):  
Xin Zhang ◽  
Chetan B. Sangani ◽  
Li-Xin Jia ◽  
Pi-Xian Gong ◽  
Fang Wang ◽  
...  

Series of novel Schiff's base derivatives have been synthesized. Compound 10q showed the most potent inhibitory activity (IC50 = 2.6883 μM).


Chemotherapy ◽  
1980 ◽  
Vol 26 (5) ◽  
pp. 316-322 ◽  
Author(s):  
Barbara Grytzmann ◽  
M. Morr ◽  
R. Wigand

2007 ◽  
Vol 62 (4) ◽  
pp. 580-586 ◽  
Author(s):  
Kalhari S. Kosmulalage ◽  
Shamsulhaq Zahid ◽  
Chibuike C. Udenigwe ◽  
Sarfraz Akhtar ◽  
Athar Ata ◽  
...  

Phytochemical studies on the ethanolic extract of Barleria prionitis of Sri Lankan origin have resulted in the isolation of a new compound, balarenone (1), along with three known compounds, pipataline (2), lupeol (3) and 13,14-seco-stigmasta-5,14-diene-3-α-ol (4). The structures of 1 - 4 were elucidated with the aid of extensive NMR spectroscopic studies. Compounds 1 - 4 showed moderate inhibitory activity against glutathione S-transferase (GST) and acetylcholinesterase (AChE). Compounds 1, 2 and 4 also exhibited antibacterial activity against Bacillus cereus and Pseudomonas aeruginosa (25 μg/disk). Three different derivatives of compound (2), 7,8-epoxypipataline (5), 8- amino-7-hydroxypipataline (6) and 7,8-dibromopipataline (7) were synthesized to evaluate them for GST and AChE inhibitory activities. Household microwave radiations were used to synthesize compound (6). Among all tested compounds, 8-amino-7-hydroxypipataline (6) exhibited a significant AChE inhibitory activity with an IC50 value of 36.8 μM.


2010 ◽  
Vol 12 (7) ◽  
pp. 549-556 ◽  
Author(s):  
Xiao-Xia Liang ◽  
Geng-Tao Liu ◽  
Qiao-Hong Chen ◽  
Hua Sun ◽  
Dong-Lin Chen ◽  
...  

Synlett ◽  
2015 ◽  
Vol 26 (08) ◽  
pp. 1131-1134 ◽  
Author(s):  
Hyoungsu Kim ◽  
Seung-Hoon Baek ◽  
Hongjun Jang

The derivatives of macakurzin C containing a modified D ring and protected C(3)/C(5)-hydroxyl groups were synthesized and their in vitro AChE inhibitory activity and neurotoxicity were evaluated to identify the structural requirements for the activities. The results indicated that C(3)-benzyl-protected derivative has a more potent AChE inhibitory activity (IC50, 2.6 μM) and a less neurotoxicity (GI50, >100 μM) than synthetic macakurzin C (IC50, 9.1 μM; GI50, 16.6 μM).


MedChemComm ◽  
2012 ◽  
Vol 3 (11) ◽  
pp. 1449-1454 ◽  
Author(s):  
Mayya G. Korochkina ◽  
Alexandra D. Nikitashina ◽  
Ravil N. Khaybullin ◽  
Konstantin A. Petrov ◽  
Irina Yu. Strobykina ◽  
...  

Derivatives of isosteviol and steviol possessing choline moieties have been synthesized and assayed for AchE and BchE inhibitory activity.


Synthesis ◽  
2014 ◽  
Vol 46 (09) ◽  
pp. 1217-1223 ◽  
Author(s):  
Guillermo Negrón-Silva ◽  
Deysi Cruz-Gonzalez ◽  
Rodrigo González-Olvera ◽  
Leticia Lomas-Romero ◽  
Atilano Gutiérrez-Carrillo ◽  
...  

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