Synthesis and Antiinflammatoryand Anticancer Activity Evaluation of Some Condensed Pyrimidines

2000 ◽  
Vol 131 (5) ◽  
pp. 0501-0509 ◽  
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Sham M. Sondhi ◽  
Nidhi Singhal ◽  
Rajeshwar P. Verma ◽  
Sudershan K. Arora ◽  
Rakesh Shukla ◽  
...  
2010 ◽  
Vol 45 (2) ◽  
pp. 555-563 ◽  
Author(s):  
Sham M. Sondhi ◽  
Jaiveer Singh ◽  
Reshma Rani ◽  
P.P. Gupta ◽  
S.K. Agrawal ◽  
...  

Author(s):  
Lan Luo ◽  
Jing Jing Jia ◽  
Qiu Zhong ◽  
Xue Zhong ◽  
Shilong Zheng ◽  
...  

2019 ◽  
Vol 141 (12) ◽  
pp. 4849-4860 ◽  
Author(s):  
Hem Raj Khatri ◽  
Bijay Bhattarai ◽  
Will Kaplan ◽  
Zhongzheng Li ◽  
Marcus John Curtis Long ◽  
...  

MedChemComm ◽  
2014 ◽  
Vol 5 (4) ◽  
pp. 528 ◽  
Author(s):  
Deepak Kumar ◽  
K. Kranthi Raj ◽  
Sanjay V. Malhotra ◽  
Diwan S. Rawat

2020 ◽  
Vol 104 ◽  
pp. 104309
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Anita Bułakowska ◽  
Jarosław Sławiński ◽  
Kamila Siedlecka-Kroplewska ◽  
Grzegorz Stasiłojć ◽  
Marcin Serocki ◽  
...  

2019 ◽  
Vol 35 (2) ◽  
pp. 723-731
Author(s):  
Weerachai Phutdhawong ◽  
Sopita Rattanopas ◽  
Jitnapa Sirirak ◽  
Thongchai Taechowisan ◽  
Waya S. Phutdhawong

Azepinobisindole derivatives, the isomeric Iheyamine skeleton, was prepared and its anticancer activity evaluation were investigated against two human cancer cell lines, Hepatocellular carcinoma (HepG2) and human cervical cancer line (Hela) as well as the normal cell line (Vero cell line) using MTT assay. The anticancer activity results indicated that 2-methoxy-5-methyl-5H-azepino[2,3-b:4,5-bʹ]diindole was the most active derivative against tested cell lines. Additionally, molecular docking study in silico the possible inhibitory effect of cyclin-dependent kinase 2 (CDK2) by the azepinoindole revealed that all synthesized compounds fit well in the binding cavity of CDK2.


2014 ◽  
Vol 24 (5) ◽  
pp. 1942-1951 ◽  
Author(s):  
Surbhi Arya ◽  
Anuj Kumar ◽  
Nikhil Kumar ◽  
Partha Roy ◽  
S. M. Sondhi

2019 ◽  
Vol 28 (4) ◽  
pp. 580-590 ◽  
Author(s):  
Tonghui Huang ◽  
Xin Wu ◽  
Tianya Liu ◽  
Lin An ◽  
Xiaoxing Yin

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