scholarly journals Modular Total Synthesis and Cell-Based Anticancer Activity Evaluation of Ouabagenin and Other Cardiotonic Steroids with Varying Degrees of Oxygenation

2019 ◽  
Vol 141 (12) ◽  
pp. 4849-4860 ◽  
Author(s):  
Hem Raj Khatri ◽  
Bijay Bhattarai ◽  
Will Kaplan ◽  
Zhongzheng Li ◽  
Marcus John Curtis Long ◽  
...  
2000 ◽  
Vol 131 (5) ◽  
pp. 0501-0509 ◽  
Author(s):  
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 131 (9) ◽  
pp. 2760-2764 ◽  
Author(s):  
Yongfeng Tao ◽  
Keighley Reisenauer ◽  
Joseph H. Taube ◽  
Daniel Romo

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

ChemInform ◽  
2013 ◽  
Vol 44 (12) ◽  
pp. no-no
Author(s):  
Narayan Chakor ◽  
Ganesh Patil ◽  
Diana Writer ◽  
Giridharan Periyasamy ◽  
Rajiv Sharma ◽  
...  

2020 ◽  
Vol 104 ◽  
pp. 104309
Author(s):  
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.


2013 ◽  
Vol 8 (7) ◽  
pp. 1934578X1300800 ◽  
Author(s):  
Takuya Imaoka ◽  
Makoto Iwata ◽  
Takafumi Akimoto ◽  
Kazuo Nagasawa

Oroidin derived pyrrole imidazole marine alkaloids (PIAs) are attractive targets for synthetic organic chemists because of their structural complexity and diversity as well as their interesting biological activities. A number of efforts have been carried out to develop strategies for the synthesis of these natural products. Members of PIAs ( eg., 2-7) which contain tetracyclic ring systems possessing characteristic cyclic guanidine or urea moieties show significant biological activities including anticancer activity and agonistic activity against the adrenoceptor. In this review investigations of the total synthesis of the representative tetracyclic PIAs dibromophakellin (2) and dibromophakellstatin (3) are described.


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