scholarly journals Multicomponent Synthesis, Binding Mode, and Structure–Activity Relationship of Selective Histone Deacetylase 6 (HDAC6) Inhibitors with Bifurcated Capping Groups

2020 ◽  
Vol 63 (18) ◽  
pp. 10339-10351 ◽  
Author(s):  
Nina Reßing ◽  
Melf Sönnichsen ◽  
Jeremy D. Osko ◽  
Andrea Schöler ◽  
Julian Schliehe-Diecks ◽  
...  
Molecules ◽  
2019 ◽  
Vol 24 (15) ◽  
pp. 2780
Author(s):  
Fanxun Zeng ◽  
Lina Quan ◽  
Guantian Yang ◽  
Tiantian Qi ◽  
Letian Zhang ◽  
...  

Human dihydroorotate dehydrogenase (hDHODH), one of the attractive targets for the development of immunosuppressive drugs, is also a potential target of anticancer drugs and anti-leukemic drugs. The development of promising hDHODH inhibitors is in high demand. Based on the unique binding mode of our previous reported 4-thiazolidinone derivatives, via molecular docking method, three new series 4-thiazolidinone derivatives were designed and synthesized as hDHODH inhibitors. The preliminary structure–activity relationship was investigated. Compound 9 of biphenyl series and compound 37 of amide series displayed IC50 values of 1.32 μM and 1.45 μM, respectively. This research will provide valuable reference for the research of new structures of hDHODH inhibitors.


2013 ◽  
Vol 56 (24) ◽  
pp. 9969-9981 ◽  
Author(s):  
Quaovi H. Sodji ◽  
Vishal Patil ◽  
James R. Kornacki ◽  
Milan Mrksich ◽  
Adegboyega K. Oyelere

2016 ◽  
Vol 22 (5) ◽  
pp. 352-359 ◽  
Author(s):  
Julia Sindlinger ◽  
Jan Bierlmeier ◽  
Lydia-Christina Geiger ◽  
Katharina Kramer ◽  
Iris Finkemeier ◽  
...  

Planta Medica ◽  
2008 ◽  
Vol 74 (09) ◽  
Author(s):  
MA Brenzan ◽  
CV Nakamura ◽  
BPD Filho ◽  
T Ueda-Nakamura ◽  
MCM Young ◽  
...  

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