Synthesis and Biological Evaluation of Analogs of Didehydroepiandrosterone as Potential New Anticancer Agents
The synthesis, cytotoxicity and inhibition of CDK8 by thirteen analogs of cortistatin A are reported. These efforts revealed that the analogs with either a 6- or 7-isoquinoline or 5-indole side chain in the 17-position are the most promising anti-proliferative agents. These compounds showed potent c...
Main Authors: | Eirik J. Solum, Sandra Liekens, Trond Vidar Hansen |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2020-07-01
|
Series: | Molecules |
Subjects: | |
Online Access: | https://www.mdpi.com/1420-3049/25/13/3052 |
Similar Items
-
Mediator Kinase Phosphorylation of STAT1 S727 Promotes Growth of Neoplasms With JAK-STAT Activation
by: Ioana I. Nitulescu, et al.
Published: (2017-12-01) -
Synthesis, Biological Evaluation and In Silico Studies of Certain Oxindole–Indole Conjugates as Anticancer CDK Inhibitors
by: Tarfah Al-Warhi, et al.
Published: (2020-04-01) -
Evaluation of a Novel DNA Vaccine Double Encoding Somatostatin and Cortistatin for Promoting the Growth of Mice
by: Xuan Luo, et al.
Published: (2022-06-01) -
Selinexor inhibits growth of patient derived chordomas in vivo as a single agent and in combination with abemaciclib through diverse mechanisms
by: Christopher J. Walker, et al.
Published: (2022-08-01) -
In-silico molecular design of heterocyclic benzimidazole scaffolds as prospective anticancer agents
by: Sumit Tahlan, et al.
Published: (2019-07-01)