Benzo[b]carbazolediones Synthesis and Inhibitory Effects on Nucleotide Pyrophosphatases/Phosphodiesterases. Issue 9 (8th March 2019)
- Record Type:
- Journal Article
- Title:
- Benzo[b]carbazolediones Synthesis and Inhibitory Effects on Nucleotide Pyrophosphatases/Phosphodiesterases. Issue 9 (8th March 2019)
- Main Title:
- Benzo[b]carbazolediones Synthesis and Inhibitory Effects on Nucleotide Pyrophosphatases/Phosphodiesterases
- Authors:
- Huy Do, Hoang
Ejaz, Syeda Abida
Molenda, Ricardo
Ohlendorf, Lars
Villinger, Alexander
Khan, Shafi Ullah
Lecka, Joanna
Sévigny, Jean
Iqbal, Jamshed
Ehlers, Peter
Langer, Peter - Abstract:
- Abstract: Two new and efficient methods for the synthesis of benzo[ b ]carbazolediones have been developed. Various derivatives were synthesized by either a three‐component one‐pot reaction or a two‐component domino reaction in moderate to good yield. Moreover, inhibition studies of these compounds against nucleotide pyrophosphatases (NPPs) have been carried out. An interesting and promising inhibitory effect was observed by the influence of different substituents. Substitution with a methyl group located at the indole moiety was found sensitive towards h ‐NPP1 (4b; IC50 ±SEM = 0.57 ± 0.05 μM), while the unsubstituted derivative exhibited a higher sensitivity towards h ‐NPP3 (4a; IC50 ± SEM = 0.16 ± 0.06 μM). Both derivatives presented non‐selective inhibition of both isozymes. Among all the derivatives, two derivatives with anisyl groups showed the highest selectivity towards h ‐NPP3 and no interaction with h ‐NPP1. Finally, the free binding energies were calculated and molecular docking studies were performed in order to provide an insight into putative binding modes of these inhibitors. Abstract : Two new and efficient methods for the synthesis of benzo[ b ]carbazolediones have been developed. Various derivatives were synthesized by either a three‐component one‐pot reaction or a two‐component domino reaction in moderate to good yield. Moreover, inhibition studies of these compounds against nucleotide pyrophosphatases (NPPs) have been carried out. An interesting andAbstract: Two new and efficient methods for the synthesis of benzo[ b ]carbazolediones have been developed. Various derivatives were synthesized by either a three‐component one‐pot reaction or a two‐component domino reaction in moderate to good yield. Moreover, inhibition studies of these compounds against nucleotide pyrophosphatases (NPPs) have been carried out. An interesting and promising inhibitory effect was observed by the influence of different substituents. Substitution with a methyl group located at the indole moiety was found sensitive towards h ‐NPP1 (4b; IC50 ±SEM = 0.57 ± 0.05 μM), while the unsubstituted derivative exhibited a higher sensitivity towards h ‐NPP3 (4a; IC50 ± SEM = 0.16 ± 0.06 μM). Both derivatives presented non‐selective inhibition of both isozymes. Among all the derivatives, two derivatives with anisyl groups showed the highest selectivity towards h ‐NPP3 and no interaction with h ‐NPP1. Finally, the free binding energies were calculated and molecular docking studies were performed in order to provide an insight into putative binding modes of these inhibitors. Abstract : Two new and efficient methods for the synthesis of benzo[ b ]carbazolediones have been developed. Various derivatives were synthesized by either a three‐component one‐pot reaction or a two‐component domino reaction in moderate to good yield. Moreover, inhibition studies of these compounds against nucleotide pyrophosphatases (NPPs) have been carried out. An interesting and promising inhibitory effect was observed by the influence of different substituents. … (more)
- Is Part Of:
- ChemistrySelect. Volume 4:Issue 9(2019)
- Journal:
- ChemistrySelect
- Issue:
- Volume 4:Issue 9(2019)
- Issue Display:
- Volume 4, Issue 9 (2019)
- Year:
- 2019
- Volume:
- 4
- Issue:
- 9
- Issue Sort Value:
- 2019-0004-0009-0000
- Page Start:
- 2545
- Page End:
- 2550
- Publication Date:
- 2019-03-08
- Subjects:
- Benzocarbazoldione, Buchwald-Hartwig, Domino Reaction, Nucleotide Pyrophosphatase, Palladium
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.201803061 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17277.xml