Poonam Bhadja
Poonam Bhadja has a total of 9 co-authors. Here are the top co-authors by number of shared publications:
Abdullah Alarifi
Department of Chemistry
1 shared publicationAbhishek Dhar
Department of Chemical Engineering, University of Calcutta 700 009, 92, Acharya Prafulla Chandra Road, Kolkata, India
1 shared publicationChetan B. Sangani
Shri Maneklal M. Patel Institute of Sciences and Research, Kadi Sarva Vishwavidyalaya University, Gandhinagar, India
1 shared publication- Kunjal Soni
Sri M. M. Patel Institute of Sciences & Research, Kadi Sarva Vishwavidhyalaya, Gandhinagar 382023, India
1 shared publication Mohd. Afzal
Department of Chemistry
1 shared publication- Mohd. Muddassir
Department of Chemistry, College of Sciences, King Saud University, Riyadh 11451, Saudi Arabia
1 shared publication
Latest Publications
- Open Access
- 24 December 2020
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 11 (2) , 612-636
Bromodomain and BET family proteins as epigenetic targets in cancer therapy: their degradation, present drugs, and possible PROTACs
Alteration in the pattern of epigenetic marking leads to cancer, neurological disorders, inflammatory problems etc. These changes are due to aberration in histone modification enzymes that function as readers, writers and erasers. Bromodomains (BDs) and BET proteins that recognize acetylation of chromatin regulate gene expression. To block the function of any of these BrDs and/or BET protein can be a controlling agent in disorders such as cancer. BrDs and BET proteins are now emerging as targets for new therapeutic development. Traditional drugs like enzyme inhibitors and protein–protein inhibitors have many limitations. Recently Proteolysis-Targeting Chimeras (PROTACs) have become an advanced tool in therapeutic intervention as they remove disease causing proteins. This review provides an overview of the development and mechanisms of PROTACs for BRD and BET protein regulation in cancer and advanced possibilities of genetic technologies in therapeutics.
- 24 December 2020
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 11 (2) , 612-636
Open AccessBromodomain and BET family proteins as epigenetic targets in cancer therapy: their degradation, present drugs, and possible PROTACs
Alteration in the pattern of epigenetic marking leads to cancer, neurological disorders, inflammatory problems etc. These changes are due to aberration in histone modification enzymes that function as readers, writers and erasers. Bromodomains (BDs) and BET proteins that recognize acetylation of chromatin regulate gene expression. To block the function of any of these BrDs and/or BET protein can be a controlling agent in disorders such as cancer. BrDs and BET proteins are now emerging as targets for new therapeutic development. Traditional drugs like enzyme inhibitors and protein–protein inhibitors have many limitations. Recently Proteolysis-Targeting Chimeras (PROTACs) have become an advanced tool in therapeutic intervention as they remove disease causing proteins. This review provides an overview of the development and mechanisms of PROTACs for BRD and BET protein regulation in cancer and advanced possibilities of genetic technologies in therapeutics.
- Open Access
- 1 January 2018
- Published by Taylor & Francis in Cogent Chemistry
- Vol. 4 (1)
n-Alkane isomerization by catalysis—a method of industrial importance: An overview
This review article provides an overview of the advances in the field of hydro-conversion of n-alkanes with particular stress on the promising ways to meet the requirements for improved quality of motor fuels and oils, which have been marked during the past decades. Particular attention is given to a catalyst formulation for conversion of n-alkanes to branched hydrocarbons. The particular challenge is to find an effective catalyst, which favors the isomerization of n-alkanes without too much cracking. The regulation of active sites and adsorption properties, as well as the topology of support surfaces, allows a potential predictive design of novel catalysts for conversion of n-alkanes into their branched isomers. Graphical Abstract
- 1 January 2018
- Published by Taylor & Francis in Cogent Chemistry
- Vol. 4 (1)
Open Accessn-Alkane isomerization by catalysis—a method of industrial importance: An overview
This review article provides an overview of the advances in the field of hydro-conversion of n-alkanes with particular stress on the promising ways to meet the requirements for improved quality of motor fuels and oils, which have been marked during the past decades. Particular attention is given to a catalyst formulation for conversion of n-alkanes to branched hydrocarbons. The particular challenge is to find an effective catalyst, which favors the isomerization of n-alkanes without too much cracking. The regulation of active sites and adsorption properties, as well as the topology of support surfaces, allows a potential predictive design of novel catalysts for conversion of n-alkanes into their branched isomers. Graphical Abstract