Crafting Carbazole-Based Vorinostat and Tubastatin-A-like Histone Deacetylase (HDAC) Inhibitors with Potent in Vitro and in Vivo Neuroactive Functions
Crafting Carbazole-Based Vorinostat and Tubastatin-A-like Histone Deacetylase (HDAC) Inhibitors with Potent in Vitro and in Vivo Neuroactive Functions
| dc.contributor.author | Reddy, R. Gajendra | |
| dc.contributor.author | Surineni, Goverdhan | |
| dc.contributor.author | Bhattacharya, Dwaipayan | |
| dc.contributor.author | Marvadi, Sandeep Kumar | |
| dc.contributor.author | Sagar, Arpita | |
| dc.contributor.author | Kalle, Arunasree M. | |
| dc.contributor.author | Kumar, Arvind | |
| dc.contributor.author | Kantevari, Srinivas | |
| dc.contributor.author | Chakravarty, Sumana | |
| dc.date.accessioned | 2022-03-27T01:01:42Z | |
| dc.date.available | 2022-03-27T01:01:42Z | |
| dc.date.issued | 2019-10-22 | |
| dc.description.abstract | Small-molecule inhibitors of HDACs (HDACi) induce hyperacetylation of histone and nonhistone proteins and have emerged as potential therapeutic agents in most animal models tested. The established HDACi vorinostat and tubastatin-A alleviate neurodegenerative and behavioral conditions in animal models of neuropsychiatric disorders restoring the neurotrophic milieu. In spite of the neuroactive pharmacological role of HDACi (vorinostat and tubastatin-A), they are limited by efficacy and toxicity. Considering these limitations and concern, we have designed novel compounds 3-11 as potential HDACi based on the strategic crafting of the key pharmacophoric elements of vorinostat and tubastatin-A into architecting a single molecule. The molecules 3-11 were synthesized through a multistep reaction sequence starting from carbazole and were fully characterized by NMR and mass spectral analysis. The novel molecules 3-11 showed remarkable pan HDAC inhibition and the potential to increase the levels of acetyl H3 and acetyl tubulin. In addition, few novel HDAC inhibitors 4-8, 10, and 11 exhibited significant neurite outgrowth-promoting activity with no observable cytotoxic effects, and interestingly, compound 5 has shown comparably more neurite growth than the parent compounds vorinostat and tubastatin-A. Also, compound 5 was evaluated for possible mood-elevating effects in a chronic unpredictable stress model of Zebrafish. It showed potent anxiolytic and antidepressant-like effects in the novel tank test and social interaction test, respectively. Furthermore, the potent in vitro and in vivo neuroactive compound 5 has shown selectivity for class II over class I HDACs. Our results suggest that the novel carbazole-based HDAC inhibitors, crafted with vorinostat and tubastatin-A pharmacophoric moieties, have potent neurite outgrowth activity and potential to be developed as therapeutics to treat depression and related psychiatric disorders. | |
| dc.identifier.citation | ACS Omega. v.4(17) | |
| dc.identifier.uri | 10.1021/acsomega.9b01950 | |
| dc.identifier.uri | https://pubs.acs.org/doi/10.1021/acsomega.9b01950 | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/3904 | |
| dc.title | Crafting Carbazole-Based Vorinostat and Tubastatin-A-like Histone Deacetylase (HDAC) Inhibitors with Potent in Vitro and in Vivo Neuroactive Functions | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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