SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL IMIDAZOQUINAZOLINONE DERIVATIVES AS HDAC6 ISOFORM-SELECTIVE INHIBITORS

Synthesis and SAR of Isoform selective HDAC6 inhibitors of novel imidazoquinazolinones is shown. It demonstrates HDAC6 selective pharmacokinetic properties and has clean off-target profile. It shows efficacy comparable to approved HDAC inhibitors.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2026-06-29
DOI
https://doi.org/10.5281/zenodo.21033572
Primary Topic
Histone Deacetylase Inhibitors Research
Type
article
Field-Weighted Citation Impact
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article

SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL IMIDAZOQUINAZOLINONE DERIVATIVES AS HDAC6 ISOFORM-SELECTIVE INHIBITORS

Abhijit Roychowdhury, Srinivas Gullapalli, Krishna Anand Putta, Kaivalya G. Kulkarni et al.
Zenodo (CERN European Organization for Nuclear Research)
Histone Deacetylase Inhibitors Research
article

SYNTHESIS AND BIOLOGICAL EVALUATION OF NOVEL IMIDAZOQUINAZOLINONE DERIVATIVES AS HDAC6 ISOFORM-SELECTIVE INHIBITORS

Abhijit Roychowdhury, Srinivas Gullapalli, Krishna Anand Putta, Kaivalya G. Kulkarni, Pankaj Kumar Singh, Tushar Khaladkar, Dhananjay Magar, Jayanarayan Kulathingal, Kailas Shikhare, Rammohana Reddy Lekkala
article en

Abstract

Synthesis and SAR of Isoform selective HDAC6 inhibitors of novel imidazoquinazolinones is shown. It demonstrates HDAC6 selective pharmacokinetic properties and has clean off-target profile. It shows efficacy comparable to approved HDAC inhibitors.

Zenodo (CERN European Organization for Nuclear Research)
Emcure Pharmaceuticals (India) (IN)
Industry, innovation and infrastructure
Openalex Percentile: Top 12%
Histone Deacetylase Inhibitors Research
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