A decennary update on diverse heterocycles and their intermediates as privileged scaffolds for cathepsin B inhibition

B Saroha, G Kumar, M Kumari, R Kaur… - International Journal of …, 2022 - Elsevier
The identification of x-ray crystal structure of cathepsin B (CTSB) in the early 90's enabled
researchers to embark on a journey to understand and demystify its multiple catalytic …

Some morpholine tethered novel aurones: Design, synthesis, biological, kinetic and molecular docking studies

B Saroha, G Kumar, P Arya, N Raghav, S Kumar - Bioorganic Chemistry, 2023 - Elsevier
Enzymes are the biological macromolecules that have emerged as an important drug target
as their upregulation/imbalance leads to various pathological conditions, such as …

Synthesis and biological evaluation of substituted aurone derivatives as potential tyrosinase inhibitors: in vitro, kinetic, QSAR, docking and drug-likeness studies

NA Alshaye, EU Mughal, EB Elkaeed… - Journal of …, 2023 - Taylor & Francis
Tyrosinase enzyme plays an essential role in melanin biosynthesis and enzymatic browning
of fruits and vegetables. To discover potent tyrosinase inhibitors, the present studies were …

1, 2, 3-triazole clubbed and dichloro substituted novel aurones as potential anticancer agents targeting digestive enzymes: Design, synthesis, DFT, ADME and …

G Kumar, B Saroha, P Arya, S Ghosh, B Kumari… - Journal of Molecular …, 2025 - Elsevier
In the present investigation, we engineered some 1, 2, 3-triazole clubbed and dichloro
substituted novel aurones as potential anticancer agents well capable of targeting digestive …

[HTML][HTML] Ultrasound assisted a one pot multicomponent and greener synthesis of 1, 2, 3-triazole incorporated aurone hybrids: Cathepsin B inhibition, anti-cancer …

B Saroha, G Kumar, S Kumar, M Kumari, M Rani… - Current Research in …, 2022 - Elsevier
Cathepsin B represents a group of lysosomal-encapsulated cellular cysteine proteases,
whose upregulation is the critical risk factor for cancer progression and in the regulation of …

[HTML][HTML] Novel 1, 2, 3-triazole-aurone hybrids as cathepsin B inhibitors: One-pot synthesis, anti-proliferative, and drug modeling studies

B Saroha, G Kumar, S Kumar, M Kumari, M Rani… - European Journal of …, 2022 - Elsevier
In the present study, we have designed a series of novel 1, 2, 3-triazole-aurone hybrids,
which were synthesized by a one-pot click reaction between a terminal alkyne and an in-situ …

Design, synthesis, biological evaluation, and molecular docking studies of some novel N,N‐dimethylaminopropoxy‐substituted aurones

G Kumar, B Saroha, R Kumar, M Kumari… - Journal of …, 2022 - Wiley Online Library
In continuation of our ongoing research on the discovery of novel and potentially bioactive
aurones, we have designed and synthesized some novel N, N‐dimethylaminopropoxy …

Synthetic and Biological Studies of Some Pyrrolidine-Tethered Novel Aurones against Digestive Enzymes

S Kumar, B Saroha, E Lathwal, G Kumar… - Current Organic …, 2023 - ingentaconnect.com
Amylase, lipase, and trypsin are crucial digestive enzymes, whose activation or inhibition is
of potent therapeutic approach for treating various body disorders. In this work, we have …

Cinnamaldehyde hydrazone derivatives as potential cathepsin B inhibitors: A parallel in-vitro investigation in liver and cerebrospinal fluid

C Vashisth, T Kaushik, N Vashisth, N Raghav - International Journal of …, 2024 - Elsevier
The emergence of cathepsins as a potential target for anticancer drugs has led to extensive
research in the development of their inhibitors. In the present study, we designed …

Design, synthesis, molecular docking and biological studies of some novel pyrrolidine-triazole-aurone hybrids against digestive enzymes

S Kumar, E Lathwal, B Saroha, G Kumar… - Research on Chemical …, 2024 - Springer
Here in this work we successfully designed and synthesized a library of some novel
pyrrolidine-triazole-aurone hybrids ie (Z)-2-benzylidene-6-((1-(2-(pyrrolidin-1-yl) ethyl)-1 H …