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In-vitro studies of Curcumin-β-cyclodextrin inclusion complex as sustained release system

Journal of molecular structure, 2021-03, Vol.1228, p.129774, Article 129774

2021

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

Research on chemical intermediates, 2024-03, Vol.50 (3), p.1249-1271

2024

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Design and development of carboxymethylcellulose ester of curcumin as sustained release delivery system in liver

International journal of biological macromolecules, 2023-03, Vol.231, p.123296-123296, Article 123296

2023

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In-vitro simulation of modified-alginate ester as sustained release delivery system for curcumin

Journal of molecular structure, 2023-07, Vol.1283, p.135307, Article 135307

2023

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

European journal of medicinal chemistry reports, 2022-08, Vol.5, p.100056, Article 100056

2022

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Comparative study of covalent and hydrophobic interactions for α-amylase immobilization on cellulose derivatives

International journal of biological macromolecules, 2021-03, Vol.174, p.134-143

2021

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Usage of nanocrystalline cellulose phosphate as novel sustained release system for anti-inflammatory drugs

Journal of molecular structure, 2021-06, Vol.1233, p.130108, Article 130108

2021

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Alginate hydrogels: Sustained release system to analyze the effect of traditional excipients on curcumin availability

Bioorganic chemistry, 2021-02, Vol.107, p.104513-104513, Article 104513

2021

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In-silico identification of lysine residue for lysozyme immobilization on dialdehyde cellulose

International journal of biological macromolecules, 2023-07, Vol.244, p.125367-125367, Article 125367

2023

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Ultrasound assisted a one pot multicomponent and greener synthesis of 1,2,3-triazole incorporated aurone hybrids: Cathepsin B inhibition, anti-cancer activity against AGS cell line, and in-silico docking evaluation

Current research in green and sustainable chemistry, 2022, Vol.5, p.100295, Article 100295

2022

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Cellulose tosylate as support for α-amylase immobilization

International journal of biological macromolecules, 2022-12, Vol.222, p.413-420

2022

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SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H

Bioorganic & medicinal chemistry, 2014-08, Vol.22 (15), p.4233-4245

2014

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A biomimetic study of aliphatic and aromatic dicarboxylic acids engineered β-CD targeted for intestinal maladies

Chemical engineering journal (Lausanne, Switzerland : 1996), 2023-04, Vol.461, p.141929, Article 141929

2023

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Study on enhanced serum protein protecting and anti-cathepsin activities of various curcumin formulations containing traditional excipients and bio-enhancers

Bioorganic chemistry, 2020-11, Vol.104, p.104177, Article 104177

2020

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Design, synthesis and docking studies of bischalcones based quinazoline-2(1H)-ones and quinazoline-2(1H)-thiones derivatives as novel inhibitors of cathepsin B and cathepsin H

European journal of pharmaceutical sciences, 2014-04, Vol.54, p.28-39

2014

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Some thiocarbamoyl based novel anticathepsin agents

Bioorganic chemistry, 2020-11, Vol.104, p.104174, Article 104174

2020

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In-silico identification of lysine residue for α-Amylase immobilization on dialdehyde cellulose

International journal of biological macromolecules, 2022-03, Vol.200, p.618-625

2022

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Acyl hydrazides and triazoles as novel inhibitors of mammalian cathepsin B and cathepsin H

European journal of medicinal chemistry, 2014-04, Vol.77, p.231-242

2014

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Chalcones, semicarbazones and pyrazolines as inhibitors of cathepsins B, H and L

International journal of biological macromolecules, 2015-09, Vol.80, p.710-724

2015

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Curcumin analogs as anti-cathepsins agents: Designing, virtual screening, and molecular docking analysis

Computational toxicology, 2021-08, Vol.19, p.100174, Article 100174

2021

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2,5-Diaryloxadiazoles and their precursors as novel inhibitors of cathepsins B, H and L

Bioorganic chemistry, 2016-08, Vol.67, p.64-74

2016

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Ligand-based modeling of semicarbazones and thiosemicarbazones derivatives as Cathepsin B, H, and L inhibitors: A multi-target approach

Journal of molecular structure, 2022-06, Vol.1257, p.132612, Article 132612

2022

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Carboxymethyl β-cyclodextrin: Box-behnken model optimized synthesis, modification with cetyltrimethylammonium bromide and usage as sustained release system for curcumin

Journal of molecular structure, 2023-04, Vol.1277, p.134820, Article 134820

2023

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Revolutionizing industrial wastewater Treatment: MXenes conquer organic pollutants in a paradigm shifting breakthrough towards Sustainability

Chemical engineering journal (Lausanne, Switzerland : 1996), 2024-06, Vol.490, p.151373, Article 151373

2024

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SAR studies of some acetophenone phenylhydrazone based pyrazole derivatives as anticathepsin agents

Bioorganic chemistry, 2017-12, Vol.75, p.38-49

2017

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In-vitro studies of Curcumin-β-cyclodextrin inclusion complex as sustained release system

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

Design and development of carboxymethylcellulose ester of curcumin as sustained release delivery system in liver

In-vitro simulation of modified-alginate ester as sustained release delivery system for curcumin

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

Comparative study of covalent and hydrophobic interactions for α-amylase immobilization on cellulose derivatives

Usage of nanocrystalline cellulose phosphate as novel sustained release system for anti-inflammatory drugs

Alginate hydrogels: Sustained release system to analyze the effect of traditional excipients on curcumin availability

In-silico identification of lysine residue for lysozyme immobilization on dialdehyde cellulose

Ultrasound assisted a one pot multicomponent and greener synthesis of 1,2,3-triazole incorporated aurone hybrids: Cathepsin B inhibition, anti-cancer activity against AGS cell line, and in-silico docking evaluation

Cellulose tosylate as support for α-amylase immobilization

SAR studies of differently functionalized chalcones based hydrazones and their cyclized derivatives as inhibitors of mammalian cathepsin B and cathepsin H

A biomimetic study of aliphatic and aromatic dicarboxylic acids engineered β-CD targeted for intestinal maladies

Study on enhanced serum protein protecting and anti-cathepsin activities of various curcumin formulations containing traditional excipients and bio-enhancers

Design, synthesis and docking studies of bischalcones based quinazoline-2(1H)-ones and quinazoline-2(1H)-thiones derivatives as novel inhibitors of cathepsin B and cathepsin H

Some thiocarbamoyl based novel anticathepsin agents

In-silico identification of lysine residue for α-Amylase immobilization on dialdehyde cellulose

Acyl hydrazides and triazoles as novel inhibitors of mammalian cathepsin B and cathepsin H

Chalcones, semicarbazones and pyrazolines as inhibitors of cathepsins B, H and L

Curcumin analogs as anti-cathepsins agents: Designing, virtual screening, and molecular docking analysis

2,5-Diaryloxadiazoles and their precursors as novel inhibitors of cathepsins B, H and L

Ligand-based modeling of semicarbazones and thiosemicarbazones derivatives as Cathepsin B, H, and L inhibitors: A multi-target approach

Carboxymethyl β-cyclodextrin: Box-behnken model optimized synthesis, modification with cetyltrimethylammonium bromide and usage as sustained release system for curcumin

Revolutionizing industrial wastewater Treatment: MXenes conquer organic pollutants in a paradigm shifting breakthrough towards Sustainability

SAR studies of some acetophenone phenylhydrazone based pyrazole derivatives as anticathepsin agents

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