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A simple sequential one-pot synthesis of 4-aryl thiazole-based Schiff bases

Synthetic communications, 2024-01, Vol.54 (2), p.111-120

2024

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Formulation and characterization of chitosan nanoparticles loaded with neuroprotective flavonoid from Phyllanthusniruri Linn

Macromolecular research, 2023, Vol.31 (1), p.13-24

2023

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Chalcone-Thiazole Hybrids: Rational Design, Synthesis, and Lead Identification against 5‑Lipoxygenase

ACS medicinal chemistry letters, 2019-10, Vol.10 (10), p.1415-1422

2019

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Bio-guided isolation of anti-Alzheimer’s compounds from Phyllanthus niruri and role of niruriflavone in the reversal of aluminum chloride-induced neurobehavioral and biochemical changes in an animal model

Medicinal chemistry research, 2022-10, Vol.31 (10), p.1740-1753

2022

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Indoles — A promising scaffold for drug development

European journal of pharmaceutical sciences, 2016-08, Vol.91, p.1-10

2016

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Novel approach of multi-targeted thiazoles and thiazolidenes toward anti-inflammatory and anticancer therapy—dual inhibition of COX-2 and 5-LOX enzymes

Medicinal chemistry research, 2021, Vol.30 (1), p.236-257

2021

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5-Lipoxygenase as a drug target: A review on trends in inhibitors structural design, SAR and mechanism based approach

Bioorganic & medicinal chemistry, 2019-09, Vol.27 (17), p.3745-3759

2019

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Design, synthesis and identification of novel substituted 2-amino thiazole analogues as potential anti-inflammatory agents targeting 5-lipoxygenase

European journal of medicinal chemistry, 2018-10, Vol.158, p.34-50

2018

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Safer anti-inflammatory therapy through dual COX-2/5-LOX inhibitors: A structure-based approach

European journal of pharmaceutical sciences, 2018-08, Vol.121, p.356-381

2018

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Identification of novel indole-based dyes as active photo-sensitizers: Synthesis, photophysical, electrochemical and computational investigation

Optical materials, 2023-11, Vol.145, p.114391, Article 114391

2023

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Identification and development of thiazole leads as COX-2/5-LOX inhibitors through in-vitro and in-vivo biological evaluation for anti-inflammatory activity

Bioorganic chemistry, 2020-07, Vol.100, p.103882-103882, Article 103882

2020

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Formulation and characterization of chitosan nanoparticles loaded with neuroprotective flavonoid from Phyllanthus niruri Linn

Macromolecular Research, 2023, 31(1), , pp.13-24

2023

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A novel class of tyrosine derivatives as dual 5-LOX and COX-2/mPGES1 inhibitors with PGE2 mediated anticancer properties

New journal of chemistry, 2019-01, Vol.43 (2), p.834

2019

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2-Amino-4-aryl thiazole: a promising scaffold identified as a potent 5-LOX inhibitor

RSC advances, 2016-01, Vol.6 (23), p.19271-19279

2016

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Synthesis and Fluorescence Properties of Novel indol-3yl-thiazolo[3,2-a][1,3,5]triazines and indole-3-carbaldehyde Schiff Bases

Journal of fluorescence, 2015-11, Vol.25 (6), p.1727-1738

2015

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Synthesis, docking, and evaluation of novel thiazoles for potent antidiabetic activity

Medicinal chemistry research, 2017-06, Vol.26 (6), p.1306-1315

2017

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Isolation, structural elucidation and anti-inflammatory activity of astragalin, ( − )hinokinin, aristolactam I and aristolochic acids (I & II) from Aristolochia indica

Natural product research, 2014-01, Vol.28 (17), p.1413-1417

2014

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Synthesis and biological evaluation of some novel substituted 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxamides

IOP conference series. Materials Science and Engineering, 2017-11, Vol.263 (2), p.22019

2017

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Development of D-D-π-A structured 5-aryl indoles as photosensitizers

Journal of molecular structure, 2024-05, Vol.1304, p.137662, Article 137662

2024

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A review on phyto-nanotechnology for therapy of alzheimer’s disease

Indian journal of biochemistry & biophysics, 2022-09

2022

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Formulation and Standardization of Polyherbal Antihyperlipidemic Formulation

Journal of natural remedies, 2021-01, Vol.20 (4), p.228

2021

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HPLC Quantification and Stability Study of Antilipidemic Polyherbal Formulation

Journal of natural remedies, 2022-07, p.380-392

2022

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A novel class of tyrosine derivatives as dual 5-LOX and COX-2/mPGES1 inhibitors with PGE 2 mediated anticancer properties

New journal of chemistry, 2019-01, Vol.43 (2), p.834-846

2019

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A novel class of tyrosine derivatives as dual 5-LOX and COX-2/mPGES1 inhibitors with PGE2 mediated anticancer propertiesElectronic supplementary information (ESI) available. See DOI: 10.1039/c8nj04385j

2019-01

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ChemInform Abstract: An Improved Bischler Indole Synthesis to Obtain 2-Arylindole Scaffolds

ChemInform, 2015-11, Vol.46 (46), p.no-no

2015

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A simple sequential one-pot synthesis of 4-aryl thiazole-based Schiff bases

Formulation and characterization of chitosan nanoparticles loaded with neuroprotective flavonoid from Phyllanthusniruri Linn

Chalcone-Thiazole Hybrids: Rational Design, Synthesis, and Lead Identification against 5‑Lipoxygenase

Bio-guided isolation of anti-Alzheimer’s compounds from Phyllanthus niruri and role of niruriflavone in the reversal of aluminum chloride-induced neurobehavioral and biochemical changes in an animal model

Indoles — A promising scaffold for drug development

Novel approach of multi-targeted thiazoles and thiazolidenes toward anti-inflammatory and anticancer therapy—dual inhibition of COX-2 and 5-LOX enzymes

5-Lipoxygenase as a drug target: A review on trends in inhibitors structural design, SAR and mechanism based approach

Design, synthesis and identification of novel substituted 2-amino thiazole analogues as potential anti-inflammatory agents targeting 5-lipoxygenase

Safer anti-inflammatory therapy through dual COX-2/5-LOX inhibitors: A structure-based approach

Identification of novel indole-based dyes as active photo-sensitizers: Synthesis, photophysical, electrochemical and computational investigation

Identification and development of thiazole leads as COX-2/5-LOX inhibitors through in-vitro and in-vivo biological evaluation for anti-inflammatory activity

Formulation and characterization of chitosan nanoparticles loaded with neuroprotective flavonoid from Phyllanthus niruri Linn

A novel class of tyrosine derivatives as dual 5-LOX and COX-2/mPGES1 inhibitors with PGE2 mediated anticancer properties

2-Amino-4-aryl thiazole: a promising scaffold identified as a potent 5-LOX inhibitor

Synthesis and Fluorescence Properties of Novel indol-3yl-thiazolo[3,2-a][1,3,5]triazines and indole-3-carbaldehyde Schiff Bases

Synthesis, docking, and evaluation of novel thiazoles for potent antidiabetic activity

Isolation, structural elucidation and anti-inflammatory activity of astragalin, ( − )hinokinin, aristolactam I and aristolochic acids (I & II) from Aristolochia indica

Synthesis and biological evaluation of some novel substituted 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxamides

Development of D-D-π-A structured 5-aryl indoles as photosensitizers

A review on phyto-nanotechnology for therapy of alzheimer’s disease

Formulation and Standardization of Polyherbal Antihyperlipidemic Formulation

HPLC Quantification and Stability Study of Antilipidemic Polyherbal Formulation

A novel class of tyrosine derivatives as dual 5-LOX and COX-2/mPGES1 inhibitors with PGE 2 mediated anticancer properties

A novel class of tyrosine derivatives as dual 5-LOX and COX-2/mPGES1 inhibitors with PGE2 mediated anticancer propertiesElectronic supplementary information (ESI) available. See DOI: 10.1039/c8nj04385j

ChemInform Abstract: An Improved Bischler Indole Synthesis to Obtain 2-Arylindole Scaffolds

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