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Electric Vehicles Charging Stations’ Architectures, Criteria, Power Converters, and Control Strategies in Microgrids

Electronics (Basel), 2021-08, Vol.10 (16), p.1895

2021

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Structure–Activity Relationship Studies on 6-Chloro-1-phenylbenzazepines Leads to the Identification of a New Dopamine D1 Receptor Antagonist

Molecules (Basel, Switzerland), 2023-08, Vol.28 (16), p.6010

2023

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Synthesis and cancer cell cytotoxicity of substituted xanthenes

Bioorganic & medicinal chemistry, 2010-02, Vol.18 (4), p.1456-1463

2010

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Diverse Approaches and Recent Advances in the Synthesis of Tetrahydroprotoberberines

Current organic chemistry, 2018-01, Vol.22 (19), p.1893-1905

2018

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Novel theranostic agent for PET imaging and targeted radiopharmaceutical therapy of tumour-infiltrating immune cells in glioma

EBioMedicine, 2021-09, Vol.71 (C), p.103571-103571, Article 103571

2021

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Synthesis and evaluation of quinazolinone derivatives as inhibitors of NF-κB, AP-1 mediated transcription and eIF-4E mediated translational activation: Inhibitors of multi-pathways involve in cancer

European journal of medicinal chemistry, 2010-09, Vol.45 (9), p.3558-3563

2010

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Synthesis, pharmacological evaluations, and molecular docking studies on a new 1,3,4,11b‐tetrahydro‐1 H ‐fluoreno[9,1‐ cd ]azepine framework: Rigidification of D 1 receptor selective 1‐phenylbenzazepines and discovery of a new 5‐HT 6 receptor scaffold

Chemical biology & drug design, 2020-08, Vol.96 (2), p.825-835

2020

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Synthetic and Biological Studies on Benzazepine Derivatives as Dopamine Receptor Ligands

Giri, Rajan

2021

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Synthesis and dopamine receptor pharmacological evaluations on ring C ortho halogenated 1-phenylbenzazepines

Bioorganic & medicinal chemistry letters, 2020-08, Vol.30 (16), p.127305-127305, Article 127305

2020

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Synthesis and dopamine receptor pharmacological evaluations on ring C ortho halogenated 1-phenyl-benzazepines

Bioorganic & medicinal chemistry letters, 2020-06, Vol.30 (16), p.127305-127305

2020

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Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents

European journal of medicinal chemistry, 2009-05, Vol.44 (5), p.2184-2189

2009

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Synthesis, pharmacological evaluations, and molecular docking studies on a new 1,3,4,11b-tetrahydro-1H-fluoreno[9,1-cd]azepine framework: Rigidification of D 1 receptor selective 1-phenylbenzazepines and discovery of a new 5-HT 6 receptor scaffold

Chemical biology & drug design, 2020-08, Vol.96 (2), p.825

2020

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Further studies on C2′-substituted 1-phenylbenzazepines as dopamine D1 receptor ligands

Bioorganic chemistry, 2022-10, Vol.127, p.105953-105953, Article 105953

2022

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Synthesis, pharmacological evaluations, and molecular docking studies on a new 1,3,4,11b‐tetrahydro‐1H‐fluoreno[9,1‐cd]azepine framework: Rigidification of D1 receptor selective 1‐phenylbenzazepines and discovery of a new 5‐HT6 receptor scaffold

Chemical biology & drug design, 2020-08, Vol.96 (2), p.825-835

2020

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Monitoring the decolourisation efficacy of advanced membrane fabricated phytosilica nanoparticles in textile effluent water treatment

Chemosphere (Oxford), 2021-06, Vol.273, p.129681, Article 129681

2021

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FUZZY INFERENCE SYSTEM BASED POWER FACTOR CORRECTION OF THREE PHASE DIODE RECTIFIER USING FIELD PROGRAMABLE GATE ARRAY

American journal of applied sciences, 2013-09, Vol.10 (9), p.986-999

2013

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9-Amino acridine pharmacokinetics, brain distribution, and in vitro/in vivo efficacy against malignant glioma

Cancer chemotherapy and pharmacology, 2012-06, Vol.69 (6), p.1519-1527

2012

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Corrigendum to “Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents” [Eur J Med Chem 44 (2009) 2184–2189]

European journal of medicinal chemistry, 2009-11, Vol.44 (11), p.4783

2009

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Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-кB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents

Bioorganic & medicinal chemistry, 2010-04, Vol.18 (7), p.2796-2808

2010

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Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-kB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents

Bioorganic & medicinal chemistry, 2010, Vol.18 (7), p.2796-2808

2010

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Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-KB and AP-1 mediated transcription activation and as potential anti-inflammatory agents

European journal of medicinal chemistry, 2009, Vol.44 (5), p.2184-2189

2009

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Corrigendum to “Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3 H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents” [Eur J Med Chem 44 (2009) 2184–2189]

European journal of medicinal chemistry, 2009, Vol.44 (11), p.4783-4783

2009

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Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3 H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents

European journal of medicinal chemistry, 2009, Vol.44 (5), p.2184-2189

2009

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Synthesis and evaluation of quinazolinone derivatives as inhibitors of NF-kappaB, AP-1 mediated transcription and eIF-4E mediated translational activation: inhibitors of multi-pathways involve in cancer

European journal of medicinal chemistry, 2010-09, Vol.45 (9), p.3558-3563

2010

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Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-kappaB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents

Bioorganic & medicinal chemistry, 2010-04, Vol.18 (7), p.2796-2808

2010

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Electric Vehicles Charging Stations’ Architectures, Criteria, Power Converters, and Control Strategies in Microgrids

Structure–Activity Relationship Studies on 6-Chloro-1-phenylbenzazepines Leads to the Identification of a New Dopamine D1 Receptor Antagonist

Synthesis and cancer cell cytotoxicity of substituted xanthenes

Diverse Approaches and Recent Advances in the Synthesis of Tetrahydroprotoberberines

Novel theranostic agent for PET imaging and targeted radiopharmaceutical therapy of tumour-infiltrating immune cells in glioma

Synthesis and evaluation of quinazolinone derivatives as inhibitors of NF-κB, AP-1 mediated transcription and eIF-4E mediated translational activation: Inhibitors of multi-pathways involve in cancer

Synthesis, pharmacological evaluations, and molecular docking studies on a new 1,3,4,11b‐tetrahydro‐1 H ‐fluoreno[9,1‐ cd ]azepine framework: Rigidification of D 1 receptor selective 1‐phenylbenzazepines and discovery of a new 5‐HT 6 receptor scaffold

Synthetic and Biological Studies on Benzazepine Derivatives as Dopamine Receptor Ligands

Synthesis and dopamine receptor pharmacological evaluations on ring C ortho halogenated 1-phenylbenzazepines

Synthesis and dopamine receptor pharmacological evaluations on ring C ortho halogenated 1-phenyl-benzazepines

Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents

Synthesis, pharmacological evaluations, and molecular docking studies on a new 1,3,4,11b-tetrahydro-1H-fluoreno[9,1-cd]azepine framework: Rigidification of D 1 receptor selective 1-phenylbenzazepines and discovery of a new 5-HT 6 receptor scaffold

Further studies on C2′-substituted 1-phenylbenzazepines as dopamine D1 receptor ligands

Synthesis, pharmacological evaluations, and molecular docking studies on a new 1,3,4,11b‐tetrahydro‐1H‐fluoreno[9,1‐cd]azepine framework: Rigidification of D1 receptor selective 1‐phenylbenzazepines and discovery of a new 5‐HT6 receptor scaffold

Monitoring the decolourisation efficacy of advanced membrane fabricated phytosilica nanoparticles in textile effluent water treatment

FUZZY INFERENCE SYSTEM BASED POWER FACTOR CORRECTION OF THREE PHASE DIODE RECTIFIER USING FIELD PROGRAMABLE GATE ARRAY

9-Amino acridine pharmacokinetics, brain distribution, and in vitro/in vivo efficacy against malignant glioma

Corrigendum to “Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents” [Eur J Med Chem 44 (2009) 2184–2189]

Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-кB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents

Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-kB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents

Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3H-quinazoline-4-one derivatives as inhibitors of NF-KB and AP-1 mediated transcription activation and as potential anti-inflammatory agents

Corrigendum to “Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3 H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents” [Eur J Med Chem 44 (2009) 2184–2189]

Design, synthesis and characterization of novel 2-(2,4-disubstituted-thiazole-5-yl)-3-aryl-3 H-quinazoline-4-one derivatives as inhibitors of NF-κB and AP-1 mediated transcription activation and as potential anti-inflammatory agents

Synthesis and evaluation of quinazolinone derivatives as inhibitors of NF-kappaB, AP-1 mediated transcription and eIF-4E mediated translational activation: inhibitors of multi-pathways involve in cancer

Design, synthesis and evaluation of novel 2-thiophen-5-yl-3H-quinazolin-4-one analogues as inhibitors of transcription factors NF-kappaB and AP-1 mediated transcriptional activation: Their possible utilization as anti-inflammatory and anti-cancer agents

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