Synthesis of Pyrroles and Condensed Pyrroles as Anti-Inflammatory Agents with Multiple Activities and Their Molecular Docking Study

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Open Journal of Medicinal Chemistry

ISSN Print: 2164-3121
ISSN Online: 2164-313X
www.scirp.org/journal/ojmc
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"Synthesis of Pyrroles and Condensed Pyrroles as Anti-Inflammatory Agents with Multiple Activities and Their Molecular Docking Study"
written by M. T. Sarg, M. M. Koraa, A. H. Bayoumi, S. M. Abd El Gilil,
published by Open Journal of Medicinal Chemistry, Vol.5 No.4, 2015

has been cited by the following article(s):

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[6]	Design, synthesis, computational molecular docking studies of novel heterocyclics bearing 1, 2, 4–triazole, 1, 3, 4–oxadiazole conjugates as potent antibacterial and …
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[7]	New Pyrrole Derivatives as Promising Biological Agents: Design, Synthesis, Characterization, In Silico, and Cytotoxicity Evaluation
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[8]	Acetic Acid‐Catalyzed Selective Synthesis of N‐Substituted 2‐Amino‐3‐Cyanopyrroles via a Three‐Component Reaction Between Carbohydrates, Primary Amines …
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[10]	Synthesis of densely functionalized pyrroles from unprotected carbohydrates
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[11]	10.09-Bicyclic 5-6 systems: four heteroatoms 1: 3
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[13]	Synthesis of novel pyrroles and fused pyrroles as antifungal and antibacterial agents
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[14]	Contemporary advances of cyclic molecules proposed for inflammation
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[15]	E/Z isomerization of ethyl 2-amino-1-(3-(ethoxycarbonyl)-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)-4-oxo-5-(2-oxo-2-phenylethylidene)-4,5-dihydro-1H-pyrrole-3 …
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[16]	E/Z isomerization of ethyl 2-amino-1-(3-(ethoxycarbonyl)-4, 5, 6, 7-tetrahydrobenzo [b] thiophen-2-yl)-4-oxo-5-(2-oxo-2-phenylethylidene)-4, 5-dihydro-1H-pyrrole-3 …
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[17]	Synthesis and Anticancer Activity Study of Some Novel Substituted and Fused Pyridotriazepine Derivatives
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[18]	Synthesis and highly potent anti-inflammatory activity of licofelone-and ketorolac-based 1-arylpyrrolizin-3-ones
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[19]	Design, synthesis, molecular docking and biological screening of N-ethyl-N-methylbenzenesulfonamide derivatives as effective antimicrobial and antiproliferative …
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[20]	Assessment of Anti-inflammatory Activity of Novel Compound of Indole Derivatives and Elucidation of Possible Mechanisms of Action
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[21]	Evaluation of novel pyrrolopyrimidine derivatives as antiviral against gastroenteric viral infections
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[22]	Synthesis and structure activity relationship of some indole derivatives as potential anti-inflammatory agents.
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[23]	Pyrrole and Fused Pyrrole Compounds with Bioactivity against Inflammatory Mediators
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[24]	Preparation of novel pyrrol-2-one derivatives via an effective synthesis of new oxazole scaffold
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[25]	Synthesis and Structure Activity Relationship of Some Indole Derivatives as Potential Anti-inflammatory Agents
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[26]	Formation of 1, 5-Disubstituted 2-hydroxypyrroles via Reaction of 2-(Triphenylphosphoranylidene) succinic Anhydride with Schiff's Bases
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[27]	4, 5, 6-7-ТЕТРАГИДРОБЕНЗО [b] ТИОФЕН-2-ИЛ) 4, 5-ДИГИДРО-1Н-ПИРРОЛ-3-КАРБОНОВОЙ КИСЛОТЫ, ОБЛАДАЮЩИЙ ПРОТИВОМИКРОБНОЙ …
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[1]	Design, synthesis, computational molecular docking studies of novel heterocyclics bearing 1,2,4–triazole, 1,3,4–oxadiazole conjugates as potent antibacterial and antitubercular agents Journal of Biomolecular Structure and Dynamics, 2024 DOI:10.1080/07391102.2023.2226743

[2]	Synthesis and biological evaluation of 1, 2, 3-triazole incorporated pyrrole derivatives as anticancer agents Synthetic Communications, 2024 DOI:10.1080/00397911.2024.2408605

[3]	1,3 Dipolar Cycloaddition of Münchnones: Factors behind the Regioselectivity The Journal of Physical Chemistry A, 2023 DOI:10.1021/acs.jpca.2c06472

[4]	1,3 Dipolar Cycloaddition of Münchnones: Factors behind the Regioselectivity The Journal of Physical Chemistry A, 2023 DOI:10.1021/acs.jpca.2c06472

[5]	Design, synthesis, computational molecular docking studies of novel heterocyclics bearing 1,2,4–triazole, 1,3,4–oxadiazole conjugates as potent antibacterial and antitubercular agents Journal of Biomolecular Structure and Dynamics, 2023 DOI:10.1080/07391102.2023.2226743

[6]	(E)-1-(3-Benzoyl-4-phenyl-1H-pyrrol-1-yl)-3-phenylprop-2-en-1-one Molbank, 2022 DOI:10.3390/M1314

[7]	New Pyrrole Derivatives as Promising Biological Agents: Design, Synthesis, Characterization, In Silico, and Cytotoxicity Evaluation International Journal of Molecular Sciences, 2022 DOI:10.3390/ijms23168854

[8]	E/Z isomerization of ethyl 2-amino-1-(3-(ethoxycarbonyl)-4,5,6,7-tetrahydrobenzo[b]thiophen-2-yl)-4-oxo-5-(2-oxo-2-phenylethylidene)-4,5-dihydro-1H-pyrrole-3-carboxylate PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019, 2020 DOI:10.1063/5.0018490

[9]	Evaluation of novel pyrrolopyrimidine derivatives as antiviral against gastroenteric viral infections European Journal of Pharmaceutical Sciences, 2019 DOI:10.1016/j.ejps.2018.10.022

[10]	Design, synthesis, molecular docking and biological screening of N-ethyl-N-methylbenzenesulfonamide derivatives as effective antimicrobial and antiproliferative agents Journal of Molecular Structure, 2019 DOI:10.1016/j.molstruc.2019.04.048

[11]	Synthesis and highly potent anti-inflammatory activity of licofelone- and ketorolac-based 1-arylpyrrolizin-3-ones Bioorganic & Medicinal Chemistry, 2019 DOI:10.1016/j.bmc.2019.115053

[12]	Pyrrole and Fused Pyrrole Compounds with Bioactivity against Inflammatory Mediators Molecules, 2017 DOI:10.3390/molecules22030461

[13]	Pyrrole and Fused Pyrrole Compounds with Bioactivity against Inflammatory Mediators Molecules, 2017 DOI:10.3390/molecules22030461

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