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Identification of new benzofuran derivatives as STING agonists with broad-spectrum antiviral activity

Virus research, 2024-09, Vol.347, p.199432, Article 199432

2024

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Enhancing drug discovery through in silico screening: strategies to increase true positives retrieval rates

Current medicinal chemistry, 2008-08, Vol.15 (20), p.2040

2008

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Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase

European journal of medicinal chemistry, 2010-10, Vol.45 (10), p.4490-4498

2010

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Synthesis and biological activity evaluation of differently substituted 1,4-dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides

Journal of heterocyclic chemistry, 2003-11, Vol.40 (6), p.1011-1015

2003

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Synthesis and anti-microbial activity evaluation of some new 1-benzoyl-isothiosemicarbazides

Farmaco (Società chimica italiana : 1989), 2004-12, Vol.59 (12), p.945-952

2004

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Synthesis, Molecular Modeling Studies, and Selective Inhibitory Activity against Monoamine Oxidase of 1-Thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)- pyrazole Derivatives

Journal of medicinal chemistry, 2005-11, Vol.48 (23), p.7113-7122

2005

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An investigation of the biological effect of structural modifications of isothiosemicarbazones and their cyclic analogues

Farmaco (Società chimica italiana : 1989), 2003-09, Vol.58 (9), p.951-959

2003

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Synthesis and Biological Activity Evaluation of Differently Substituted 1,4-Dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides

ChemInform, 2004-05, Vol.35 (19), p.no-no

2004

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Matter and Method: The Quest for a New‐Materialist Methodology in Management Studies

British journal of management, 2024-01, Vol.35 (1), p.86-98

2024

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Evaluation of the performance of 3D virtual screening protocols: RMSD comparisons, enrichment assessments, and decoy selection—What can we learn from earlier mistakes?

Journal of computer-aided molecular design, 2008-03, Vol.22 (3-4), p.213-228

2008

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Quercetin Blocks Ebola Virus Infection by Counteracting the VP24 Interferon-Inhibitory Function

Antimicrobial agents and chemotherapy, 2020-06, Vol.64 (7)

2020

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Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea

Journal of enzyme inhibition and medicinal chemistry, 2024-12, Vol.39 (1), p.2287420-2287420

2024

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Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase

Journal of enzyme inhibition and medicinal chemistry, 2017-01, Vol.32 (1), p.130-136

2017

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How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information

Journal of Chemical Information and Modeling, 2009-03, Vol.49 (3), p.678-692

2009

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2-(2-Methyl-2-nitrovinyl)furan but Not Furvina Interfere with Staphylococcus aureus Agr Quorum-Sensing System and Potentiate the Action of Fusidic Acid against Biofilms

International journal of molecular sciences, 2021-01, Vol.22 (2), p.613

2021

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Ribonuclease H/DNA Polymerase HIV-1 Reverse Transcriptase Dual Inhibitor: Mechanistic Studies on the Allosteric Mode of Action of Isatin-Based Compound RMNC6

PloS one, 2016-01, Vol.11 (1), p.e0147225

2016

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Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.685-692

2021

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2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms

Journal of enzyme inhibition and medicinal chemistry, 2023-12, Vol.38 (1), p.2270183-2270183

2023

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Coumarins from Magydaris pastinacea as inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.539-548

2020

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Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors

Journal of enzyme inhibition and medicinal chemistry, 2017-01, Vol.32 (1), p.68-73

2017

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5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action

Frontiers in cellular and infection microbiology, 2023-06, Vol.13, p.1193280-1193280

2023

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Flavonoids and Acid-Hydrolysis derivatives of Neo-Clerodane diterpenes from Teucrium flavum subsp. glaucum as inhibitors of the HIV-1 reverse transcriptase-associated RNase H function

Journal of enzyme inhibition and medicinal chemistry, 2021-01, Vol.36 (1), p.749-757

2021

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Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions

Molecules (Basel, Switzerland), 2021-06, Vol.26 (13), p.3821

2021

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Molecular aspects of the RT/drug interactions. Perspective of dual inhibitors

Current pharmaceutical design, 2013, Vol.19 (10), p.1850

2013

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Ebola virus disease: In vivo protection provided by the PAMP restricted TLR3 agonist rintatolimod and its mechanism of action

Antiviral research, 2023-04, Vol.212, p.105554-105554, Article 105554

2023

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Identification of new benzofuran derivatives as STING agonists with broad-spectrum antiviral activity

Enhancing drug discovery through in silico screening: strategies to increase true positives retrieval rates

Synthesis of new 3-aryl-4,5-dihydropyrazole-1-carbothioamide derivatives. An investigation on their ability to inhibit monoamine oxidase

Synthesis and biological activity evaluation of differently substituted 1,4-dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides

Synthesis and anti-microbial activity evaluation of some new 1-benzoyl-isothiosemicarbazides

Synthesis, Molecular Modeling Studies, and Selective Inhibitory Activity against Monoamine Oxidase of 1-Thiocarbamoyl-3,5-diaryl-4,5-dihydro-(1H)- pyrazole Derivatives

An investigation of the biological effect of structural modifications of isothiosemicarbazones and their cyclic analogues

Synthesis and Biological Activity Evaluation of Differently Substituted 1,4-Dioxo-3,4-dihydrophthalazine-2(1H)-carboxamides and -carbothioamides

Matter and Method: The Quest for a New‐Materialist Methodology in Management Studies

Evaluation of the performance of 3D virtual screening protocols: RMSD comparisons, enrichment assessments, and decoy selection—What can we learn from earlier mistakes?

Quercetin Blocks Ebola Virus Infection by Counteracting the VP24 Interferon-Inhibitory Function

Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea

Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase

How To Optimize Shape-Based Virtual Screening: Choosing the Right Query and Including Chemical Information

2-(2-Methyl-2-nitrovinyl)furan but Not Furvina Interfere with Staphylococcus aureus Agr Quorum-Sensing System and Potentiate the Action of Fusidic Acid against Biofilms

Ribonuclease H/DNA Polymerase HIV-1 Reverse Transcriptase Dual Inhibitor: Mechanistic Studies on the Allosteric Mode of Action of Isatin-Based Compound RMNC6

Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives

2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms

Coumarins from Magydaris pastinacea as inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation

Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors

5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action

Flavonoids and Acid-Hydrolysis derivatives of Neo-Clerodane diterpenes from Teucrium flavum subsp. glaucum as inhibitors of the HIV-1 reverse transcriptase-associated RNase H function

Exploring New Scaffolds for the Dual Inhibition of HIV-1 RT Polymerase and Ribonuclease Associated Functions

Molecular aspects of the RT/drug interactions. Perspective of dual inhibitors

Ebola virus disease: In vivo protection provided by the PAMP restricted TLR3 agonist rintatolimod and its mechanism of action

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