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Effects of docosanyl ferulate, a constituent of Withania somnifera, on ethanol- and morphine-elicited conditioned place preference and ERK phosphorylation in the accumbens shell of CD1 mice

Psychopharmacology, 2022-03, Vol.239 (3), p.795-806

2022

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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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The biologically active compound of Withania somnifera (L.) Dunal, docosanyl ferulate, is endowed with potent anxiolytic properties but devoid of typical benzodiazepine-like side effects

Journal of psychopharmacology (Oxford), 2021-10, Vol.35 (10), p.1277-1284

2021

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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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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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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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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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Targeting Tumor Associated Carbonic Anhydrases IX and XII: Highly Isozyme Selective Coumarin and Psoralen Inhibitors

ACS medicinal chemistry letters, 2018-07, Vol.9 (7), p.725-729

2018

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Limonoids from Melia azedarach Fruits as Inhibitors of Flaviviruses and Mycobacterium tubercolosis

PloS one, 2015-10, Vol.10 (10), p.e0141272-e0141272

2015

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Lumichrome and Phenyllactic Acid as Chemical Markers of Thistle (Galactites tomentosa Moench) Honey

Journal of agricultural and food chemistry, 2011-01, Vol.59 (1), p.364-369

2011

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Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases

Journal of enzyme inhibition and medicinal chemistry, 2019-01, Vol.34 (1), p.1526-1533

2019

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Formulation and In Vitro Efficacy Assessment of Teucrium marum Extract Loading Hyalurosomes Enriched with Tween 80 and Glycerol

Nanomaterials (Basel, Switzerland), 2022-03, Vol.12 (7), p.1096

2022

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Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B

Journal of enzyme inhibition and medicinal chemistry, 2017-01, Vol.32 (1), p.264-270

2017

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Antiherpevirus activity of Artemisia arborescens essential oil and inhibition of lateral diffusion in Vero cells

Annals of clinical microbiology and antimicrobials, 2007-09, Vol.6 (1), p.10-10, Article 10

2007

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Cytotoxic tirucallane triterpenoids from Melia azedarach fruits

Molecules (Basel, Switzerland), 2010-08, Vol.15 (9), p.5866-5877

2010

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Benzophenones from the roots of the Popoluca Amerindian medicinal plant Securidaca diversifolia (L.) S.F. Blake

Phytochemistry letters, 2010-12, Vol.3 (4), p.226-229

2010

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Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase

European journal of medicinal chemistry, 2017-04, Vol.130, p.248-260

2017

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(3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro-1H-indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptase

European journal of medicinal chemistry, 2015-03, Vol.93, p.452-460

2015

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A pterocarpan from the seeds of Bituminaria morisiana

Journal of natural medicines, 2010-07, Vol.64 (3), p.354-357

2010

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Cytotoxic diacetylenic spiroketal enol ethers from Plagius flosculosus

Journal of natural products (Washington, D.C.), 2006-02, Vol.69 (2), p.295-298

2006

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Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold

European journal of medicinal chemistry, 2016-01, Vol.108, p.542-552

2016

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Effects of docosanyl ferulate, a constituent of Withania somnifera, on ethanol- and morphine-elicited conditioned place preference and ERK phosphorylation in the accumbens shell of CD1 mice

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

The biologically active compound of Withania somnifera (L.) Dunal, docosanyl ferulate, is endowed with potent anxiolytic properties but devoid of typical benzodiazepine-like side effects

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

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

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

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

Targeting Tumor Associated Carbonic Anhydrases IX and XII: Highly Isozyme Selective Coumarin and Psoralen Inhibitors

Limonoids from Melia azedarach Fruits as Inhibitors of Flaviviruses and Mycobacterium tubercolosis

Lumichrome and Phenyllactic Acid as Chemical Markers of Thistle (Galactites tomentosa Moench) Honey

Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases

Formulation and In Vitro Efficacy Assessment of Teucrium marum Extract Loading Hyalurosomes Enriched with Tween 80 and Glycerol

Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B

Antiherpevirus activity of Artemisia arborescens essential oil and inhibition of lateral diffusion in Vero cells

Cytotoxic tirucallane triterpenoids from Melia azedarach fruits

Benzophenones from the roots of the Popoluca Amerindian medicinal plant Securidaca diversifolia (L.) S.F. Blake

Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase

(3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro-1H-indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptase

A pterocarpan from the seeds of Bituminaria morisiana

Cytotoxic diacetylenic spiroketal enol ethers from Plagius flosculosus

Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold

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