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Synthesis of Some Unique Carbamate Derivatives bearing 2-Furoyl-1-piperazine as a Valuable Therapeutic Agents

Acta chimica Slovenica, 2017-01, Vol.64 (1), p.159-169

2017

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Phytohormones Producing Acinetobacter bouvetii P1 Mitigates Chromate Stress in Sunflower by Provoking Host Antioxidant Response

Antioxidants, 2021-11, Vol.10 (12), p.1868

2021

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Biscoumarin: new class of urease inhibitors; economical synthesis and activity

Bioorganic & medicinal chemistry, 2004-04, Vol.12 (8), p.1963-1968

2004

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Inhibition of Acetylcholinesterase with Novel 1, 3, 4, Oxadiazole Derivatives: A Kinetic, In Silico, and In Vitro Approach

ACS omega, 2023-12, Vol.8 (49), p.46816-46829

2023

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Urease inhibitor from Datisca cannabina linn

Journal of enzyme inhibition and medicinal chemistry, 2008-01, Vol.23 (3), p.386-390

2008

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Halosterols A and B, Chymotrypsin Inhibitory Sterols from Haloxylon recurvum

Chemical and Pharmaceutical Bulletin, 2006, Vol.54(5), pp.623-625

2006

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First Natural Urease Inhibitor from Euphorbia decipiens

Chemical and Pharmaceutical Bulletin, 2003, Vol.51(6), pp.719-723

2003

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Tyrosinase Inhibitory Activity of S-Naproxen Derivatives

Letters in drug design & discovery, 2019-01, Vol.16 (11), p.1276-1285

2019

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Hyperinols A and B, Chymotrypsin Inhibiting Triterpenes from Hypericum oblongifolium

Chemical and Pharmaceutical Bulletin, 2006, Vol.54(8), pp.1088-1090

2006

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Convergent synthesis of new N -substituted 2-{[5-(1H -indol-3-ylmethyl)-1,3,4-oxadiazol-2-yl]sulfanyl}acetamides as suitable therapeutic agents

Brazilian Journal of Pharmaceutical Sciences, 2015-12, Vol.51 (4), p.931-947

2015

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Chemistry, Urease Inhibition, and Phytotoxic Studies of Binuclear Vanadium(IV) Complexes

Chemistry & biodiversity, 2007-01, Vol.4 (1), p.58-71

2007

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Two New Protease-Inhibiting Glycosphingolipids from Buddleja crispa

Chemistry & biodiversity, 2007-05, Vol.4 (5), p.917-924

2007

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Synthesis and in silico study of 2-furyl(4-{4-[(substituted)sulfonyl]benzyl}-1-piperazinyl)methanone derivatives as suitable therapeutic agents

Brazilian Journal of Pharmaceutical Sciences, 2017-01, Vol.53 (1)

2017

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Three-dimensional quantitative structure–activity relationship (CoMSIA) analysis of bis-coumerine analogues as urease inhibitors

Medicinal chemistry research, 2013, Vol.22 (1), p.498-504

2013

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Nicotinonitriles as potential inhibitors of α-glucosidase, tyrosinase, and urease enzymes: Synthesis, characterization, in vitro, and in silico studies

Journal of molecular structure, 2024-06, Vol.1305, p.137742, Article 137742

2024

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α-Chymotrypsin inhibition studies on the lignans from Vitex negundo Linn

Journal of enzyme inhibition and medicinal chemistry, 2008-06, Vol.23 (3), p.400-405

2008

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Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico

Bioorganic & medicinal chemistry, 2019-03, Vol.27 (6), p.1009-1022

2019

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Elaeagnoside, chymotrypsin inhibiting steroidal glucoside from Elaeagnus orientalis

Natural product research, 2009-01, Vol.23 (5), p.409-414

2009

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Synthesis and anti-inflammatory activity of some selected aminothiophene analogs

Journal of enzyme inhibition and medicinal chemistry, 2006-04, Vol.21 (2), p.139-143

2006

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Structural basis of binding and justification for the urease inhibitory activity of acetamide hybrids of N-substituted 1,3,4-oxadiazoles and piperidines

Journal of molecular structure, 2021-01, Vol.1223, p.129141, Article 129141

2021

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Phosphodiesterase and thymidine phosphorylase-inhibiting salirepin derivatives from Symplocos racemosa

Planta medica, 2004-12, Vol.70 (12), p.1189-1194

2004

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5-Acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones: As potent urease inhibitors; synthesis, in vitro screening, and molecular modeling study

Bioorganic chemistry, 2018-02, Vol.76, p.37-52

2018

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Thiadiazine thione derivatives as anti-leishmanial agents: synthesis, biological evaluation, structure activity relationship, ADMET, molecular docking and molecular dynamics simulation studies

Journal of biomolecular structure & dynamics, 2024-09, Vol.42 (15), p.7758-7772

2024

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Enzyme inhibition and radical scavenging activities of aerial parts of Paeonia emodi Wall. (Paeoniaceae)

Journal of enzyme inhibition and medicinal chemistry, 2005-06, Vol.20 (3), p.245-249

2005

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Novel urease inhibitors from Daphne oleoids

Journal of enzyme inhibition and medicinal chemistry, 2006-10, Vol.21 (5), p.527-529

2006

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Synthesis of Some Unique Carbamate Derivatives bearing 2-Furoyl-1-piperazine as a Valuable Therapeutic Agents

Phytohormones Producing Acinetobacter bouvetii P1 Mitigates Chromate Stress in Sunflower by Provoking Host Antioxidant Response

Biscoumarin: new class of urease inhibitors; economical synthesis and activity

Inhibition of Acetylcholinesterase with Novel 1, 3, 4, Oxadiazole Derivatives: A Kinetic, In Silico, and In Vitro Approach

Urease inhibitor from Datisca cannabina linn

Halosterols A and B, Chymotrypsin Inhibitory Sterols from Haloxylon recurvum

First Natural Urease Inhibitor from Euphorbia decipiens

Tyrosinase Inhibitory Activity of S-Naproxen Derivatives

Hyperinols A and B, Chymotrypsin Inhibiting Triterpenes from Hypericum oblongifolium

Convergent synthesis of new N -substituted 2-{[5-(1H -indol-3-ylmethyl)-1,3,4-oxadiazol-2-yl]sulfanyl}acetamides as suitable therapeutic agents

Chemistry, Urease Inhibition, and Phytotoxic Studies of Binuclear Vanadium(IV) Complexes

Two New Protease-Inhibiting Glycosphingolipids from Buddleja crispa

Synthesis and in silico study of 2-furyl(4-{4-[(substituted)sulfonyl]benzyl}-1-piperazinyl)methanone derivatives as suitable therapeutic agents

Three-dimensional quantitative structure–activity relationship (CoMSIA) analysis of bis-coumerine analogues as urease inhibitors

Nicotinonitriles as potential inhibitors of α-glucosidase, tyrosinase, and urease enzymes: Synthesis, characterization, in vitro, and in silico studies

α-Chymotrypsin inhibition studies on the lignans from Vitex negundo Linn

Synthesis and urease inhibitory potential of benzophenone sulfonamide hybrid in vitro and in silico

Elaeagnoside, chymotrypsin inhibiting steroidal glucoside from Elaeagnus orientalis

Synthesis and anti-inflammatory activity of some selected aminothiophene analogs

Structural basis of binding and justification for the urease inhibitory activity of acetamide hybrids of N-substituted 1,3,4-oxadiazoles and piperidines

Phosphodiesterase and thymidine phosphorylase-inhibiting salirepin derivatives from Symplocos racemosa

5-Acetyl-6-methyl-4-aryl-3,4-dihydropyrimidin-2(1H)-ones: As potent urease inhibitors; synthesis, in vitro screening, and molecular modeling study

Thiadiazine thione derivatives as anti-leishmanial agents: synthesis, biological evaluation, structure activity relationship, ADMET, molecular docking and molecular dynamics simulation studies

Enzyme inhibition and radical scavenging activities of aerial parts of Paeonia emodi Wall. (Paeoniaceae)

Novel urease inhibitors from Daphne oleoids

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