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Discovery of neurotrophic agents based on hydroxycinnamic acid scaffold.
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- Chemical Biology & Drug Design, 2016, v. 88, n. 6, p. 926, doi. 10.1111/cbdd.12829
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- Article
QSAR Study of 4-Aryl-4 H-Chromenes as a New Series of Apoptosis Inducers Using Different Chemometric Tools.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 4, p. 442, doi. 10.1111/j.1747-0285.2011.01284.x
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- Article
5-Oxo-hexahydroquinoline Derivatives and Their Tetrahydroquinoline Counterparts as Multidrug Resistance Reversal Agents.
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- Molecules, 2020, v. 25, n. 8, p. 1839, doi. 10.3390/molecules25081839
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- Article
Response surface methodology in docking study of small molecule BACE-1 inhibitors.
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- Journal of Molecular Modeling, 2012, v. 18, n. 10, p. 4567, doi. 10.1007/s00894-012-1424-1
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- Article
Synthesis and Cytotoxic Activity of Some Novel Dihyrobenzo[ h]pyrano[3,2- c]chromene Derivatives.
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- Journal of Heterocyclic Chemistry, 2015, v. 52, n. 1, p. 97, doi. 10.1002/jhet.1991
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- Article
Novel N‐benzylpiperidine derivatives of 5‐arylisoxazole‐3‐carboxamides as anti‐Alzheimer's agents.
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- Archiv der Pharmazie, 2021, v. 354, n. 3, p. 1, doi. 10.1002/ardp.202000258
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- Article
Thieno[2,3‐b]pyridine amines: Synthesis and evaluation of tacrine analogs against biological activities related to Alzheimer's disease.
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- Archiv der Pharmazie, 2020, v. 353, n. 10, p. 1, doi. 10.1002/ardp.202000101
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- Article
1,2,3‐Triazole‐linked 5‐benzylidene (thio)barbiturates as novel tyrosinase inhibitors and free‐radical scavengers.
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- Archiv der Pharmazie, 2020, v. 353, n. 10, p. 1, doi. 10.1002/ardp.202000058
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- Article
Novel cinnamic acid–tryptamine hybrids as potent butyrylcholinesterase inhibitors: Synthesis, biological evaluation, and docking study.
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- Archiv der Pharmazie, 2018, v. 351, n. 10, p. 1, doi. 10.1002/ardp.201800115
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- Article
Novel Tacrine-Based Pyrano[3',4':5,6]pyrano[2,3- b]quinolinones: Synthesis and Cholinesterase Inhibitory Activity.
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- Archiv der Pharmazie, 2016, v. 349, n. 12, p. 915, doi. 10.1002/ardp.201600123
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- Article
N-(2-(Piperazin-1-yl)phenyl)arylamide Derivatives as β-Secretase (BACE1) Inhibitors: Simple Synthesis by Ugi Four-Component Reaction and Biological Evaluation.
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- Archiv der Pharmazie, 2015, v. 348, n. 5, p. 330, doi. 10.1002/ardp.201400322
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- Article
Synthesis, biological evaluation and molecular docking analysis of vaniline–benzylidenehydrazine hybrids as potent tyrosinase inhibitors.
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- BMC Chemistry, 2020, v. 14, n. 1, p. 1, doi. 10.1186/s13065-020-00679-1
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- Article
Novel 5-oxo-hexahydroquinoline derivatives: design, synthesis, in vitro P-glycoprotein-mediated multidrug resistance reversal profile and molecular dynamics simulation study.
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- Drug Design, Development & Therapy, 2017, v. 11, p. 407, doi. 10.2147/dddt.s119995
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- Article
Design, synthesis, in vitro and in silico studies of novel Schiff base derivatives of 2‐hydroxy‐4‐methoxybenzamide as tyrosinase inhibitors.
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- Drug Development Research, 2021, v. 82, n. 4, p. 533, doi. 10.1002/ddr.21771
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- Article
Synthesis and In vitro cytotoxic activity evaluation of (E)-16-(substituted benzylidene) derivatives of dehydroepiandrosterone.
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- DARU: Journal of Pharmaceutical Sciences, 2013, v. 21, p. 1, doi. 10.1186/2008-2231-21-34
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- Article
Synthesis and biological evaluation of novel benzyl piperazine derivatives of 5-(5-nitroaryl)-1,3,4-thiadiazoles as Anti-Helicobacter pylori agents.
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- DARU: Journal of Pharmaceutical Sciences, 2013, v. 21, p. 66, doi. 10.1186/2008-2231-21-66
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- Article
2-Imino 2 H-chromene and 2-(phenylimino) 2 H-chromene 3-aryl carboxamide derivatives as novel cytotoxic agents: synthesis, biological assay, and molecular docking study.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 12, p. 2163, doi. 10.1007/s13738-016-0934-7
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- Article
5-Oxo-hexahydroquinoline and 5-oxo-tetrahydrocyclopentapyridine derivatives as promising antiproliferative agents with potential apoptosis-inducing capacity.
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- Molecular Diversity, 2022, v. 26, n. 3, p. 1481, doi. 10.1007/s11030-021-10281-9
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- Article
Synthesis and evaluation of novel arylisoxazoles linked to tacrine moiety: in vitro and in vivo biological activities against Alzheimer's disease.
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- Molecular Diversity, 2022, v. 26, n. 1, p. 409, doi. 10.1007/s11030-021-10248-w
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- Article
5,6-Diphenyl triazine-thio methyl triazole hybrid as a new Alzheimer's disease modifying agents.
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- Molecular Diversity, 2020, v. 24, n. 3, p. 641, doi. 10.1007/s11030-019-09970-3
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- Article
Design, synthesis, in vivo and in vitro studies of 1,2,3,4-tetrahydro-9H-carbazole derivatives, highly selective and potent butyrylcholinesterase inhibitors.
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- Molecular Diversity, 2020, v. 24, n. 1, p. 211, doi. 10.1007/s11030-019-09943-6
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- Article
5-Oxo-hexahydroquinoline: an attractive scaffold with diverse biological activities.
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- Molecular Diversity, 2019, v. 23, n. 2, p. 471, doi. 10.1007/s11030-018-9886-4
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- Article
Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1- $$c$$ ][1,2,4]triazin-6-amines.
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- Molecular Diversity, 2015, v. 19, n. 2, p. 273, doi. 10.1007/s11030-015-9566-6
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- Article
Correction: Cinnamomum verum J. Presl. Bark essential oil: in vitro investigation of anti-cholinesterase, anti-BACE1, and neuroprotective activity.
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- 2022
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- Correction Notice
Cinnamomum verum J. Presl. Bark essential oil: in vitro investigation of anti-cholinesterase, anti-BACE1, and neuroprotective activity.
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- BMC Complementary Medicine & Therapies, 2022, v. 22, n. 1, p. 1, doi. 10.1186/s12906-022-03767-y
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- Article
Design, synthesis, and biological evaluation of new series of 2-amido-1,3,4-thiadiazole derivatives as cytotoxic agents.
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- Zeitschrift für Naturforschung B: A Journal of Chemical Sciences, 2016, v. 71, n. 3, p. 205, doi. 10.1515/znb-2015-0138
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- Article
Phenoxyethyl Piperidine/Morpholine Derivatives as PAS and CAS Inhibitors of Cholinesterases: Insights for Future Drug Design.
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- Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-56463-2
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- Article
In Silico Screening of IL-1β Production Inhibitors Using Chemometric Tools.
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- Iranian Journal of Pharmaceutical Research, 2017, v. 16, n. 2, p. 513
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- Article
Comparative QSAR Analysis of 3,5-bis (Arylidene)-4-Piperidone Derivatives: the Development of Predictive Cytotoxicity Models.
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- Iranian Journal of Pharmaceutical Research, 2016, v. 15, n. 2, p. 425
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- Article
Novel N-2-(Furyl)-2-(Chlorobenzyloxyimino) Ethyl Piperazinyl Quinolones: Synthesis, Cytotoxic Evaluation and Structure-Activity Relationship.
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- Iranian Journal of Pharmaceutical Research, 2015, v. 14, n. 4, p. 1095
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- Article
Oxidative Aromatization, Cytotoxic Activity Evaluation and Conformational Study of Novel 7-aryl-10, 11-dihydro-7H-chromeno [4, 3-b]quinoline-6, 8(9H, 12H)-dione Derivatives.
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- Iranian Journal of Pharmaceutical Research, 2014, v. 13, n. 1, p. 103
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- Article
Fragment-based Binding Efficiency Indices in Bioactive Molecular Design: A Computational Approach to BACE-1 Inhibitors.
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- Iranian Journal of Pharmaceutical Research, 2013, v. 12, n. 3, p. 423
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- Article
Anti-Helicobacter pylori activity and Structure-Activity Relationship study of 2-Alkylthio-5-(nitroaryl)-1,3,4-thiadiazole Derivatives.
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- Iranian Journal of Pharmaceutical Research, 2013, v. 12, n. 3, p. 281
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- Publication type:
- Article
Exploring QSAR for Substituted 2-Sulfonyl-Phenyl-Indol Derivatives as Potent and Selective COX-2 Inhibitors Using Different Chemometrics Tools.
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- Chemical Biology & Drug Design, 2008, v. 72, n. 6, p. 564, doi. 10.1111/j.1747-0285.2008.00735.x
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- Article
QSAR Study of Phenoxypyrimidine Derivatives as Potent Inhibitors of p38 Kinase Using different Chemometric Tools.
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- Chemical Biology & Drug Design, 2007, v. 70, n. 6, p. 530, doi. 10.1111/j.1747-0285.2007.00597.x
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- Article
Synthesis, QSAR and Calcium Channel Modulator Activity of New Hexahydroquinoline Derivatives Containing Nitroimidazole.
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- Chemical Biology & Drug Design, 2007, v. 70, n. 4, p. 329, doi. 10.1111/j.1747-0285.2007.00565.x
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- Publication type:
- Article
Imidazopyridine hydrazone derivatives exert antiproliferative effect on lung and pancreatic cancer cells and potentially inhibit receptor tyrosine kinases including c-Met.
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- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-83069-4
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- Publication type:
- Article
Benzylidene-6-hydroxy-3,4-dihydronaphthalenone chalconoids as potent tyrosinase inhibitors.
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- Research in Pharmaceutical Sciences, 2021, v. 16, n. 4, p. 425, doi. 10.4103/1735-5362.319580
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- Article
Design, synthesis, cytotoxicity evaluation and docking studies of 1,2,4- triazine derivatives bearing different arylidene-hydrazinyl moieties as potential mTOR inhibitors.
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- Research in Pharmaceutical Sciences, 2018, v. 13, n. 1, p. 1, doi. 10.4103/1735-5362.220962
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- Article
Investigation of anti-Alzheimer's activity of aqueous extract of areca nuts (Areca catechu L.): In vitro and in vivo studies.
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- Boletín Latinoamericano y del Caribe de Plantas Medicinales y Aromáticas, 2021, v. 20, n. 4, p. 406, doi. 10.37360/blacpma.21.20.4.30
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- Article
Inhibitors of Alzheimer's BACE-1 with 3,5-bis- N-(aryl/heteroaryl) carbamoyl-4-aryl-1,4-dihydropyridine structure.
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- Archives of Pharmacal Research, 2015, v. 38, n. 4, p. 456, doi. 10.1007/s12272-014-0401-x
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- Article
Synthesis and antiproliferative activity evaluation of imidazole-based indeno[1,2-b]quinoline-9,11-dione derivatives.
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- Archives of Pharmacal Research, 2013, v. 36, n. 4, p. 436, doi. 10.1007/s12272-013-0032-7
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- Article
Cytotoxic activity evaluation and QSAR study of chromene-based chalcones.
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- Archives of Pharmacal Research, 2012, v. 35, n. 12, p. 2117, doi. 10.1007/s12272-012-1208-2
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- Article
Unsymmetric dihydropyridines bearing 2-pyridyl methyl carboxylate as modulators of P-glycoprotein; synthesis and biological evaluation in resistant and non-resistant cancer cells.
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- Canadian Journal of Chemistry, 2019, v. 97, n. 8, p. 603, doi. 10.1139/cjc-2018-0351
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- Article
Synthesis and cytotoxic activity evaluation of novel imidazopyridine carbohydrazide derivatives.
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- BMC Chemistry, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13065-023-01073-3
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- Article
Benzyl‐Triazole Derivatives of Hydrazinecarbothiamide Derivatives as Potent Tyrosinase Inhibitors: Synthesis, Biological Evaluation, Structure‐Activity Relationship and Docking Study.
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- ChemistrySelect, 2023, v. 8, n. 8, p. 1, doi. 10.1002/slct.202203382
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- Article
Design, synthesis, and evaluation of novel cinnamic acid-tryptamine hybrid for inhibition of acetylcholinesterase and butyrylcholinesterase.
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- DARU: Journal of Pharmaceutical Sciences, 2020, v. 28, p. 463, doi. 10.1007/s40199-020-00346-9
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- Article
Bioassay-guided purification of α-glucosidase inhibitor fatty acids from Padina tetrastromatica.
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- Journal of Applied Phycology, 2024, v. 36, n. 1, p. 359, doi. 10.1007/s10811-023-03125-6
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- Article
Novel quinazoline-1,2,3-triazole hybrids with anticancer and MET kinase targeting properties.
- Published in:
- Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-41283-2
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- Article
Imino‐2H‐Chromene Based Derivatives as Potential Anti‐Alzheimer's Agents: Design, Synthesis, Biological Evaluation and in Silico Study.
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- Chemistry & Biodiversity, 2022, v. 19, n. 1, p. 1, doi. 10.1002/cbdv.202100599
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- Article