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Rational Design, Synthesis, in Vitro, and in Silico Studies of Chlorophenylquinazolin‐4(3H)‐One Containing Different Aryl Acetohydrazides as Tyrosinase Inhibitors.
- Published in:
- Chemistry & Biodiversity, 2022, v. 19, n. 7, p. 1, doi. 10.1002/cbdv.202100964
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- Publication type:
- 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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- 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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- Publication type:
- Article
Synthesis and cytotoxic activity evaluation of novel imidazopyridine carbohydrazide derivatives.
- Published in:
- BMC Chemistry, 2024, v. 18, n. 1, p. 1, doi. 10.1186/s13065-023-01073-3
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- Publication type:
- Article
Design, synthesis, and biological evaluation of symmetrical azine derivatives as novel tyrosinase inhibitors.
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- BMC Chemistry, 2021, v. 15, n. 1, p. 1, doi. 10.1186/s13065-021-00780-z
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- Publication type:
- 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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- Publication type:
- Article
Ultrasound-assisted synthesis of kojic acid-1,2,3-triazole based dihydropyrano[3,2-b]pyran derivatives using Fe<sub>3</sub>O<sub>4</sub>@CQD@CuI as a novel nanomagnetic catalyst.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-24089-6
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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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- Publication type:
- Article
Anti-Toxoplasma gondii activity of 5-oxo-hexahydroquinoline derivatives: synthesis, in vitro and in vivo evaluations, and molecular docking analysis.
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- Research in Pharmaceutical Sciences, 2020, v. 15, n. 4, p. 367, doi. 10.4103/1735-5362.293515
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- Publication type:
- 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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- Publication type:
- Article
A Series of Benzylidenes Linked to Hydrazine‐1‐carbothioamide as Tyrosinase Inhibitors: Synthesis, Biological Evaluation and Structure−Activity Relationship.
- Published in:
- Chemistry & Biodiversity, 2020, v. 17, n. 8, p. 1, doi. 10.1002/cbdv.202000285
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- Publication type:
- Article
Synthesis of New Benzimidazole‐1,2,3‐triazole Hybrids as Tyrosinase Inhibitors.
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- Chemistry & Biodiversity, 2018, v. 15, n. 7, p. 1, doi. 10.1002/cbdv.201800120
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- Publication type:
- Article
Synthesis, QSAR and Calcium Channel Modulator Activity of New Hexahydroquinoline Derivatives Containing Nitroimidazole.
- Published in:
- 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
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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- Publication type:
- Article
In Silico Screening of IL-1β Production Inhibitors Using Chemometric Tools.
- Published in:
- Iranian Journal of Pharmaceutical Research, 2017, v. 16, n. 2, p. 513
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- Publication type:
- Article
Synthesis and Antidiabetic Evaluation of Benzenesulfonamide Derivatives.
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- Iranian Journal of Pharmaceutical Research, 2013, v. 12, n. 2, p. 325
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- Publication type:
- 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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- Publication type:
- Article
Antimicrobial Activity of Isoniazid in Conjugation with Surface-Modified Magnetic Nanoparticles against Mycobacterium tuberculosis and Nonmycobacterial Microorganisms.
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- Journal of Nanomaterials, 2020, p. 1, doi. 10.1155/2020/7372531
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- Publication type:
- 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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- Publication type:
- Article
N-(2-(Piperazin-1-yl)phenyl)arylamide Derivatives as β-Secretase (BACE1) Inhibitors: Simple Synthesis by Ugi Four-Component Reaction and Biological Evaluation.
- Published in:
- Archiv der Pharmazie, 2015, v. 348, n. 5, p. 330, doi. 10.1002/ardp.201400322
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- Publication type:
- Article
Synthesis of Novel Triazole Incorporated Thiazolone Motifs Having Promising Antityrosinase Activity through Green Nanocatalyst CuI‐Fe<sub>3</sub>O<sub>4</sub>@SiO<sub>2</sub> (TMS‐EDTA).
- Published in:
- Applied Organometallic Chemistry, 2020, v. 34, n. 12, p. 1, doi. 10.1002/aoc.5962
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- Publication type:
- Article
Effect of different physical factors on the synthesis of spherical gold nanoparticles towards cost‐effective biomedical applications.
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- IET Nanobiotechnology (Wiley-Blackwell), 2023, v. 17, n. 1, p. 1, doi. 10.1049/nbt2.12100
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- Publication type:
- Article
Synthesis, biological evaluation and molecular docking analysis of vaniline–benzylidenehydrazine hybrids as potent tyrosinase inhibitors.
- Published in:
- BMC Chemistry, 2020, v. 14, n. 1, p. 1, doi. 10.1186/s13065-020-00679-1
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- Publication type:
- 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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- Publication type:
- Article
Rational Design, Synthesis, In Vitro, and In Silico Studies of Dihydropyrimidinone Derivatives as β-Glucuronidase Inhibitors.
- Published in:
- Journal of Chemistry, 2021, p. 1, doi. 10.1155/2021/6664756
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- Publication type:
- Article
Magnetic silica nanoparticle-supported copper complex as an efficient catalyst for the synthesis of novel triazolopyrazinylacetamides with improved antibacterial activity.
- Published in:
- Chemistry of Heterocyclic Compounds, 2020, v. 56, n. 4, p. 488, doi. 10.1007/s10593-020-02685-6
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- Publication type:
- Article
Efficient copper-catalyzed synthesis of 2-arylbenzimidazole derivatives by reaction of 1-fluoro-2-nitrobenzene with benzamidine hydrochlorides.
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- Chemistry of Heterocyclic Compounds, 2018, v. 54, n. 3, p. 351, doi. 10.1007/s10593-018-2272-4
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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.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-83069-4
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- Publication type:
- 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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- Publication type:
- Article
Viral 3CL<sup>pro</sup> as a Target for Antiviral Intervention Using Milk-Derived Bioactive Peptides.
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- International Journal of Peptide Research & Therapeutics, 2021, v. 27, n. 4, p. 2703, doi. 10.1007/s10989-021-10284-y
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- Publication type:
- Article
5,6-Diphenyl triazine-thio methyl triazole hybrid as a new Alzheimer's disease modifying agents.
- Published in:
- Molecular Diversity, 2020, v. 24, n. 3, p. 641, doi. 10.1007/s11030-019-09970-3
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- Publication type:
- 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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- Publication type:
- 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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- Publication type:
- Article
Design, synthesis, in vitro and in silico studies of novel Schiff base derivatives of 2‐hydroxy‐4‐methoxybenzamide as tyrosinase inhibitors.
- Published in:
- Drug Development Research, 2021, v. 82, n. 4, p. 533, doi. 10.1002/ddr.21771
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- Publication type:
- Article
6‐(Hydroxymethyl)‐8‐oxo‐4,8‐dihydropyrano[3,2‐b]pyrans as New Tyrosinase Inhibitors and Antioxidant Agents.
- Published in:
- ChemistrySelect, 2023, v. 8, n. 43, p. 1, doi. 10.1002/slct.202302990
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- Publication type:
- Article
Benzylidine‐N‐phenylhydrazine‐1‐carboxamide Derivatives as Tyrosinase Inhibitors: Design, Preparation, Molecular Docking, and Biological Activity.
- Published in:
- ChemistrySelect, 2023, v. 8, n. 39, p. 1, doi. 10.1002/slct.202300836
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- Publication type:
- Article
Benzyl‐Triazole Derivatives of Hydrazinecarbothiamide Derivatives as Potent Tyrosinase Inhibitors: Synthesis, Biological Evaluation, Structure‐Activity Relationship and Docking Study.
- Published in:
- ChemistrySelect, 2023, v. 8, n. 8, p. 1, doi. 10.1002/slct.202203382
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- Publication type:
- Article
6‐Methoxy‐1‐tetralone Derivatives Bearing an N‐Arylpyridinium Moiety as Cholinesterase Inhibitors: Design, Synthesis, Biological Evaluation, and Molecular Docking Study.
- Published in:
- ChemistrySelect, 2022, v. 7, n. 27, p. 1, doi. 10.1002/slct.202201977
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- Publication type:
- Article
Exploring quantitative structure-activity relationship (QSAR) models for some biologically active catechol structures using PC-LS-SVM and PC-ANFIS.
- Published in:
- Applied Biological Chemistry, 2016, v. 59, n. 3, p. 433, doi. 10.1007/s13765-016-0180-9
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- Publication type:
- Article
5-Oxo-hexahydroquinoline Derivatives and Their Tetrahydroquinoline Counterparts as Multidrug Resistance Reversal Agents.
- Published in:
- Molecules, 2020, v. 25, n. 8, p. 1839, doi. 10.3390/molecules25081839
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- Publication type:
- Article
5-Oxo-hexahydroquinoline and 5-oxo-tetrahydrocyclopentapyridine derivatives as promising antiproliferative agents with potential apoptosis-inducing capacity.
- Published in:
- Molecular Diversity, 2022, v. 26, n. 3, p. 1481, doi. 10.1007/s11030-021-10281-9
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- Publication type:
- Article
4H-benzochromene derivatives as novel tyrosinase inhibitors and radical scavengers: synthesis, biological evaluation, and molecular docking analysis.
- Published in:
- Molecular Diversity, 2021, v. 25, n. 4, p. 2339, doi. 10.1007/s11030-020-10123-0
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- Publication type:
- 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
- By:
- Publication type:
- Article
A simple one-pot synthesis of 2,4-diaryl- 9 H-pyrido[2,3- b]indoles under solvent-free conditions.
- Published in:
- Heterocyclic Communications, 2017, v. 23, n. 4, p. 293, doi. 10.1515/hc-2016-0222
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- Publication type:
- Article
Novel 9-(alkylthio)-Acenaphtho[1,2-e]-1,2,4-triazine derivatives: synthesis, cytotoxic activity and molecular docking studies on B-cell lymphoma 2 (Bcl-2)
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- 2014
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- Publication type:
- Journal Article
Novel 9-(alkylthio)-Acenaphtho[1,2-e]-1,2,4-triazine derivatives: synthesis, cytotoxic activity and molecular docking studies on B-cell lymphoma 2 (Bcl-2).
- Published in:
- DARU: Journal of Pharmaceutical Sciences, 2014, v. 22, p. 1, doi. 10.1186/2008-2231-22-2
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- Publication type:
- Article
Comparative amino acid decomposition analysis of potent type I p38α inhibitors.
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- DARU: Journal of Pharmaceutical Sciences, 2013, v. 21, p. 1, doi. 10.1186/2008-2231-21-41
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- Publication type:
- Article
Synthesis and In vitro cytotoxic activity evaluation of (E)-16-(substituted benzylidene) derivatives of dehydroepiandrosterone.
- Published in:
- DARU: Journal of Pharmaceutical Sciences, 2013, v. 21, p. 1, doi. 10.1186/2008-2231-21-34
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- Publication type:
- Article