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Exploring hydrophilic 2,2-di(indol-3-yl)ethanamine derivatives against Leishmania infantum.
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- PLoS ONE, 2024, v. 19, n. 6, p. 1, doi. 10.1371/journal.pone.0301901
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- Article
Sugar-Based Monoester Surfactants: Synthetic Methodologies, Properties, and Biological Activities.
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- Antibiotics (2079-6382), 2023, v. 12, n. 10, p. 1500, doi. 10.3390/antibiotics12101500
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- Article
Synthesis and Biological Evaluation of 6- O -Sucrose Monoester Glycolipids as Possible New Antifungal Agents.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 2, p. 136, doi. 10.3390/ph16020136
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- Article
Synthesis and Properties of Sucrose- and Lactose-Based Aromatic Ester Surfactants as Potential Drugs Permeability Enhancers.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 2, p. 223, doi. 10.3390/ph16020223
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- Article
Synthetic Methodologies and Therapeutic Potential of Indole-3-Carbinol (I3C) and Its Derivatives.
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- Pharmaceuticals (14248247), 2023, v. 16, n. 2, p. 240, doi. 10.3390/ph16020240
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- Article
Special issue: Chirality in pharmaceutical research and development.
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- Chirality, 2022, v. 34, n. 12, p. 1491, doi. 10.1002/chir.23510
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- Article
A recent update on new synthetic chiral compounds with antileishmanial activity.
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- Chirality, 2022, v. 34, n. 10, p. 1279, doi. 10.1002/chir.23494
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- Article
Morpho‐functional analyses reveal that changes in the chemical structure of a marine bisindole alkaloid alter the cytotoxic effect of its derivatives.
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- Microscopy Research & Technique, 2022, v. 85, n. 7, p. 2381, doi. 10.1002/jemt.24092
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- Article
Synthesis and Biological Characterization of the New Glycolipid Lactose Undecylenate (URB1418).
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- Pharmaceuticals (14248247), 2022, v. 15, n. 4, p. N.PAG, doi. 10.3390/ph15040456
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- Article
6′- O -Lactose Ester Surfactants as an Innovative Opportunity in the Pharmaceutical Field: From Synthetic Methods to Biological Applications.
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- Pharmaceuticals (14248247), 2021, v. 14, n. 12, p. 1306, doi. 10.3390/ph14121306
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- Article
A Fluorinated Analogue of Marine Bisindole Alkaloid 2,2-Bis(6-bromo-1H-indol-3-yl)ethanamine as Potential Anti-Biofilm Agent and Antibiotic Adjuvant Against Staphylococcus aureus.
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- Pharmaceuticals (14248247), 2020, v. 13, n. 9, p. 210, doi. 10.3390/ph13090210
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- Article
Total Synthesis of Natural Disaccharide Sambubiose.
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- Pharmaceuticals (14248247), 2020, v. 13, n. 8, p. 198, doi. 10.3390/ph13080198
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- Article
Synthesis and Evaluation of Saccharide-Based Aliphatic and Aromatic Esters as Antimicrobial and Antibiofilm Agents †.
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- Pharmaceuticals (14248247), 2019, v. 12, n. 4, p. 186, doi. 10.3390/ph12040186
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- Article
Marine bisindole alkaloid 2,2-bis(6-bromo-3-indolyl)ethylamine to control and prevent fungal growth on building material: a potential antifungal agent.
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- Applied Microbiology & Biotechnology, 2019, v. 103, n. 14, p. 5607, doi. 10.1007/s00253-019-09895-9
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- Article
Marine Alkaloid 2,2-Bis(6-bromo-3-indolyl) Ethylamine and Its Synthetic Derivatives Inhibit Microbial Biofilms Formation and Disaggregate Developed Biofilms.
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- Microorganisms, 2019, v. 7, n. 2, p. 28, doi. 10.3390/microorganisms7020028
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- Article
Polycyclic Indolines by an Acid‐Mediated Intramolecular Dearomative Strategy: Reversing Indole Reactivity in the Pictet‐Spengler‐Type Reaction.
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- Advanced Synthesis & Catalysis, 2018, v. 360, n. 21, p. 4060, doi. 10.1002/adsc.201800981
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- Article
Synthesis, Structure–Activity Relationships and In Vitro Toxicity Profile of Lactose-Based Fatty Acid Monoesters as Possible Drug Permeability Enhancers.
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- Pharmaceutics, 2018, v. 10, n. 3, p. 81, doi. 10.3390/pharmaceutics10030081
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- Article
Marine bisindole alkaloid: A potential apoptotic inducer in human cancer cells.
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- European Journal of Histochemistry, 2018, v. 62, n. 2, p. 111, doi. 10.4081/ejh.2018.2881
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- Article
One-Pot Synthesis of Biheterocycles Based on Indole and Azole Scaffolds Using Tryptamines and 1,2-Diaza-1,3-dienes as Building Blocks.
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- European Journal of Organic Chemistry, 2016, v. 2016, n. 19, p. 3193, doi. 10.1002/ejoc.201600210
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- Article
Potent, Metabolically Stable 2-Alkyl-8-(2 H-1,2,3-triazol-2-yl)-9 H-adenines as Adenosine A<sub>2A</sub> Receptor Ligands.
- Published in:
- ChemMedChem, 2015, v. 10, n. 7, p. 1149, doi. 10.1002/cmdc.201500113
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- Article
Synthesis of Boron- and Silicon-Containing Amino Acids through Copper-Catalysed Conjugate Additions to Dehydroalanine Derivatives.
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- European Journal of Organic Chemistry, 2015, p. 3352, doi. 10.1002/ejoc.201500362
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- Article
Synthesis of Boron- and Silicon-Containing Amino Acids through Copper-Catalysed Conjugate Additions to Dehydroalanine Derivatives.
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- European Journal of Organic Chemistry, 2015, v. 2015, n. 15, p. 3352, doi. 10.1002/ejoc.201500362
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- Article
Brønsted Acid Catalyzed Bisindolization of α-Amido Acetals: Synthesis and Anticancer Activity of Bis(indolyl)ethanamino Derivatives.
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- European Journal of Organic Chemistry, 2014, v. 2014, n. 18, p. 3822, doi. 10.1002/ejoc.201402055
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- Article
MT<sub>1</sub>-Selective Melatonin Receptor Ligands: Synthesis, Pharmacological Evaluation, and Molecular Dynamics Investigation of N-{[(3- O-Substituted)anilino]alkyl}amides.
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- ChemMedChem, 2012, v. 7, n. 11, p. 1954, doi. 10.1002/cmdc.201200303
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- Article
The indole-3-carbinol cyclic tetrameric derivative CTet inhibits cell proliferation via overexpression of p21/CDKN1A in both estrogen receptor-positive and triple-negative breast cancer cell lines.
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- Breast Cancer Research, 2011, v. 13, n. 1, p. 1, doi. 10.1186/bcr2855
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- Article
The indole-3-carbinol cyclic tetrameric derivative CTet inhibits cell proliferation via overexpression of p21/CDKN1A in both estrogen receptor-positive and triple-negative breast cancer cell lines.
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- 2011
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- Publication type:
- journal article
Synthesis and Biological Evaluation of a γ-Cyclodextrin-based Formulation of the Anticancer Agent 5,6,11,12,17,18,23,24-Octahydrocyclododeca[1,2-b:4,5-b′:7,8-b′′:10,11-b′′′]tetraindole (CTet).
- Published in:
- Molecules, 2010, v. 15, n. 6, p. 4085, doi. 10.3390/molecules15064085
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- Article
Diastereo- and Enantioselective Hydrogenation of a Challenging Enamide Derived from 4-Phenyl-2-tetralone: An Appealing Shortcut Towards Enantiopure cis-2-Aminotetraline Derivatives.
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- Chemistry - An Asian Journal, 2010, v. 5, n. 3, p. 550, doi. 10.1002/asia.200900441
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- Article
N-(Anilinoethyl)amides: Design and Synthesis of Metabolically Stable, Selective Melatonin Receptor Ligands.
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- ChemMedChem, 2009, v. 4, n. 10, p. 1746, doi. 10.1002/cmdc.200900240
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- Article