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Enantioselective catalytic Strecker reaction on cyclic (Z)-aldimines in flow: reaction optimization and sustainability aspects.
- Published in:
- Journal of Flow Chemistry, 2024, v. 14, n. 1, p. 197, doi. 10.1007/s41981-023-00279-9
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- Article
Unveiling the modulation of Pseudomonas aeruginosa virulence and biofilm formation by selective histone deacetylase 6 inhibitors.
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- Frontiers in Microbiology, 2024, p. 1, doi. 10.3389/fmicb.2024.1340585
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- Article
Editorial: Multi-target directed ligands for the treatment of cancer.
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- Frontiers in Oncology, 2022, v. 12, p. 1, doi. 10.3389/fonc.2022.980141
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- Article
Amide Bonds Meet Flow Chemistry: A Journey into Methodologies and Sustainable Evolution.
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- ChemSusChem, 2022, v. 15, n. 6, p. 1, doi. 10.1002/cssc.202102708
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- Article
Amide Bonds Meet Flow Chemistry: A Journey into Methodologies and Sustainable Evolution.
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- ChemSusChem, 2022, v. 15, n. 6, p. 1, doi. 10.1002/cssc.202102708
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- Article
Front Cover: Amide Bonds Meet Flow Chemistry: A Journey into Methodologies and Sustainable Evolution (ChemSusChem 6/2022).
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- ChemSusChem, 2022, v. 15, n. 6, p. 1, doi. 10.1002/cssc.202200302
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- Article
Amide Bonds Meet Flow Chemistry: A Journey into Methodologies and Sustainable Evolution.
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- ChemSusChem, 2022, v. 15, n. 6, p. 1, doi. 10.1002/cssc.202102708
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- Publication type:
- Article
Coupling Interrupted Fischer and Multicomponent Joullié‐Ugi to Chase Chemical Diversity: from Batch to Sustainable Flow Synthesis of Peptidomimetics.
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- ChemMedChem, 2021, v. 16, n. 24, p. 3795, doi. 10.1002/cmdc.202100474
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- Article
Design, Synthesis, and Anticancer Screening for Repurposed Pyrazolo[3,4-d]pyrimidine Derivatives on Four Mammalian Cancer Cell Lines.
- Published in:
- Molecules, 2021, v. 26, n. 10, p. 2961, doi. 10.3390/molecules26102961
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- Article
Development of CDK4/6 Inhibitors: A Five Years Update.
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- Molecules, 2021, v. 26, n. 5, p. 1488, doi. 10.3390/molecules26051488
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- Article
Design, Synthesis, Molecular Docking, and Tumor Resistance Reversal Activity Evaluation of Matrine Derivative with Thiophene Structure.
- Published in:
- Molecules, 2021, v. 26, n. 2, p. 417, doi. 10.3390/molecules26020417
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- Article
Targeting Endocannabinoid Metabolism: an Arrow with Multiple Tips Against Multiple Sclerosis.
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- ChemMedChem, 2020, v. 15, n. 21, p. 1985, doi. 10.1002/cmdc.202000310
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- Article
Synthesis of Novel Chalcone-Based Phenothiazine Derivatives as Antioxidant and Anticancer Agents.
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- Molecules, 2020, v. 25, n. 19, p. 4566, doi. 10.3390/molecules25194566
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- Article
Anticancer and Antiviral Properties of Cardiac Glycosides: A Review to Explore the Mechanism of Actions.
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- Molecules, 2020, v. 25, n. 16, p. 3596, doi. 10.3390/molecules25163596
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- Article
Protective Effects of Polyphenols against Ischemia/Reperfusion Injury.
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- Molecules, 2020, v. 25, n. 15, p. 3469, doi. 10.3390/molecules25153469
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- Article
Drug Development and Medicinal Chemistry Efforts toward SARS‐Coronavirus and Covid‐19 Therapeutics.
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- ChemMedChem, 2020, v. 15, n. 11, p. 907, doi. 10.1002/cmdc.202000223
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- Article
Synthesis and Characterization of New Series of 1,3-5-Triazine Hydrazone Derivatives with Promising Antiproliferative Activity.
- Published in:
- Molecules, 2020, v. 25, n. 11, p. 2708, doi. 10.3390/molecules25112708
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- Article
Autophagy modulators for the treatment of oral and esophageal squamous cell carcinomas.
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- Medicinal Research Reviews, 2020, v. 40, n. 3, p. 1002, doi. 10.1002/med.21646
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- Article
Cover Feature: Highly Selective and Potent Human β‐Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X‐ray Structure and Structure–Activity Relationship Studies (ChemMedChem 5/2019).
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- ChemMedChem, 2019, v. 14, n. 5, p. 513, doi. 10.1002/cmdc.201900100
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- Article
Highly Selective and Potent Human β‐Secretase 2 (BACE2) Inhibitors against Type 2 Diabetes: Design, Synthesis, X‐ray Structure and Structure–Activity Relationship Studies.
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- ChemMedChem, 2019, v. 14, n. 5, p. 545, doi. 10.1002/cmdc.201900100
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- Article
The Curtius Rearrangement: Applications in Modern Drug Discovery and Medicinal Chemistry.
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- ChemMedChem, 2018, v. 13, n. 22, p. 2351, doi. 10.1002/cmdc.201800518
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- Article
Development of Potent Inhibitors of Fatty Acid Amide Hydrolase Useful for the Treatment of Neuropathic Pain.
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- ChemMedChem, 2018, v. 13, n. 19, p. 2090, doi. 10.1002/cmdc.201800397
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- Article
Nature Inspired Molecular Design: Stereoselective Synthesis of Bicyclic and Polycyclic Ethers for Potent HIV‐1 Protease Inhibitors.
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- Asian Journal of Organic Chemistry, 2018, v. 7, n. 8, p. 1448, doi. 10.1002/ajoc.201800255
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- Article
Front Cover: Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants (ChemMedChem 8/2018).
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- ChemMedChem, 2018, v. 13, n. 8, p. 762, doi. 10.1002/cmdc.201800226
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- Article
Design of Highly Potent, Dual‐Acting and Central‐Nervous‐System‐Penetrating HIV‐1 Protease Inhibitors with Excellent Potency against Multidrug‐Resistant HIV‐1 Variants.
- Published in:
- ChemMedChem, 2018, v. 13, n. 8, p. 803, doi. 10.1002/cmdc.201700824
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- Article
Development of Potent Inhibitors of the <italic>Mycobacterium tuberculosis</italic> Virulence Factor Zmp1 and Evaluation of Their Effect on Mycobacterial Survival inside Macrophages.
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- ChemMedChem, 2018, v. 13, n. 5, p. 422, doi. 10.1002/cmdc.201700759
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- Article
Activation of the Wnt Pathway by Small Peptides: Rational Design, Synthesis and Biological Evaluation.
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- ChemMedChem, 2017, v. 12, n. 24, p. 2074, doi. 10.1002/cmdc.201700551
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- Article
Design, Synthesis, Biological Evaluation, and X-ray Studies of HIV-1 Protease Inhibitors with Modified P2′ Ligands of Darunavir.
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- ChemMedChem, 2017, v. 12, n. 23, p. 1942, doi. 10.1002/cmdc.201700614
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- Article
Dopamine D3 Receptor Antagonists as Potential Therapeutics for the Treatment of Neurological Diseases.
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- Frontiers in Neuroscience, 2016, v. 10, p. 1, doi. 10.3389/fnins.2016.00451
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- Article
Site-directed Mutagenesis of Key Residues Unveiled a Novel Allosteric Site on Human Adenosine Kinase for Pyrrolobenzoxa(thia)zepinone Non-Nucleoside Inhibitors.
- Published in:
- Chemical Biology & Drug Design, 2016, v. 87, n. 1, p. 112, doi. 10.1111/cbdd.12630
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- Article
Structure-based discovery of the first non-covalent inhibitors of Leishmania major tryparedoxin peroxidase by high throughput docking.
- Published in:
- Scientific Reports, 2015, p. 9705, doi. 10.1038/srep09705
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- Article
Disease-Modifying Anti-Alzheimer's Drugs: Inhibitors of Human Cholinesterases Interfering with β-Amyloid Aggregation.
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- CNS Neuroscience & Therapeutics, 2014, v. 20, n. 7, p. 624, doi. 10.1111/cns.12290
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- Article
Developing β-secretase inhibitors for treatment of Alzheimer's disease.
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- Journal of Neurochemistry, 2012, v. 120, p. 71, doi. 10.1111/j.1471-4159.2011.07476.x
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- Article