Microwave-assisted rapid synthesis of spirooxindole-pyrrolizidine analogues and their activity as anti-amyloidogenic agents
Published 2021 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
Microwave-assisted rapid synthesis of spirooxindole-pyrrolizidine analogues and their activity as anti-amyloidogenic agents
Authors
Keywords
Spicocyclics, Alzheimer’s disease, Neuroprotection, Amyloid beta, Protein misfolding, Fluorescence inhibition
Journal
BIOORGANIC CHEMISTRY
Volume 114, Issue -, Pages 105128
Publisher
Elsevier BV
Online
2021-06-30
DOI
10.1016/j.bioorg.2021.105128
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Natural spirocyclic alkaloids and polyphenols as multi target dementia leads
- (2021) Helmut M. Hügel et al. BIOORGANIC & MEDICINAL CHEMISTRY
- N-1,2,3-triazole-isatin derivatives for cholinesterase and β-amyloid aggregation inhibition: A comprehensive bioassay study
- (2020) Carolina S. Marques et al. BIOORGANIC CHEMISTRY
- Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes
- (2020) Emmanuelle Lautié et al. Frontiers in Pharmacology
- Bioavailability enhancement of EGCG by structural modification and nano-delivery: A review
- (2019) Wenzhong Dai et al. Journal of Functional Foods
- Recent advances in the neurobiology and neuropharmacology of Alzheimer’s disease
- (2018) Kushal Kumar et al. BIOMEDICINE & PHARMACOTHERAPY
- Rhynchophylline suppresses soluble Aβ 1-42 -induced impairment of spatial cognition function via inhibiting excessive activation of extrasynaptic NR2B-containing NMDA receptors
- (2018) Yang Yang et al. NEUROPHARMACOLOGY
- In Search of an Identity for Amyloid Plaques
- (2018) Tien-Phat V. Huynh et al. TRENDS IN NEUROSCIENCES
- Enhanced oral bioavailability of EGCG using pH-sensitive polymeric nanoparticles: characterization and in vivo investigation on nephrotic syndrome rats
- (2018) Guojuan Zhang et al. Drug Design Development and Therapy
- Nitro-Group-Containing Drugs
- (2018) Kunal Nepali et al. JOURNAL OF MEDICINAL CHEMISTRY
- Plaque formation and the intraneuronal accumulation of β-amyloid in Alzheimer's disease
- (2017) Reisuke H. Takahashi et al. PATHOLOGY INTERNATIONAL
- Oxidized epigallocatechin gallate inhibited lysozyme fibrillation more strongly than the native form
- (2017) Ting-Ting An et al. Redox Biology
- Certain (−)-epigallocatechin-3-gallate (EGCG) auto-oxidation products (EAOPs) retain the cytotoxic activities of EGCG
- (2016) Yaqing Wei et al. FOOD CHEMISTRY
- Discovery of Novel Spiro[3H-indole-3,2′-pyrrolidin]-2(1H)-one Compounds as Chemically Stable and Orally Active Inhibitors of the MDM2–p53 Interaction
- (2016) Andreas Gollner et al. JOURNAL OF MEDICINAL CHEMISTRY
- A convenient and rapid microwave-assisted synthesis of spirooxindoles in aqueous medium and their antimicrobial activities
- (2016) Prakash R. Mali et al. NEW JOURNAL OF CHEMISTRY
- Spiroindole Alkaloids and Spiroditerpenoids from Aspergillus duricaulis and Their Potential Neuroprotective Effects
- (2015) Jaeyoung Kwon et al. JOURNAL OF NATURAL PRODUCTS
- Polyphenols for the prevention and treatment of dementia diseases
- (2015) HelmutM Hügel et al. Neural Regeneration Research
- Rhynchophylline Protects Against the Amyloid β-Induced Increase of Spontaneous Discharges in the Hippocampal CA1 Region of Rats
- (2015) Hui Shao et al. NEUROCHEMICAL RESEARCH
- Determination of protein-unbound rhynchiphylline brain distribution by microdialysis and ultra-performance liquid chromatography with tandem mass spectrometry
- (2014) Chia-Jung Lee et al. BIOMEDICAL CHROMATOGRAPHY
- What does the aromatic ring number mean for drug design?
- (2014) Simon E Ward et al. Expert Opinion on Drug Discovery
- A brief overview of amyloids and Alzheimer's disease
- (2014) Sian-Yang Ow et al. PROTEIN SCIENCE
- A facile chemo-, regio- and stereoselective synthesis and cholinesterase inhibitory activity of spirooxindole–pyrrolizine–piperidine hybrids
- (2013) Yalda Kia et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- Regio- and stereoselective synthesis of spirooxindole 1′-nitro pyrrolizidines with five concurrent stereocenters under aqueous medium and their bioprospection using the zebrafish (Danio rerio) embryo model
- (2013) Carlos E. Puerto Galvis et al. ORGANIC & BIOMOLECULAR CHEMISTRY
- Enantioselective synthesis of the spirotryprostatin A scaffold
- (2011) Andrey P. Antonchick et al. TETRAHEDRON
- Antimycobacterial activity of spirooxindolo-pyrrolidine, pyrrolizine and pyrrolothiazole hybrids obtained by a three-component regio- and stereoselective 1,3-dipolar cycloaddition
- (2011) Stephen Michael Rajesh et al. MedChemComm
- Antihypertensive and neuroprotective activities of rhynchophylline: The role of rhynchophylline in neurotransmission and ion channel activity
- (2010) Jiyin Zhou et al. JOURNAL OF ETHNOPHARMACOLOGY
- Safety and Tolerability of Donepezil, Rivastigmine and Galantamine for Patients with Alzheimer’s Disease: Systematic Review of the ‘Real-World’ Evidence
- (2009) I.A. Lockhart et al. DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
- The impact of aromatic ring count on compound developability – are too many aromatic rings a liability in drug design?
- (2009) Timothy J. Ritchie et al. DRUG DISCOVERY TODAY
- From Nature to Drug Discovery: The Indole Scaffold as a ‘Privileged Structure’
- (2009) Fernando de Sa Alves et al. MINI-REVIEWS IN MEDICINAL CHEMISTRY
- Synthesis of novel spiropyrrolizidines as potent antimicrobial agents for human and plant pathogens
- (2008) Govindasami Periyasami et al. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS
- On the binding of Thioflavin-T to HET-s amyloid fibrils assembled at pH 2
- (2008) Raimon Sabaté et al. JOURNAL OF STRUCTURAL BIOLOGY
- EGCG redirects amyloidogenic polypeptides into unstructured, off-pathway oligomers
- (2008) Dagmar E Ehrnhoefer et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
Create your own webinar
Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.
Create NowAsk a Question. Answer a Question.
Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.
Get Started