Cargando…

Clarifying the Use of Benzylidene Protecting Group for D-(+)-Ribono-1,4-Lactone, an Essential Building Block in the Synthesis of C-Nucleosides

In the last two years, nucleosides analogues, a class of well-established bioactive compounds, have been the subject of renewed interest from the scientific community thanks to their antiviral activity. The COVID-19 global pandemic, indeed, spread light on the antiviral drug Remdesivir, an adenine C...

Descripción completa

Detalles Bibliográficos
Autores principales:	Casati, Silvana, Rota, Paola, Allevi, Pietro, Mingione, Alessandra, Ottria, Roberta, Ciuffreda, Pierangela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2021
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8587313/ https://www.ncbi.nlm.nih.gov/pubmed/34770855 http://dx.doi.org/10.3390/molecules26216447

Ejemplares similares

Small-Molecules as Chemiluminescent Probes to Detect Lipase Activity
por: La Rocca, Paolo, et al.
Publicado: (2022)

2,3-O-(S)-Benzylidene-2-C-methyl-d-ribono-1,4-lactone
por: Booth, K. Victoria, et al.
Publicado: (2009)

5-O-Acetyl-d-ribono-1,4-lactone
por: Bortoluzzi, Adailton J., et al.
Publicado: (2011)

A New Ultrasensitive Bioluminescence-Based Method for Assaying Monoacylglycerol Lipase
por: Miceli, Matteo, et al.
Publicado: (2021)

2-Arachidonoylglycerol Synthesis: Facile and Handy Enzymatic Method That Allows to Avoid Isomerization
por: Ottria, Roberta, et al.
Publicado: (2022)

Simple Synthesis of 17-β-O-hemisuccinate of Stanozolol for Immunoanalytical Methods
por: Casati, Silvana, et al.
Publicado: (2020)

Crystal structure of 5-O-benzoyl-2,3-O-isopropylidene-d-ribono-1,4-lactone
por: Bortoluzzi, Adailton J., et al.
Publicado: (2017)

Chios Mastic Gum: Chemical Profile and Pharmacological Properties in Inflammatory Bowel Disease: From the Past to the Future
por: Ottria, Roberta, et al.
Publicado: (2023)

Intramolecular Lactones of Sialic Acids
por: Rota, Paola, et al.
Publicado: (2020)

Quantitative Characterization of Olaparib in Nanodelivery System and Target Cell Compartments by LC-MS/MS
por: Ottria, Roberta, et al.
Publicado: (2019)

Correction: Ottria, R., et al. Quantitative Characterization of Olaparib in Nanodelivery System and Target Cell Compartments by LC-MS/MS. Molecules 2019, 24, 989
por: Ottria, Roberta, et al.
Publicado: (2019)

Set-Up and Validation of a High Throughput Screening Method for Human Monoacylglycerol Lipase (MAGL) Based on a New Red Fluorescent Probe
por: Miceli, Matteo, et al.
Publicado: (2019)

2-O-Benzhydryl-3,4-(S)-O-benzylidene-d-xylono-1,4-lactone
por: Jenkinson, Sarah F., et al.
Publicado: (2008)

2-O-Benzhydryl-3,4-(S)-O-benzylidene-d-lyxono-1,4-lactone
por: Jenkinson, Sarah F., et al.
Publicado: (2008)

Urine Endocannabinoids as Novel Non-Invasive Biomarkers for Bladder Cancer at Early Stage
por: Vago, Riccardo, et al.
Publicado: (2020)

Nucleoside Triphosphates — Building Blocks for the Modification of Nucleic Acids
por: Hollenstein, Marcel
Publicado: (2012)

Quantitative Lipidomic Analysis of Osteosarcoma Cell-Derived Products by UHPLC-MS/MS
por: Casati, Sara, et al.
Publicado: (2020)

Unambiguous Characterization of p-Cresyl Sulfate, a Protein-Bound Uremic Toxin, as Biomarker of Heart and Kidney Disease
por: Paroni, Rita, et al.
Publicado: (2019)

(1S)-1,2-O-Benzylidene-α-d-glucurono-6,3-lactone
por: Jenkinson, Sarah F., et al.
Publicado: (2009)

Toward Upscaled Biocatalytic Preparation of Lactone Building Blocks for Polymer Applications
por: Delgove, Marie A. F., et al.
Publicado: (2018)

Isoxazole Nucleosides as Building Blocks for a Plausible Proto‐RNA
por: Xu, Felix, et al.
Publicado: (2022)

Analysis of the intramolecular 1,7-lactone of N-acetylneuraminic acid using HPLC–MS: relationship between detection and stability
por: La Rocca, Paolo, et al.
Publicado: (2023)

Recent Advances Clarifying the Structure and Function of Plant Apyrases (Nucleoside Triphosphate Diphosphohydrolases)
por: Clark, Greg, et al.
Publicado: (2021)

2-C-Hydroxymethyl-2,3-O-isopropylidene-d-ribono-1,5-lactam. Corrigendum
por: Newton, Christopher R., et al.
Publicado: (2010)

A green, economical synthesis of β-ketonitriles and trifunctionalized building blocks from esters and lactones
por: Pienaar, Daniel P, et al.
Publicado: (2019)

A bicyclic S-adenosylmethionine regeneration system applicable with different nucleosides or nucleotides as cofactor building blocks
por: Popadić, Désirée, et al.
Publicado: (2021)

2-C-Phenylerythrono-1,4-lactone
por: Robinson, Tony V., et al.
Publicado: (2009)

An Approach to Modify 14-Membered Lactone Macrolide Antibiotic Scaffolds
por: Janas, Anna, et al.
Publicado: (2022)

Potential Building Blocks for 1,4‐Dihydro‐N‐heteroacenes
por: John Plater, M., et al.
Publicado: (2022)

Clarifying Water
Publicado: (1867)

Clarifying Water
Publicado: (1879)

ADME studies of [5‐(3)H]‐2′‐O‐methyluridine nucleoside in mice: a building block in siRNA therapeutics
por: Lozac'h, Frederic, et al.
Publicado: (2016)

Functional Annotation and Structural Characterization of a Novel Lactonase Hydrolyzing d-Xylono-1,4-lactone-5-phosphate and l-Arabino-1,4-lactone-5-phosphate
por: Korczynska, Magdalena, et al.
Publicado: (2014)

A novel route to a chiral building block for the preparation of cyclopentenyl carbocyclic nucleosides. Synthesis and anticancer activity of enantiomeric neplanocins A
por: Łukasik, Beata, et al.
Publicado: (2020)

An atypical mechanism of pseudo mitral isthmus block clarified by the high-resolution mapping system
por: Takigawa, Masateru, et al.
Publicado: (2017)

Clarifying the Mechanisms of Antidepressants
por: Tucker, Don M.
Publicado: (2015)

Clarifying the origin of Houzao
por: Zhao, Zhongzhen, et al.
Publicado: (2018)

2-(4-Isopropylbenzylidene)propanoic acid
por: Muhammad, Niaz, et al.
Publicado: (2008)

Discovery, Semisynthesis, Antiparasitic and Cytotoxic Evaluation of 14-Membered Resorcylic Acid Lactones and Their Derivatives
por: Zhang, Xue-Qing, et al.
Publicado: (2017)

The building blocks
Publicado: (2008)

Cannot write session to /tmp/vufind_sessions/sess_7396mkf3nc7r34nhtfqved47r2