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Roberto Cighetti

Roberto Cighetti
Istituto di Istruzione Superiore A. Cesaris

Ph.D.

About

9
Publications
9,267
Reads
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235
Citations
Introduction
Science teaching, Science communication, Social media usage in Science communication, Laboratory teaching, Osteology teaching
Additional affiliations
October 2016 - present
IIS Cesaris
Position
  • High School Science Teacher
Description
  • High School teacher of Biology, Chemistry, Earth Sciences, Anatomy and Pathology
September 2015 - September 2016
IIS Codogno
Position
  • High School Science Teacher
Description
  • High School teacher of Food Chemistry Support teacher for students of the Accountability School
February 2014 - June 2014
Liceo G. Novello, Codogno, Italy
Position
  • High School Science Teacher
Description
  • High School teacher of Biology, Chemistry, Earth Sciences, Astronomy
Education
January 2011 - December 2013
Università degli Studi di Milano-Bicocca
Field of study
  • Industrial Biotechnology
November 2008 - November 2010
Università degli Studi di Milano-Bicocca
Field of study
  • Industrial Biotechnology
October 2005 - November 2008

Publications

Publications (9)
Data
📢 Last Chance Alert! 📢 Due to unforeseen circumstances, two spots have opened up for our upcoming field school! If you've been eager to join us for an unforgettable learning experience, now's your chance! Field School Details: Location: Crkveno Brdo (medieval period), Senta, Serbia Dates: from 22nd of July till 10th of August Activities: Excav...
Article
An increasing number of pathologies have been linked to Toll-like Receptor 4 (TLR4) activation and signaling. New hit and lead compounds that target the TLR4 activation process are urgently needed. We report on the synthesis and biological properties of protonatable glycolipids based on glucose and trehalose scaffolds. Some of these compounds poten...
Article
A growing body of data suggests that therapies based on Toll-like receptors (TLR) targeting, in particular TLR4, holds promise in curing autoimmune and inflammatory pathologies still lacking specific treatment, included several rare diseases. While TLR4 activators (agonists) have already found successful clinical application as vaccine adjuvants, t...
Article
Monosaccharide lipid A mimetics based on a glucosamine core linked to two fatty acid chains and bearing one or two phosphate groups have been synthesized. Compounds 1 and 2, each with one phosphate group, were practically inactive in inhibiting LPS-induced TLR4 signaling and cytokine production in HEK-blue cells and murine macrophages, but compound...
Article
The sincerest form of flattery! A novel, symmetric lipid A mimetic (D1) formed by two glucose units linked through a 6-6' succinic diamide linker is active in modulating the activity of human TLR4. D1 inhibits endotoxin-stimulated TLR4 activation by inhibiting interaction of endotoxin with both receptors CD14 and MD-2 (associated to TLR4). D1 also...
Article
Toll-like receptor 4 (TLR4), the receptor of bacterial endotoxins in mammalians, plays a pivotal role in the induction of innate immunity and inflammation. TLR4 activation by bacterial lipopolysaccharide (LPS) is achieved by the coordinate and sequential action of three other proteins, the lipopolysaccharide binding protein (LBP), the cluster diffe...
Chapter
The identification of the bacterial endotoxin receptors for innate immunity, most notably the Toll-like receptor 4 (TLR4), has sparked great interest in therapeutic manipulation of innate immune system. In this chapter, several natural and synthetic molecules that modulate the TLR4-mediated LPS signalling in animals and humans are presented, and th...
Article
Full-text available
The identification of the bacterial endotoxin receptors for innate immunity, most notably TLR4 (Toll-like receptor 4), has sparked great interest in therapeutic manipulation of the innate immune system. In the present mini-review, several natural and synthetic molecules that modulate the TLR4-mediated LPS (lipopolysaccharide) signalling in animals...

Questions

Question (1)
Question
I'd like to protect a secondary amine group (on Glucosamine-HCl) with a silyl group.
Did you ever do that? Did you use a chlorosilane? Does it get attached two times to the amine? Is the resulting nitrogen on -NH-Si-R more activated as a nucleophile?
How is it removed? Acids only or also fluoride ions? Does it work only for trimethylsilanes or also more bulky/resistent silanes (TBDMS, TBDPS, ...)?
Thank you in advance
RC

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