Hallo! Tracked shipping to Austria with Delivery Duty Paid for just €3.99  

Ship to
Austria
0
  • argentina
  • chile
  • colombia
  • españa
  • méxico
  • perú
  • estados unidos
  • internacional

Select your country

Americas

Europe

Rest of the world

portada Substituted Methanimine Derivatives: Neurodegenerative Disease
Type
Physical Book
Language
English
Pages
52
Format
Paperback
Dimensions
22.9 x 15.2 x 0.3 cm
ISBN13
9786209575709

Substituted Methanimine Derivatives: Neurodegenerative Disease

Swaminathan, Gomathi; M, Navinkumar; Rajagopal, Kalirajan (Author) · LAP Lambert Academic Publishing · Paperback

Substituted Methanimine Derivatives: Neurodegenerative Disease - Swaminathan, Gomathi; M, Navinkumar; Rajagopal, Kalirajan

Cheaper New Book Imported to Austria
Delivery: 27 Aug - 01 Sep Shipping: 13 to 14 business days.
57,36 €
Faster New Book Imported to Austria
Delivery: 14 Aug - 18 Aug Shipping: 4 to 5 business days.
61,68 €
Import costs and 10% VAT included in the price ✅
57,36 €

Synopsis "Substituted Methanimine Derivatives: Neurodegenerative Disease"

Parkinson's disease (PD) is a progressive neurodegenerative disorder marked by the degeneration of dopaminergic neurons in the striatum and the presence of Lewy bodies composed mainly of α-synuclein. Sirtuin 2 (SIRT2), a class III histone deacetylase, is known to influence key cellular functions such as genome integrity, mitochondrial regulation, autophagy, and apoptosis. Increased SIRT2 expression in aging and PD models highlights its relevance as a potential therapeutic target. In this study, a set of Benzoxazole-based methanimine derivatives, (E)-1-Phenyl-N-(2-Phenyl)-1,3-benzoxazol-6-yl) methanimine analogues (NOV 1-3), were designed and evaluated for their inhibitory potential against SIRT2. The target protein (PDB ID: 5YQL) was obtained from the RCSB PDB database, refined through loop modelling, and energy-minimized before molecular docking analysis. Docking studies showed that NOV 1-3 exhibited strong binding affinities and key interactions within the SIRT2 active site, suggesting effective inhibition. The synthesized compounds were structurally confirmed using IR, NMR, and mass spectroscopy.

Customers reviews

Frequently Asked Questions about the Book

All books in our catalog are Original.
The book is written in English.
The binding of this edition is Paperback.

Questions and Answers about the Book

Do you have a question about the book? Login to be able to add your own question.

Opinions about Bookdelivery

More customer reviews