Zobrazeno 1 - 10
of 42
pro vyhledávání: '"N. André Sasaki"'
Publikováno v:
Pharmaceuticals, Vol 12, Iss 4, p 162 (2019)
There is an urgent need to propose effective treatments for Alzheimer’s disease (AD). Although the origin of the disease is poorly understood, several therapeutic options have been proposed. The new therapeutic approaches targeting biometal-mediate
Externí odkaz:
https://doaj.org/article/5348536f07954cd78c2b0de9cd104866
Autor:
N André Sasaki, Pascal Sonnet
Publikováno v:
Future medicinal chemistry. 13(24)
Instead of a conventional ‘one-drug-one-target approach’, this article presents a novel multi-target approach with a concept of trapping simultaneously as many detrimental factors as possible involved in the progression of Parkinson's disease. Th
Publikováno v:
Pharmaceuticals
Volume 12
Issue 4
Pharmaceuticals, Vol 12, Iss 4, p 162 (2019)
Volume 12
Issue 4
Pharmaceuticals, Vol 12, Iss 4, p 162 (2019)
There is an urgent need to propose effective treatments for Alzheimer&rsquo
s disease (AD). Although the origin of the disease is poorly understood, several therapeutic options have been proposed. The new therapeutic approaches targeting biometa
s disease (AD). Although the origin of the disease is poorly understood, several therapeutic options have been proposed. The new therapeutic approaches targeting biometa
Publikováno v:
Proceedings of 4th International Electronic Conference on Medicinal Chemistry.
Publikováno v:
Proceedings of 3rd International Electronic Conference on Medicinal Chemistry.
Reactive carbonyl species (RCS) such as methylglyoxal (MGO) or malondialdehyde (MDA) are endogenously formed during the sugar glycoxidation and lipid peroxidation of polyunsaturated fatty acids induced by oxidative stress exacerbation. Their condensa
Publikováno v:
European journal of medicinal chemistry. 122
An important part of pathogenesis of Alzheimer's disease (AD) is attributed to the contribution of AGE (Advanced Glycation Endproducts) and ALE (Advanced Lipid peroxidation Endproducts). In order to attenuate the progression of AD, we designed a new
Publikováno v:
International Journal of Peptide and Protein Research. 27:366-372
An optically active, alkynyl analogue of norleucine (Nle), L-2-amino-4-hexynoic acid (Aha), was substituted for Met in the solution synthesis of the Boc-protected C-terminal heptapeptide analogue of substance P. Treatment of the resulting alkynyl pep
Publikováno v:
International Journal of Peptide and Protein Research. 27:360-365
A synthesis is described of optically pure L-2-amino-4-hexynoic acid and its derivatives, which can serve as potentially useful precursors for the preparation of highly tritium labeled norleucine-containing peptides, as well as other side-chain modif
Publikováno v:
Tetrahedron. 63:2084-2092
Convergent syntheses of N-functionalized (3S,4S)-3-amino-4-vinyl-piperidin-2-one 10, trans-3-substituted proline 18 and (3S)-3-amino-piperidin-2-one 28 are developed. By incorporating these building blocks to an appropriate position, conformationally
Autor:
Rajesh Dave, N. André Sasaki
Publikováno v:
Tetrahedron: Asymmetry
Tetrahedron: Asymmetry, Elsevier, 2006, 17(3), pp.388-401. ⟨10.1016/j.tetasy.2005.12.027⟩
Tetrahedron: Asymmetry, Elsevier, 2006, 17(3), pp.388-401. ⟨10.1016/j.tetasy.2005.12.027⟩
A broad variety of chiral C/N-functionalized morpholine alcohols sharing a common structural motif in the 3-(hydroxymethyl)morpholine 6 were prepared from enantiomerically pure serine for the purpose of studying their catalytic ligand properties. The