Novel Hydrazine Molecules as Tools To Understand the Flexibility of Vascular Adhesion Protein-1 Ligand-Binding Site: Toward More Selective Inhibitors-Reference-Cited by-同舟云学术

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Novel Hydrazine Molecules as Tools To Understand the Flexibility of Vascular Adhesion Protein-1 Ligand-Binding Site: Toward More Selective Inhibitors

Published:2011-03-15 Issue:7 Volume:54 Page:2143-2154
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Nurminen Elisa M.¹,Pihlavisto Marjo²,Lázár László³,Pentikäinen Ulla¹,Fülöp Ferenc³,Pentikäinen Olli T.¹

Affiliation:

1. Department of Biological and Environmental Science and Nanoscience Center, University of Jyväskylä, P.O. Box 35, FI-40014 Jyväskylä, Finland

2. BioTie Therapies Corporation, Tykistökatu 6, FI-20520 Turku, Finland

3. Institute of Pharmaceutical Chemistry, University of Szeged, H-6720 Eotvos 6, Szeged, Hungary

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm200059p

Reference63 articles.

1. Vascular amine oxidases are needed for leukocyte extravasation into inflamed joints in vivo

2. Induction and function of vascular adhesion protein-1 at sites of inflammation.

3. Semicarbazide-sensitive amine oxidase activity exerts insulin-like effects on glucose metabolism and insulin-signaling pathways in adipose cells

4. Semicarbazide-sensitive amine oxidase in aortic smooth muscle cells mediates synthesis of a methylglyoxal-AGE: implications for vascular complications in diabetes

5. Expression of Vascular Adhesion Protein-1 in Atopic Eczema

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