A Novel Insulin Secretagogue Based on a Dinucleoside Polyphosphate Scaffold-Reference-Cited by-同舟云学术

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A Novel Insulin Secretagogue Based on a Dinucleoside Polyphosphate Scaffold

Published:2010-02-22 Issue:6 Volume:53 Page:2472-2481
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Eliahu Shay¹,Barr Haim M.²,Camden Jean³,Weisman Gary A.³,Fischer Bilha¹

Affiliation:

1. Department of Chemistry, Bar-Ilan University, Ramat-Gan 52900, Israel

2. BioLineRx Ltd., 23 Hillel Street, Jerusalem, 91450, Israel

3. Biochemistry Department, 540E Bond Life Sciences Center, University of Missouri-Columbia, Columbia, Missouri 65211

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm901621h

Reference46 articles.

1. Fischer, B.; Nahum, V.Dinucleoside poly(borano)phosphate derivatives and uses thereof. U.S. Patent 7,368,439, 2008.

2. Type 2 diabetes mellitus: not quite exciting enough?

3. Type 2 diabetes: principles of pathogenesis and therapy

4. Intensive blood-glucose control with sulphonylureas or insulin compared with conventional treatment and risk of complications in patients with type 2 diabetes (UKPDS 33)

Cited by 16 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Ball‐Milling to Access Dinucleoside Polyphosphates and Analogues;Advanced Synthesis & Catalysis;2024-03-19

2. The Synthesis of Nucleoside 2′,3′‐Cyclic Monophosphate Analogs with Regio‐ and Stereospecificity;Current Protocols;2021-11

3. Addressing regio- and stereo-specificity challenges in the synthesis of nucleoside 2′,3′-cyclic monophosphate analogs – a rapid and facile synthesis of nucleoside-2′,3′-O,O-phosphoro-thioate or -selenoate, and elucidation of the origin of the rare specificity;Chemical Communications;2020

4. Regulation of glucose and lipid metabolism in health and disease;Science China Life Sciences;2019-10-31

5. How To Form a Phosphate Anhydride Linkage in Nucleotide Derivatives;ChemBioChem;2015-10-30

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