Aberrant Cyclization Affords a C-6 Modified Cyclic Adenosine 5′-Diphosphoribose Analogue with Biological Activity in Jurkat T Cells-Reference-Cited by-同舟云学术

Aberrant Cyclization Affords a C-6 Modified Cyclic Adenosine 5′-Diphosphoribose Analogue with Biological Activity in Jurkat T Cells

Published:2012-02-08 Issue:4 Volume:55 Page:1478-1489
ISSN:0022-2623
Container-title:Journal of Medicinal Chemistry
language:en
Short-container-title:J. Med. Chem.

Author:

Moreau Christelle¹,Kirchberger Tanja²,Zhang Bo¹,Thomas Mark P.¹,Weber Karin²,Guse Andreas H.²,Potter Barry V. L.¹

Affiliation:

1. Wolfson Laboratory of Medicinal Chemistry, Department of Pharmacy and Pharmacology, University of Bath, Claverton Down, Bath, BA2 7AY, United Kingdom

2. Calcium Signalling Group, Department of Biochemistry and Signal Transduction, Center of Experimental Medicine, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, D-20246 Hamburg, Germany

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

Link

https://pubs.acs.org/doi/pdf/10.1021/jm201127y

Reference71 articles.

1. Pyridine nucleotide metabolites stimulate calcium release from sea urchin egg microsomes desensitized to inositol trisphosphate.

2. Comparison of Ca2+ mobilizing activities of cyclic ADP-ribose and inositol trisphosphate.

3. Biochemistry, Biology, and Pharmacology of Cyclic Adenosine Diphosphoribose (cADPR)

4. Second messenger function and the structure-activity relationship of cyclic adenosine diphosphoribose (cADPR)

5. Regulation of Calcium Signaling by the Second Messenger Cyclic Adenosine Diphosphoribose (cADPR)

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