Advanced search
Publication Cover
Nucleosides and Nucleotides Volume 14, 1995 - Issue 6
Journal homepage
28
Views
8
CrossRef citations to date
0
Altmetric
Original Articles

Synthesis of 2′,5′-Dideoxy-adenosine-3′-monophosphate Derivatives as Allosteric Inhibitors of Adenylyl Cyclase

Laurent Désaubry Department of Physiology and Biophysics, Health Sciences Center, State University of New-York at Stony Brook, Stony Brook, NY, 11794-8661
,
Ilana Shoshani Department of Physiology and Biophysics, Health Sciences Center, State University of New-York at Stony Brook, Stony Brook, NY, 11794-8661
&
Roger A. Johnson Department of Physiology and Biophysics, Health Sciences Center, State University of New-York at Stony Brook, Stony Brook, NY, 11794-8661
Pages 1453-1460 | Received 12 Oct 1994, Accepted 16 Feb 1995, Published online: 24 Sep 2006

Citations (8)

Keep up to date with the latest research on this topic with citation updates for this article.

Subscribe to citation updates

Read on this site (2)

F. Gavazza, F. Daverio, A.T. Chaytor, T.M. Griffith & C. McGuigan. (2005) PHOSPHORAMIDATE DERIVATIVES OF 2′,5′-DIDEOXYADENOSINE AS POTENTIAL INHIBITORS OF THE EDHF PHENOMENON. Nucleosides, Nucleotides & Nucleic Acids 24:5-7, pages 553-555.
Read now
MaciejB. Szczepanik, Laurent Désaubry & RogerA. Johnson. (1999) Synthesis of Nucleoside 3′-Thiophosphates in One Step Procedure. Nucleosides and Nucleotides 18:4-5, pages 951-953.
Read now

Articles from other publishers (6)

Bhavini Kumari, Alaa Huwaidi, Gabriel Robert, Pierre Cloutier, Andrew D. Bass, Léon Sanche & J. Richard Wagner. (2022) Shape Resonances in DNA: Nucleobase Release, Reduction, and Dideoxynucleoside Products Induced by 1.3 to 2.3 eV Electrons. The Journal of Physical Chemistry B 126:28, pages 5175-5184.
Crossref
Wolfgang H.G. Laux, Praveen Pande, Ilana Shoshani, Junyuan Gao, Valérie Boudou-Vivet, Gilles Gosselin & Roger A. Johnson. (2004) Pro-nucleotide Inhibitors of Adenylyl Cyclases in Intact Cells. Journal of Biological Chemistry 279:14, pages 13317-13332.
Crossref
Ilana Shoshani, Ronald Taussig, Ravi Iyengar & Roger A. Johnson. (2000) Synthesis and Use of 3′-(Azidoiodosalicyl) Derivatives of 2′,5′-Dideoxyadenosine as Photoaffinity Ligands for Adenylyl Cyclase. Archives of Biochemistry and Biophysics 376:1, pages 221-228.
Crossref
Azeddine Ibrahimi, Nada Abumrad, Hengameh Maghareie, Michael Golia, Ilana Shoshani, Laurent Désaubry & Roger A. Johnson. (1999) Adenylyl cyclase P-site ligands accelerate differentiation in Ob1771 preadipocytes. American Journal of Physiology-Cell Physiology 276:2, pages C487-C496.
Crossref
Szczepanik B Maciej, Laurent Désaubry & Roger A Johnson. (1998) One-pot synthesis of deoxyadenosine 3′-thiophosphates. Tetrahedron Letters 39:41, pages 7455-7458.
Crossref
Laurent Désaubry, Ilana Shoshani & Roger A. Johnson. (1996) Inhibition of Adenylyl Cyclase by a Family of Newly Synthesized Adenine Nucleoside 3′-Polyphosphates. Journal of Biological Chemistry 271:24, pages 14028-14034.
Crossref

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Order Reprints Request Corporate Permissions

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

Request Academic Permissions

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.

Related research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.