Synthesis and biological properties of 7α-cyano derivatives of the (17α,20E/Z)-[125I]iodovinyl- and 16α-[125I]iodo-estradiols-Reference-Cited by-同舟云学术

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Synthesis and biological properties of 7α-cyano derivatives of the (17α,20E/Z)-[125I]iodovinyl- and 16α-[125I]iodo-estradiols

Published:2003-12 Issue:14 Volume:68 Page:1189-1200
ISSN:0039-128X
Container-title:Steroids
language:en
Short-container-title:Steroids

Author:

Ali Hasrat,Rousseau Jacques,Paquette Benoit,Dubé Charlotte,Marko Bernadette,van Lier Johan E

Publisher

Elsevier BV

Subject

Organic Chemistry,Clinical Biochemistry,Pharmacology,Endocrinology,Molecular Biology,Biochemistry

Reference31 articles.

1. Katzenellenbogen JA. Receptor imaging of tumors (non-peptide). In: Welch MJ, Redvaly CS, editors. Handbook of radiopharmaceuticals. West Sussex: Wiley; 2003. p. 715–50.

2. Katzenellenbogen JA, Heiman DF, Carlson KE, Lloyd JE. In vivo and in vitro steroid receptor assays in the design of estrogen pharmaceuticals. In: Eckelman WC, editor. Receptor binding radiotracers. Boca Raton, FL: CRC Press; 1982. p. 93–126.

3. Iodine-125-labeled estradiol: a gamma emitting analog of estradiol that binds to the estrogen receptor;Hochberg;Science,1979

4. Synthesis and evaluation of (17α,20E)-21-[125I]iodo-19-norpregna-1,3,5(10),20-tetraene-3,17-diol and (17α,20E)-21-[125II]iodo-11β-methoxy-19-norpregna-1,3,5(10),20-tetraene-3,17-diol (17α-(iodovinyl)estradiol derivatives) as high specific activity potential radiopharmaceuticals;Nakatsuka;J. Med. Chem.,1984

5. Synthesis, receptor binding and tissue distribution of (17α,20E)- and (7α,20Z)-21-[125I]iodo-19-norpregna-1,3,5(10),20-tetraene-3,17-diol;Ali;J. Med. Chem.,1988

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