Synthesis and biological evaluation of a fluorine-18 labeled estrogen receptor-alpha selective ligand: [18F] propyl pyrazole triol (Q44454355)

3 December 2017

title

Synthesis and biological evaluation of a fluorine-18 labeled estrogen receptor-alpha selective ligand: [18F] propyl pyrazole triol (English)

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3 December 2017

Dange Vijaykumar

1

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3 December 2017

Mohammed H Al-Qahtani

series ordinal

2

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3 December 2017

Michael J Welch

series ordinal

3

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3 December 2017

John A Katzenellenbogen

series ordinal

4

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3 December 2017

publication date

1 May 2003

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Nuclear Medicine and Biology

3 December 2017

published in

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3 December 2017

volume

30

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3 December 2017

issue

4

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3 December 2017

page(s)

397-404

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Electronic Substituent Effects on the Acid-Catalyzed [4+ + 2] Cycloaddition of Isopyrazoles with Cyclopentadiene and the Photochemical and Thermal Denitrogenation of the Resulting 1,4-Diaryl-7,7-dimethyl-2,3-diazabicyclo[2.2.1]hept-2-ene Azoalkanes t

3 December 2017

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Estrogen receptor subtype-selective ligands: asymmetric synthesis and biological evaluation of cis- and trans-5,11-dialkyl- 5,6,11, 12-tetrahydrochrysenes

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Methodology for the synthesis and specific activity determination of 16 alpha-[77Br]-bromoestradiol-17 beta and 16 alpha-[77Br]-11 beta-methoxyestradiol-17 beta, two estrogen receptor-binding radiopharmaceuticals

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Pyrazole ligands: structure-affinity/activity relationships and estrogen receptor-alpha-selective agonists.

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Solid-phase synthesis of tetrasubstituted pyrazoles, novel ligands for the estrogen receptor

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Acyclic amides as estrogen receptor ligands: synthesis, binding, activity and receptor interaction

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Identifiers

DOI

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3 December 2017

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