(Q56764589)

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Synthesis of a First Estradiol-Adenosine Hybrid Compound

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Synthesis of a First Estradiol-Adenosine Hybrid Compound (English)

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Sheng-Xiang Lin

4

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author name string

Donald Poirier

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1

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Roch P. Boivin

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2

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Marie Bérubé

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3

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publication date

September 2003

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published in

Synthetic Communications

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volume

33

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issue

18

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page(s)

3183-3192

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cites work

Estrogenic regulation of growth and polypeptide growth factor secretion in human breast carcinoma

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Characteristics of human types 1, 2 and 3 17 beta-hydroxysteroid dehydrogenase activities: oxidation/reduction and inhibition

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The key role of 17 beta-hydroxysteroid dehydrogenases in sex steroid biology

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Chemical synthesis of 16beta-propylaminoacyl derivatives of estradiol and their inhibitory potency on type 1 17beta-hydroxysteroid dehydrogenase and binding affinity on steroid receptors.

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Overview of a rational approach to design type I 17beta-hydroxysteroid dehydrogenase inhibitors without estrogenic activity: chemical synthesis and biological evaluation

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N-butyl, N-methyl, 11-[3',17' beta-(dihydroxy)-1',3',5'(10')-estratrien-16' alpha-yl]-9(R/S)-bromo undecanamide: synthesis and 17 beta-HSD inhibiting, estrogenic and antiestrogenic activities

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Nucleic acids. 11. Synthesis of 5'-esters of 1-.beta.-D-arabinofuranosylcytosine possessing antileukemic and immunosuppressive activity

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Estradiol binding and metabolism in human endometrial hyperplasia and adenocarcinoma

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A 6beta-(thiaheptanamide) derivative of estradiol as inhibitor of 17beta-hydroxysteroid dehydrogenase type 1

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The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products

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10.1081/SCC-120023440

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(Q56764589)

Synthesis of a First Estradiol-Adenosine Hybrid Compound

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