Chemical Synthesis, Characterisation and Biological Evaluation of Furanic- Estradiol Derivatives as Inhibitors of 17&bgr;-Hydroxysteroid Dehydrogenase Type 1

Publisher： Bentham Science Publishers

E-ISSN： 1875-6638|7|2|80-91

ISSN： 1573-4064

Source： Medicinal Chemistry, Vol.7, Iss.2, 2011-03, pp. : 80-91

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Design, Synthesis and In Vitro Evaluation of 4-Androstene-3,17-dione/Adenosine Hybrid Compounds as Bisubstrate Inhibitors of Type 3 17&bgr;-Hydroxysteroid Dehydrogenase

By  

Medicinal Chemistry, Vol. 2, Iss. 4, 2006-01 ,pp. : 329-347

Bentham Science Publishers

Access to resources Recommend Favorite

Type 1 11 &bgr;-hydroxysteroid Dehydrogenase as Universal Drug Target in Metabolic Diseases?

By  

Endocrine, Metabolic & Immune Disorders-Drug Targets (Formerly Current Drug Targets - Immune, Endocrine & Metabolic Disorders), Vol. 6, Iss. 3, 2006-09 ,pp. : 259-269

Bentham Science Publishers

Access to resources Recommend Favorite

Synthesis and Biological Evaluation of Spiro-δ-lactones as Inhibitors of 17&bgr;-Hydroxysteroid Dehydrogenase Type 2 (17&bgr;-HSD2)

By  

Letters in Drug Design & Discovery, Vol. 8, Iss. 5, 2011-06 ,pp. : 406-421

Bentham Science Publishers

Access to resources Recommend Favorite

Inhibitors of 17&bgr;-Hydroxysteroid Dehydrogenase Type 1

By  

Current Medicinal Chemistry, Vol. 15, Iss. 2, 2008-01 ,pp. : 137-150

Bentham Science Publishers

Access to resources Recommend Favorite

Synthesis, Biochemical Evaluation and Rationalisation of a Series of (3-O-Sulfonate) Derivatives of Estrone (E1) as Probes of the Active Site of Type 3 of the 17&bgr;-Hydroxysteroid Dehydrogenase (17&bgr;-HSD) Family of Enzymes

By  

Letters in Drug Design & Discovery, Vol. 9, Iss. 1, 2012-01 ,pp. : 69-76

Bentham Science Publishers

Access to resources Recommend Favorite