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 Novel &bgr;-Carboline Derivatives as Antiproliferative Agents

By  

Letters in Drug Design & Discovery, Vol. 10, Iss. 9, 2013-11 ,pp. : 879-885

Bentham Science Publishers

Access to resources Recommend Favorite

Synthesis and Characterization of 3&bgr;-Substituted Amides of 17a-Aza-Dhomo- 4-androsten-17-one as Potent 5&agr;-Reductase Inhibitors and Antimicrobial Agents

By  

Current Topics in Medicinal Chemistry, Vol. 13, Iss. 16, 2013-08 ,pp. : 2047-2061

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