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Letters in Drug Design & Discovery, Vol. 6, Iss. 7, 2009-10 ,pp. : 518-523

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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

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

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Synthesis, Biochemical Evaluation and Rationalisation of a Series of 3,5- Dibromo Derivatives of 4-Hydroxyphenyl Ketone-Based Compounds as Probes of the Active Site of Type 3 of 17&bgr;-Hydroxysteroid Dehydrogenase (17&bgr;-HSD3) and the Role of Hydrogen Bonding Interaction in the Inhibition of 17&bgr;-HSD3

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Letters in Drug Design & Discovery, Vol. 9, Iss. 6, 2012-07 ,pp. : 604-610

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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

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Esters of Dehydroepiandrosterone (DHEA) as Probes for the Active Site of Type 3 17&bgr;-Hydroxysteroid Dehydrogenase (17&bgr;-HSD3)

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Letters in Drug Design & Discovery, Vol. 7, Iss. 5, 2010-06 ,pp. : 365-369

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