Supplemental material
Journal of Enzyme Inhibition and Medicinal Chemistry
Volume 33, 2018 - Issue 1
Related Research Data
Synthesis and structure-activity relationships of 6-substituted androst-4-ene analogs as aromatase inhibitors.
Source:
American Chemical Society (ACS)
Diverse function of aromatase and the N-terminal sequence deleted form.
Source:
Elsevier BV
The Important Roles of Steroid Sulfatase and Sulfotransferases in Gynecological Diseases.
Source:
Frontiers Media SA
By-Products Produced by the Reaction of Estrogens with Hypochlorous Acid and their Estrogen Activities
Source:
Pharmaceutical Society of Japan
17β-Hydroxysteroid dehydrogenases (17β-HSDs) as therapeutic targets: protein structures, functions, and recent progress in inhibitor development.
Source:
Elsevier BV
Synthesis and in vitro pharmacological evaluation of N-[(1-benzyl-1,2,3-triazol-4-yl)methyl]-carboxamides on d-secoestrone scaffolds
Source:
Informa UK Limited
The structure of a complex of human 17β-hydroxysteroid dehydrogenase with estradiol and NADP+ identifies two principal targets for the design of inhibitors
Source:
Elsevier Science Ltd.
Synthesis of A-ring halogenated 13α-estrone derivatives as potential 17β-HSD1 inhibitors.
Source:
Elsevier BV
Inhibition of human placental 17β-hydroxysteroid dehydrogenase by steroids and nonsteroidal alcohols: Aspects of inhibitor structure and binding specificity
Source:
Elsevier BV
Diverse function of aromatase and the N-terminal sequence deleted form.
Source:
Elsevier BV
Synthesis and structure–activity relationships of 2- and/or 4-halogenated 13β- and 13α-estrone derivatives as enzyme inhibitors of estrogen biosynthesis
Source:
Taylor & Francis
Human sulfatases: a structural perspective to catalysis.
Source:
Springer Science and Business Media LLC
Impact of estradiol structural modifications (18-methyl and/or 17-hydroxy inversion of configuration) on the in vitro and in vivo estrogenic activity
Source:
Elsevier BV
Estrogen O-sulfamates and their analogues: Clinical steroid sulfatase inhibitors with broad potential.
Source:
Elsevier BV
The estradiol pharmacophore: Ligand structure-estrogen receptor binding affinity relationships and a model for the receptor binding site
Source:
Elsevier BV
Pd-Catalyzed microwave-assisted synthesis of phosphonated 13α-estrones as potential OATP2B1, 17β-HSD1 and/or STS inhibitors
Source:
Beilstein Institut
Steroid sulfatase inhibitors
Source:
Informa Healthcare
Linking provided by
