# | Title | Journal | Year | Citations |
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1 | Peripheral cannabinoid receptor, CB2, regulates bone mass | Proceedings of the National Academy of Sciences of the United States of America | 2006 | 492 |
2 | Steroid Sulfatase: Molecular Biology, Regulation, and Inhibition | Endocrine Reviews | 2005 | 468 |
3 | Regulation of calcium signalling in T lymphocytes by the second messenger cyclic ADP-ribose | Nature | 1999 | 317 |
4 | Estrone sulfamates: potent inhibitors of estrone sulfatase with therapeutic potential | Journal of Medicinal Chemistry | 1994 | 215 |
5 | Structure of the PH domain from Bruton's tyrosine kinase in complex with inositol 1,3,4,5-tetrakisphosphate | Structure | 1999 | 204 |
6 | Nicotinic Acid Adenine Dinucleotide Phosphate (Naadp+) Is an Essential Regulator of T-Lymphocyte Ca2+-Signaling | Journal of Cell Biology | 2000 | 166 |
7 | Class III β-tubulin expression and in vitro resistance to microtubule targeting agents | British Journal of Cancer | 2010 | 163 |
8 | Identification of Mammalian Vps24p as an Effector of Phosphatidylinositol 3,5-Bisphosphate-dependent Endosome Compartmentalization | Journal of Biological Chemistry | 2003 | 154 |
9 | Steroidal and Nonsteroidal Sulfamates as Potent Inhibitors of Steroid Sulfatase | Journal of Medicinal Chemistry | 1998 | 147 |
10 | Determination of neo- and d-chiro-Inositol Hexakisphosphate in Soils by Solution 31P NMR Spectroscopy | Environmental Science & Technology | 2012 | 124 |
11 | Pharmacokinetics and efficacy of 2-methoxyoestradiol and 2-methoxyoestradiol-bis-sulphamate in vivo in rodents | British Journal of Cancer | 2004 | 108 |
12 | Induction of Hippocampal LTD Requires Nitric-Oxide-Stimulated PKG Activity and Ca2+Release From Cyclic ADP-Ribose-Sensitive Stores | Journal of Neurophysiology | 1999 | 106 |
13 | NAADP-mediated Ca 2+ signaling via type 1 ryanodine receptor in T cells revealed by a synthetic NAADP antagonist | Proceedings of the National Academy of Sciences of the United States of America | 2009 | 101 |
14 | InsP4 facilitates store-operated calcium influx by inhibition of InsP3 5-phosphatase | Nature | 2000 | 99 |
15 | 17β‐hydroxysteroid dehydrogenase Type 1, and not Type 12, is a target for endocrine therapy of hormone‐dependent breast cancer | International Journal of Cancer | 2008 | 99 |
16 | Quinazolinone-Based Anticancer Agents: Synthesis, Antiproliferative SAR, Antitubulin Activity, and Tubulin Co-crystal Structure | Journal of Medicinal Chemistry | 2018 | 99 |
17 | 2-Substituted Estradiol Bis-sulfamates, Multitargeted Antitumor Agents: Synthesis, In Vitro SAR, Protein Crystallography, and In Vivo Activity† | Journal of Medicinal Chemistry | 2006 | 98 |
18 | Steroid Sulfatase: A New Target for the Endocrine Therapy of Breast Cancer | Oncologist | 2007 | 94 |
19 | The advantages and limitations of protein crystal structures | Trends in Pharmacological Sciences | 2005 | 93 |
20 | Inositol pentakisphosphate promotes apoptosis through the PI 3-K/Akt pathway | Oncogene | 2004 | 91 |
21 | Olefin metathesis in non-degassed solvent using a recyclable, polymer supported alkylideneruthenium | Chemical Communications | 2001 | 84 |
22 | Simple pyrazoline and pyrazole “turn on” fluorescent sensors selective for Cd2+ and Zn2+ in MeCN | Organic and Biomolecular Chemistry | 2012 | 82 |
23 | Chiral Aromatase and Dual Aromatase−Steroid Sulfatase Inhibitors from the Letrozole Template: Synthesis, Absolute Configuration, and In Vitro Activity | Journal of Medicinal Chemistry | 2008 | 81 |
24 | E-Ring Modified Steroids as Novel Potent Inhibitors of 17β-Hydroxysteroid Dehydrogenase Type 1 | Journal of Medicinal Chemistry | 2005 | 78 |
25 | α-Methylacyl-CoA racemase (AMACR): Metabolic enzyme, drug metabolizer and cancer marker P504S | Progress in Lipid Research | 2013 | 78 |
26 | Multiple DNA binding modes of anthracene-9-carbonyl-N1-spermine | Bioorganic and Medicinal Chemistry | 1995 | 77 |
27 | First Dual Aromatase-Steroid Sulfatase Inhibitors | Journal of Medicinal Chemistry | 2003 | 76 |
28 | Highly Potent First Examples of Dual Aromatase−Steroid Sulfatase Inhibitors based on a Biphenyl Template | Journal of Medicinal Chemistry | 2010 | 76 |
29 | In vivo inhibition of oestrone sulphatase and dehydroepiandrosterone sulphatase by oestrone-3-O-sulphamate | International Journal of Cancer | 1995 | 75 |
30 | Dual Aromatase−Steroid Sulfatase Inhibitors | Journal of Medicinal Chemistry | 2007 | 75 |
31 | Discovery and Development of the Aryl O-Sulfamate Pharmacophore for Oncology and Women’s Health | Journal of Medicinal Chemistry | 2015 | 74 |
32 | 7-Deaza-8-bromo-cyclic ADP-ribose, the First Membrane-permeant, Hydrolysis-resistant Cyclic ADP-ribose Antagonist | Journal of Biological Chemistry | 1997 | 73 |
33 | The effect of 2-methoxyoestrone-3-O-sulphamate on the growth of breast cancer cells and induced mammary tumours | International Journal of Cancer | 2000 | 70 |
34 | Modification of Estrone at the 6, 16, and 17 Positions: Novel Potent Inhibitors of 17β-Hydroxysteroid Dehydrogenase Type 1 | Journal of Medicinal Chemistry | 2006 | 70 |
35 | Active Site Directed Inhibition of Estrone Sulfatase by Nonsteroidal Coumarin Sulfamates | Journal of Medicinal Chemistry | 1996 | 69 |
36 | A-Ring-Substituted Estrogen-3-O-sulfamates: Potent Multitargeted Anticancer Agents | Journal of Medicinal Chemistry | 2005 | 69 |
37 | Synthetic partial agonists reveal key steps in IP3 receptor activation | Nature Chemical Biology | 2009 | 69 |
38 | 2′-Deoxyadenosine 5′-diphosphoribose is an endogenous TRPM2 superagonist | Nature Chemical Biology | 2017 | 68 |
39 | Structure–Activity Relationship of Adenosine 5′-diphosphoribose at the Transient Receptor Potential Melastatin 2 (TRPM2) Channel: Rational Design of Antagonists | Journal of Medicinal Chemistry | 2013 | 64 |
40 | Synthesis of Selective Non-Ca2+ Mobilizing Inhibitors of D-myo-Inositol 1,4,5-Trisphosphate 5-Phosphatase | Journal of Medicinal Chemistry | 1994 | 61 |
41 | Inhibition ofin vitro angiogenesis by 2-methoxy- and 2-ethyl-estrogen sulfamates | International Journal of Cancer | 2004 | 61 |
42 | Regulation of Ins(3,4,5,6)P4 Signaling by a Reversible Kinase/Phosphatase | Current Biology | 2002 | 60 |
43 | D-Ring Modified Estrone Derivatives as Novel Potent Inhibitors of Steroid Sulfatase | Bioorganic and Medicinal Chemistry | 2003 | 59 |
44 | Dual aromatase–sulfatase inhibitors based on the anastrozole template: synthesis, in vitro SAR, molecular modelling and in vivo activity | Organic and Biomolecular Chemistry | 2007 | 58 |
45 | Chemical genetics suggests a critical role for lysyl oxidase in zebrafish notochord morphogenesis | Molecular BioSystems | 2007 | 58 |
46 | Aromatase and Dual Aromatase‐Steroid Sulfatase Inhibitors from the Letrozole and Vorozole Templates | ChemMedChem | 2011 | 58 |
47 | Structure–Activity Relationship for the First‐in‐Class Clinical Steroid Sulfatase Inhibitor Irosustat (STX64, BN83495) | ChemMedChem | 2011 | 58 |
48 | Fluorescence Lifetime Imaging and FRET‐Induced Intracellular Redistribution of Tat‐Conjugated Quantum Dot Nanoparticles through Interaction with a Phthalocyanine Photosensitiser | Small | 2014 | 58 |
49 | Synthetic Inositol Phosphate Analogs Reveal that PPIP5K2 Has a Surface-Mounted Substrate Capture Site that Is a Target for Drug Discovery | Chemistry and Biology | 2014 | 58 |
50 | Benzothiazole derivatives as novel inhibitors of human 11β-hydroxysteroid dehydrogenase type 1 | Molecular and Cellular Endocrinology | 2006 | 57 |