12699377 24044724 31757413 23580166 34328178 34648283 23946113 29271936 21129978 23113794 14617632 15860255 31782213 17451940 12559047 23332519 23033157 17827713 18384086 15052541 16373394 18511229 17185393 16533016 29566679 26286148 18599548 1524850 - Search Results

Year	Number of Results
2002	9
2003	36
2004	30
2005	27
2006	22
2007	29
2008	25
2009	17
2010	17
2011	12
2012	14
2013	17
2014	10
2015	17
2016	6
2017	5
2018	9
2019	9
2020	8
2021	10
2022	3
2023	0

1

Bridged bicyclic cores containing a 1,1-diarylethylene motif are high-affinity subtype-selective ligands for the estrogen receptor.

Muthyala RS, Sheng S, Carlson KE, Katzenellenbogen BS, Katzenellenbogen JA. Muthyala RS, et al. J Med Chem. 2003 Apr 24;46(9):1589-602. doi: 10.1021/jm0204800. J Med Chem. 2003. PMID: 12699377

2

Effects of HO-/MeO-PBDEs on androgen receptor: in vitro investigation and helix 12-involved MD simulation.

Wang X, Yang H, Hu X, Zhang X, Zhang Q, Jiang H, Shi W, Yu H. Wang X, et al. Environ Sci Technol. 2013 Oct 15;47(20):11802-9. doi: 10.1021/es4029364. Epub 2013 Oct 2. Environ Sci Technol. 2013. PMID: 24044724

3

Rational approaches of drug design for the development of selective estrogen receptor modulators (SERMs), implicated in breast cancer.

Makar S, Saha T, Swetha R, Gutti G, Kumar A, Singh SK. Makar S, et al. Bioorg Chem. 2020 Jan;94:103380. doi: 10.1016/j.bioorg.2019.103380. Epub 2019 Oct 24. Bioorg Chem. 2020. PMID: 31757413

4

Designer antiandrogens join the race against drug resistance.

Josan JS, Katzenellenbogen JA. Josan JS, et al. Elife. 2013 Apr 9;2:e00692. doi: 10.7554/eLife.00692. Elife. 2013. PMID: 23580166 Free PMC article.

5

Current and emerging estrogen receptor-targeted therapies for the treatment of breast cancer.

Haines CN, Wardell SE, McDonnell DP. Haines CN, et al. Essays Biochem. 2021 Dec 17;65(6):985-1001. doi: 10.1042/EBC20200174. Essays Biochem. 2021. PMID: 34328178

6

Human Estrogen Receptor α Antagonists. Part 1: 3-D QSAR-Driven Rational Design of Innovative Coumarin-Related Antiestrogens as Breast Cancer Suppressants through Structure-Based and Ligand-Based Studies.

Mihović N, Tomašević N, Matić S, Mitrović MM, Kostić DA, Sabatino M, Antonini L, Ragno R, Mladenović M. Mihović N, et al. J Chem Inf Model. 2021 Oct 25;61(10):5028-5053. doi: 10.1021/acs.jcim.1c00530. Epub 2021 Oct 14. J Chem Inf Model. 2021. PMID: 34648283

7

Aerobic iron-based cross-dehydrogenative coupling enables efficient diversity-oriented synthesis of coumestrol-based selective estrogen receptor modulators.

Kshirsagar UA, Parnes R, Goldshtein H, Ofir R, Zarivach R, Pappo D. Kshirsagar UA, et al. Chemistry. 2013 Sep 27;19(40):13575-83. doi: 10.1002/chem.201300389. Epub 2013 Aug 14. Chemistry. 2013. PMID: 23946113

8

Label-Free Biosensor Detection of Endocrine Disrupting Compounds Using Engineered Estrogen Receptors.

La Spina R, Ferrero VEV, Aiello V, Pedotti M, Varani L, Lettieri T, Calzolai L, Haasnoot W, Colpo P. La Spina R, et al. Biosensors (Basel). 2017 Dec 22;8(1):1. doi: 10.3390/bios8010001. Biosensors (Basel). 2017. PMID: 29271936 Free PMC article.

9

New hydroxystilbenoid derivatives endowed with neuroprotective activity and devoid of interference with estrogen and aryl hydrocarbon receptor-mediated transcription.

Villalonga-Barber C, Meligova AK, Alexi X, Steele BR, Kouzinos CE, Screttas CG, Katsanou ES, Micha-Screttas M, Alexis MN. Villalonga-Barber C, et al. Bioorg Med Chem. 2011 Jan 1;19(1):339-51. doi: 10.1016/j.bmc.2010.11.018. Epub 2010 Nov 11. Bioorg Med Chem. 2011. PMID: 21129978

10

Aryllithiums with increasing steric crowding and lipophilicity prepared from chlorides in diethyl ether. The first directly prepared room-temperature-stable dilithioarenes.

Screttas CG, Steele BR, Micha-Screttas M, Heropoulos GA. Screttas CG, et al. Org Lett. 2012 Nov 16;14(22):5680-3. doi: 10.1021/ol302672n. Epub 2012 Oct 31. Org Lett. 2012. PMID: 23113794

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