35566172 19014882 19967775 22283328 22517684 23608764 23149805 22293490 34710747 19293997 33966620 21342564 20053559 20519201 23531218 30108860 27467155 31215379 36325400 30448715 18344977 23061562 22002344 21481497 - Search Results

Year	Number of Results
2008	2
2009	3
2010	2
2011	5
2012	5
2013	3
2017	1
2018	1
2019	2
2021	2
2022	3
2023	0

1

Human Estrogen Receptor Alpha Antagonists, Part 3: 3-D Pharmacophore and 3-D QSAR Guided Brefeldin A Hit-to-Lead Optimization toward New Breast Cancer Suppressants.

Kurtanović N, Tomašević N, Matić S, Proia E, Sabatino M, Antonini L, Mladenović M, Ragno R. Kurtanović N, et al. Molecules. 2022 Apr 28;27(9):2823. doi: 10.3390/molecules27092823. Molecules. 2022. PMID: 35566172 Free PMC article.

2

Analogs of methyl-piperidinopyrazole (MPP): antiestrogens with estrogen receptor alpha selective activity.

Zhou HB, Carlson KE, Stossi F, Katzenellenbogen BS, Katzenellenbogen JA. Zhou HB, et al. Bioorg Med Chem Lett. 2009 Jan 1;19(1):108-10. doi: 10.1016/j.bmcl.2008.11.006. Epub 2008 Nov 6. Bioorg Med Chem Lett. 2009. PMID: 19014882 Free PMC article.

3

Estrogen receptor β ligands: recent advances and biomedical applications.

Minutolo F, Macchia M, Katzenellenbogen BS, Katzenellenbogen JA. Minutolo F, et al. Med Res Rev. 2011 May;31(3):364-442. doi: 10.1002/med.20186. Med Res Rev. 2011. PMID: 19967775 Review.

4

Identification and structure-activity relationships of a novel series of estrogen receptor ligands based on 7-thiabicyclo[2.2.1]hept-2-ene-7-oxide.

Wang P, Min J, Nwachukwu JC, Cavett V, Carlson KE, Guo P, Zhu M, Zheng Y, Dong C, Katzenellenbogen JA, Nettles KW, Zhou HB. Wang P, et al. J Med Chem. 2012 Mar 8;55(5):2324-41. doi: 10.1021/jm201556r. Epub 2012 Feb 21. J Med Chem. 2012. PMID: 22283328 Free PMC article.

5

Development of selective estrogen receptor modulator (SERM)-like activity through an indirect mechanism of estrogen receptor antagonism: defining the binding mode of 7-oxabicyclo[2.2.1]hept-5-ene scaffold core ligands.

Zheng Y, Zhu M, Srinivasan S, Nwachukwu JC, Cavett V, Min J, Carlson KE, Wang P, Dong C, Katzenellenbogen JA, Nettles KW, Zhou HB. Zheng Y, et al. ChemMedChem. 2012 Jun;7(6):1094-100. doi: 10.1002/cmdc.201200048. Epub 2012 Apr 19. ChemMedChem. 2012. PMID: 22517684 Free PMC article.

6

Discovery of natural estrogen receptor modulators with structure-based virtual screening.

Cao X, Jiang J, Zhang S, Zhu L, Zou J, Diao Y, Xiao W, Shan L, Sun H, Zhang W, Huang J, Li H. Cao X, et al. Bioorg Med Chem Lett. 2013 Jun 1;23(11):3329-33. doi: 10.1016/j.bmcl.2013.03.105. Epub 2013 Apr 3. Bioorg Med Chem Lett. 2013. PMID: 23608764

7

Discovery of novel SERMs with a ferrocenyl entity based on the oxabicyclo[2.2.1]heptene scaffold and evaluation of their antiproliferative effects in breast cancer cells.

Zheng Y, Wang C, Li C, Qiao J, Zhang F, Huang M, Ren W, Dong C, Huang J, Zhou HB. Zheng Y, et al. Org Biomol Chem. 2012 Dec 28;10(48):9689-99. doi: 10.1039/c2ob26226f. Epub 2012 Nov 14. Org Biomol Chem. 2012. PMID: 23149805

8

Synthesis of 2-phenylbenzofuran derivatives and selective binding activities on estrogen receptor.

Zhang P, Yang Y, Zheng X, Huang W, Ma Z, Shen Z. Zhang P, et al. Chem Pharm Bull (Tokyo). 2012;60(2):270-4. doi: 10.1248/cpb.60.270. Chem Pharm Bull (Tokyo). 2012. PMID: 22293490 Free article.

9

Human estrogen receptor α antagonists, part 2: Synthesis driven by rational design, in vitro antiproliferative, and in vivo anticancer evaluation of innovative coumarin-related antiestrogens as breast cancer suppressants.

Kurtanović N, Tomašević N, Matić S, Mitrović MM, Kostić DA, Sabatino M, Antonini L, Ragno R, Mladenović M. Kurtanović N, et al. Eur J Med Chem. 2022 Jan 5;227:113869. doi: 10.1016/j.ejmech.2021.113869. Epub 2021 Sep 29. Eur J Med Chem. 2022. PMID: 34710747

10

Docking study of triphenylphosphonium cations as estrogen receptor alpha modulators.

Salisbury JP, Williams JC Jr. Salisbury JP, et al. Bioinformation. 2009;3(7):303-7. doi: 10.6026/97320630003303. Epub 2009 Feb 28. Bioinformation. 2009. PMID: 19293997 Free PMC article.

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