Synthesis and estrogen receptor binding affinities of 7-hydroxy-3-(4-hydroxyphenyl)-4 H -1-benzopyran-4-ones containing a basic side chain
Bioorganic & Medicinal Chemistry Letters, ISSN: 0960-894X, Vol: 13, Issue: 8, Page: 1475-1478
2003
- 26Citations
- 9Captures
Metric Options: Counts1 Year3 YearSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations26
- Citation Indexes26
- 26
- CrossRef19
- Captures9
- Readers9
Article Description
Two isoflavones containing a sulfur or oxygen hinge with an amine-bearing side chain have been designed and synthesized as potential selective estrogen receptor modulators. The target compounds exhibited low affinities for estrogen receptors (ERs), and binding affinity data indicate that oxygen hinge is more favorable than sulfur for binding. These compounds also displayed selectivity for ERα over ERβ.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0960894X0300132X; http://dx.doi.org/10.1016/s0960-894x(03)00132-x; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0037451845&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/12668015; http://linkinghub.elsevier.com/retrieve/pii/S0960894X0300132X; http://api.elsevier.com/content/article/PII:S0960894X0300132X?httpAccept=text/xml; http://api.elsevier.com/content/article/PII:S0960894X0300132X?httpAccept=text/plain; https://linkinghub.elsevier.com/retrieve/pii/S0960894X0300132X; http://dx.doi.org/10.1016/s0960-894x%2803%2900132-x; https://dx.doi.org/10.1016/s0960-894x%2803%2900132-x
Elsevier BV
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