Zobrazeno 1 - 10
of 128
pro vyhledávání: '"Robert N. Hanson"'
Autor:
Robert N. Hanson, Nisal Gajadeera
Publikováno v:
Steroids. 145:39-46
A set of derivatives of 11β-(4-oxyphenyl)estradiol were prepared as potential fluorescent imaging agents for the evaluation of the estrogen receptor. The compounds were designed based on the established affinity and selectivity of 11β-[4-(dimethyle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4112f49b3a7792ff3bdf9ce23c43bbd
https://doi.org/10.1016/j.steroids.2019.02.013
https://doi.org/10.1016/j.steroids.2019.02.013
Autor:
Nisal Gajadeera, Robert N. Hanson
Publikováno v:
Steroids. 144:30-46
The development of fluorescent ligands for the estrogen receptor (ER) continues to be of interest. Over the past 20 years, most efforts have focused on appending an expanding variety of fluorophores to the B-, C- and D-rings of the steroidal scaffold
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::467da22385923051ebddc2a988c6255c
https://doi.org/10.1016/j.steroids.2019.02.002
https://doi.org/10.1016/j.steroids.2019.02.002
Autor:
Timothy A. Coulther, David Labaree, Jessa L. Silver, Robert Dilis, Edward Hua, Richard B. Hochberg, Emmett McCaskill, Robert N. Hanson, Mary Jo Ondrechen, Pakamas Tongcharoensirikul
Publikováno v:
Steroids. 144:15-20
A series consisting of substituted benzoylbenzamide derivatives of 17α-E-vinyl estradiol 6a-i and 7a-d was prepared in good overall yields from the corresponding novel iodinated benzoylbenzamide precursors using Pd(0)-catalyzed Stille coupling. Biol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd16f6deaa0e9a5ccb0c5f49b75c6cfc
https://doi.org/10.1016/j.steroids.2019.02.003
https://doi.org/10.1016/j.steroids.2019.02.003
Autor:
Kelton Barnsley, Robert N. Hanson, Mary Jo Ondrechen, Eugene R. DeSombre, Alun Hughes, Pakamas Tongcharoensirikul
Publikováno v:
Steroids. 96:50-62
A series of three 1,1-bis(4-hydroxyphenyl)-2-(3-hydroxyphenyl)-ethylene derivatives was prepared and evaluated as potential estrogen receptor imaging agents. The compounds display high binding affinity compared to estradiol, with the 2-iodo and 2-bro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aa49a86722fa343f0b8eb067462724c8
https://doi.org/10.1016/j.steroids.2015.01.013
https://doi.org/10.1016/j.steroids.2015.01.013
Publikováno v:
Bioorganic & Medicinal Chemistry. 22:917-926
A series of unsymmetrically substituted biphenyl compounds was designed as alpha helical proteomimetics with the aim of inhibiting the binding of coactivator proteins to the nuclear hormone receptor coactivator binding domain. These compounds were sy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::58f5b02d331237cb56456a33b171b864
https://doi.org/10.1016/j.bmc.2013.10.051
https://doi.org/10.1016/j.bmc.2013.10.051
Autor:
Emily B. Corcoran, Robert N. Hanson
Publikováno v:
Medicinal Research Reviews. 34:596-643
In an effort to discover a noninvasive method for predicting which cancer patients will benefit from therapy targeting the EGFR and HER2 proteins, a large body of the research has been conducted toward the development of PET and SPECT imaging agents,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f51b1bee69e283496da13414cd6240df
https://doi.org/10.1002/med.21299
https://doi.org/10.1002/med.21299
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 22:6587-6590
A series of bipolar biphenyl compounds was synthesized as proteomimetic analogs of the LXXLL penta-peptide motif responsible for the binding of coactivator proteins to the nuclear hormone receptor coactivator binding domain. These compounds were subj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0d7248ef52b5c2cea6124412d44e6ec
https://doi.org/10.1016/j.bmcl.2012.09.007
https://doi.org/10.1016/j.bmcl.2012.09.007
Autor:
Anna B. Williams, Robert N. Hanson
Publikováno v:
Tetrahedron. 68:5406-5414
As part of our ongoing project to develop new molecular probes for estrogen receptor-alpha, we are exploring the utility of internally-substituted asymmetric biphenyls as a proteomimetic scaffold. In this study, we describe synthetic methods for prep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8150c7284dd99ca0371a32fdf426ef64
https://doi.org/10.1016/j.tet.2012.04.106
https://doi.org/10.1016/j.tet.2012.04.106
Autor:
Robert Dilis, Emmett McCaskill, David Labaree, Robert N. Hanson, Pakamas Tongcharoensirikul, Richard B. Hochberg
Publikováno v:
Steroids. 77:471-476
As part of our program to explore the influence of small structural modifications on the biological response of the estrogen receptor-α (ERα), we prepared and evaluated a series of mono-and di-substituted phenyl vinyl estradiols. The target compoun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9e2a36dbf45d8de5937d49724e7a65c
https://doi.org/10.1016/j.steroids.2012.01.003
https://doi.org/10.1016/j.steroids.2012.01.003