Zobrazeno 1 - 10
of 100
pro vyhledávání: '"Terefenko, Eugene A."'
Publikováno v:
In Microporous and Mesoporous Materials August 2023 358
Autor:
Peter I. Ravikovitch, Tom Willhammar, Terefenko Eugene, Elina Kapaca, Lucas Koziol, Hongyi Xu, Xiaodong Zou, Allen W. Burton, Charanjit S. Paur, Hilda B. Vroman, Mobae Afeworki, Simon C. Weston, Meghan L. Nines Kochersperger
Publikováno v:
Inorganic Chemistry. 58:12854-12858
A new aluminosilicate zeolite, denoted EMM-37, with a 3D small pore channel system, has been synthesized using a diquaternary ammonium molecule as the structure directing agent (SDA) and metakaolin as the aluminum source. The structures of both as-ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bbcbda3b90e4d88ee53185cb96a7d6ad
https://doi.org/10.1021/acs.inorgchem.9b01798
https://doi.org/10.1021/acs.inorgchem.9b01798
Autor:
Zhang, Puwen, Kern, Jeffrey C., Terefenko, Eugene A., Fensome, Andrew, Unwalla, Ray, Zhang, Zhiming, Cohen, Jeffrey, Berrodin, Thomas J., Yudt, Matthew R., Winneker, Richard C., Wrobel, Jay
Publikováno v:
In Bioorganic & Medicinal Chemistry 2008 16(13):6589-6600
Autor:
Zhang, Puwen, Terefenko, Eugene, Kern, Jeffrey, Fensome, Andrew, Trybulski, Eugene, Unwalla, Ray, Wrobel, Jay, Lockhead, Susan, Zhu, Yuan, Cohen, Jeffrey, LaCava, Margaret, Winneker, Richard C., Zhang, Zhiming
Publikováno v:
In Bioorganic & Medicinal Chemistry 2007 15(20):6556-6564
Akademický článek
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Autor:
Casey Cameron Mccomas, Jenifer A. Bray, Cheryl A. Mugford, Puwen Zhang, Terefenko Eugene Anthony, Eugene John Trybulski, An T. Vu, Andrew Fensome, Garth T. Whiteside, Elizabeth Koury, Lilly Mark, Jim Harrison, Darlene C. Deecher, Paige Erin Mahaney, Kim Callain Younghee
Publikováno v:
Journal of Medicinal Chemistry. 52:5703-5711
Sequential structural modifications of the aryloxypropanamine template (e.g., atomoxetine, 2) led to a novel series of 1-(3-amino-2-hydroxy-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors (NRIs). In
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::afc387e88a81026305a6f4d591b56022
https://doi.org/10.1021/jm900888c
https://doi.org/10.1021/jm900888c
Autor:
Darlene C. Deecher, Puwen Zhang, An T. Vu, Jenifer A. Bray, Rebecca Dooley, Stephen Todd Cohn, Igor Goljer, Paige Erin Mahaney, Grace H. Johnston, Jennifer Leiter, Terefenko Eugene Anthony, Eugene John Trybulski, William Jay Moore
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 19:2464-2467
A series of 3-(arylamino)-3-phenylpropan-2-olamines was prepared and screened for their ability to inhibit monoamine reuptake. A number of analogues displayed significant dual norepinephrine and serotonin reuptake inhibition. Compounds in this class
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7db3ef438ffaa46e586b95753deb71
https://doi.org/10.1016/j.bmcl.2009.03.054
https://doi.org/10.1016/j.bmcl.2009.03.054
Autor:
Casey Cameron Mccomas, Paige E. Mahaney, Darlene C. Deecher, Grace H. Johnston, Terefenko Eugene Anthony, Eugene John Trybulski, Elizabeth Koury, Puwen Zhang, An Vu, Jenifer A. Bray
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 18:6067-6070
A series of novel 1- or 3-(3-amino-1-phenyl propyl)-1,3-dihydro-2H-benzimidazol-2-ones as selective norepinephrine reuptake inhibitors was discovered. Several compounds such as 15 and 20 showed good hNET potency. Compounds 15 and 20 also displayed ex
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f10d315d14d5a7dfa8fd5b0e8d81e04c
https://doi.org/10.1016/j.bmcl.2008.10.026
https://doi.org/10.1016/j.bmcl.2008.10.026
Autor:
Richard C. Winneker, Puwen Zhang, Terefenko Eugene Anthony, Zhiming Zhang, Andrew Fensome, Jeffrey I. Cohen, Ray Unwalla, Jay E. Wrobel, Matthew R. Yudt, Thomas J. Berrodin, Jeffrey Curtis Kern
Publikováno v:
Bioorganic & Medicinal Chemistry. 16:6589-6600
Novel 7-aryl benzo[1,4]oxazepin-2-ones were synthesized and evaluated as non-steroidal progesterone receptor (PR) modulators. The structure activity relationship of 7-aryl benzo[1,4]oxazepinones was examined using the T47D cell alkaline phosphatase a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b3496fa932622954dc632d097a2020c1
https://doi.org/10.1016/j.bmc.2008.05.018
https://doi.org/10.1016/j.bmc.2008.05.018
Autor:
Jay Wrobel, Zhiming Zhang, Terefenko Eugene Anthony, Jeffrey A. Cohen, Jeffrey A. Kern, Puwen Zhang, Andrew Fensome, Richard C. Winneker, Yuan Zhu
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 15:3600-3603
We have previously reported that the aryl substituted benzimidazolones, benzoxazinones, and oxindoles (e.g., 1-3) are progesterone receptor (PR) antagonists and have recently disclosed that the nature of 5- and 6-aryl moieties played a critical role
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::61f99fa78e8412682740ef4f47ea0746
https://doi.org/10.1016/j.bmcl.2005.05.082
https://doi.org/10.1016/j.bmcl.2005.05.082