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- [1] Tetraiodobenzimidazoles are potent inhibitors of protein kinase CK2BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (20) : 7281 - 7289Gianoncelli, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandCozza, Giorgio论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandOrzeszko, Andrzej论文数: 0 引用数: 0 h-index: 0机构: Mil Univ Technol, PL-00908 Warsaw, Poland Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandMeggio, Flavio论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandKazimierczuk, Zygmunt论文数: 0 引用数: 0 h-index: 0机构: Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, Poland Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandPinna, Lorenzo A.论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, Poland
- [2] Novel 2-benzylidene benzothiazolidinones as potent and selective inhibitors of protein kinase CK2 and PIM kinasesABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2014, 248Pallela, Venkat R.论文数: 0 引用数: 0 h-index: 0机构: Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USASubbaiah, D. R. C. Venkata论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Deapartment Oncol Sci, New York, NY 10029 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USAMallireddigari, Muralidhar R.论文数: 0 引用数: 0 h-index: 0机构: Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USAAkula, Balireddy论文数: 0 引用数: 0 h-index: 0机构: Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USAPatti, Revathi论文数: 0 引用数: 0 h-index: 0机构: Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USABharathi, Vijaya E.论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Deapartment Oncol Sci, New York, NY 10029 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USACosenza, Stephen C.论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Deapartment Oncol Sci, New York, NY 10029 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USAReddy, E. Premkumar论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Deapartment Oncol Sci, New York, NY 10029 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USAReddy, M. V. Ramana论文数: 0 引用数: 0 h-index: 0机构: Icahn Sch Med Mt Sinai, Deapartment Oncol Sci, New York, NY 10029 USA Onconova Therapeut Inc, Dept Med Chem, Newtown, PA 18940 USA
- [3] Structure-Based Design Of Novel Potent Protein Kinase CK2 (CK2) Inhibitors with Phenyl-azole ScaffoldsJOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (06) : 2899 - 2903Hou, Zengye论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanNakanishi, Isao论文数: 0 引用数: 0 h-index: 0机构: Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanKinoshita, Takayoshi论文数: 0 引用数: 0 h-index: 0机构: Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, Japan论文数: 引用数: h-index:机构:Yasue, Misato论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanMisu, Ryosuke论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanSuzuki, Yamato论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanNakamura, Shinya论文数: 0 引用数: 0 h-index: 0机构: Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanKure, Tatsuhide论文数: 0 引用数: 0 h-index: 0机构: Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanOhno, Hiroald论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanMurata, Katsumi论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanKitaura, Kazuo论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanHirasawa, Akira论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, JapanTsujimoto, Gozoh论文数: 0 引用数: 0 h-index: 0机构: Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan Kinki Univ, Fac Pharm, Higashiosaka, Osaka 5778502, Japan论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:
- [4] Potent and Selective CK2 Kinase Inhibitors with Effects on Wnt Pathway Signaling in VivoACS MEDICINAL CHEMISTRY LETTERS, 2016, 7 (03): : 300 - 305Dowling, James E.论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAAlimzhanov, Marat论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USABao, Larry论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAChuaqui, Claudio论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USADenz, Christopher R.论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAJenkins, Emma论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USALarsen, Nicholas A.论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USALyne, Paul D.论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAPontz, Timothy论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAYe, Qing论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAHoldgate, Geoff A.论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Discovery Sci, Struct & Biophys, Darwin Bldg,310 Cambridge Sci Pk,Milton Rd, Cambridge CB4 0WG, England AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USASnow, Lindsay论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Discovery Sci, Struct & Biophys, Darwin Bldg,310 Cambridge Sci Pk,Milton Rd, Cambridge CB4 0WG, England AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAO'Connell, Nichole论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Discovery Sci, Struct & Biophys, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USAFerguson, Andrew D.论文数: 0 引用数: 0 h-index: 0机构: AstraZeneca R&D, Discovery Sci, Struct & Biophys, 35 Gatehouse Dr, Waltham, MA 02451 USA AstraZeneca R&D, Oncol Innovat Med Unit, 35 Gatehouse Dr, Waltham, MA 02451 USA
- [5] Quinalizarin as a potent, selective and cell-permeable inhibitor of protein kinase CK2BIOCHEMICAL JOURNAL, 2009, 421 : 387 - 395Cozza, Giorgio论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyMazzorana, Marco论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy VIMM, I-35129 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyPapinutto, Elena论文数: 0 引用数: 0 h-index: 0机构: VIMM, I-35129 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyBain, Jenny论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland Univ Dundee, MRC, Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyElliott, Matthew论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland Univ Dundee, MRC, Prot Phosphorylat Unit, Dundee DD1 5EH, Scotland Univ Padua, Dept Biol Chem, I-35121 Padua, Italy论文数: 引用数: h-index:机构:Gianoncelli, Alessandra论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, Italy论文数: 引用数: h-index:机构:Sarno, Stefania论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy VIMM, I-35129 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, Italy论文数: 引用数: h-index:机构:Battistutta, Roberto论文数: 0 引用数: 0 h-index: 0机构: VIMM, I-35129 Padua, Italy Univ Padua, Dept Chem Sci, I-35131 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyMeggio, Flavio论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyMoro, Stefano论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Pharmaceut Sci, MMS, I-35131 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyZagotto, Giuseppe论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Pharmaceut Sci, MMS, I-35131 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, ItalyPinna, Lorenzo A.论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35121 Padua, Italy Univ Padua, CNR, Inst Neurosci, I-35121 Padua, Italy VIMM, I-35129 Padua, Italy Univ Padua, Dept Biol Chem, I-35121 Padua, Italy
- [6] Selected flavonoid compounds as promising inhibitors of protein kinase CK2α and CK2α', the catalytic subunits of CK2PHYTOCHEMISTRY, 2017, 136 : 39 - 45Baier, Andrea论文数: 0 引用数: 0 h-index: 0机构: John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, PolandGalicka, Anna论文数: 0 引用数: 0 h-index: 0机构: Med Univ Bialystok, Dept Med Chem, Ul Mickiewicza 2a, PL-15089 Bialystok, Poland John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, PolandNazaruk, Jolanta论文数: 0 引用数: 0 h-index: 0机构: Med Univ Bialystok, Dept Pharmacognosy, Ul Mickiewicza 2a, PL-15089 Bialystok, Poland John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, PolandSzyszka, Ryszard论文数: 0 引用数: 0 h-index: 0机构: John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland John Paul II Catholic Univ Lublin, Dept Mol Biol, Ul Konstantynow 1I, PL-20708 Lublin, Poland
- [7] The selectivity of inhibitors of protein kinase CK2: an updateBIOCHEMICAL JOURNAL, 2008, 415 (353-365) : 353 - 365论文数: 引用数: h-index:机构:Bain, Jenny论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Prot Phosphorylat Unit, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland Univ Dundee, Prot Phosphorylat Unit, MRC, Dundee DD1 5EH, Scotland Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandKazimierczuk, Zygmunt论文数: 0 引用数: 0 h-index: 0机构: Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, Poland Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandSarno, Stefania论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35131 Padua, Italy Univ Padua, Inst Neurosci, CNR, I-35131 Padua, Italy VIMM, I-35129 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, Poland论文数: 引用数: h-index:机构:论文数: 引用数: h-index:机构:Elliott, Matthew论文数: 0 引用数: 0 h-index: 0机构: Univ Dundee, Prot Phosphorylat Unit, Div Signal Transduct Therapy, Dundee DD1 5EH, Scotland Univ Dundee, Prot Phosphorylat Unit, MRC, Dundee DD1 5EH, Scotland Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandOrzeszko, Andrzej论文数: 0 引用数: 0 h-index: 0机构: Mil Univ Technol, PL-00908 Warsaw, Poland Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandCozza, Giorgio论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35131 Padua, Italy Univ Padua, Inst Neurosci, CNR, I-35131 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandMeggio, Flavio论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35131 Padua, Italy Univ Padua, Inst Neurosci, CNR, I-35131 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, PolandPinna, Lorenzo A.论文数: 0 引用数: 0 h-index: 0机构: Univ Padua, Dept Biol Chem, I-35131 Padua, Italy Univ Padua, Inst Neurosci, CNR, I-35131 Padua, Italy VIMM, I-35129 Padua, Italy Polish Acad Sci, Med Res Ctr, Lab Expt Pharmacol, PL-02106 Warsaw, Poland
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