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Two novel SHP-1 agonists, SC-43 and SC-78, are more potent than regorafenib in suppressing the in vitro stemness of human colorectal cancer cells.

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Title: Two novel SHP-1 agonists, SC-43 and SC-78, are more potent than regorafenib in suppressing the in vitro stemness of human colorectal cancer cells.
Authors: Chung SY; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China., Chen YH; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China., Lin PR; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China., Chao TC; 2Division of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, TAIPEI, Republic of China.; Faculty of Medicine, School of Medicine, National Yang-Min University, TAIPEI, Republic of China., Su JC; 4Faculty of Pharmacy, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China., Shiau CW; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China., Su Y; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.
Source: Cell death discovery [Cell Death Discov] 2018 Aug 13; Vol. 4, pp. 25. Date of Electronic Publication: 2018 Aug 13 (Print Publication: 2018).
Publication Type: Journal Article
Journal Info: Publisher: Nature Publishing Group Country of Publication: United States NLM ID: 101665035 Publication Model: eCollection Cited Medium: Print ISSN: 2058-7716 (Print) Linking ISSN: 20587716 NLM ISO Abbreviation: Cell Death Discov Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
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  Data: Two novel SHP-1 agonists, SC-43 and SC-78, are more potent than regorafenib in suppressing the in vitro stemness of human colorectal cancer cells.
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  Data: <searchLink fieldCode="AU" term="%22Chung+SY%22">Chung SY</searchLink>; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.<br /><searchLink fieldCode="AU" term="%22Chen+YH%22">Chen YH</searchLink>; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.<br /><searchLink fieldCode="AU" term="%22Lin+PR%22">Lin PR</searchLink>; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.<br /><searchLink fieldCode="AU" term="%22Chao+TC%22">Chao TC</searchLink>; 2Division of Medical Oncology, Department of Oncology, Taipei Veterans General Hospital, TAIPEI, Republic of China.; Faculty of Medicine, School of Medicine, National Yang-Min University, TAIPEI, Republic of China.<br /><searchLink fieldCode="AU" term="%22Su+JC%22">Su JC</searchLink>; 4Faculty of Pharmacy, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.<br /><searchLink fieldCode="AU" term="%22Shiau+CW%22">Shiau CW</searchLink>; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.<br /><searchLink fieldCode="AU" term="%22Su+Y%22">Su Y</searchLink>; 1Institute of Biopharmaceutical Sciences, School of Pharmaceutical Sciences, National Yang-Ming University, TAIPEI, Republic of China.
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  Data: <searchLink fieldCode="JN" term="%22101665035%22">Cell death discovery</searchLink> [Cell Death Discov] 2018 Aug 13; Vol. 4, pp. 25. <i>Date of Electronic Publication: </i>2018 Aug 13 (<i>Print Publication: </i>2018).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Nature+Publishing+Group%22">Nature Publishing Group </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101665035 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2058-7716 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2220587716%22">20587716 </searchLink><i>NLM ISO Abbreviation: </i>Cell Death Discov <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1038/s41420-018-0084-z
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      – TitleFull: Two novel SHP-1 agonists, SC-43 and SC-78, are more potent than regorafenib in suppressing the in vitro stemness of human colorectal cancer cells.
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              Text: 2018 Aug 13
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