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Items for Author "Lu, CT"
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Showing 14 items.
Collection
Date
Title
Relation
Bitstream
[蔣維棠] 期刊論文
2011-02
Synthesis of 3,3-dimethylglutamic acid derivatives as DPP-IV inhibitors and evaluation of their chemical stability
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[蔣維棠] 期刊論文
2019-12
Identification of a multitargeted tyrosine kinase inhibitor for the treatment of gastrointestinal stromal tumors and acute myeloid leukemia
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[蔣維棠] 期刊論文
2012-06-07
3-Phenyl-1H-5-pyrazolylamine-based derivatives as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
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[蔣維棠] 期刊論文
2011-07
Discovery and evaluation of 3-phenyl-1H-5-pyrazolylamine-based derivatives as potent, selective and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
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[謝興邦] 期刊論文
2013-06-28
Optimization of ligand and lipophilic efficiency to identify an in vivo active furano-pyrimidine aurora kinase inhibitor
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[伍素瑩] 期刊論文
2016-04-12
Pyrazolylamine derivatives reveal the conformational switching between type I and type II binding modes of Anaplastic Lymphoma Kinase (ALK)
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[楊采菱] 期刊論文
2018-01
Clinical and molecular features of MDR livestock-associated MRSA ST9 with staphylococcal cassette chromosome mecXII in humans
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[伍素瑩] 期刊論文
2019-04-10
Discovery of Conformational Control Inhibitors Switching off the Activated c-KIT and Targeting a Broad Range of Clinically Relevant c-KIT Mutants
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[郭靜娟] 期刊論文
2021-08-12
Xanthine derivatives reveal an allosteric binding site in methylenetetrahydrofolate dehydrogenase 2 (MTHFD2)
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[蔣維棠] 期刊論文
2009-03-15
Novel trans-2-aryl-cyclopropylamine analogues as potent and selective dipeptidyl peptidase IV inhibitors
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[蔣維棠] 期刊論文
2021-01
Potent and orally active purine-based fetal hemoglobin inducers for treating Beta-thalassemia and sickle cell disease
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[羅秀容] 期刊論文
2024-08-31
Surveillance of pathogenic yeasts in hospital environments in Taiwan in 2020
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[蔣維棠] 期刊論文
2015-07
Identification of a potent 5-phenyl-thiazol-2-ylamine-based inhibitor of FLT3 with activity against drug resistance-conferring point mutations
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[蔣維棠] 期刊論文
2013-06
Discovery of 3-phenyl-1H-5-pyrazolylamine derivatives containing a urea pharmacophore as potent and efficacious inhibitors of FMS-like tyrosine kinase-3 (FLT3)
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