하정미

전체 201건 중 101번부터 110번까지의 결과를 표시합니다.

2019

Patent

Imidazole derivative having JNK inhibitory activity and use thereof

Article

Chemistry-oriented synthesis (ChOS) and target deconvolution on neuroprotective effect of a novel scaffold, oxaza spiroquinone

Article

Design, synthesis, and in vitro evaluation of N-(3-(3-alkyl-1H-pyrazol-5-yl) phenyl)-aryl amide for selective RAF inhibition

Patent

비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 제해제인 신규 (2-oxo-2,3-dihydro-1H-thieno[3,4-b][1,4]diazepin-4-yl)phenyl) 유도체

Article

Computer-aided design and synthesis of 3-carbonyl-5-phenyl-1H-pyrazole as highly selective and potent BRAFV600E and CRAF inhibitor

Article

Conformational restriction of a type II FMS inhibitor leading to discovery of 5-methyl-N-(2-aryl-1H-benzo[d]imidazo-5-yl)isoxazole-4-carboxamide analogues as selective FLT3 inhibitors

2018

Conference

Optimaization of novel JNK3 inhibitors as a potential therapeutics for neurodegenerative diseases

Conference

Design and syntheses of 3-carbonyl-5-phenyl-1H pyrazole analogues as selective BRAF V600E Inhibitor

Conference

Discovery of FLT3 inhibitors from conformational rigidification of FMS inhibitors

Patent

2-(1-(2-(Alkylamino)4-heteroaryl)-2-Aryl-1H-imidazol-5-yl)acetonitrile 유도체와 이의 약학적으로 허용 가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 단백질 카이네이즈 저해제

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Imidazole derivative having JNK inhibitory activity and use thereof

Chemistry-oriented synthesis (ChOS) and target deconvolution on neuroprotective effect of a novel scaffold, oxaza spiroquinone

Design, synthesis, and in vitro evaluation of N-(3-(3-alkyl-1H-pyrazol-5-yl) phenyl)-aryl amide for selective RAF inhibition

비정상 세포 성장 질환의 치료를 위한 단백질 키나아제 제해제인 신규 (2-oxo-2,3-dihydro-1H-thieno[3,4-b][1,4]diazepin-4-yl)phenyl) 유도체

Computer-aided design and synthesis of 3-carbonyl-5-phenyl-1H-pyrazole as highly selective and potent BRAFV600E and CRAF inhibitor

Conformational restriction of a type II FMS inhibitor leading to discovery of 5-methyl-N-(2-aryl-1H-benzo[d]imidazo-5-yl)isoxazole-4-carboxamide analogues as selective FLT3 inhibitors

Optimaization of novel JNK3 inhibitors as a potential therapeutics for neurodegenerative diseases

Design and syntheses of 3-carbonyl-5-phenyl-1H pyrazole analogues as selective BRAF V600E Inhibitor

Discovery of FLT3 inhibitors from conformational rigidification of FMS inhibitors

2-(1-(2-(Alkylamino)4-heteroaryl)-2-Aryl-1H-imidazol-5-yl)acetonitrile 유도체와 이의 약학적으로 허용 가능한 염, 이의 제조방법 및 이를 유효성분으로 함유하는 단백질 카이네이즈 저해제