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Cryo_fit: Democratization of flexible fitting for cryo-EM

Journal of structural biology, 2019-10, Vol.208 (1), p.1-6

2019

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Identification of TG100-115 as a new and potent TRPM7 kinase inhibitor, which suppresses breast cancer cell migration and invasion

Biochimica et biophysica acta. General subjects, 2017-04, Vol.1861 (4), p.947-957

2017

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15-Deoxy-Δ12,14-prostaglandin J2 activates PI3K-Akt signaling in human breast cancer cells through covalent modification of the tumor suppressor PTEN at cysteine 136

Cancer letters, 2018-06, Vol.424, p.30-45

2018

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Identification of a novel 5-amino-3-(5-cyclopropylisoxazol-3-yl)-1-isopropyl-1H-pyrazole-4-carboxamide as a specific RET kinase inhibitor

European journal of medicinal chemistry, 2017-01, Vol.125, p.1145-1155

2017

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15-Deoxy-Δ 12,14 -prostaglandin J 2 activates PI3K-Akt signaling in human breast cancer cells through covalent modification of the tumor suppressor PTEN at cysteine 136

Cancer letters, 2018-06, Vol.424, p.30

2018

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Discovery of enantioselectivity of urea inhibitors of soluble epoxide hydrolase

European journal of medicinal chemistry, 2016-07, Vol.117, p.113-124

2016

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Myeloid differentiation 2 as a therapeutic target of inflammatory disorders

Pharmacology & therapeutics (Oxford), 2012-03, Vol.133 (3), p.291-298

2012

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Design, synthesis, and antitumor evaluation of 2,4,6-triaryl pyridines containing chlorophenyl and phenolic moiety

European journal of medicinal chemistry, 2012-06, Vol.52, p.123-136

2012

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Expression and purification of biologically active recombinant human paraoxonase 1 from a Drosophila S2 stable cell line

Protein expression and purification, 2017-03, Vol.131, p.34-41

2017

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Structure-based virtual screening of novel tubulin inhibitors and their characterization as anti-mitotic agents

Bioorganic & medicinal chemistry, 2010-10, Vol.18 (19), p.7092-7100

2010

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A Small Molecule Inhibitor of ATPase Activity of HSP70 Induces Apoptosis and Has Antitumor Activities

Chemistry & biology, 2015-03, Vol.22 (3), p.391-403

2015

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Identification of a novel small molecule targeting UQCRB of mitochondrial complex III and its anti-angiogenic activity

Bioorganic & medicinal chemistry letters, 2011-02, Vol.21 (3), p.1052-1056

2011

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Rhodium-catalyzed reductive cyclization of 1,6-enynes and stereoselective synthesis of the putative structure of lucentamycin A and its stereoisomers

Tetrahedron, 2012-02, Vol.68 (7), p.1918-1925

2012

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Discovery of novel HCV polymerase inhibitors using pharmacophore-based virtual screening

Bioorganic & medicinal chemistry letters, 2011-06, Vol.21 (11), p.3329-3334

2011

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QSAR analysis of pyrazolidine-3,5-diones derivatives as Dyrk1A inhibitors

Bioorganic & medicinal chemistry letters, 2009-04, Vol.19 (8), p.2324-2328

2009

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Identification of novel inhibitors of HCV RNA-dependent RNA polymerase by pharmacophore-based virtual screening and in vitro evaluation

Bioorganic & medicinal chemistry, 2009-04, Vol.17 (8), p.2975-2982

2009

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Different spectrum of mutations of isovaleryl-CoA dehydrogenase ( IVD) gene in Korean patients with isovaleric acidemia

Molecular genetics and metabolism, 2007-09, Vol.92 (1), p.71-77

2007

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Design and synthesis of 4-quinolinone 2-carboxamides as calpain inhibitors

Bioorganic & medicinal chemistry letters, 2008, Vol.18 (1), p.205-209

2008

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Design and synthesis of 4-aryl-4-oxobutanoic acid amides as calpain inhibitors

Bioorganic & medicinal chemistry letters, 2009-01, Vol.19 (2), p.502-507

2009

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Identification of α-amanitin effector proteins in hepatocytes by limited proteolysis-coupled mass spectrometry

Chemico-biological interactions, 2023-12, Vol.386, p.110778-110778, Article 110778

2023

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Putative therapeutic agents for the learning and memory deficits of people with Down syndrome

Bioorganic & medicinal chemistry letters, 2006-07, Vol.16 (14), p.3772-3776

2006

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Structural modeling of V299L and E459K Bcr-Abl mutation, and sequential therapy of tyrosine kinase inhibitors for the compound mutations

Leukemia research, 2009-09, Vol.33 (9), p.1260-1265

2009

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Celastrol blocks binding of lipopolysaccharides to a Toll-like receptor4/myeloid differentiation factor2 complex in a thiol-dependent manner

Journal of ethnopharmacology, 2015-08, Vol.172, p.254-260

2015

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Sulforaphane inhibits the engagement of LPS with TLR4/MD2 complex by preferential binding to Cys133 in MD2

Biochemical and biophysical research communications, 2013-05, Vol.434 (3), p.600-605

2013

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Ex situ target strength of yellow croaker (Larimichthys polyactis) in a seawater tank

Fisheries research, 2023-04, Vol.260, p.106610, Article 106610

2023

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Cryo_fit: Democratization of flexible fitting for cryo-EM

Identification of TG100-115 as a new and potent TRPM7 kinase inhibitor, which suppresses breast cancer cell migration and invasion

15-Deoxy-Δ12,14-prostaglandin J2 activates PI3K-Akt signaling in human breast cancer cells through covalent modification of the tumor suppressor PTEN at cysteine 136

Identification of a novel 5-amino-3-(5-cyclopropylisoxazol-3-yl)-1-isopropyl-1H-pyrazole-4-carboxamide as a specific RET kinase inhibitor

15-Deoxy-Δ 12,14 -prostaglandin J 2 activates PI3K-Akt signaling in human breast cancer cells through covalent modification of the tumor suppressor PTEN at cysteine 136

Discovery of enantioselectivity of urea inhibitors of soluble epoxide hydrolase

Myeloid differentiation 2 as a therapeutic target of inflammatory disorders

Design, synthesis, and antitumor evaluation of 2,4,6-triaryl pyridines containing chlorophenyl and phenolic moiety

Expression and purification of biologically active recombinant human paraoxonase 1 from a Drosophila S2 stable cell line

Structure-based virtual screening of novel tubulin inhibitors and their characterization as anti-mitotic agents

A Small Molecule Inhibitor of ATPase Activity of HSP70 Induces Apoptosis and Has Antitumor Activities

Identification of a novel small molecule targeting UQCRB of mitochondrial complex III and its anti-angiogenic activity

Rhodium-catalyzed reductive cyclization of 1,6-enynes and stereoselective synthesis of the putative structure of lucentamycin A and its stereoisomers

Discovery of novel HCV polymerase inhibitors using pharmacophore-based virtual screening

QSAR analysis of pyrazolidine-3,5-diones derivatives as Dyrk1A inhibitors

Identification of novel inhibitors of HCV RNA-dependent RNA polymerase by pharmacophore-based virtual screening and in vitro evaluation

Different spectrum of mutations of isovaleryl-CoA dehydrogenase ( IVD) gene in Korean patients with isovaleric acidemia

Design and synthesis of 4-quinolinone 2-carboxamides as calpain inhibitors

Design and synthesis of 4-aryl-4-oxobutanoic acid amides as calpain inhibitors

Identification of α-amanitin effector proteins in hepatocytes by limited proteolysis-coupled mass spectrometry

Putative therapeutic agents for the learning and memory deficits of people with Down syndrome

Structural modeling of V299L and E459K Bcr-Abl mutation, and sequential therapy of tyrosine kinase inhibitors for the compound mutations

Celastrol blocks binding of lipopolysaccharides to a Toll-like receptor4/myeloid differentiation factor2 complex in a thiol-dependent manner

Sulforaphane inhibits the engagement of LPS with TLR4/MD2 complex by preferential binding to Cys133 in MD2

Ex situ target strength of yellow croaker (Larimichthys polyactis) in a seawater tank

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