81 |
Cyclo(d-Pro-L-Val), a specific β-glucosidase inhibitor produced by Aspergillus sp. F70609 /
Oh Sung Kwon;
Sang Ho Park;
Bong Sik Yun;
Yu Ryang Pyun;
Chang Jin Kim
, 2001
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82 |
Cyclopentenediones, inhibitors of farnesyl protein transferase and anti-tumor compounds, isolated from the fruit of Lindera erythrocarpa Makino /
Hyun Mi Oh;
Sung Kyu Choi;
Ji Min Lee;
Su Kyung Lee;
H Y Kim;
Dong Cho Han;
Hwan Mook Kim;
Kwang Hee Son;
Byoung-Mog Kwon
, 2005
|
83 |
Cytoplasmic localization and ubiquitination of p21Cip1 by reactive oxygen species /
C Y Hwang;
I Y Kim;
Ki Sun Kwon
, 2007
|
84 |
des-Asp⁴-amastatin, MRK-22 as an inhibitor of aminopeptidase M produced by Streptomyces sp. SL20209 /
Hack Ryong Ko;
Hyo Kon Chun;
Seung Ho Kim;
NACK-KIE SUNG;
Yung Hee Kho
, 1995
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85 |
Design, synthesis and biological evaluation of 1,3-diphenylbenzo[f][1,7]naphthyrdines /
S K Arepalli;
B Park;
K Lee;
H Jo;
K Y Jun;
Y Kwon;
Jong Soon Kang;
J K Jung;
H Lee
, 2017
|
86 |
Design, synthesis and evaluation of novel 3/4-((substituted benzamidophenoxy) methyl)-N-hydroxybenzamides/propenamides as histone deacetylase inhibitors and antitumor agents /
D T Anh;
N T Thuan;
P T Hai;
L T T Huong;
N T K Yen;
B W Han;
E J Park;
Y J Choi;
Jong Soon Kang;
V T M Hue;
S B Han;
N H Nam
, 2019
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87 |
Design and synthesis of 3,4-dihydro-2H-benzo[h]chromene derivatives as potential NF-κB inhibitors /
M Choi;
Y S Hwang;
A S Kumar;
H Jo;
Y Jeong;
Y Oh;
J Lee;
Jieun Yun;
Y Kim;
S B Han;
J K Jung;
J Cho;
H Lee
, 2014
|
88 |
Design and synthesis of novel 2,4-Diamino-5-pyrazol-4-yl pyrimidine derivatives as selective Tyro3 kinase inhibitors /
D Kim;
Kyung Won Lee;
H Jung;
Miok Kim;
J Y Lee;
Y Lee;
Jong Yeon Hwang;
Y Min;
Chang Hoon Lee;
Sung Yun Cho
, 2018
|
89 |
Development of ELISA system for screening of specific binding inhibitors for Src homology (SH)2 domain and phosphotyrosine interactions /
Sang Seop Lee;
Kyung Im Lee;
Ji Yun Yoo;
Moon Jin Jeong;
Young Mee Park;
Byoung-Mog Kwon;
Yun Soo Bae;
Mi Young Han
, 2001
|
90 |
Development of tripeptidyl farnesyltransferase inhibitors /
Hee Yoon Lee;
Jeong Hun Sohn;
Byoung-Mog Kwon
, 2002
|
91 |
Development of cyclic peptomer inhibitors targeting the polo-box domain of polo-like kinase 1 /
R N Murugan;
J E Park;
D Lim;
M Ahn;
C Cheong;
T Kwon;
K Y Nam;
S H Choi;
Bo Yeon Kim;
D Y Yoon;
M B Yaffe;
Dae Yeul Yu;
K S Lee;
J K Bang
, 2013
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92 |
Diacylglycerol acyltransferase-inhibitory compounds from Erythrina senegalensis /
W K Oh;
Chul Ho Lee;
J H Seo;
M Y Chung;
L Cui;
T Fomum;
J S Kang;
Hyun Sun Lee
, 2009
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93 |
Differential effects of genistein and staurosporin on IL-1 receptor signaling pathway during T cell activation /
Mi Young Han;
Do Young Yoon;
Eun Sook Oh;
Woo Suk Koh;
Sun Young Yoon;
Tai Wha Chung
, 1996
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94 |
Differential gene expression common to acquired and intrinsic resistance to BRAF inhibitor revealed by RNA-Seq analysis /
J H Ahn;
S H Hwang;
Hyun Soo Cho;
M Lee
, 2019
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95 |
Direct exposure to 2,3,7,8-tetrachlodibenzo-p-dioxin(TCDD) increases infectivity of human erythrocytes to a malarial parasite /
Hwan Mook Kim;
In Pyo Choi;
M P Holsapple
, 1994
|
96 |
Discovery of VHR phosphatase inhibitors with micromolar activity based on structure-based virtual screening /
H Park;
Suk Kyeong Jung;
Dae Gwin Jeong;
Seong Eon Ryu;
Seung Jun Kim
, 2008
|
97 |
Discovery of novel Cdc25 phosphatase inhibitors with micromolar activity based on the structure-based virtual screening /
H Park;
Young Jae Bahn;
Suk Kyeong Jung;
Dae Gwin Jeong;
S H Lee;
Il Seo;
Tae-Sung Yoon;
Seung Jun Kim;
Seong Eon Ryu
, 2008
|
98 |
Discovery of novel and potent Cdc25 phosphatase inhibitors based on the structure-based de novo design /
H Park;
Suk-Kyeong Jung;
Young Jae Bahn;
Dae Gwin Jeong;
S E Ryu;
Seung Jun Kim
, 2009
|
99 |
Discovery of novel PRL-3 inhibitors based on the structure-based virtual screening /
H Park;
S K Jung;
Dae Gwin Jeong;
Seong Eon Ryu;
Seung Jun Kim
, 2008
|
100 |
Discovery of novel inhibitors of dual-specificity phosphatase pyst2 with structure-based virtual screening /
H Park;
J Y Jeon;
S E Ryu;
Seung Jun Kim
, 2011
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