Resultados da pesquisa - ((muro x) OR (((((eun j) OR (eun ju))) OR (((eun j) OR (eun ju))i)))) med chem

Pesquisas alternativas:
muro x » muro k (Expandir a Pesquisa), muro _ (Expandir a Pesquisa)
eun ju » eun jung (Expandir a Pesquisa)
eun j » eun ji (Expandir a Pesquisa), sun j (Expandir a Pesquisa), jun j (Expandir a Pesquisa)
chem » chen (Expandir a Pesquisa)

1

Effect of cinnamamides on atopic dermatitis through regulation of IL-4 in CD4(+) cells

Effect of cinnamamides on atopic dermatitis through regulation of IL-4 in CD4(+) cells

Por Choi, Eun-Ju, Ryu, Young Bae, Tang, Yujiao, Kim, Bo Ram, Lee, Woo Song, Debnath, Trishna, Fan, Meiqi, Kim, Eun-Kyung, Lee, Hyun-Su
Publicado no J Enzyme Inhib Med Chem (2019)

“...) levels and expression of T-helper (Th)1/Th2 cytokines. Moreover, cinnamamides suppressed interleukin (IL...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

2

Use of Ionically Tagged Glycosyl Donors in the Synthesis of Oligosaccharide Libraries

Use of Ionically Tagged Glycosyl Donors in the Synthesis of Oligosaccharide Libraries

Por Kim, Eun Ju, Gray, Gary R.
Publicado em 2009

Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

3

Structure Activity Relationships of 1,4-Dihydropyridines That Act as Enhancers of the Vanilloid Receptor 1 (TRPV1)

Structure Activity Relationships of 1,4-Dihydropyridines That Act as Enhancers of the Vanilloid Receptor 1 (TRPV1)

Por Roh, Eun Joo, Keller, Jason M., Olah, Zoltan, Iadarola, Michael J., Jacobson, Kenneth A.
Publicado em 2008

“...Vanilloid agonists such as capsaicin activate ion flux through the TRPV1 channel, a heat...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

4

Simultaneous determination of methylcarbamate and ethylcarbamate in fermented foods and beverages by derivatization and GC-MS analysis

Simultaneous determination of methylcarbamate and ethylcarbamate in fermented foods and beverages by derivatization and GC-MS analysis

Por Shin, Ho-Sang, Yang, Eun-Young
Publicado em 2012

“.../kg and 0.03-0.1 μg/kg, respectively, and the interday relative standard deviation was less than 12...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

5

Tat-DJ-1 inhibits oxidative stress-mediated RINm5F cell death through suppression of NF-κB and MAPK activation

Tat-DJ-1 inhibits oxidative stress-mediated RINm5F cell death through suppression of NF-κB and MAPK activation

Por Jo, Hyo Sang, Cha, Hyun Ju, Kim, Sang Jin, Yeo, Hyeon Ji, Cho, Su Bin, Park, Jung Hwan, Lee, Chi Hern, Yeo, Eun Ji, Choi, Yeon Joo, Eum, Won Sik, Choi, Soo Young
Publicado no Med Chem Res (2016)

“... of pancreatic β-cells. DJ-1 is an antioxidant protein and DJ-1 expression levels are known to be reduced...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

6

Non-proteinogenic amino acids in the pThr-2 position of a pentamer peptide that confer high binding affinity for the polo box domain (PBD) of polo-like kinase 1 (Plk1)

Non-proteinogenic amino acids in the pThr-2 position of a pentamer peptide that confer high binding affinity for the polo box domain (PBD) of polo-like kinase 1 (Plk1)

Por Qian, Wen-Jian, Park, Jung-Eun, Lee, Kyung S., Burke, Terrence R.
Publicado em 2012

“... in place of His at the pT-2 position of the parent polo-like kinase 1 (Plk1) polo box domain (PBD)-binding...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

7

OGA inhibition by GlcNAc-selenazoline

OGA inhibition by GlcNAc-selenazoline

Por Kim, Eun Ju, Love, Dona C., Darout, Etzer, Abdo, Mohannad, Rempel, Brian, Withers, Stephen G., Rablen, Paul R., Hanover, John A., Knapp, Spencer
Publicado em 2010

Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

8

Effects on Polo-like Kinase 1 Polo-box Domain Binding Affinities of Peptides Incurred by Structural Variation at the Phosphoamino Acid Position

Effects on Polo-like Kinase 1 Polo-box Domain Binding Affinities of Peptides Incurred by Structural Variation at the Phosphoamino Acid Position

Por Qian, Wenjian, Park, Jung-Eun, Liu, Fa, Lee, Kyung S., Burke, Terrence R.
Publicado em 2012

“...Protein-protein interactions (PPIs) mediated by the polo-box domain (PBD) of polo-like kinase 1...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

9

(S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5

(S)-4-Trimethylsilyl-3-butyn-2-ol as an auxiliary for stereocontrolled synthesis of salinosporamide analogs with modifications at positions C2 and C5

Por Blasdel, Landy K., Lee, DongEun, Sun, Binyuan, Myers, Andrew G.
Publicado em 2013

“... the chiral 5-tert-butyldimethylsiloxy-3-methyl-1H-pyrrole-2-carboxylic ester depicted and various aldehyde...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

10

Elucidation of New Binding Interactions with the Human Tsg101 Protein Using Modified HIV-1 Gag-p6 Derived Peptide Ligands

Elucidation of New Binding Interactions with the Human Tsg101 Protein Using Modified HIV-1 Gag-p6 Derived Peptide Ligands

Por Kim, Sung-Eun, Liu, Fa, Im, Young Jun, Stephen, Andrew G., Fivash, Matthew J., Waheed, Abdul A., Freed, Eric O., Fisher, Robert J., Hurley, James H., Burke, Terrence R.
Publicado em 2011

“... domain of the nascent viral Gag protein is required for HIV-1 particle budding and release...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

11

Optimization of Thiazole Analogues of Resveratrol for Induction of NAD(P)H:quinone Reductase 1 (QR1)

Optimization of Thiazole Analogues of Resveratrol for Induction of NAD(P)H:quinone Reductase 1 (QR1)

Por Mayhoub, Abdelrahman S., Marler, Laura, Kondratyuk, Tamara P., Park, Eun-Jung, Pezzuto, John M., Cushman, Mark
Publicado em 2012

“...NAD(P)H:quinone reductase 1 (QR1) belongs to a class of enzymes called cytoprotective enzymes...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

12

Inhibition of atherosclerosis-promoting microRNAs via targeted polyelectrolyte complex micelles

Inhibition of atherosclerosis-promoting microRNAs via targeted polyelectrolyte complex micelles

Por Kuo, Cheng-Hsiang, Leon, Lorraine, Chung, Eun Ji, Huang, Ru-Ting, Sontag, Timothy J., Reardon, Catherine A., Getz, Godfrey S., Tirrell, Matthew, Fang, Yun
Publicado no J Mater Chem B Mater Biol Med (2014)

“... sequences to our miRNA inhibitor containing polyelectrolyte complex micelles. One of the peptides (Arginine...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

13

A POTENT AND SELECTIVE INHIBITOR TARGETING HUMAN AND MURINE 12/15-LOX

A POTENT AND SELECTIVE INHIBITOR TARGETING HUMAN AND MURINE 12/15-LOX

Por Armstrong, Michelle M., Freedman, Cody J., Jung, Joo Eun, Zheng, Yi, Kalyanaraman, Chakrapani, Jacobson, Matthew P., Simeonov, Anton, Maloney, David J., van Leyen, Klaus, Jadhav, Ajit, Holman, Theodore R.
Publicado no Bioorg Med Chem (2016)

“... inhibitor with a K(ic) of 1.0 ± 0.08 µM and a K(iu) of 6.0 ± 3.3 µM. These data indicate that 99089...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

14

Optimizing Thiadiazole Analogues of Resveratrol vs. Three Chemopreventive Targets

Optimizing Thiadiazole Analogues of Resveratrol vs. Three Chemopreventive Targets

Por Mayhoub, Abdelrahman S., Marler, Laura, Kondratyuk, Tamara, Park, Eun-Jung, Pezzuto, John M., Cushman, Mark
Publicado em 2011

“.... Replacement of the stilbene ethylenic bridge of resveratrol with a 1,2,4-thiadiazole heterocycle...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

15

Structural Basis of Wee Kinases Functionality and Inactivation by Diverse Small Molecule Inhibitors

Structural Basis of Wee Kinases Functionality and Inactivation by Diverse Small Molecule Inhibitors

Por Zhu, Jin-Yi, Cuellar, Rebecca A., Berndt, Norbert, Lee, Hee Eun, Olesen, Sanne H., Martin, Mathew P., Jensen, Jeffrey T., Georg, Gunda I., Schönbrunn, Ernst
Publicado no J Med Chem (2017)

“...Members of the Wee family of kinases negatively regulate the cell cycle via phosphorylation of CDK1...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

16

Structure-activity relationships and docking studies of synthetic 2-arylindole derivatives determined with aromatase and quinone reductase 1

Structure-activity relationships and docking studies of synthetic 2-arylindole derivatives determined with aromatase and quinone reductase 1

Por Prior, Allan M., Yu, Xufen, Park, Eun-Jung, Kondratyuk, Tamara P., Lin, Yan, Pezzuto, John M., Sun, Dianqing
Publicado no Bioorg Med Chem Lett (2017)

“...-arylindole derivatives were synthesized and evaluated toward aromatase and quinone reductase 1 (QR1...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

17

The effects of phenolic glycosides from Betula platyphylla var. japonica on adipocyte differentiation and mature adipocyte metabolism

The effects of phenolic glycosides from Betula platyphylla var. japonica on adipocyte differentiation and mature adipocyte metabolism

Por Huh, Joo Young, Lee, Seulah, Ma, Eun-Bi, Eom, Hee Jeong, Baek, Jiwon, Ko, Yoon-Joo, Kim, Ki Hyun
Publicado no J Enzyme Inhib Med Chem (2018)

“.... platyphylla, that shows inhibition on adipocyte differentiation and induces lipolysis in 3T3-L1 cells. Based...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

18

Synthesis and SAR of Thiazolylmethylphenyl Glucoside as Novel C-Aryl Glucoside SGLT2 Inhibitors

Synthesis and SAR of Thiazolylmethylphenyl Glucoside as Novel C-Aryl Glucoside SGLT2 Inhibitors

Por Song, Kwang-Seop, Lee, Suk Ho, Kim, Min Ju, Seo, Hee Jeong, Lee, Junwon, Lee, Sung-Han, Jung, Myung Eun, Son, Eun-Jung, Lee, MinWoo, Kim, Jeongmin, Lee, Jinhwa
Publicado em 2010

Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

19

Synthesis and evaluation of quinoxaline derivatives as potential influenza NS1A protein inhibitors

Synthesis and evaluation of quinoxaline derivatives as potential influenza NS1A protein inhibitors

Por You, Lei, Cho, Eun Jeong, Leavitt, John, Ma, Li-Chung, Montelione, Gaetano T., Anslyn, Eric V., Krug, Robert M., Ellington, Andrew, Robertus, Jon D.
Publicado em 2011

“...A library of quinoxaline derivatives were prepared to target non-structural protein 1 of influenza...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

20

Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X(7) receptor

Synthesis and structure–activity relationship studies of tyrosine-based antagonists at the human P2X(7) receptor

Por Lee, Ga Eun, Joshi, Bhalchandra V., Chen, Wangzhong, Jeong, Lak Shin, Moon, Hyung Ryong, Jacobson, Kenneth A., Kim, Yong-Chul
Publicado em 2007

“...Analogues of the P2X(7) receptor antagonist KN-62, modified at the piperazine and arylsulfonyl...”
Obter o texto integral
Obter o texto integral
Obter o texto integral

Artigo

1
2
3
Seguinte
[3]