Resultados da pesquisa - ((((((eum j) OR (lum j))) OR (mur j))) OR (eun j)) med chem

Pesquisas alternativas:
med chem » med cem (Expandir a Pesquisa), med chi (Expandir a Pesquisa), od chem (Expandir a Pesquisa)
eum j » gum j (Expandir a Pesquisa)
lum j » blum j (Expandir a Pesquisa), lim j (Expandir a Pesquisa), lam j (Expandir a Pesquisa)
eun j » eun ju (Expandir a Pesquisa), eun ji (Expandir a Pesquisa), sun j (Expandir a Pesquisa)

1

Transient-state Kinetic Analysis of Transcriptional Activator·DNA Complexes Interacting with a Key Coactivator

Transient-state Kinetic Analysis of Transcriptional Activator·DNA Complexes Interacting with a Key Coactivator

Por Wands, Amberlyn M., Wang, Ningkun, Lum, Jenifer K., Hsieh, John, Fierke, Carol A., Mapp, Anna K.
Publicado em 2011

“..., Gcn4, and VP16 interact with the key coactivator Med15 (Gal11) during transcription initiation despite...”
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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

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3

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

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4

Development of a triazole class of highly potent Porcn inhibitors

Development of a triazole class of highly potent Porcn inhibitors

Por You, Lin, Zhang, Chengwei, Yarravarapu, Nageswari, Morlock, Lorraine, Wang, Xiaolei, Zhang, Lishu, Williams, Noelle S., Lum, Lawrence, Chen, Chuo
Publicado no Bioorg Med Chem Lett (2016)

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5

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

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6

The Development of Highly Potent Inhibitors for Porcupine

The Development of Highly Potent Inhibitors for Porcupine

Por Wang, Xiaolei, Moon, Jesung, Dodge, Michael E., Pan, Xinchao, Zhang, Lishu, Hanson, Jordan M., Tuladhar, Rubina, Ma, Zhiqiang, Shi, Heping, Williams, Noelle S., Amatruda, James F., Carroll, Thomas J., Lum, Lawrence, Chen, Chuo
Publicado em 2013

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7

Structure/Activity Relationship Studies of Small-Molecule Inhibitors of Wnt Response

Structure/Activity Relationship Studies of Small-Molecule Inhibitors of Wnt Response

Por Lu, Jianming, Ma, Zhiqiang, Hsieh, Jen-Chieh, Fan, Chih-Wei, Chen, Baozhi, Longgood, Jamie C., Williams, Noelle S., Amatruda, James F., Lum, Lawrence, Chen, Chuo
Publicado em 2009

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8

Synthesis and antioxidant properties of dendritic polyphenols

Synthesis and antioxidant properties of dendritic polyphenols

Por Lee, Choon Young, Sharma, Ajit, Cheong, Jae Eun, Nelson, Julie L.
Publicado em 2009

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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

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10

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

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11

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

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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)

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13

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

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14

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)

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15

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

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16

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

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17

Polymer-Protein Hydrogel Nanomatrix for Stabilization of Indocyanine Green towards Targeted Fluorescence and Photoacoustic Bio-imaging

Polymer-Protein Hydrogel Nanomatrix for Stabilization of Indocyanine Green towards Targeted Fluorescence and Photoacoustic Bio-imaging

Por Yoon, Hyung Ki, Ray, Aniruddha, Lee, Yong-Eun Koo, Kim, Gwangseong, Wang, Xueding, Kopelman, Raoul
Publicado em 2013

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18

Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia Pestis Outer Protein H (YopH) Phosphatase, ,

Utilization of Nitrophenylphosphates and Oxime-Based Ligation for the Development of Nanomolar Affinity Inhibitors of the Yersinia Pestis Outer Protein H (YopH) Phosphatase, ,

Por Bahta, Medhanit, Lountos, George T., Dyas, Beverly, Kim, Sung-Eun, Ulrich, Robert G., Waugh, David S., Burke, Terrence R.
Publicado em 2011

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19

Identificaiton of Shc Src Homology 2 Domain-Binding Peptoid – Peptide Hybrids

Identificaiton of Shc Src Homology 2 Domain-Binding Peptoid – Peptide Hybrids

Por Choi, Won Jun, Kim, Sung Eun, Stephen, Andrew G., Weidlich, Iwona, Giubellino, Alessio, Liu, Fa, Worthy, Karen M., Bindu, Lakshman, Fivash, Matthew J., Nicklaus, Marc C., Bottaro, Donald P., Fisher, Robert J., Burke, Terrence R.
Publicado em 2009

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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

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