Resultados da pesquisa - ((((eur j) OR (luo j))) OR (((eun mi) OR (eun miu)))) ((med chem) OR (od chem))

Pesquisas alternativas:
eun miu » eun min (Expandir a Pesquisa), jun miu (Expandir a Pesquisa)
eun mi » eun ji (Expandir a Pesquisa)
eur j » eun j (Expandir a Pesquisa), eus j (Expandir a Pesquisa), mur j (Expandir a Pesquisa)
luo j » guo j (Expandir a Pesquisa)

1

Epigenetic Modification of Histone 3 Lysine 27: MEDIATOR SUBUNIT MED25 IS REQUIRED FOR THE DISSOCIATION OF POLYCOMB REPRESSIVE COMPLEX 2 FROM THE PROMOTER OF CYTOCHROME P450 2C9

Epigenetic Modification of Histone 3 Lysine 27: MEDIATOR SUBUNIT MED25 IS REQUIRED...

Por Englert, Neal A., Luo, George, Goldstein, Joyce A., Surapureddi, Sailesh
Publicado no J Biol Chem (2015)

“... polymerase II. Here, we examine the involvement of Mediator subunit MED25 in the epigenetic regulation...”
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2

Identification of BRAF inhibitors through in silico screening

Identification of BRAF inhibitors through in silico screening

Por Luo, Cheng, Xie, Peng, Marmorstein, Ronen
Publicado em 2008

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3

Profiling Protein Arginine Deiminase 4 (PAD4): A novel screen to identify PAD4 inhibitors

Profiling Protein Arginine Deiminase 4 (PAD4): A novel screen to identify PAD4 inhibitors

Por Knuckley, Bryan, Luo, Yuan, Thompson, Paul R.
Publicado em 2007

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4

α-Conotoxin [S9A]TxID Potently discriminates between α3β4 and α6/α3β4 Nicotinic Acetylcholine Receptors

α-Conotoxin [S9A]TxID Potently discriminates between α3β4 and α6/α3β4 Nicotinic Acetylcholine Receptors

Por Wu, Yong, Zhangsun, Dongting, Zhu, Xiaopeng, Kaas, Quentin, Zhangsun, Manqi, Harvey, Peta J., Craik, David J., McIntosh, J. Michael, Luo, Sulan
Publicado no J Med Chem (2017)

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5

Characterization of a Novel Alpha-Conotoxin TxID from Conus textile that Potently Blocks rat Alpha3beta4 Nicotinic Acetylcholine Receptors

Characterization of a Novel Alpha-Conotoxin TxID from Conus textile that Potently Blocks rat Alpha3beta4 Nicotinic Acetylcholine Receptors

Por Luo, Sulan, Zhangsun, Dongting, Zhu, Xiaopeng, Wu, Yong, Hu, Yuanyan, Christensen, Sean, Harvey, Peta J., Akcan, Muharrem, Craik, David J., McIntosh, J. Michael
Publicado em 2013

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6

Optimization of ultrasonic extraction of polysaccharides from Ziziphus jujuba Mill. by response surface methodology

Optimization of ultrasonic extraction of polysaccharides from Ziziphus jujuba Mill. by response surface methodology

Por Qu, Chenling, Yu, Songcheng, Luo, Li, Zhao, Yan, Huang, Yawei
Publicado em 2013

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7

Pure Graphene Oxide Doped Conducting Polymer Nanocomposite for Bio-interfacing

Pure Graphene Oxide Doped Conducting Polymer Nanocomposite for Bio-interfacing

Por Luo, Xiliang, Weaver, Cassandra L., Tan, Susheng, Cui, Xinyan Tracy
Publicado no J Mater Chem B Mater Biol Med (2013)

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8

Chemical composition and in vitro evaluation of the cytotoxic and antioxidant activities of supercritical carbon dioxide extracts of pitaya (dragon fruit) peel

Chemical composition and in vitro evaluation of the cytotoxic and antioxidant activities of supercritical carbon dioxide extracts of pitaya (dragon fruit) peel

Por Luo, Hui, Cai, Yongqiang, Peng, Zhijun, Liu, Tao, Yang, Shengjie
Publicado em 2014

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9

Design and Synthesis of Neuroprotective Methylthiazoles and Modification as NO-Chimeras for Neurodegenerative Therapy

Design and Synthesis of Neuroprotective Methylthiazoles and Modification as NO-Chimeras for Neurodegenerative Therapy

Por Qin, Zhihui, Luo, Jia, VandeVrede, Lawren, Tavassoli, Ehsan, Fa’, Mauro, Teich, Andrew, Arancio, Ottavio, Thatcher, Gregory R. J.
Publicado em 2012

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10

Synthesis and Evaluation of Novel Erlotinib–NSAID Conjugates as More Comprehensive Anticancer Agents

Synthesis and Evaluation of Novel Erlotinib–NSAID Conjugates as More Comprehensive Anticancer Agents

Por Zhang, Yanmei, Tortorella, Micky D., Liao, Jinxi, Qin, Xiaochu, Chen, Tingting, Luo, Jinfeng, Guan, Jiantong, Talley, John J., Tu, Zhengchao
Publicado no ACS Med Chem Lett (2015)

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11

Corrigendum to “Synthesis and cytotoxic activity of novel Aring cleaved ursolic acid derivatives in human nonsmall cell lung cancer cells” [Eur. J. Med. Chem. 123 (2016) 317–331]

Corrigendum to “Synthesis and cytotoxic activity of novel Aring cleaved ursolic acid derivatives in human nonsmall cell lung cancer cells” [Eur. J. Med. Chem. 123 (2016) 317–331]

Por Mendes, Vanessa I. S., Bartholomeusz, Geoffrey A., Ayres, Mary, Gandhi, Varsha, Salvador, Jorge A. R.
Publicado no Eur J Med Chem (2016)

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12

Perturbing pro-survival proteins using quinoxaline derivatives: A structure activity relationship study

Perturbing pro-survival proteins using quinoxaline derivatives: A structure activity relationship study

Por Rajule, Rajkumar, Bryant, Vashti C., Lopez, Hernando, Luo, Xu, Natarajan, Amarnath
Publicado em 2012

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13

Design and Synthesis of Novel Quinone Inhibitors Targeted to the Redox Function of Apurinic/Apyrimidinic Endonuclease 1/Redox Enhancing Factor-1 (Ape1/Ref-1)

Design and Synthesis of Novel Quinone Inhibitors Targeted to the Redox Function of Apurinic/Apyrimidinic Endonuclease 1/Redox Enhancing Factor-1 (Ape1/Ref-1)

Por Nyland, Rodney L., Luo, Meihua, Kelley, Mark R., Borch, Richard F.
Publicado em 2010

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14

Insight into binding of phosphodiesterase-9A selective inhibitors by crystal structures and mutagenesis

Insight into binding of phosphodiesterase-9A selective inhibitors by crystal structures and mutagenesis

Por Wang, Huanchen, Luo, Xuan, Ye, Mengchun, Hou, Jing, Robinson, Howard, Ke, Hengming
Publicado em 2010

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15

Discovery of histone deacetylase 8 selective inhibitors

Discovery of histone deacetylase 8 selective inhibitors

Por Tang, Weiping, Luo, Tuoping, Greenberg, Edward F., Bradner, James E., Schreiber, Stuart L.
Publicado em 2011

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16

2,3-Substituted quinoxalin-6-amine analogs as antiproliferatives: A structure activity relationship study

2,3-Substituted quinoxalin-6-amine analogs as antiproliferatives: A structure activity relationship study

Por Chen, Qianyi, Bryant, Vashti C., Lopez, Hernando, Kelly, David L., Luo, Xu, Natarajan, Amarnath
Publicado em 2011

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17

Development of Novel ACK1/TNK2 Inhibitors Using a Fragment-Based Approach

Development of Novel ACK1/TNK2 Inhibitors Using a Fragment-Based Approach

Por Lawrence, Harshani R., Mahajan, Kiran, Luo, Yunting, Zhang, Daniel, Tindall, Nathan, Huseyin, Miles, Gevariya, Harsukh, Kazi, Sakib, Ozcan, Sevil, Mahajan, Nupam P., Lawrence, Nicholas J.
Publicado no J Med Chem (2015)

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18

Positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4). Part II: Challenges in hit-to-lead

Positive allosteric modulators of the metabotropic glutamate receptor subtype 4 (mGluR4). Part II: Challenges in hit-to-lead

Por Williams, Richard, Niswender, Colleen M., Luo, Qingwei, Le, Uyen, Conn, P. Jeffrey, Lindsley, Craig W.
Publicado em 2008

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19

Supramolecular assembly of crosslinkable monomers for degradable and fluorescent polymer nanoparticles

Supramolecular assembly of crosslinkable monomers for degradable and fluorescent polymer nanoparticles

Por Yuan, Conghui, Chang, Ying, Mao, Jie, Yu, Shirong, Luo, Weiang, Xu, Yiting, Thayumanavan, S., Dai, Lizong
Publicado no J Mater Chem B Mater Biol Med (2015)

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20

Synthesis and biological evaluation of lycorine derivatives as dual inhibitors of human acetylcholinesterase and butyrylcholinesterase

Synthesis and biological evaluation of lycorine derivatives as dual inhibitors of human acetylcholinesterase and butyrylcholinesterase

Por Wang, Yue-Hu, Wan, Qin-Li, Gu, Cheng-Ding, Luo, Huai-Rong, Long, Chun-Lin
Publicado em 2012

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