Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Roya Zoraghi"'
Autor:
Roya Zoraghi, Neil E. Reiner, James P. Morrison, Clinton G. L. Veale, Kevin A. Lobb, Raymond J. Andersen, Michael T. Davies-Coleman
Publikováno v:
Tetrahedron. 70:7845-7853
The public health care crisis caused by the emergence of drug resistant bacterial strains, e.g., methicillin resistant Staphylococcus aureus (MRSA) has underlined the urgent need to accelerate the discovery of new chemical entities active against ant
Autor:
Robert N. Young, B. Brett Finlay, Neil E. Reiner, Anthony R. Richardson, J. Jon Paul Selvam, Roya Zoraghi, Sara Campbell, Lisa Thorson, Nag S. Kumar, Nicholas P. Vitko, Huansheng Gong, Edie Dullaghan
Publikováno v:
Bioorganic & Medicinal Chemistry. 22:1708-1725
A novel series of bis-indoles derived from naturally occurring marine alkaloid 4 were synthesized and evaluated as inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase (PK). PK is not only critical for bacterial survival w
Autor:
Roya Zoraghi, Neil E. Reiner
Publikováno v:
Current Opinion in Microbiology. 16:566-572
Novel classes of antimicrobials are needed to address the challenge of multidrug-resistant bacteria. Current bacterial drug targets mainly consist of specific proteins or subsets of proteins without regard for either how these targets are integrated
Autor:
Emily Amandoron, B. Brett Finlay, Liam J. Worrall, Nag S. Kumar, Sukhbir Kaur, Lisa Thorson, Huansheng Gong, Roya Zoraghi, Neil E. Reiner, Edwin W. Y. Wong, Raymond H. See, Christophe Labriere, Artem Cherkasov, Anne Moreau, Natalie C. J. Strynadka, Robert N. Young, Linda A. Jackson, Tian Lian
Publikováno v:
Bioorganic & Medicinal Chemistry. 20:7069-7082
A novel series of hydrazones were synthesized and evaluated as inhibitors of methicillin-resistant Staphylococcus aureus (MRSA) pyruvate kinase (PK). PK has been identified as one of the most highly connected 'hub proteins' in MRSA. PK has been shown
Autor:
Nikolay Stoynov, Artem Cherkasov, Natalie C. J. Strynadka, Sukhbir Kaur, Michael Hsing, Robert N. Young, Jihong Jiang, Emily Amandoron, Leonard J. Foster, Nag S. Kumar, Anne Moreau, Linda A. Jackson, B. Brett Finlay, Liam Worral, Huansheng Gong, Rick Swayze, William R. McMaster, Peter Axerio-Cilies, Roya Zoraghi, Raymond H. See, Tian Lian, Neil E. Reiner
Publikováno v:
ACS Chemical Biology. 7:350-359
We have recently mapped the protein interaction network of methicillin-resistant Staphylococcus aureus (MRSA), which revealed its scale-free organization with characteristic presence of highly connected hub proteins that are critical for bacterial su
Autor:
Sukhbir Kaur, B. Brett Finlay, Phuong Dao, Cenk Sahinalp, William R. McMaster, Emily Amandoron, Rick Swayze, Leonard J. Foster, Raymond H. See, Robert C. Brunham, Peter Axerio-Cilies, Neil E. Reiner, Farhad Hormozdiari, Nikolay Stoynov, Artem Cherkasov, Huansheng Gong, Tian Lian, Linda A. Jackson, Osvaldo A. Santos-Filho, Michael Hsing, Roya Zoraghi, Kendall G. Byler, Jihong Jiang
Publikováno v:
Journal of Proteome Research. 10:1139-1150
Mortality attributable to infection with methicillin-resistant Staphylococcus aureus (MRSA) has now overtaken the death rate for AIDS in the United States, and advances in research are urgently needed to address this challenge. We report the results
Publikováno v:
Biochemistry. 46:10353-10364
The phosphodiesterase-11A (PDE11) family consists of four splice variants (PDE11A1-PDE11A4) that contain a conserved carboxyl-terminal (C-terminal) catalytic domain that hydrolyzes cAMP and cGMP; the amino-termini (N-termini) vary in length and amino
Autor:
Knut Ohlsen, Mardia Telep El-Sayed, Michael Lalk, Sibel Suzen, Roya Zoraghi, Nurten Altanlar, Neil E. Reiner, Andreas Hilgeroth
Novel bisindolyl-cycloalkane indoles resulted from the reaction of aliphatic dialdehydes and indole. As bisindolyl-natural alkaloid compounds have recently been reported as inhibitors of the methicillin-resistant Staphylococcus aureus (MRSA)-pyruvate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67fee4cc61be459b348f72dd1b0f6098
Autor:
Jiwen Cai, Roya Zoraghi, Howard Robinson, Yudong Liu, Qing Huai, Huanchen Wang, Jackie D. Corbin, Guiting Lin, Sharron H. Francis, Zhongcheng Xin, Hengming Ke
Publikováno v:
Journal of Biological Chemistry. 281:21469-21479
Phosphodiesterase-5 (PDE5) is the target for sildenafil, vardenafil, and tadalafil, which are drugs for treatment of erectile dysfunction and pulmonary hypertension. We report here the crystal structures of a fully active catalytic domain of unligand
Publikováno v:
Journal of Biological Chemistry. 281:5553-5558
The side group of an invariant Gln in cGMP- and cAMP-specific phosphodiesterases (PDE) is held in different orientations by bonds with other amino acids and purportedly discriminates between guanine and adenine in cGMP and cAMP. In cGMP-specific PDE5