Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Howard E, Morton"'
Autor:
Thomas W von Geldern, Howard E Morton, Rick F Clark, Brian S Brown, Kelly L Johnston, Louise Ford, Sabine Specht, Robert A Carr, Deanne F Stolarik, Junli Ma, Matthew J Rieser, Dominique Struever, Stefan J Frohberger, Marianne Koschel, Alexandra Ehrens, Joseph D Turner, Marc P Hübner, Achim Hoerauf, Mark J Taylor, Stephen A Ward, Kennan Marsh, Dale J Kempf
Publikováno v:
PLoS Neglected Tropical Diseases, Vol 13, Iss 2, p e0007159 (2019)
There is a significant need for improved treatments for onchocerciasis and lymphatic filariasis, diseases caused by filarial worm infection. In particular, an agent able to selectively kill adult worms (macrofilaricide) would be expected to substanti
Externí odkaz:
https://doaj.org/article/68bed1add1a349b9b6bff6345f18be14
Autor:
Sabine Specht, Thomas W. von Geldern, Kelly L. Johnston, Franziska Lenz, Samuel Wanji, Joseph D. Turner, Nicolas Pionnier, Abdel Jelil Njouendou, Dominique Bloemker, Darren A. N. Cook, Robert A. Carr, Louise Ford, Stephen A. Ward, Mark J. Taylor, Kennan C. Marsh, Marianne Koschel, Hanna T. Sjoberg, Howard E. Morton, Dale J. Kempf, John Archer, Hayley E. Tyrer, Haelly M. Metuge, Fanny Fri Fombad, Ghaith Aljayyoussi, Valerinne C. Chunda, Patrick W. N. Chounna, Rachel H. Clare, Marc P. Hübner, Alexandra Ehrens, Achim Hoerauf, Andrew Steven, Emma A Murphy
Publikováno v:
Science Translational Medicine. 11(483)
There is an urgent global need for a safe macrofilaricide drug to accelerate elimination of the neglected tropical diseases onchocerciasis and lymphatic filariasis. From an anti-infective compound library, the macrolide veterinary antibiotic, tylosin
Autor:
Mark J, Taylor, Thomas W, von Geldern, Louise, Ford, Marc P, Hübner, Kennan, Marsh, Kelly L, Johnston, Hanna T, Sjoberg, Sabine, Specht, Nicolas, Pionnier, Hayley E, Tyrer, Rachel H, Clare, Darren A N, Cook, Emma, Murphy, Andrew, Steven, John, Archer, Dominique, Bloemker, Franziska, Lenz, Marianne, Koschel, Alexandra, Ehrens, Haelly M, Metuge, Valerinne C, Chunda, Patrick W, Ndongmo Chounna, Abdel J, Njouendou, Fanny F, Fombad, Robert, Carr, Howard E, Morton, Ghaith, Aljayyoussi, Achim, Hoerauf, Samuel, Wanji, Dale J, Kempf, Joseph D, Turner, Stephen A, Ward
Publikováno v:
Science translational medicine. 11(483)
There is an urgent global need for a safe macrofilaricide drug to accelerate elimination of the neglected tropical diseases onchocerciasis and lymphatic filariasis. From an anti-infective compound library, the macrolide veterinary antibiotic, tylosin
Publikováno v:
Tetrahedron Letters. 48:1059-1062
ABT-578, an anti-restenosis agent exists as two isomers, a major pyran form and a minor oxepane form. The existence of the two isomeric forms was established by isolation and equilibration studies under buffered and physiological conditions. Finally
Autor:
John E. Lallaman, Jianguo Ji, Wenke Li, Howard E. Morton, Ji Zhang, Francis A. J. Kerdesky, M. Robert Leanna
Publikováno v:
Organic Process Research & Development. 10:512-517
An efficient chemical process for the multikilogram synthesis of ABT-963 (3) is described. The potent and selective COX-2 inhibitor was prepared in four steps in 36% overall isolated yield from commercially available 3,4-difluoroaniline (4). The chem
Autor:
Gregory S. Wayne, John E. Lallaman, Lakshmi Bhagavatula, Jonathan P. Pease, Ramiya H. Premchandran, Steven A. King, William H. Arnold, Francis A. J. Kerdesky, Howard E. Morton, Sou-Jen Chang
Publikováno v:
Organic Process Research & Development. 6:869-875
An efficient and practical synthesis of 2‘-O-benzoyl-3-keto-6-O-propargyl-11,12-carbamoyl erythromycin A (4) is described. The semisynthetic macrolide was prepared on large scale in seven steps in 38% overall isolated yield from the readily availab
Autor:
Seble Wagaw, Jianguo Ji, Michael A Fitzgerald, Michael G. Fickes, David M. Barnes, Frederick A. Plagge, Margo Preskill, Steven A. King, Steven J. Wittenberger, Ji Zhang, Howard E. Morton
Publikováno v:
Journal of the American Chemical Society. 124:13097-13105
The enantioselective synthesis of endothelin-A antagonist ABT-546 has been accomplished via the discovery and development of a highly selective catalytic asymmetric conjugate addition of ketoesters to nitroolefins. Employing just 4 mol % bis(oxazolin
Autor:
William A. Arnold, Lynch John K, Mark W. Holladay, Keith B. Ryther, Daniel A. Dickman, Chi-Nung Hsiao, Hao Bai, Howard E. Morton, Steven A. King
Publikováno v:
Tetrahedron: Asymmetry. 9:2791-2794
A concise asymmetric synthesis of ( R )-2-chloro-5-(2-azetidinylmethoxy)pyridine (ABT-594) is presented in which the key intermediate t -butoxycarbonyl protected (2 R )-azetidinylalcohol is obtained in three steps from the dibenzyl ester of D-asparti
Autor:
Thomas Albert, Sanjay R. Chemburkar, Howard E. Morton, Daniel A. Dickman, David P. Sawick, Daniel J. Plata, Hemantkumar H. Patel, Yi-Yin Ku
Publikováno v:
Tetrahedron: Asymmetry. 8:1791-1795
A convergent, high yielding, and scalable synthesis of A-79175, with a key step involving a mild and efficient CuPd catalyzed coupling reaction of a terminal acetylene with a substituted 2-iodofuran is discussed.
Autor:
Mike Rozema, Padam Sharma, Tim Grieme, Yi-Yin Ku, Howard E. Morton, Prasad S. Raje, Steve A. King
Publikováno v:
The Journal of Organic Chemistry. 68:3238-3240
A practical and scaleable synthesis of a novel nonsteroidal ligand for the glucocorticoid receptor A-224817.0 1A is described. The synthesis proceeds in seven steps starting from 1,3-dimethoxybenzene. The biaryl intermediate 5 was prepared by an opti