Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Natan A. Kogan"'
Autor:
Rui Liang, Chunguang Wang, Kiho Han, Nicole T. Hatzenbuhler, Buwen Huang, Muthoni G. Kamau, Helena R. Axelrod, Jan A. Anderson, Ramesh Kakarla, Neil Bristol, Anna Chen, Domingos J. Silva, Arthur Branstrom, Robert D. Goldman, Richard G. Dulina, Huiming Wang, Feng Chi, David Gange, Clifford B. Longley, Michael J. Sofia, Nigel M. Allanson, Dashan Liu, Rakesh K. Jain, Eugene R. Baizman, Natan A. Kogan, Sunita Midha
Publikováno v:
Journal of Medicinal Chemistry. 42:3193-3198
The increase in bacterial resistance to conventional chemotherapy has resulted in a resurgent interest in the discovery and development of antibacterial agents.1-4 The search for novel antibiotics active against resistant phenotypes is increasingly f
Autor:
Natan A. Kogan, Y. W. Hui, Richard G. Dulina, Michael J. Sofia, Dashan Liu, Thomas Wagler, Ramesh Kakarla, Anna Chen, Nicole T. Hatzenbuhler
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 7:2251-2254
The drug transport reagent, methyl 3-β-amino-7α, 12α-di(1′α-glucosyl)-5β-cholate (TC002) 1 was prepared in 15% overall yield from pentaacetyl glucose and methyl cholate. Pentaacetyl glucose was converted to glucosyl sulfoxide 2 in 56% overall
Autor:
Babu Suresh D, Leigh Wierichs, Suzanne Walker, Natan A. Kogan, Michael J. Sofia, Karen Bruker, Ramesh Kakarla, Helena R. Axelrod, Clifford B. Longley, Sunita Midha, Daniel Kahne
Publikováno v:
Proceedings of the National Academy of Sciences. 93:1585-1590
A promising class of compounds for DNA transfection have been designed by conjugating various polyamines to bile-acid-based amphiphiles. Formulations containing these compounds were tested for their ability to facilitate the uptake of a beta-galactos
Autor:
Michael J. Sofia, Nicole T. Hatzenbuhler, Y. W. Hui, Richard G. Dulina, Anna Chen, Natan A. Kogan, Ramesh Kakarla, Thomas Wagler, Dashan Liu
Publikováno v:
ChemInform. 29
The drug transport reagent, methyl 3-β-amino-7α, 12α-di(1′α-glucosyl)-5β-cholate (TC002) 1 was prepared in 15% overall yield from pentaacetyl glucose and methyl cholate. Pentaacetyl glucose was converted to glucosyl sulfoxide 2 in 56% overall