Kilogram-scale synthesis of the CXCR4 antagonist GSK812397

S Boggs, VI Elitzin, K Gudmundsson…

Index: Boggs, Sharon; Elitzin, Vassil I.; Gudmundsson, Kristjan; Martin, Michael T.; Sharp, Matthew J. Organic Process Research and Development, 2009 , vol. 13, # 4 p. 781 - 785

Full Text: HTML

Citation Number: 17

Abstract

CXC chemokine receptor 4 (CXCR4) is a 7-transmembrane protein which functions in part as a host co-receptor for a number of HIV-1 strains.(1) It is believed that targeting CXCR4 would be beneficial in suppressing the replication of several cytopathic late-stage viruses; therefore, CXCR4 antagonists are among the most promising new classes of experimental anti-HIV drugs.(2, 3) GSK812397 is a potent antagonist of CXCR4,(4) and thus a ...

Related Articles:

Synthesis of some unsymmetrical bridged terpyridines

[Kelly, T. Ross; Lebedev, Rimma L. Journal of Organic Chemistry, 2002 , vol. 67, # 7 p. 2197 - 2205]

Convenient Synthesis of 5, 6, 7, 8-Tetrahydroquinolin-8-ylamine and 6, 7-Dihydro-5 H-quinolin-8-one

[McEachern; Yang; Chen; Skerlj; Bridger Synthetic Communications, 2003 , vol. 33, # 20 p. 3497 - 3502]

Synthesis of a novel tricyclic 1, 2, 3, 4, 4a, 5, 6, 10b-octahydro-1, 10-phenanthroline ring system and CXCR4 antagonists with potent activity against HIV-1

[Catalano, John G.; Gudmundsson, Kristjan S.; Svolto, Angilique; Boggs, Sharon D.; Miller, John F.; Spaltenstein, Andrew; Thomson, Michael; Wheelan, Pat; Minick, Doug J.; Phelps, Dean P.; Jenkinson, Stephen Bioorganic and Medicinal Chemistry Letters, 2010 , vol. 20, # 7 p. 2186 - 2190]

… -mediated preparation of 2-arylquinoline and 4-aryl-1-azaanthraquinone derivatives. X-Ray crystal structure of 1, 2-dihydro-3H-indazolo [2, 3-a] quinolin-4-one

[Molina; Molina, Pedro; Pastor; Pastor, Aurelia; Vilaplana; Vilaplana, Maria Jesus; Foces-Foces; Foces-Foces, Concepcion Tetrahedron, 1995 , vol. 51, # 4 p. 1265 - 1276]

More Articles...