Structure-activity relationship analysis of the selective inhibition of transglutaminase 2 by dihydroisoxazoles
RE Watts, M Siegel, C Khosla
Index: Journal of Medicinal Chemistry, , vol. 49, # 25 p. 7493 - 7501
Full Text: HTML
Citation Number: 62
Abstract
... Journal of Medicinal Chemistry. ... Departments of Chemistry and Chemical Engineering, Stanford University, Stanford, California 94305. J. Med. Chem. , 2006, 49 (25), pp 7493–7501. DOI: 10.1021/jm060839a. Publication ...
Related Articles:
[Lin, Songnian; Yang, Zhi-Qiang; Kwok, Benjamin H. B.; Koldobskiy, Michael; Crews, Craig M.; Danishefsky, Samuel J. Journal of the American Chemical Society, 2004 , vol. 126, # 20 p. 6347 - 6355]
Synthesis and biological activity of new potential agonists for the human adenosine A2A receptor
[Bosch, M. Pilar; Campos, Francisco; Niubo, Itziar; Rosell, Gloria; Diaz, J. Luis; Brea; Loza, M. Isabel; Guerrero, Angel Journal of Medicinal Chemistry, 2004 , vol. 47, # 16 p. 4041 - 4053]
[Journal of the American Chemical Society, , vol. 126, # 20 p. 6347 - 6355]
[Sajiki, Hironao; Hirota, Kosaku Chemical and Pharmaceutical Bulletin, 2003 , vol. 51, # 3 p. 320 - 324]
[Allevi, Pietro; Cighetti, Giuliana; Anastasia, Mario Tetrahedron Letters, 2001 , vol. 42, # 31 p. 5319 - 5321]