161045-48-3Relevant academic research and scientific papers
Design and synthesis of a heparanase inhibitor with pseudodisaccharide structure
Takahashi, Shunya,Kuzuhara, Hiroyoshi,Nakajima, Motowo
, p. 6915 - 6926 (2007/10/03)
Aza-analogue of the basic disaccharide unit of heparane sulfate was designed as a potent inhibitor against heparanase produced by solid tumors cell, and synthesized via a coupling reaction of phenyl 2-azide-1-thio-D-glucopyranoside derivatives with a partially protected 1-deoxynojirimycin derived from D-glucose. The azapseudodisaccharide inhibited tumor cell heparanase with IC50 value of 58-63 μM.
