Volume 26, Issue 6
Natural Products
Full Access

ChemInform Abstract: Isofagomine, a Potent, New Glycosidase Inhibitor.

T. M. JESPERSEN

T. M. JESPERSEN

Chem. Biochem. Eng., Univ. Md. Baltimore County, Baltimore, MD 21228- 5398, USA

Search for more papers by this author
W. DONG

W. DONG

Chem. Biochem. Eng., Univ. Md. Baltimore County, Baltimore, MD 21228- 5398, USA

Search for more papers by this author
M. R. SIERKS

M. R. SIERKS

Chem. Biochem. Eng., Univ. Md. Baltimore County, Baltimore, MD 21228- 5398, USA

Search for more papers by this author
T. SKRYDSTRUP

T. SKRYDSTRUP

Chem. Biochem. Eng., Univ. Md. Baltimore County, Baltimore, MD 21228- 5398, USA

Search for more papers by this author
I. LUNDT

I. LUNDT

Chem. Biochem. Eng., Univ. Md. Baltimore County, Baltimore, MD 21228- 5398, USA

Search for more papers by this author
M. BOLS

M. BOLS

Chem. Biochem. Eng., Univ. Md. Baltimore County, Baltimore, MD 21228- 5398, USA

Search for more papers by this author
First published: February 7, 1995

Abstract

ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.

ChemInform Abstract

Replacing the anomeric C atom of 2-deoxy-O-glucose with an N atom and the ring O atom with a C atom leads to the title compound (V), the most potent β-glycosidase inhibitor known to date. This synthetic monosaccharide derivative also inhibits other glucosidases better than naturally occurring sugar derivatives in which only the O atom in the ring is exchanged for an N atom.

chemical structure image

    The full text of this article hosted at iucr.org is unavailable due to technical difficulties.