Bioorganic & Medicinal Chemistry Letters 1999-11-01

Revised structure of a homonojirimycin isomer from Aglaonema treubii: first example of a naturally occurring alpha-homoallonojirimycin.

O R Martin, P Compain, H Kizu, N Asano

Index: Bioorg. Med. Chem. Lett. 9(21) , 3171-4, (1999)

Full Text: HTML

Abstract

The structure of a homonojirimycin isomer isolated from Aglaonema treublii and originally proposed as alpha-3,4-di-epi-homonojirimycin was revised to alpha-4-epi-homonojirimycin 3 ("alpha-homoallonojirimycin") on the basis of NMR analysis and synthetic studies. Its activity as a glycosidase inhibitor is compared to that of other homonojirimycin isomers.


Related Compounds

Related Articles:

In vitro inhibition of glycogen-degrading enzymes and glycosidases by six-membered sugar mimics and their evaluation in cell cultures

2008-01-01

[Bioorg. Chem. 16 , 7330-7336, (2008)]

Homonojirimycin analogues and their glucosides from Lobelia sessilifolia and Adenophora spp. (Campanulaceae).

2000-01-12

[Carbohydr. Res. 323(1-4) , 73-80, (2000)]

Eight stereoisomers of homonojirimycin from D-mannose.

2012-04-20

[Org. Lett. 14(8) , 2050-3, (2012)]

Synthesis and evaluation of glycosidase inhibitory activity of N-butyl 1-deoxy-D-gluco-homonojirimycin and N-butyl 1-deoxy-L-ido-homonojirimycin.

2006-08-15

[Bioorg. Med. Chem. 14(16) , 5535-9, (2006)]

More Articles...