Inhibition of naringinase (L-rhamnosidase) by piperidine analogues of L-rhamnose: Scaffolds for libraries incorporating trihydroxypipecolic acids-Reference-Cited by-同舟云学术

Inhibition of naringinase (L-rhamnosidase) by piperidine analogues of L-rhamnose: Scaffolds for libraries incorporating trihydroxypipecolic acids

Published:1996-11 Issue:47 Volume:37 Page:8569-8572
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Shilvock John P.,Wheatley Joseph R.,Davis Benjamin,Nash Robert J.,Griffiths Rhodri C.,Jones M.George,Müller Matthias,Crook Sarah,Watkin David J.,Smith Colin,Besra Gurdyal S.,Brennan Patrick J.,Fleet George W.J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference16 articles.

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2. The structural basis of the inhibition of human α-mannosidases by azafuranose analogues of mannose

3. Synthesis of, and lack of inhibition of a rhamnosidase by, both enantiomers of deoxyrhamnojirimycin and rhamnolactam: β-mannosidase inhibition by δ-lactams

4. A chemoenzymic synthesis of 1,5-dideoxy-1,5-imino-l-mannitol and l-rhamnitol and investigation of their effects on glycosidases

5. Five-membered ring azasugars as potent inhibitors of α-L-rhamnosidase (naringinase) from Penicillium decumbens

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