Abstract:
:A highly practicable synthesis of both enantiomers of 3-hydroxypipecolic acid derivatives 1, 2, 3, 4 is described. Screening of these molecules for glycosidase inhibition has been examined. Compound 3 was shown to be a potent inhibitor of beta-N-acetylglucosaminidase as well as Escherichia coli beta-glucuronidase.
journal_name
Bioorg Med Chem Lettjournal_title
Bioorganic & medicinal chemistry lettersauthors
Ohara C,Takahashi R,Miyagawa T,Yoshimura Y,Kato A,Adachi I,Takahata Hdoi
10.1016/j.bmcl.2008.02.028subject
Has Abstractpub_date
2008-03-15 00:00:00pages
1810-3issue
6eissn
0960-894Xissn
1464-3405pii
S0960-894X(08)00210-2journal_volume
18pub_type
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