Synthesis and biological evaluation of four stereoisomers of PDMP-analogue, N-(2-decylamino-3-hydroxy-3-phenylprop-1-yl)-β-valienamine, and related compounds
- 22 July 1997
- journal article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 7 (14) , 1915-1920
- https://doi.org/10.1016/s0960-894x(97)00341-7
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Synthesis of potent β-D-glucocerebrosidase inhibitors: N-alkyl-β-valienaminesBioorganic & Medicinal Chemistry Letters, 1996
- Glucosylceramide synthetase inhibitor, d-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol exhibits a novel decarcinogenic activity against Shope carcinoma cellsCancer Letters, 1996
- Pseudosugars, 35. Synthesis of glycosylceramide analogs composed of imino‐linked unsaturated 5a‐carbaglycosyl residues: Potent and specific gluco‐ and galactocerebrosidase inhibitorsEuropean Journal of Organic Chemistry, 1995
- Pseudosugars, 34. Synthesis of 5a‐carba‐β‐D‐glycosylceramide analogs linked by imino, ether and sulfide bridgesEuropean Journal of Organic Chemistry, 1995
- Alternative synthesis and enzyme-inhibitory activity of methyl 1′-epiacarviosin and its 6-hydroxy analogCarbohydrate Research, 1992
- Total synthesis of acarbose and adiposin-2Carbohydrate Research, 1989
- Total synthesis of acarbose and adiposin-2Journal of the Chemical Society, Chemical Communications, 1988