Results 111 to 120 of about 665,601 (180)

Expeditious Synthesis of Tri- and Tetrahydroxyazepanes from d-(−)-Quinic Acid as Potent Glycosidase Inhibitors

open access: yes, 2016
Several new stereoisomers of 3,4,6-trihydroxyazepanes and 7-hydroxymethyl-3,4,5-trihydroxyazepanes as well as known 3,4,5-trihydroxyazepanes were synthesized as potent glycosidase inhibitors from d-(−)-quinic acid in an efficient manner.
Chun-Hung Lin (296934)   +4 more
core   +1 more source

Expeditious Synthesis of Tri- and Tetrahydroxyazepanes from d-(−)-Quinic Acid as Potent Glycosidase Inhibitors

open access: yes, 2009
Several new stereoisomers of 3,4,6-trihydroxyazepanes and 7-hydroxymethyl-3,4,5-trihydroxyazepanes as well as known 3,4,5-trihydroxyazepanes were synthesized as potent glycosidase inhibitors from D-(-)-quinic acid in an efficient manner.
Shih, Tzenge-lien; Yang, Ru-ying; Li, Shiou-ting; Chiang, Cheng-fan; Lin, Chun-hung   +1 more
core   +1 more source

Effective α-glycosidase inhibitors based on polyphenolic benzothiazole heterocycles

open access: yes
α-Glycosidase inhibition is one of the main approaches to treat Diabetes mellitus. Polyphenolic moieties are known to be responsible for yielding exhibit potent α-glycosidase inhibitory effects.
SEYHAN, GÖKÇE   +5 more
core   +1 more source

Convergent, stereoselective syntheses of the glycosidase inhibitors broussonetines C, O and P

open access: yes, 2009
The first syntheses of the polyhydroxylated alkaloids (iminosugars) broussonetines O and P, glycosidase inhibitors of the pyrrolidine class, have been performed in a convergent, stereocontrolled way from d-serine as the chiral starting material.
Falomir, Eva   +9 more
core   +1 more source

Chiron approaches to polyhydroxylated piperidines: promising glycosidase inhibitors

open access: yesARKIVOC, 2002
Dilip D. Dhavale   +3 more
doaj   +1 more source

From Sugars to Sugar Mimics:Stereoselective synthesis of aminocyclopentanols as glycosidase inhibitors

open access: yes, 2005
The mechanism of enzymatic cleavage of glycosides has been continuously under debate and design of new glycosidase inhibitors has been based on structural similarity of putative intermediates or transition states.
Lundt, Inge
core  

The chemistry of antipredator defense by secondary compounds in neotropical lepidoptera: facts, perspectives and caveats

open access: yesJournal of the Brazilian Chemical Society, 2000
Chemical defense against predation in butterflies and moths has been studied since nineteenth century. A classical example is that of the larvae of the monarch butterfly Danaus plexippus, which feed on leaves of Asclepias curassavica (Asclepiadaceae ...
Trigo José R.
doaj  

Direct Stereoselective Aziridination of Cyclohexenols with 3-Amino-2-(trifluoromethyl)quinazolin-4(3H)-one in the Synthesis of Cyclitol Aziridine Glycosidase Inhibitors. [PDF]

open access: yesEuropean J Org Chem, 2019
Artola M   +10 more
europepmc   +1 more source

From Mechanism-Based Retaining Glycosidase Inhibitors to Activity-Based Glycosidase Profiling. [PDF]

open access: yesJ Am Chem Soc
Artola M   +6 more
europepmc   +1 more source

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