Thiamet G
Chemical Name: (3aR,5R,6S,7R,7aR)-2-(Ethylamino)-3a,6,7,7a-tetrahydro-5-(hydroxymethyl)-5H-pyrano[3,2-d]thiazole-6,7-diol
Biological Activity
Thiamet G is a potent, selective inhibitor of O-GlcNAcase (Ki = 21 nM for human O-GlcNAcase). Decreases the phosphorylation of tau protein in vivo. Promotes autophagy independently of mTOR pathway and reduces toxic protein species in mouse tauopathy model. Orally bioavailable and blood brain barrier permeable.Technical Data
The technical data provided above is for guidance only.
For batch specific data refer to the Certificate of Analysis.
Tocris products are intended for laboratory research use only, unless stated otherwise.
Background References
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A potent mechanism-inspired O-GlcNAcase inhibitor that blocks phosphorylation of tau in vivo.
Yuzwa et al.
Nat.Chem.Biol., 2008;4:483 -
Pharmacological inhibition of O-GlcNAcase enhances autophagy in brain through an mTOR-independent pathway
Zhu et al.
ACS Chem.Neurosci., 2018;9:1366
Product Datasheets
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Citations for Thiamet G
The citations listed below are publications that use Tocris products. Selected citations for Thiamet G include:
4 Citations: Showing 1 - 4
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O-GlcNAcylation is required for mutant KRAS-induced lung tumorigenesis.
Authors: Taparra Et al.
J Clin Invest 2018;128:4924
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Tau post-translational modifications in wild-type and human amyloid precursor protein transgenic mice.
Authors: Jonathan C Et al.
Nat Neurosci 2015;18:1183-9
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Epigenetic switching by the metabolism-sensing factors in the generation of orexin neurons from mouse embryonic stem cells.
Authors: Hayakawa Et al.
J Biol Chem 2013;288:17099
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Excess of O-linked N-acetylglucosamine modifies human pluripotent stem cell differentiation.
Authors: Maury Et al.
Stem Cell Res 2013;11:926
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