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Thiamet G

Chemical Structure : Thiamet G

CAS No.: 1009816-48-1

Thiamet G (Thiamet-G)

Catalog No.: PC-43111Not For Human Use, Lab Use Only.

Thiamet-G is a potent, selective O-GlcNAcase inhibitor with Ki of 21 nM for human O-GlcNAcase, blocks phosphorylation of tau both in vitro and in vivo.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

Thiamet-G is a potent, selective O-GlcNAcase inhibitor with Ki of 21 nM for human O-GlcNAcase, blocks phosphorylation of tau both in vitro and in vivo.
Thiamet-G decreases phosphorylation of tau in PC-12 cells at pathologically relevant sites including Thr231 and Ser396.
Thiamet-G also efficiently reduces phosphorylation of tau at Thr231, Ser396 and Ser422 in both rat cortex and hippocampus, which reveals the rapid and dynamic relationship between O-GlcNAc and phosphorylation of tau in vivo.
Thiamet-G stimulates chondrogenic differentiation both in vitro and in vivo.

Physicochemical Properties

M.Wt 248.2993
Formula C9H16N2O4S
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

DMSO: ≥ 45 mg/mL

Chemical Name/SMILES

5H-Pyrano[3,2-d]thiazole-6,7-diol, 2-(ethylamino)-3a,6,7,7a-tetrahydro-5-(hydroxymethyl)-, (3aR,5R,6S,7R,7aR)-

References

1. Yuzwa SA, et al. Nat Chem Biol. 2008 Aug;4(8):483-90.

2. Goldberg H, et al. Am J Physiol Endocrinol Metab. 2011 Oct;301(4):E713-26.

3. Yuzwa SA, et al. Nat Chem Biol. 2012 Feb 26;8(4):393-9.

4. Andrés-Bergós J, et al. J Biol Chem. 2012 Sep 28;287(40):33615-28.

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