Chemical Structure : Thiamet G
CAS No.: 1009816-48-1
货号: PC-43111Not For Human Use, Lab Use Only.
Thiamet-G (Thiamet G) is a potent, selective O-GlcNAcase (OGA) inhibitor with Ki of 21 nM for human O-GlcNAcase, blocks phosphorylation of tau both in vitro and in vivo.
规格 | 价格 | 库存 | 数量 |
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5 mg | ¥580 | In stock | |
10 mg | ¥880 | In stock | |
25 mg | ¥1480 | In stock | |
50 mg | ¥2480 | In stock | |
100 mg | Get quote |
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Thiamet-G (Thiamet G) is a potent, selective O-GlcNAcase (OGA) 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.
分子量 | 248.2993 | |
分子式 | C9H16N2O4S | |
外观性状 | Solid | |
储存条件 |
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Solubility |
DMSO: ≥ 45 mg/mL |
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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)- |
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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