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PF-04802367

  Cat. No.:  DC21484   Featured
Chemical Structure
1962178-27-3
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More than 5000 active chemicals with high quality for research!
Field of application
PF04802367 is a potent, highly selective GSK-3 inhibitor with IC50 of 2.1 nM for human GSK-3β in enzyme assays; shows equal effectivity against GSK-3α and GSK-3β with IC50 of 10.0 and 9.0 nM respectively in mobility shift assays, inhibits phosphorylation of tau with an IC50 of 466 nM in a stable inducible CHO cell line over-expressing GSK-3β and substrate tau; modulates tau phosphorylation in vitro and in vivo.
Cas No.: 1962178-27-3
Chemical Name: PF-04802367
Synonyms: 5-(3-Chloranyl-4-Methoxy-Phenyl)-~{n}-[3-(1,2,4-Triazol-1-Yl)propyl]-1,3-Oxazole-4-Carboxamide;N-(3-(1h-1,2,4-triazol-1-yl)propyl)-5-(3-chloro-4-methoxyphenyl)oxazole-4-carboxamide;Q27456523;6QH;PF-04802367
SMILES: ClC1=C(C=CC(=C1)C1=C(C(NCCCN2C=NC=N2)=O)N=CO1)OC
Formula: C16H16ClN5O3
M.Wt: 361.782941818237
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Publication: . Liang SH, et al. Angew Chem Int Ed Engl. 2016 Aug 8;55(33):9601-5. View Related Products by Target GSK-3
Description: A potent, highly selective GSK-3 inhibitor with IC50 of 2.1 nM for human GSK-3β in enzyme assays; shows equal effectivity against GSK-3α and GSK-3β with IC50 of 10.0 and 9.0 nM respectively in mobility shift assays, inhibits phosphorylation of tau with an IC50 of 466 nM in a stable inducible CHO cell line over-expressing GSK-3β and substrate tau; modulates tau phosphorylation in vitro and in vivo.
References: . Liang SH, et al. Angew Chem Int Ed Engl. 2016 Aug 8;55(33):9601-5. View Related Products by Target GSK-3
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