1257256-44-2

1257256-44-2 structure
1257256-44-2 structure
  • Name: TC-G 24
  • Chemical Name: N-(3-Chloro-4-methylphenyl)-5-(4-nitrophenyl)-1,3,4-oxadiazol-2-a mine
  • CAS Number: 1257256-44-2
  • Molecular Formula: C15H11ClN4O3
  • Molecular Weight: 330.73
  • Catalog: Signaling Pathways PI3K/Akt/mTOR GSK-3
  • Create Date: 2016-05-22 21:27:56
  • Modify Date: 2025-08-31 17:42:46
  • TC-G 24 (Compound 24) is a potent, selective glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 of 17.1 nM. TC-G 24 can cross the BBB and can be used for studying many diseases such as type 2 diabetes mellitus, stroke, Alzheimer, and other related diseases[1].

Name N-(3-Chloro-4-methylphenyl)-5-(4-nitrophenyl)-1,3,4-oxadiazol-2-a mine
Synonyms 3-Pyridinecarboxamide,N-(3-chloro-4-isoquinolinyl)-2-(cyclopropylamino)
N-(3-CHLOROISOQUINOLIN-4-YL)-2-CYCLOPROPYLAMINONICOTINAMIDE
N-(3-chloro-4-methylphenyl)-5-(4-nitrophenyl)-1,3,4-oxadiazol-2-amine
N-(3-chloro-4-methyl-phenyl)-3-methyl-benzamide
N-(3-chloro-4-isoquinolinyl)-2-cyclopropylamino-3-pyridinecarboxamide
Description TC-G 24 (Compound 24) is a potent, selective glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 of 17.1 nM. TC-G 24 can cross the BBB and can be used for studying many diseases such as type 2 diabetes mellitus, stroke, Alzheimer, and other related diseases[1].
Related Catalog
Target

GSK-3β:17.1 nM (IC50)

In Vitro TC-G 24 (Compound 24) binds to the ATP binding site of GSK-3β[1]. TC-G 24 (1 µM, 4 h) blocks the FBW7α-mediated degradation of TPP1 in human embryonic kidney (HEK) 293T cells[2]. Western Blot Analysis[2] Cell Line: 293T cells Concentration: 1 μM Incubation Time: 4 h Result: Blocked the FBW7α-mediated degradation of TPP1
In Vivo TC-G 24 (Compound 24) (0-15 mg/kg; i.p.; once) significantly raises liver glycogen content in a dose-dependent manner without obvious toxicity and can cross the BBB[1]. Animal Model: Six-week-old male C57BL/6N mice with weights averaging 22 g[1] Dosage: 1, 5, and 15 mg/kg Administration: Intraperitoneal injection, once Result: Significantly raised liver glycogen content in a dose-dependent manner without obvious toxicity. Was detected in the brain at concentrations higher than in plasma for all three tested doses (38 ± 6, 113 ± 54 and 286 ± 58 ng/g brain tissue at 1, 5 and 15 mg/kg, respectively).
References

[1]. Khanfar MA, et al. Discovery of novel GSK-3β inhibitors with potent in vitro and in vivo activities and excellent brain permeability using combined ligand- and structure-based virtual screening. J Med Chem. 2010 Dec 23;53(24):8534-45.

[2]. Lihui Wang, et al. FBW7 Mediates Senescence and Pulmonary Fibrosis through Telomere Uncapping. Cell Metab. 2020 Nov 3;32(5):860-877.e9.

Molecular Formula C15H11ClN4O3
Molecular Weight 330.73
Exact Mass 330.05200
PSA 100.00000
LogP 4.29530
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