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  • DC Chemicals Limited
  • China
  • Product Name: TC-DAPK-6
  • Price: $400.0/100mg $800.0/250mg $1600.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

315694-89-4

315694-89-4 structure
315694-89-4 structure
  • Name: TC-DAPK 6
  • Chemical Name: (4E)-2-[(E)-2-phenylethenyl]-4-(pyridin-3-ylmethylidene)-1,3-oxazol-5-one
  • CAS Number: 315694-89-4
  • Molecular Formula: C17H12N2O2
  • Molecular Weight: 276.289
  • Catalog: Signaling Pathways Apoptosis DAPK
  • Create Date: 2016-07-15 07:50:57
  • Modify Date: 2024-01-12 13:41:19
  • TC-DAPK 6 is a potent, ATP-competitive, and highly selective DAPK inhibitor (IC50=69 and 225 nM against DAPK1 and DAPK3, respectively, with 10 μM ATP).

Name (4E)-2-[(E)-2-phenylethenyl]-4-(pyridin-3-ylmethylidene)-1,3-oxazol-5-one
Synonyms (4Z)-2-[(E)-2-Phenylvinyl]-4-(3-pyridinylmethylene)-1,3-oxazol-5(4H)-one
tc-dapk 6
5(4H)-Oxazolone, 2-[(E)-2-phenylethenyl]-4-(3-pyridinylmethylene)-, (4Z)-
cs-1062
Description TC-DAPK 6 is a potent, ATP-competitive, and highly selective DAPK inhibitor (IC50=69 and 225 nM against DAPK1 and DAPK3, respectively, with 10 μM ATP).
Related Catalog
Target

IC50: 69 nM (DAPK1), 225 nM (DAPK3)[1]

In Vitro TC-DAPK 6 is found to be the most potent Death-associated protein kinase (DAPK) inhibitor with enzyme selectivity. When assayed with 10 μM ATP, the IC50 values for DAPK1 and DAPK3 are 69 and 225 nM, respectively. TC-DAPK 6 also inhibits p70S6K (1 μM < IC50< 10 μM)[1].
Kinase Assay Kinase assay is performed using the Z’-LYTE kinase assay kit Ser/Thr 13 peptide. The standard reaction for compound screening contained 1 mM peptide substrate, 10 mM ATP, 50 mM HEPES (pH 7.4), 10 mM MgCl2, 0.01% Brij-35, and 0.5% DMSO. Human recombinant DAPK1 is used at a final concentration of 2.6 μg/mL, and recombinant DAPK3 is used at a final concentration 1.5 mg/mL. To test the enzyme selectively of the inhibitors (e.g., TC-DAPK 6), ProfilerPro kits are used in the protocol[1].
References

[1]. Okamoto M, et al. Identification of death-associated protein kinases inhibitors using structure-based virtual screening. J Med Chem. 2009 Nov 26;52(22):7323-7.

Density 1.2±0.1 g/cm3
Boiling Point 439.6±55.0 °C at 760 mmHg
Molecular Formula C17H12N2O2
Molecular Weight 276.289
Flash Point 219.7±31.5 °C
Exact Mass 276.089874
PSA 51.55000
LogP 3.62
Vapour Pressure 0.0±1.1 mmHg at 25°C
Index of Refraction 1.615
Storage condition 2-8℃
HS Code 2934999090
HS Code 2934999090
Summary 2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%