Basic information Safety Supplier Related

AP-III-a4

Basic information Safety Supplier Related

AP-III-a4 Basic information

Product Name:
AP-III-a4
Synonyms:
  • AP-III-a4
  • ENOblock (AP-III-a4)
  • AP-III-A4 Benzeneacetamide, N-[2-[2-(2-aminoethoxy)ethoxy]ethyl]-4-[[4-[(cyclohexylmethyl)amino]-6-[[(4-fluorophenyl)methyl]amino]-1,3,5-triazin-2-yl]amino]-
  • N-[2-[2-(2-Aminoethoxy)ethoxy]ethyl]-4-[[4-[(cyclohexylmethyl)amino]-6-[[(4-fluorophenyl)methyl]amino]-1,3,5-triazin-2-yl]amino]benzeneacetamide
  • AP-III-a4(ENOblock), >98%
  • ENOBLOCK
  • CS-1077
  • ENOBLOCK HYDROCHLORIDE
CAS:
1177827-73-4
MF:
C31H43FN8O3
MW:
594.72
Mol File:
1177827-73-4.mol
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AP-III-a4 Chemical Properties

Density 
1.250±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
solubility 
Soluble in DMSO
form 
Powder
pka
15.25±0.46(Predicted)
color 
Off-white to light yellow
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AP-III-a4 Usage And Synthesis

Uses

AP-III-a4 (ENOblock) is a nonsubstrate analogue enolase inhibitor with an IC50 of 0.576 uM. AP-III-a4 can be used for the research of cancer and diabetic[1].

in vivo

AP-III-a4 (ENOblock) (10 μM; 96 h) inhibits cancer cell metastasis and suppresses the gluconeogenesis regulator PEPCK in zebrafish[1].

Animal Model:The zebrafish cancer cell HCT116 xenograft model[1]
Dosage:10 μM
Administration:96 h
Result:Reduced cancer cell dissemination. Inhibited PEPCK expression and induced glucose uptake. Inhibited adipogenesis and foam cell formation.

References

[1] Da-Woon Jung, et al. A Unique Small Molecule Inhibitor of Enolase Clarifies Its Role in Fundamental Biological Processes.ACS Chem. Biol., 2013, 8 (6), pp 1271–1282 DOI:10.1021/cb300687k

AP-III-a4Supplier

Shanghai Boyle Chemical Co., Ltd.
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BOC Sciences
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MedChemexpress LLC
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AdooQ BioScience, LLC
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AdooQ Bioscience CHINA
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025-58849295 18951903616;
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