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2-(4-TERT-BUTYLPHENOXY)CYCLOHEXANOL

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2-(4-TERT-BUTYLPHENOXY)CYCLOHEXANOL Basic information

Product Name:
2-(4-TERT-BUTYLPHENOXY)CYCLOHEXANOL
Synonyms:
  • 2-(4-tert-butylphenoxy)-1-cyclohexanol
  • 2-(4-TERT-BUTYLPHENOXY)CYCLOHEXANOL
  • 2-(p-t-butylphenoxy)cyclohexanol
  • 2-(p-tert-butylphenoxy)-cyclohexano
  • CYCLOHEXANOL-2-(4-TERT-BUTYL-PHENOXY)
  • 2-(4-tert-butylphenoxy)cyclohexan-1-ol
  • 2-[4-(1,1-DIMETHYLETHYL)PHENOXY]CYCLOHEXANOL
  • propargite metab.
CAS:
1942-71-8
MF:
C16H24O2
MW:
248.36
EINECS:
217-732-3
Mol File:
1942-71-8.mol
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2-(4-TERT-BUTYLPHENOXY)CYCLOHEXANOL Chemical Properties

Melting point:
93-95 °C
Boiling point:
365.7±42.0 °C(Predicted)
Density 
1.036±0.06 g/cm3(Predicted)
storage temp. 
Store at 4℃
solubility 
24.84mg/ml in DMSO, 24.84mg/ml in Ethanol
form 
powder
pka
14.60±0.40(Predicted)
color 
white to beige
EPA Substance Registry System
2-(p-tert-Butylphenoxy)cyclohexanol (1942-71-8)
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Safety Information

Hazardous Substances Data
1942-71-8(Hazardous Substances Data)
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2-(4-TERT-BUTYLPHENOXY)CYCLOHEXANOL Usage And Synthesis

Uses

tBPC is a selective positive allosteric modulator for human Y4 receptor (Y4R), which enhances the activation of Y4R in G protein signaling and arrestin3 recruitment[1].

Biological Activity

tBPC is a postitive allosteric modulator of the neuropeptide Y (NPY) Y4 receptor, which is predominantly expressed in the gastrointestinal tract and activated most strongly by pancreatic polypeptide (PP). tBPC was shown to potentiate Y4R activity in G-Protein signaling and arrestin3 recruitment and to potentiate the native PP response. tBPC was selective for Y4R over other Neuropeptide Y receptors and showed no effect on the efficacy (Emax) or potency (EC50) of the NPY signal response at the Y1, Y2, or Y5 receptors at 30 μM.

References

[1] Schubert M, et al., Identification and Characterization of the First Selective Y4 Receptor Positive Allosteric Modulator. J Med Chem. 2017 Sep 14;60(17):7605-7612. DOI:10.1021/acs.jmedchem.7b00976

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