ChemicalBook > CAS DataBase List > HJC-0350

HJC-0350

Product Name
HJC-0350
CAS No.
885434-70-8
Chemical Name
HJC-0350
Synonyms
CS-1879;HJC0350;HJC 0350;HJC-0350;HJC0350 ,S7500;HJC0350, 10 mM in DMSO;HJC-0350;HJC0350;HJC 0350;1-(Mesitylsulfonyl)-2,4-diMethyl-1H-pyrrole;inhibit,HJC-0350,Inhibitor,HJC 0350,HJC0350;2,4-dimethyl-1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-pyrrole
CBNumber
CB72668476
Molecular Formula
C15H19NO2S
Formula Weight
277.38
MOL File
885434-70-8.mol
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HJC-0350 Property

Boiling point:
434.6±55.0 °C(Predicted)
Density 
1.13±0.1 g/cm3(Predicted)
storage temp. 
room temp
solubility 
DMSO: soluble5mg/mL, clear
pka
-6.94±0.70(Predicted)
form 
powder
color 
white to beige
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0820
Product name
HJC0350
Purity
≥98% (HPLC)
Packaging
5mg
Price
$109
Updated
2022/05/15
Sigma-Aldrich
Product number
SML0820
Product name
HJC0350
Purity
≥98% (HPLC)
Packaging
25mg
Price
$425
Updated
2022/05/15
Cayman Chemical
Product number
22949
Product name
HJC0350
Purity
≥98%
Packaging
1mg
Price
$32
Updated
2024/03/01
Cayman Chemical
Product number
22949
Product name
HJC0350
Purity
≥98%
Packaging
5mg
Price
$93
Updated
2024/03/01
Cayman Chemical
Product number
22949
Product name
HJC0350
Purity
≥98%
Packaging
10mg
Price
$139
Updated
2024/03/01
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HJC-0350 Chemical Properties,Usage,Production

Uses

HJC 0350 is a potent and selective inhibitor of EPAC2 and exhibits no inhibition of EPAC1.

Biological Activity

hjc 0350 is a potent and selective antagonist of epac2 with ic50 value of 0.3 μm [1].camp/camp regulated guanine nucleotide exchange factor (epac/camp-gef) is a guanine nucleotide exchange factor for the small gtpases rap1 and rap2 in response to intracellular camp. epac2 is mainly expressed in the central nervous system, pancreas and adrenal gland [1].hjc 0350 is a potent and selective epac2 antagonist. hjc 0350 competed with 8-nbd-camp in binding recombinant fusion protein epac2 with ic50 value of 0.3 μm and exhibited 133-fold more potent than camp, which competed with 8-nbd-camp in binding epac2 with ic50 value of 40 μm. in the presence of 25 μm camp, hjc 0350 (25 μm) inhibited epac2 gef activity but had no effect on epac1-mediated rap1-gdp exchange activity and camp-mediated pka activation, which suggested that hjc 0350 was epac2-specific antagonist. in hek293 cells expressing epac1- or epac2-based fluorescence resonance energy transfer (fret) sensor (epac2-fl or epac1-fl), hjc 0350 (10 μm) completely inhibited the 007-am (a membrane permeable epac selective camp analogue) induced decrease of fret in hek293/epac2-fl cells but had no effect on hek293/epac1-fl cells [1].

Synthesis

625-82-1

773-64-8

885434-70-8

To a 5 mL solution of 2,4-dimethyl-1H-pyrrole (24 mg, 0.25 mmol) and 2,4,6-trimethylbenzenesulfonyl chloride (218 mg, 1.0 mmol) in tetrahydrofuran (THF) was slowly added 60% sodium hydride (NaH, 40 mg, 1.0 mmol) at 0 °C. The reaction mixture was stirred at room temperature for 16 hours. After completion of the reaction, the reaction solution was diluted with ethyl acetate (EtOAc, 50 mL) and washed sequentially with 1N hydrochloric acid (HCl, aq., 10 mL) and saturated saline (10 mL). The organic layer was dried with anhydrous sodium sulfate (Na2SO4) and concentrated under reduced pressure to remove the solvent. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=10/1) to afford the target compound 2,4-dimethyl-1-((2,4,6-trimethylphenyl)sulfonyl)-1H-pyrrole as a light red solid (40 mg, 58% yield).1H NMR (600 MHz, CDCl3) δ 7.01 (s, 1H), 6.95 (s 2H), 5.77 (s, 1H), 2.49 (s, 6H), 2.31 (s, 3H), 2.00 (s, 3H), 1.99 (s, 3H).13C NMR (150 MHz, CDCl3) δ 143.8, 140.2, 133.8, 132.2, 130.2, 119.7, 119.2, 114.5, 23.4, 21.1, 114.5, 13.4, 21.1, 114.5, 114.5 23.4, 21.1, 12.6, 11.8.

storage

Store at +4°C

References

[1]. chen h, tsalkova t, chepurny og, et al. identification and characterization of small molecules as potent and specific epac2 antagonists. j med chem, 2013, 56(3): 952-962.

HJC-0350 Preparation Products And Raw materials

Raw materials

Preparation Products

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885434-70-8, HJC-0350Related Search:


  • HJC 0350
  • HJC0350
  • HJC-0350
  • 1-(Mesitylsulfonyl)-2,4-diMethyl-1H-pyrrole
  • 2,4-dimethyl-1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-pyrrole
  • 2,4-Dimethyl-1-[(2,4,6-trimethylphenyl)sulfonyl]-1H-pyrrole HJC 0350
  • HJC-0350;HJC0350;HJC 0350
  • CS-1879
  • 1H-Pyrrole, 2,4-dimethyl-1-[(2,4,6-trimethylphenyl)sulfonyl]-
  • inhibit,HJC-0350,Inhibitor,HJC 0350,HJC0350
  • HJC0350, 10 mM in DMSO
  • HJC0350 ,S7500
  • 885434-70-8
  • Inhibitors