Basic information Safety Supplier Related

7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN

Basic information Safety Supplier Related

7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN Basic information

Product Name:
7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN
Synonyms:
  • JCP 251)
  • JCP251 (JCP-251
  • JLK6
  • GAMMA-SECRETASE INHIBITOR XI
  • 7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN
  • 7-Amino-4-chloro-3-methoxy-1H-2-benzopyran
  • 7-Amino-4-chloro-3-methoxy-isochromen-1-one
  • 7-Amino-4-chloro-3-methoxy-1H-isochromen-1-one
CAS:
62252-26-0
MF:
C10H8ClNO3
MW:
225.63
Mol File:
62252-26-0.mol
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7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN Chemical Properties

Melting point:
115 °C
Boiling point:
456.1±45.0 °C(Predicted)
Density 
1.46±0.1 g/cm3(Predicted)
storage temp. 
Keep in dark place,Sealed in dry,2-8°C
solubility 
DMSO (Slightly)
pka
1.95±0.20(Predicted)
form 
Solid
color 
Yellow to Beige
Stability:
Hygroscopic
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7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN Usage And Synthesis

Uses

JLK 6 is an inhibitor of γ-secretase, selectively inhibits βAPP cleavage.

Definition

ChEBI: 7-amino-4-chloro-3-methoxy-2-benzopyran-1-one is a member of isocoumarins.

Biological Activity

Inhibitor of γ -secretase that selectively inhibits β APP cleavage without affecting other γ -secretase-mediated pathways. Prevents recovery of A β 40 and A β 42 from HEK293 cell overexpressing wild-type or Swedish-mutated β APP (IC 50 ~ 30 μ M) but displays no effect on Notch cleavage and Notch-mediated intracellular signaling. Displays no activity on BACE1, BACE2, α -secretase, the proteosome or GSK3 β .

References

[1]. petit a, pasini a, alves da costa c, et al. jlk isocoumarin inhibitors: selective γ-secretase inhibitors that do not interfere with notch pathway in vitro or in vivo. journal of neuroscience research, 2003, 74(3): 370-377.
[2]. petit a, bihel f, da costa ca, et al. new protease inhibitors prevent γ-secretase-mediated production of aβ40/42 without affecting notch cleavage. nature cell biology, 2001, 3(5): 507-511.

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