7-AMINO-4-CHLORO-3-METHOXYISOCOUMARIN
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
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
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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